View source for Article:Diabetes Mellitus and Liver Surgery: The Effect of Diabetes on Oxidative Stress and Inflammation. (5964489)

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| Wikidata_code = Q54939023
| title = Diabetes Mellitus and Liver Surgery: The Effect of Diabetes on Oxidative Stress and Inflammation.
| publication_date = 2018-05-08
| author1 = Mariana Mendes-Braz
| Generator = https://github.com/ContentMine/ScienceSourceIngest.git/442d8277d1bbe4ff10eda38334e9415eaeecf44c*
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<section><h2 id="Journal_Information">Journal Information</h2>
<p>Title: Mediators of Inflammation</p></section><section><h1 id="Diabetes_Mellitus_and_Liver_Surgery:_The_Effect_of_Diabetes_on_Oxidative_Stress_and_Inflammation">Diabetes Mellitus and Liver Surgery: The Effect of Diabetes on Oxidative Stress and Inflammation</h1>
<ul>
<li>Mariana Mendes-Braz</li>
<li>Joilson O. Martins</li>
</ul>
<p>Laboratory of Immunoendocrinology, Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences of University Sao Paulo (FCF/USP), São Paulo, SP, Brazil</p>
<p>Publication date (collection): /2018</p>
<p>Publication date (epub): 5/2018</p>
<section><h2 id="Abstract">Abstract</h2>
<p><i>Diabetes mellitus</i> (DM) is a metabolic disorder characterized by hyperglycaemia and high morbidity worldwide. The detrimental effects of hyperglycaemia include an increase in the oxidative stress (OS) response and an enhanced inflammatory response. DM compromises the ability of the liver to regenerate and is particularly associated with poor prognosis after ischaemia-reperfusion (I/R) injury. Considering the growing need for knowledge of the impact of DM on the liver following a surgical procedure, this review aims to present recent publications addressing the effects of DM (hyperglycaemia) on OS and the inflammatory process, which play an essential role in I/R injury and impaired hepatic regeneration after liver surgery.</p></section></section><h2 id="Paper">Paper</h2>
<section><h3 id="1._Introduction">1. Introduction</h3>
<p>To extirpate a macroscopic lesion or accomplish a transplant, the blood flow to the liver must be interrupted to avoid the haemorrhagic process. Despite the safety of surgical procedures that involve the interruption of blood flow to the liver (ischaemia), this interruption contributes to tissue damage, which is potentiated by the restoration of blood flow (reperfusion). This phenomenon, known as ischaemia-reperfusion (I/R) injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B1" data-mw='{"name":"ref","attrs":{"name":"B1"},"body":{"id":"mw-reference-text-cite_note-B1"}}'><a href="#cite_note-B1"><span class="mw-reflink-text">[1]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B2" data-mw='{"name":"ref","attrs":{"name":"B2"},"body":{"id":"mw-reference-text-cite_note-B2"}}'><a href="#cite_note-B2"><span class="mw-reflink-text">[2]</span></a></sup>], is associated with inflammation and oxidative stress (OS) [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B3" data-mw='{"name":"ref","attrs":{"name":"B3"},"body":{"id":"mw-reference-text-cite_note-B3"}}'><a href="#cite_note-B3"><span class="mw-reflink-text">[3]</span></a></sup>].</p>
<p>Diabetes mellitus (DM) is a metabolic disorder resulting from deficient insulin secretion and/or insulin action, leading to hyperglycaemia (high blood glucose) [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B4" data-mw='{"name":"ref","attrs":{"name":"B4"},"body":{"id":"mw-reference-text-cite_note-B4"}}'><a href="#cite_note-B4"><span class="mw-reflink-text">[4]</span></a></sup>], which causes oxidative damage and activates inflammatory signalling cascades [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B5" data-mw='{"name":"ref","attrs":{"name":"B5"},"body":{"id":"mw-reference-text-cite_note-B5"}}'><a href="#cite_note-B5"><span class="mw-reflink-text">[5]</span></a></sup>], in addition to acting as a damaging agent exacerbating the pathological conditions of DM [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B6" data-mw='{"name":"ref","attrs":{"name":"B6"},"body":{"id":"mw-reference-text-cite_note-B6"}}'><a href="#cite_note-B6"><span class="mw-reflink-text">[6]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B7" data-mw='{"name":"ref","attrs":{"name":"B7"},"body":{"id":"mw-reference-text-cite_note-B7"}}'><a href="#cite_note-B7"><span class="mw-reflink-text">[7]</span></a></sup>]. Considering the growing need for knowledge about the impact of DM on livers undergoing a surgical procedure, the present review aims to present recent data concerning the effects of DM (hyperglycaemia) on OS and the inflammatory process.</p></section><section><h3 id="2._Oxidative_Stress">2. Oxidative Stress</h3>
<p>Under normal conditions, the hepatic production of prooxidants, such as reactive oxygen species (ROS), is counterbalanced by antioxidants. An imbalance in favour of prooxidants corresponds to OS, and the direct action of ROS on cell viability and function is directly related to the occurrence of several pathological processes in the liver [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B8" data-mw='{"name":"ref","attrs":{"name":"B8"},"body":{"id":"mw-reference-text-cite_note-B8"}}'><a href="#cite_note-B8"><span class="mw-reflink-text">[8]</span></a></sup>]. OS plays an essential role in liver surgery [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B9" data-mw='{"name":"ref","attrs":{"name":"B9"},"body":{"id":"mw-reference-text-cite_note-B9"}}'><a href="#cite_note-B9"><span class="mw-reflink-text">[9]</span></a></sup>], and diabetes is generally followed by increased free radical production [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B10" data-mw='{"name":"ref","attrs":{"name":"B10"},"body":{"id":"mw-reference-text-cite_note-B10"}}'><a href="#cite_note-B10"><span class="mw-reflink-text">[10]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B13" data-mw='{"name":"ref","attrs":{"name":"B13"},"body":{"id":"mw-reference-text-cite_note-B13"}}'><a href="#cite_note-B13"><span class="mw-reflink-text">[13]</span></a></sup>] or reduced antioxidant protection [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B14" data-mw='{"name":"ref","attrs":{"name":"B14"},"body":{"id":"mw-reference-text-cite_note-B14"}}'><a href="#cite_note-B14"><span class="mw-reflink-text">[14]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B15" data-mw='{"name":"ref","attrs":{"name":"B15"},"body":{"id":"mw-reference-text-cite_note-B15"}}'><a href="#cite_note-B15"><span class="mw-reflink-text">[15]</span></a></sup>]. To better understand the effect of DM (hyperglycaemia) on OS, this section will describe research findings that help clarify the association of DM with liver surgery.</p>
<section><h3 id="2.1._Diabetes_Mellitus_and_Ischaemia-Reperfusion_Injury">2.1. Diabetes Mellitus and Ischaemia-Reperfusion Injury</h3>
<p>Hydrogen peroxide (H2O2), a mild and relatively stable oxidant that is formed in tissues exposed to I/R, has been considered a representative ROS for evaluating the response of cells to OS [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B16" data-mw='{"name":"ref","attrs":{"name":"B16"},"body":{"id":"mw-reference-text-cite_note-B16"}}'><a href="#cite_note-B16"><span class="mw-reflink-text">[16]</span></a></sup>]. Although H2O2 is not a free radical, its accumulation may promote the formation of more toxic species, such as hydroxyl radicals (•OH), through the Fenton reaction [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B17" data-mw='{"name":"ref","attrs":{"name":"B17"},"body":{"id":"mw-reference-text-cite_note-B17"}}'><a href="#cite_note-B17"><span class="mw-reflink-text">[17]</span></a></sup>]. H2O2 can cause permanent growth arrest [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B18" data-mw='{"name":"ref","attrs":{"name":"B18"},"body":{"id":"mw-reference-text-cite_note-B18"}}'><a href="#cite_note-B18"><span class="mw-reflink-text">[18]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B19" data-mw='{"name":"ref","attrs":{"name":"B19"},"body":{"id":"mw-reference-text-cite_note-B19"}}'><a href="#cite_note-B19"><span class="mw-reflink-text">[19]</span></a></sup>] and apoptosis [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B20" data-mw='{"name":"ref","attrs":{"name":"B20"},"body":{"id":"mw-reference-text-cite_note-B20"}}'><a href="#cite_note-B20"><span class="mw-reflink-text">[20]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B22" data-mw='{"name":"ref","attrs":{"name":"B22"},"body":{"id":"mw-reference-text-cite_note-B22"}}'><a href="#cite_note-B22"><span class="mw-reflink-text">[22]</span></a></sup>] in a number of cell types. Nuclear (8-hydroxy-2′-deoxyguanosine) 8-OHdG formation indicates the presence of OS in nuclei [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B23" data-mw='{"name":"ref","attrs":{"name":"B23"},"body":{"id":"mw-reference-text-cite_note-B23"}}'><a href="#cite_note-B23"><span class="mw-reflink-text">[23]</span></a></sup>]. The liver is a major organ affected by ROS [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B24" data-mw='{"name":"ref","attrs":{"name":"B24"},"body":{"id":"mw-reference-text-cite_note-B24"}}'><a href="#cite_note-B24"><span class="mw-reflink-text">[24]</span></a></sup>] and is susceptible to the effects of OS induced by hyperglycaemia, causing liver injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B25" data-mw='{"name":"ref","attrs":{"name":"B25"},"body":{"id":"mw-reference-text-cite_note-B25"}}'><a href="#cite_note-B25"><span class="mw-reflink-text">[25]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B27" data-mw='{"name":"ref","attrs":{"name":"B27"},"body":{"id":"mw-reference-text-cite_note-B27"}}'><a href="#cite_note-B27"><span class="mw-reflink-text">[27]</span></a></sup>]. Zhang et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B28" data-mw='{"name":"ref","attrs":{"name":"B28"},"body":{"id":"mw-reference-text-cite_note-B28"}}'><a href="#cite_note-B28"><span class="mw-reflink-text">[28]</span></a></sup>] found that serum H2O2 and nuclear 8-OHdG levels were higher in streptozotocin- (STZ-) induced diabetic rats subjected to I/R compared with the diabetic control group. ROS induce lipid peroxidation, which causes membrane injury, in addition to changes in ion permeability, enzyme activity, and, ultimately, cell death. Malondialdehyde (MDA), an indicator of oxidative injury produced via lipid peroxidation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B29" data-mw='{"name":"ref","attrs":{"name":"B29"},"body":{"id":"mw-reference-text-cite_note-B29"}}'><a href="#cite_note-B29"><span class="mw-reflink-text">[29]</span></a></sup>], is significantly enhanced in STZ-induced diabetic rats compared with normal rats and increases after I/R [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B28" data-mw='{"name":"ref","attrs":{"name":"B28"},"body":{"id":"mw-reference-text-cite_note-B28"}}'><a href="#cite_note-B28"><span class="mw-reflink-text">[28]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B30" data-mw='{"name":"ref","attrs":{"name":"B30"},"body":{"id":"mw-reference-text-cite_note-B30"}}'><a href="#cite_note-B30"><span class="mw-reflink-text">[30]</span></a></sup>] (Figure 1).</p>
<p>Apoptosis and necrosis can occur after I/R. An intense injury leads to initial necrotic killing, whereas late apoptosis may follow moderate injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B31" data-mw='{"name":"ref","attrs":{"name":"B31"},"body":{"id":"mw-reference-text-cite_note-B31"}}'><a href="#cite_note-B31"><span class="mw-reflink-text">[31]</span></a></sup>]. STZ-induced diabetic rats exposed to an ischaemic period present significantly increased hepatocyte degeneration, sinusoidal dilatation, nuclear pyknosis, and cellular necrosis compared with the diabetes sham group [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B30" data-mw='{"name":"ref","attrs":{"name":"B30"},"body":{"id":"mw-reference-text-cite_note-B30"}}'><a href="#cite_note-B30"><span class="mw-reflink-text">[30]</span></a></sup>]. In spite of this experimental difference, Behrends et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B32" data-mw='{"name":"ref","attrs":{"name":"B32"},"body":{"id":"mw-reference-text-cite_note-B32"}}'><a href="#cite_note-B32"><span class="mw-reflink-text">[32]</span></a></sup>] reported that necrosis is the preferential form of cell death in the liver of hyperglycemic rats (due to intraperitoneal injection of 25% glucose) subjected to I/R. The authors [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B32" data-mw='{"name":"ref","attrs":{"name":"B32"},"body":{"id":"mw-reference-text-cite_note-B32"}}'><a href="#cite_note-B32"><span class="mw-reflink-text">[32]</span></a></sup>] noted that this increased injury may be associated with the inhibition of heat shock proteins (HSPs), which is only possible through the association of hyperglycaemia and I/R. The hyperglycaemia alone was not enough for HSP32 and HSP70 downregulation. HSPs are considered to be an indispensable protective agent against I/R injury because they are able to protect the liver from OS [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B33" data-mw='{"name":"ref","attrs":{"name":"B33"},"body":{"id":"mw-reference-text-cite_note-B33"}}'><a href="#cite_note-B33"><span class="mw-reflink-text">[33]</span></a></sup>] (Figure 1).</p>
<p>Cell adaptation to OS is a consequence of the upregulation of distinct cytoprotective genes responsible for buffering the antioxidant capacity of the cell [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B34" data-mw='{"name":"ref","attrs":{"name":"B34"},"body":{"id":"mw-reference-text-cite_note-B34"}}'><a href="#cite_note-B34"><span class="mw-reflink-text">[34]</span></a></sup>]. Under physiological conditions, an antioxidant defence system protects the body against the harmful effects of free radicals [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B35" data-mw='{"name":"ref","attrs":{"name":"B35"},"body":{"id":"mw-reference-text-cite_note-B35"}}'><a href="#cite_note-B35"><span class="mw-reflink-text">[35]</span></a></sup>]. Diabetic livers are vulnerable to attack by oxygen free radicals because they present overall antioxidant depression [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B14" data-mw='{"name":"ref","attrs":{"name":"B14"},"body":{"id":"mw-reference-text-cite_note-B14"}}'><a href="#cite_note-B14"><span class="mw-reflink-text">[14]</span></a></sup>]. Release of ROS and the concurrent consumption of endogenous antioxidants and cell death (apoptosis or necrosis) occur during hepatic I/R [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B36" data-mw='{"name":"ref","attrs":{"name":"B36"},"body":{"id":"mw-reference-text-cite_note-B36"}}'><a href="#cite_note-B36"><span class="mw-reflink-text">[36]</span></a></sup>]. After I/R, nuclear factor (erythroid-derived 2)-like-2 factor (Nrf2), a transcription factor that mediates the expression of many endogenous antioxidants plays an important role in opposing hepatic injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B37" data-mw='{"name":"ref","attrs":{"name":"B37"},"body":{"id":"mw-reference-text-cite_note-B37"}}'><a href="#cite_note-B37"><span class="mw-reflink-text">[37]</span></a></sup>]. Zhang et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B28" data-mw='{"name":"ref","attrs":{"name":"B28"},"body":{"id":"mw-reference-text-cite_note-B28"}}'><a href="#cite_note-B28"><span class="mw-reflink-text">[28]</span></a></sup>] reported that, after I/R injury, hepatocytes pretreated with high glucose (25 mM) exhibited a reduction in the antioxidative ability of the Nrf2 pathway and a substantial increase in nuclear factor kappa B (NF-<i>κ</i>B) translocation; however, NF-<i>κ</i>B activation was already enhanced in these hepatocytes before I/R injury. Interestingly, NF-<i>κ</i>B, a transcription factor that reacts to redox signals, may directly repress Nrf2 signalling at the transcriptional level [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B38" data-mw='{"name":"ref","attrs":{"name":"B38"},"body":{"id":"mw-reference-text-cite_note-B38"}}'><a href="#cite_note-B38"><span class="mw-reflink-text">[38]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B39" data-mw='{"name":"ref","attrs":{"name":"B39"},"body":{"id":"mw-reference-text-cite_note-B39"}}'><a href="#cite_note-B39"><span class="mw-reflink-text">[39]</span></a></sup>]. Zhang et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B28" data-mw='{"name":"ref","attrs":{"name":"B28"},"body":{"id":"mw-reference-text-cite_note-B28"}}'><a href="#cite_note-B28"><span class="mw-reflink-text">[28]</span></a></sup>] postulated that high glucose-induced ROS overproduction could initiate the inhibitory interaction between NF-<i>κ</i>B and Nrf2 (Figure 1<b>)</b>. However, the precise mechanisms involved in the NF-<i>κ</i>B and Nrf2 interaction under hyperglycaemic conditions require further elucidation.</p>
<p>Under normal conditions, the body presents a potent antioxidant system that is responsible for protecting it from the harmful effects of ROS [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B40" data-mw='{"name":"ref","attrs":{"name":"B40"},"body":{"id":"mw-reference-text-cite_note-B40"}}'><a href="#cite_note-B40"><span class="mw-reflink-text">[40]</span></a></sup>]. Endogenous antioxidant enzymes attenuate I/R injury in the liver [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B36" data-mw='{"name":"ref","attrs":{"name":"B36"},"body":{"id":"mw-reference-text-cite_note-B36"}}'><a href="#cite_note-B36"><span class="mw-reflink-text">[36]</span></a></sup>]. In both type 1 and type 2 DM, antioxidant defence enzymes are deficient, and there is an increase in oxidative damage [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B41" data-mw='{"name":"ref","attrs":{"name":"B41"},"body":{"id":"mw-reference-text-cite_note-B41"}}'><a href="#cite_note-B41"><span class="mw-reflink-text">[41]</span></a></sup>]. High levels of ROS such as superoxide (O2−) are found in diabetes and especially during I/R injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B42" data-mw='{"name":"ref","attrs":{"name":"B42"},"body":{"id":"mw-reference-text-cite_note-B42"}}'><a href="#cite_note-B42"><span class="mw-reflink-text">[42]</span></a></sup>]. Cem Sezen et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B30" data-mw='{"name":"ref","attrs":{"name":"B30"},"body":{"id":"mw-reference-text-cite_note-B30"}}'><a href="#cite_note-B30"><span class="mw-reflink-text">[30]</span></a></sup>] showed that there is an increase in glutathione s-transferase (GST) in STZ-induced diabetic mice post-I/R with respect to diabetic rats. Between these two groups, there was no difference in the level of superoxide dismutase (SOD); however, compared with the sham group (nondiabetic), there was a marked decrease in SOD levels. The orchestrated actions of several antioxidants in mammalian cells are essential for efficiently detoxifying free radicals. Therefore, any impairment in this pathway will influence the activities of other enzymes [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B43" data-mw='{"name":"ref","attrs":{"name":"B43"},"body":{"id":"mw-reference-text-cite_note-B43"}}'><a href="#cite_note-B43"><span class="mw-reflink-text">[43]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B44" data-mw='{"name":"ref","attrs":{"name":"B44"},"body":{"id":"mw-reference-text-cite_note-B44"}}'><a href="#cite_note-B44"><span class="mw-reflink-text">[44]</span></a></sup>]. Reduction in the activity of SOD will result in an increased level of O2− [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B45" data-mw='{"name":"ref","attrs":{"name":"B45"},"body":{"id":"mw-reference-text-cite_note-B45"}}'><a href="#cite_note-B45"><span class="mw-reflink-text">[45]</span></a></sup>]. GST is known to be an early and sensitive marker of liver injury and has been shown to increase after liver ischaemia/reperfusion [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B46" data-mw='{"name":"ref","attrs":{"name":"B46"},"body":{"id":"mw-reference-text-cite_note-B46"}}'><a href="#cite_note-B46"><span class="mw-reflink-text">[46]</span></a></sup>]. This increased activity of GST could be explained as a compensatory mechanism to protect the organism against injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B47" data-mw='{"name":"ref","attrs":{"name":"B47"},"body":{"id":"mw-reference-text-cite_note-B47"}}'><a href="#cite_note-B47"><span class="mw-reflink-text">[47]</span></a></sup>]. These findings are not only in accord with the diverse signalling pathways related to postoperative liver injury associated with DM (Figure 1<b>)</b> but also indicate the importance of the determination of increased ROS production and its characteristic consequences in postischaemic tissues, permitting the identification of interventions that stimulates ROS detoxification, and consequently protect against reperfusion injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B16" data-mw='{"name":"ref","attrs":{"name":"B16"},"body":{"id":"mw-reference-text-cite_note-B16"}}'><a href="#cite_note-B16"><span class="mw-reflink-text">[16]</span></a></sup>], mainly in a diabetic context (Figure 1).</p></section><section><h3 id="2.2._Diabetes_Mellitus_and_Liver_Regeneration">2.2. Diabetes Mellitus and Liver Regeneration</h3>
<p>An increase in lipid peroxidation was found to be important for a normal proliferative process to occur in the liver remnant after partial hepatectomy (PH) [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B48" data-mw='{"name":"ref","attrs":{"name":"B48"},"body":{"id":"mw-reference-text-cite_note-B48"}}'><a href="#cite_note-B48"><span class="mw-reflink-text">[48]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B49" data-mw='{"name":"ref","attrs":{"name":"B49"},"body":{"id":"mw-reference-text-cite_note-B49"}}'><a href="#cite_note-B49"><span class="mw-reflink-text">[49]</span></a></sup>]. Francés et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B50" data-mw='{"name":"ref","attrs":{"name":"B50"},"body":{"id":"mw-reference-text-cite_note-B50"}}'><a href="#cite_note-B50"><span class="mw-reflink-text">[50]</span></a></sup>] reported that OS is increased by hyperglycaemia and is juxtaposed with the effect of PH in STZ-induced diabetic rats. Postoperative recovery depends on the regenerative capacity of the residual liver. The liver presents altered intracellular signalling pathways in type 1 DM specimens [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B51" data-mw='{"name":"ref","attrs":{"name":"B51"},"body":{"id":"mw-reference-text-cite_note-B51"}}'><a href="#cite_note-B51"><span class="mw-reflink-text">[51]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B53" data-mw='{"name":"ref","attrs":{"name":"B53"},"body":{"id":"mw-reference-text-cite_note-B53"}}'><a href="#cite_note-B53"><span class="mw-reflink-text">[53]</span></a></sup>] and a consequent deficient regenerative response [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B54" data-mw='{"name":"ref","attrs":{"name":"B54"},"body":{"id":"mw-reference-text-cite_note-B54"}}'><a href="#cite_note-B54"><span class="mw-reflink-text">[54]</span></a></sup>]. STZ-induced diabetic rats were found to present an increase in •OH production, which could result in DNA damage [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B55" data-mw='{"name":"ref","attrs":{"name":"B55"},"body":{"id":"mw-reference-text-cite_note-B55"}}'><a href="#cite_note-B55"><span class="mw-reflink-text">[55]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B56" data-mw='{"name":"ref","attrs":{"name":"B56"},"body":{"id":"mw-reference-text-cite_note-B56"}}'><a href="#cite_note-B56"><span class="mw-reflink-text">[56]</span></a></sup>] (Figure 1). Hyperglycaemia in STZ-induced diabetic rats leads to an increase in hepatic ROS production and is further enhanced after PH. STZ-induced diabetic rats subjected to PH present a decrease in the level of proliferating cell nuclear antigen (PCNA) and a significant decrease in cyclin D1 levels, suggesting that few hepatocytes are capable of entering the cell cycle [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B50" data-mw='{"name":"ref","attrs":{"name":"B50"},"body":{"id":"mw-reference-text-cite_note-B50"}}'><a href="#cite_note-B50"><span class="mw-reflink-text">[50]</span></a></sup>].</p>
<p>Hyperglycaemia enhances •OH radical levels and consequent Bax protein induction. After PH, STZ-induced diabetic rats were found to present an increase in proapoptotic events (Bax/Bcl-xL ratio, caspase-3 activity, and cytosolic cytochrome c) compared with the diabetic group [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B50" data-mw='{"name":"ref","attrs":{"name":"B50"},"body":{"id":"mw-reference-text-cite_note-B50"}}'><a href="#cite_note-B50"><span class="mw-reflink-text">[50]</span></a></sup>] (Figure 1<b>)</b>. The diversity of the results of different studies [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B30" data-mw='{"name":"ref","attrs":{"name":"B30"},"body":{"id":"mw-reference-text-cite_note-B30"}}'><a href="#cite_note-B30"><span class="mw-reflink-text">[30]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B32" data-mw='{"name":"ref","attrs":{"name":"B32"},"body":{"id":"mw-reference-text-cite_note-B32"}}'><a href="#cite_note-B32"><span class="mw-reflink-text">[32]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B50" data-mw='{"name":"ref","attrs":{"name":"B50"},"body":{"id":"mw-reference-text-cite_note-B50"}}'><a href="#cite_note-B50"><span class="mw-reflink-text">[50]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B55" data-mw='{"name":"ref","attrs":{"name":"B55"},"body":{"id":"mw-reference-text-cite_note-B55"}}'><a href="#cite_note-B55"><span class="mw-reflink-text">[55]</span></a></sup>] shows that the association of hyperglycaemia with different surgical modalities leads to differences in the type of cell death. It is imperative to identify the effects of diabetes on cell death after more complex surgical procedures leading to pronounced liver injury, such as liver transplantation and PH under I/R.</p></section></section><section><h3 id="3._Inflammation">3. Inflammation</h3>
<p>Hepatic inflammation is a complex process that is initiated in response to stressful conditions to protect hepatocytes from injury. However, overly intense inflammatory responses are followed by massive hepatocyte loss, causing irreversible parenchymal damage [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B57" data-mw='{"name":"ref","attrs":{"name":"B57"},"body":{"id":"mw-reference-text-cite_note-B57"}}'><a href="#cite_note-B57"><span class="mw-reflink-text">[57]</span></a></sup>]. Liver damage is a serious complication in DM [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B58" data-mw='{"name":"ref","attrs":{"name":"B58"},"body":{"id":"mw-reference-text-cite_note-B58"}}'><a href="#cite_note-B58"><span class="mw-reflink-text">[58]</span></a></sup>]. Surgical procedures induce acute inflammation, which is characterized by the production and release of various chemical mediators, including cytokines [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B59" data-mw='{"name":"ref","attrs":{"name":"B59"},"body":{"id":"mw-reference-text-cite_note-B59"}}'><a href="#cite_note-B59"><span class="mw-reflink-text">[59]</span></a></sup>]. In the next section, the effects of DM (hyperglycaemia) on the hepatic inflammatory process after a surgical procedure will be discussed.</p>
<section><h3 id="3.1._Diabetes_Mellitus_and_Ischaemia-Reperfusion_Injury">3.1. Diabetes Mellitus and Ischaemia-Reperfusion Injury</h3>
<p>The pathophysiology of hepatic I/R injury is not only related to the direct cell impairment caused by ischaemic insult but also results from the restoration of blood flow, which triggers the proinflammatory environment. Diabetic patients present a variety of deficient immune cell functions [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B60" data-mw='{"name":"ref","attrs":{"name":"B60"},"body":{"id":"mw-reference-text-cite_note-B60"}}'><a href="#cite_note-B60"><span class="mw-reflink-text">[60]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B61" data-mw='{"name":"ref","attrs":{"name":"B61"},"body":{"id":"mw-reference-text-cite_note-B61"}}'><a href="#cite_note-B61"><span class="mw-reflink-text">[61]</span></a></sup>], and diabetic animals exhibit abnormalities in the course of the inflammatory response, with a consequent decrease in the number of leukocytes in inflammatory injuries [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B62" data-mw='{"name":"ref","attrs":{"name":"B62"},"body":{"id":"mw-reference-text-cite_note-B62"}}'><a href="#cite_note-B62"><span class="mw-reflink-text">[62]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B63" data-mw='{"name":"ref","attrs":{"name":"B63"},"body":{"id":"mw-reference-text-cite_note-B63"}}'><a href="#cite_note-B63"><span class="mw-reflink-text">[63]</span></a></sup>], the airway inflammatory response to antigen challenge [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B64" data-mw='{"name":"ref","attrs":{"name":"B64"},"body":{"id":"mw-reference-text-cite_note-B64"}}'><a href="#cite_note-B64"><span class="mw-reflink-text">[64]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B65" data-mw='{"name":"ref","attrs":{"name":"B65"},"body":{"id":"mw-reference-text-cite_note-B65"}}'><a href="#cite_note-B65"><span class="mw-reflink-text">[65]</span></a></sup>], mast cell degranulation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B66" data-mw='{"name":"ref","attrs":{"name":"B66"},"body":{"id":"mw-reference-text-cite_note-B66"}}'><a href="#cite_note-B66"><span class="mw-reflink-text">[66]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B67" data-mw='{"name":"ref","attrs":{"name":"B67"},"body":{"id":"mw-reference-text-cite_note-B67"}}'><a href="#cite_note-B67"><span class="mw-reflink-text">[67]</span></a></sup>], superoxide generation, and tumour necrosis factor- (TNF-) <i>α</i> release by leukocytes upon exposure to lipopolysaccharides [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B68" data-mw='{"name":"ref","attrs":{"name":"B68"},"body":{"id":"mw-reference-text-cite_note-B68"}}'><a href="#cite_note-B68"><span class="mw-reflink-text">[68]</span></a></sup>]. The difficulty in arriving at any consistent conclusion is due to the conflicting views regarding the impact of hyperglycaemia on inflammatory responses between different reports. Since clinical observations have revealed that the association between hyperglycaemia and immune alterations could increase the risk for rejection in transplantation, the substantial inflammatory response associated with I/R injury appears to be mediated by an exaggerated adhesion of leukocytes to the endothelium [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B69" data-mw='{"name":"ref","attrs":{"name":"B69"},"body":{"id":"mw-reference-text-cite_note-B69"}}'><a href="#cite_note-B69"><span class="mw-reflink-text">[69]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B70" data-mw='{"name":"ref","attrs":{"name":"B70"},"body":{"id":"mw-reference-text-cite_note-B70"}}'><a href="#cite_note-B70"><span class="mw-reflink-text">[70]</span></a></sup>].</p>
<p>The hyperinflammatory phenotype associated with DM may induce a liver immune response against I/R, which could favour an increase in parenchymal damage [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B71" data-mw='{"name":"ref","attrs":{"name":"B71"},"body":{"id":"mw-reference-text-cite_note-B71"}}'><a href="#cite_note-B71"><span class="mw-reflink-text">[71]</span></a></sup>]. In the initial phase of liver injury, different events trigger a complex inflammatory pathway that leads to hepatic accumulation of neutrophils [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B72" data-mw='{"name":"ref","attrs":{"name":"B72"},"body":{"id":"mw-reference-text-cite_note-B72"}}'><a href="#cite_note-B72"><span class="mw-reflink-text">[72]</span></a></sup>]. Through the release of oxidants and proteases, hepatocytes are directly damaged by recruited neutrophils, which are involved in by the later phase of liver injury induced by I/R [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B73" data-mw='{"name":"ref","attrs":{"name":"B73"},"body":{"id":"mw-reference-text-cite_note-B73"}}'><a href="#cite_note-B73"><span class="mw-reflink-text">[73]</span></a></sup>]. In the livers of hyperglycaemic rats subjected to I/R, Behrends et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B32" data-mw='{"name":"ref","attrs":{"name":"B32"},"body":{"id":"mw-reference-text-cite_note-B32"}}'><a href="#cite_note-B32"><span class="mw-reflink-text">[32]</span></a></sup>] observed an increase in neutrophil infiltration (Figure 2<b>)</b>. Interestingly, in association with microvascular dysfunction in response to I/R, neutrophil infiltration is exacerbated in DM, suggesting that DM predisposes tissues to the detrimental consequences of I/R, which is a deleterious process that is broadly mediated by neutrophils [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B69" data-mw='{"name":"ref","attrs":{"name":"B69"},"body":{"id":"mw-reference-text-cite_note-B69"}}'><a href="#cite_note-B69"><span class="mw-reflink-text">[69]</span></a></sup>].</p>
<p>The immune system responds to liver injury and/or stress through the activation of resident Kupffer cells (KCs), which release proinflammatory cytokines and other factors [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B74" data-mw='{"name":"ref","attrs":{"name":"B74"},"body":{"id":"mw-reference-text-cite_note-B74"}}'><a href="#cite_note-B74"><span class="mw-reflink-text">[74]</span></a></sup>]. A prominent feature of liver injury is an increase in the hepatic macrophage population [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B75" data-mw='{"name":"ref","attrs":{"name":"B75"},"body":{"id":"mw-reference-text-cite_note-B75"}}'><a href="#cite_note-B75"><span class="mw-reflink-text">[75]</span></a></sup>]. Considering cellular and molecular mechanisms, Yue et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B71" data-mw='{"name":"ref","attrs":{"name":"B71"},"body":{"id":"mw-reference-text-cite_note-B71"}}'><a href="#cite_note-B71"><span class="mw-reflink-text">[71]</span></a></sup>] showed that I/R stimulates the release of advanced glycation end products (AGE) into the blood of STZ-induced diabetic mice and that KCs express higher levels of the receptor for AGE (RAGE). The authors [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B71" data-mw='{"name":"ref","attrs":{"name":"B71"},"body":{"id":"mw-reference-text-cite_note-B71"}}'><a href="#cite_note-B71"><span class="mw-reflink-text">[71]</span></a></sup>] proposed that RAGE may exhibit different functions in a cell type-specific manner. In normal mice, RAGE regulates hepatocyte proliferation during the restoration phase of I/R, whereas in diabetic mice, RAGE activates the hepatic immune system. These findings support the hypothesis that DM may be a factor involved in the course and evolution of I/R injury after liver surgery.</p>
<p>Activated KCs respond with a classic inflammatory reaction and consequent production of proinflammatory cytokines [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B76" data-mw='{"name":"ref","attrs":{"name":"B76"},"body":{"id":"mw-reference-text-cite_note-B76"}}'><a href="#cite_note-B76"><span class="mw-reflink-text">[76]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B80" data-mw='{"name":"ref","attrs":{"name":"B80"},"body":{"id":"mw-reference-text-cite_note-B80"}}'><a href="#cite_note-B80"><span class="mw-reflink-text">[80]</span></a></sup>]. At 6 hours after reperfusion, TNF-<i>α</i> and interleukin- (IL-) 6 levels were found to be increased, while the IL-10 level was decreased on STZ-induced diabetic mice [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B71" data-mw='{"name":"ref","attrs":{"name":"B71"},"body":{"id":"mw-reference-text-cite_note-B71"}}'><a href="#cite_note-B71"><span class="mw-reflink-text">[71]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B81" data-mw='{"name":"ref","attrs":{"name":"B81"},"body":{"id":"mw-reference-text-cite_note-B81"}}'><a href="#cite_note-B81"><span class="mw-reflink-text">[81]</span></a></sup>] (Figure 2), whereas in control mice, KCs not only presented increases in TNF-<i>α</i> and IL-6 but also an increase in IL-10 [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B81" data-mw='{"name":"ref","attrs":{"name":"B81"},"body":{"id":"mw-reference-text-cite_note-B81"}}'><a href="#cite_note-B81"><span class="mw-reflink-text">[81]</span></a></sup>]. The activation of IL-10 during a proinflammatory response may represent an important agent in the regulation of intensive inflammation in a stressful situation. These findings not only illustrate the defensive role of KCs during liver I/R injury in opposing the hyperinflammatory response through IL-10 expression but also show that hyperglycemic mice subjected to I/R present a significant decrease in IL-10 secretion, by KCs, which is related to uncontrolled inflammation and robust hepatic I/R injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B81" data-mw='{"name":"ref","attrs":{"name":"B81"},"body":{"id":"mw-reference-text-cite_note-B81"}}'><a href="#cite_note-B81"><span class="mw-reflink-text">[81]</span></a></sup>].</p>
<p>Several studies suggest that endoplasmic reticulum stress and CHOP signalling could be upregulated by RAGE signalling [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B82" data-mw='{"name":"ref","attrs":{"name":"B82"},"body":{"id":"mw-reference-text-cite_note-B82"}}'><a href="#cite_note-B82"><span class="mw-reflink-text">[82]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B85" data-mw='{"name":"ref","attrs":{"name":"B85"},"body":{"id":"mw-reference-text-cite_note-B85"}}'><a href="#cite_note-B85"><span class="mw-reflink-text">[85]</span></a></sup>]. After 6 hours of reperfusion, C/EBP homologous protein (CHOP) levels in KCs were found to be stimulated by I/R and were further increased in STZ-induced hyperglycemic mice. In hyperglycemic KCs, overactivation of CHOP is related to the inhibition of STAT3 and STAT6 activation. The signal transducers and activators of transcription (STATs) regulate the polarization of macrophages [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B86" data-mw='{"name":"ref","attrs":{"name":"B86"},"body":{"id":"mw-reference-text-cite_note-B86"}}'><a href="#cite_note-B86"><span class="mw-reflink-text">[86]</span></a></sup>], and diabetic mice present M2 KC phenotype inhibition, which results in increased inflammation under hepatic I/R when the rodents exhibit interruption of IL-10-secreting M2 differentiation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B81" data-mw='{"name":"ref","attrs":{"name":"B81"},"body":{"id":"mw-reference-text-cite_note-B81"}}'><a href="#cite_note-B81"><span class="mw-reflink-text">[81]</span></a></sup>]. Additionally, mice that are only subjected to ischaemia show development of M2-type macrophages, which protect livers from I/R via an IL-10-dependent mechanism [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B87" data-mw='{"name":"ref","attrs":{"name":"B87"},"body":{"id":"mw-reference-text-cite_note-B87"}}'><a href="#cite_note-B87"><span class="mw-reflink-text">[87]</span></a></sup>] <b>(</b>Figure 2<b>).</b></p>
<p>In the pathogenesis of DM, activated innate immunity and inflammation are important factors. Type 2 DM involves inflammatory elements [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B88" data-mw='{"name":"ref","attrs":{"name":"B88"},"body":{"id":"mw-reference-text-cite_note-B88"}}'><a href="#cite_note-B88"><span class="mw-reflink-text">[88]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B89" data-mw='{"name":"ref","attrs":{"name":"B89"},"body":{"id":"mw-reference-text-cite_note-B89"}}'><a href="#cite_note-B89"><span class="mw-reflink-text">[89]</span></a></sup>], and type 1 DM is regarded as an inflammatory process [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B90" data-mw='{"name":"ref","attrs":{"name":"B90"},"body":{"id":"mw-reference-text-cite_note-B90"}}'><a href="#cite_note-B90"><span class="mw-reflink-text">[90]</span></a></sup>]. NF-<i>κ</i>B is a transcription factor that is activated in the diabetic liver [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B91" data-mw='{"name":"ref","attrs":{"name":"B91"},"body":{"id":"mw-reference-text-cite_note-B91"}}'><a href="#cite_note-B91"><span class="mw-reflink-text">[91]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B93" data-mw='{"name":"ref","attrs":{"name":"B93"},"body":{"id":"mw-reference-text-cite_note-B93"}}'><a href="#cite_note-B93"><span class="mw-reflink-text">[93]</span></a></sup>] and is involved in events that lead to inflammation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B94" data-mw='{"name":"ref","attrs":{"name":"B94"},"body":{"id":"mw-reference-text-cite_note-B94"}}'><a href="#cite_note-B94"><span class="mw-reflink-text">[94]</span></a></sup>]. NF-<i>κ</i>B regulates the expression of many inflammatory cytokines, including monocyte chemotactic protein- (MCP-) 1, IL-6, and TNF-<i>α</i> [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B95" data-mw='{"name":"ref","attrs":{"name":"B95"},"body":{"id":"mw-reference-text-cite_note-B95"}}'><a href="#cite_note-B95"><span class="mw-reflink-text">[95]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B96" data-mw='{"name":"ref","attrs":{"name":"B96"},"body":{"id":"mw-reference-text-cite_note-B96"}}'><a href="#cite_note-B96"><span class="mw-reflink-text">[96]</span></a></sup>], which are proinflammatory cytokines that may activate neutrophils and KCs [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B97" data-mw='{"name":"ref","attrs":{"name":"B97"},"body":{"id":"mw-reference-text-cite_note-B97"}}'><a href="#cite_note-B97"><span class="mw-reflink-text">[97]</span></a></sup>]. Zhang et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B28" data-mw='{"name":"ref","attrs":{"name":"B28"},"body":{"id":"mw-reference-text-cite_note-B28"}}'><a href="#cite_note-B28"><span class="mw-reflink-text">[28]</span></a></sup>] showed that after 6 hours of reperfusion, the levels of these hepatic cytokines were significantly higher in STZ-induced diabetic rats and further increased after the ischaemic period. These results suggested that NF-<i>κ</i>B might also be involved in hepatic I/R in diabetic rats (Figure 2). The investigation of NF-<i>κ</i>B activation in diabetic livers subjected to surgical procedures should be extended to cell death. Between NF-<i>κ</i>B and TNF-<i>α</i>, there is an autocrine-reinforcing loop [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B98" data-mw='{"name":"ref","attrs":{"name":"B98"},"body":{"id":"mw-reference-text-cite_note-B98"}}'><a href="#cite_note-B98"><span class="mw-reflink-text">[98]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B99" data-mw='{"name":"ref","attrs":{"name":"B99"},"body":{"id":"mw-reference-text-cite_note-B99"}}'><a href="#cite_note-B99"><span class="mw-reflink-text">[99]</span></a></sup>]. The hepatic increase of TNF-<i>α</i> in STZ-induced diabetic rats leads to pronounced upregulation of the NF-<i>κ</i>B pathway [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B100" data-mw='{"name":"ref","attrs":{"name":"B100"},"body":{"id":"mw-reference-text-cite_note-B100"}}'><a href="#cite_note-B100"><span class="mw-reflink-text">[100]</span></a></sup>], and NF-<i>κ</i>B activation induced by hyperglycaemia mediates cell apoptosis [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B101" data-mw='{"name":"ref","attrs":{"name":"B101"},"body":{"id":"mw-reference-text-cite_note-B101"}}'><a href="#cite_note-B101"><span class="mw-reflink-text">[101]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B102" data-mw='{"name":"ref","attrs":{"name":"B102"},"body":{"id":"mw-reference-text-cite_note-B102"}}'><a href="#cite_note-B102"><span class="mw-reflink-text">[102]</span></a></sup>].</p>
<p>Several inflammatory cytokines (e.g., TNF-<i>α</i>) and arachidonic acid metabolites (prostaglandins and thromboxanes) are involved in liver injury induced by I/R. Cyclooxygenase (COX) regulates the production of prostanoids [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B103" data-mw='{"name":"ref","attrs":{"name":"B103"},"body":{"id":"mw-reference-text-cite_note-B103"}}'><a href="#cite_note-B103"><span class="mw-reflink-text">[103]</span></a></sup>], and inhibition of COX-2 protects against hepatic I/R injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B104" data-mw='{"name":"ref","attrs":{"name":"B104"},"body":{"id":"mw-reference-text-cite_note-B104"}}'><a href="#cite_note-B104"><span class="mw-reflink-text">[104]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B105" data-mw='{"name":"ref","attrs":{"name":"B105"},"body":{"id":"mw-reference-text-cite_note-B105"}}'><a href="#cite_note-B105"><span class="mw-reflink-text">[105]</span></a></sup>], which suggests that COX-2 is associated with organ injury and contributes to hepatic microvascular and hepatocellular injuries through TNF-<i>α</i> production [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B103" data-mw='{"name":"ref","attrs":{"name":"B103"},"body":{"id":"mw-reference-text-cite_note-B103"}}'><a href="#cite_note-B103"><span class="mw-reflink-text">[103]</span></a></sup>]. Hepatocyte apoptosis stimulated by TNF is associated with c-Jun N-terminal kinase (JNK) activation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B106" data-mw='{"name":"ref","attrs":{"name":"B106"},"body":{"id":"mw-reference-text-cite_note-B106"}}'><a href="#cite_note-B106"><span class="mw-reflink-text">[106]</span></a></sup>]. Conversely, Francés et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B107" data-mw='{"name":"ref","attrs":{"name":"B107"},"body":{"id":"mw-reference-text-cite_note-B107"}}'><a href="#cite_note-B107"><span class="mw-reflink-text">[107]</span></a></sup>] showed that STZ-induced diabetic COX-2 transgenic mice presented a substantial decrease in apoptosis and that COX-2 overexpression could prevent the increase in JNK activity stimulated by high glucose. The authors [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B107" data-mw='{"name":"ref","attrs":{"name":"B107"},"body":{"id":"mw-reference-text-cite_note-B107"}}'><a href="#cite_note-B107"><span class="mw-reflink-text">[107]</span></a></sup>] also showed that the increased expression of COX-2 in diabetic COX-2 transgenic mice induces an increase of phosphoinositide 3-kinase (PI3K) activity compared with diabetic wild-type mice, in addition to favouring the activation of Akt and producing an antiapoptotic signal [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B107" data-mw='{"name":"ref","attrs":{"name":"B107"},"body":{"id":"mw-reference-text-cite_note-B107"}}'><a href="#cite_note-B107"><span class="mw-reflink-text">[107]</span></a></sup>]. These studies call attention not only to the contradictory roles of diabetes in orchestrating hepatocyte activity but also to the necessity of clearly understanding the consequences of diabetes for cell death after liver surgery (Figure 2).</p></section><section><h3 id="3.2._Diabetes_Mellitus_and_Liver_Regeneration">3.2. Diabetes Mellitus and Liver Regeneration</h3>
<p>In a model of type 2 DM (ob/ob murine), liver regeneration was found to be impaired after 70% PH, which resulted in 90% mortality [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B108" data-mw='{"name":"ref","attrs":{"name":"B108"},"body":{"id":"mw-reference-text-cite_note-B108"}}'><a href="#cite_note-B108"><span class="mw-reflink-text">[108]</span></a></sup>]. The regenerative ability of the liver is compromised in type 1 diabetic rats subjected to PH [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B51" data-mw='{"name":"ref","attrs":{"name":"B51"},"body":{"id":"mw-reference-text-cite_note-B51"}}'><a href="#cite_note-B51"><span class="mw-reflink-text">[51]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B52" data-mw='{"name":"ref","attrs":{"name":"B52"},"body":{"id":"mw-reference-text-cite_note-B52"}}'><a href="#cite_note-B52"><span class="mw-reflink-text">[52]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B109" data-mw='{"name":"ref","attrs":{"name":"B109"},"body":{"id":"mw-reference-text-cite_note-B109"}}'><a href="#cite_note-B109"><span class="mw-reflink-text">[109]</span></a></sup>]. In patients subjected to a major hepatectomy, DM tends to induce postoperative liver failure [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B110" data-mw='{"name":"ref","attrs":{"name":"B110"},"body":{"id":"mw-reference-text-cite_note-B110"}}'><a href="#cite_note-B110"><span class="mw-reflink-text">[110]</span></a></sup>]. Considering the mechanisms of regeneration failure, diabetic and obese KK-Ay mice exhibit abnormal responses after PH [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>] and present excessive induction of hepatic TNF-<i>α</i> expression. Although TNF-<i>α</i> is important for the initiation of normal hepatic regeneration [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B112" data-mw='{"name":"ref","attrs":{"name":"B112"},"body":{"id":"mw-reference-text-cite_note-B112"}}'><a href="#cite_note-B112"><span class="mw-reflink-text">[112]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B113" data-mw='{"name":"ref","attrs":{"name":"B113"},"body":{"id":"mw-reference-text-cite_note-B113"}}'><a href="#cite_note-B113"><span class="mw-reflink-text">[113]</span></a></sup>], excess induction of TNF-<i>α</i> in KCs might interfere with the regenerative process [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>] (Figure 2).</p>
<p>Adipose tissue is involved in a number of biological functions, including inflammation, and acts as an endocrine organ through the secretion of several biologically active substances known as “adipokines” [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B114" data-mw='{"name":"ref","attrs":{"name":"B114"},"body":{"id":"mw-reference-text-cite_note-B114"}}'><a href="#cite_note-B114"><span class="mw-reflink-text">[114]</span></a></sup>]. During liver regeneration, systemic adipose stores are required as a source of various adipokines, such as adiponectin, which is an essential signal for liver regeneration [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B115" data-mw='{"name":"ref","attrs":{"name":"B115"},"body":{"id":"mw-reference-text-cite_note-B115"}}'><a href="#cite_note-B115"><span class="mw-reflink-text">[115]</span></a></sup>]. Aoyama et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>] showed that the serum adiponectin level was significantly reduced in KK-Ay mice before PH and tended to decrease gradually after PH. Adiponectin has been found to inhibit the lipopolysaccharide-dependent activation of macrophages [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B116" data-mw='{"name":"ref","attrs":{"name":"B116"},"body":{"id":"mw-reference-text-cite_note-B116"}}'><a href="#cite_note-B116"><span class="mw-reflink-text">[116]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B117" data-mw='{"name":"ref","attrs":{"name":"B117"},"body":{"id":"mw-reference-text-cite_note-B117"}}'><a href="#cite_note-B117"><span class="mw-reflink-text">[117]</span></a></sup>]. The significant hypoadiponectinemia presented by KK-Ay mice could be related to the fact that the KCs of these animals are more susceptible to certain stimuli; moreover, the hypoadiponectinemia caused by this susceptibility could be further associated with the increased production of TNF-<i>α</i> by KCs, which may interfere with regenerative responses [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>] (Figure 2). Adiponectin mediates anti-inflammatory effects. However, since this role for adiponectin was found to depend on surgical conditions, the function of adiponectin in the inflammatory process is a controversial issue [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B118" data-mw='{"name":"ref","attrs":{"name":"B118"},"body":{"id":"mw-reference-text-cite_note-B118"}}'><a href="#cite_note-B118"><span class="mw-reflink-text">[118]</span></a></sup>]. While injurious effects of adiponectin on steatotic livers subjected to warm ischaemia (60 minutes) were identified by Massip-Salcedo et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B119" data-mw='{"name":"ref","attrs":{"name":"B119"},"body":{"id":"mw-reference-text-cite_note-B119"}}'><a href="#cite_note-B119"><span class="mw-reflink-text">[119]</span></a></sup>], the beneficial (anti-inflammatory) effects of adiponectin on small fatty grafts subjected to cold ischaemia (40 minutes) were observed by Man et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B120" data-mw='{"name":"ref","attrs":{"name":"B120"},"body":{"id":"mw-reference-text-cite_note-B120"}}'><a href="#cite_note-B120"><span class="mw-reflink-text">[120]</span></a></sup>]. Although these findings were obtained in steatotic livers, these results suggest opportunities for investigation of the effect of adiponectin on diabetic livers subjected to different surgical procedures.</p>
<p>IL-6 is a protein synthesized by fibroblasts, monocytes, macrophages, T cells, and endothelial cells [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B121" data-mw='{"name":"ref","attrs":{"name":"B121"},"body":{"id":"mw-reference-text-cite_note-B121"}}'><a href="#cite_note-B121"><span class="mw-reflink-text">[121]</span></a></sup>] that plays an important role in hepatic regeneration [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B122" data-mw='{"name":"ref","attrs":{"name":"B122"},"body":{"id":"mw-reference-text-cite_note-B122"}}'><a href="#cite_note-B122"><span class="mw-reflink-text">[122]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B123" data-mw='{"name":"ref","attrs":{"name":"B123"},"body":{"id":"mw-reference-text-cite_note-B123"}}'><a href="#cite_note-B123"><span class="mw-reflink-text">[123]</span></a></sup>]. Adipokines exhibit proinflammatory or anti-inflammatory activities [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B124" data-mw='{"name":"ref","attrs":{"name":"B124"},"body":{"id":"mw-reference-text-cite_note-B124"}}'><a href="#cite_note-B124"><span class="mw-reflink-text">[124]</span></a></sup>], and leptin presents proinflammatory properties [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B125" data-mw='{"name":"ref","attrs":{"name":"B125"},"body":{"id":"mw-reference-text-cite_note-B125"}}'><a href="#cite_note-B125"><span class="mw-reflink-text">[125]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B126" data-mw='{"name":"ref","attrs":{"name":"B126"},"body":{"id":"mw-reference-text-cite_note-B126"}}'><a href="#cite_note-B126"><span class="mw-reflink-text">[126]</span></a></sup>]. IL-6 and leptin function in the Janus kinase- (JAK-) STAT3 signalling pathway [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>]. KK-Ay mice present a substantial increase in the levels of IL-6 and leptin following PH [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>]. Despite the important role of the JAK-STAT pathway in hepatic protection against different hepatic injuries [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B127" data-mw='{"name":"ref","attrs":{"name":"B127"},"body":{"id":"mw-reference-text-cite_note-B127"}}'><a href="#cite_note-B127"><span class="mw-reflink-text">[127]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B128" data-mw='{"name":"ref","attrs":{"name":"B128"},"body":{"id":"mw-reference-text-cite_note-B128"}}'><a href="#cite_note-B128"><span class="mw-reflink-text">[128]</span></a></sup>] and the evidence that IL-6, leptin, and the JAK-STAT signalling pathway are essential to liver regeneration [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B129" data-mw='{"name":"ref","attrs":{"name":"B129"},"body":{"id":"mw-reference-text-cite_note-B129"}}'><a href="#cite_note-B129"><span class="mw-reflink-text">[129]</span></a></sup>–<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B132" data-mw='{"name":"ref","attrs":{"name":"B132"},"body":{"id":"mw-reference-text-cite_note-B132"}}'><a href="#cite_note-B132"><span class="mw-reflink-text">[132]</span></a></sup>], Aoyama et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B111" data-mw='{"name":"ref","attrs":{"name":"B111"},"body":{"id":"mw-reference-text-cite_note-B111"}}'><a href="#cite_note-B111"><span class="mw-reflink-text">[111]</span></a></sup>] showed that the role of the JAK-STAT pathway in hepatic regeneration seems to be complex and dependent on the intensity of the stimulus, showing that hyperphosphorylation of STAT3 favours poor hepatic regeneration as a result of direct downregulation of cyclin D1 expression (Figure 2).</p></section></section><section><h3 id="4._Diabetes_Mellitus_in_Clinical_Situations">4. Diabetes Mellitus in Clinical Situations</h3>
<p>There is an absence of clinical studies elucidating signalling pathways related to liver damage and impaired regeneration in diabetic patients undergoing surgery. Nevertheless, it is indispensable to discuss and generate hypotheses about this issue, which is quite controversial because some studies have shown that DM patients present a poorer prognosis after hepatic surgery in comparison with non-DM patients, whereas others show no difference [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B133" data-mw='{"name":"ref","attrs":{"name":"B133"},"body":{"id":"mw-reference-text-cite_note-B133"}}'><a href="#cite_note-B133"><span class="mw-reflink-text">[133]</span></a></sup>].</p>
<p>Focusing on the issues addressed in this review (OS and inflammation), Li et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B133" data-mw='{"name":"ref","attrs":{"name":"B133"},"body":{"id":"mw-reference-text-cite_note-B133"}}'><a href="#cite_note-B133"><span class="mw-reflink-text">[133]</span></a></sup>] and Shields et al. [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B134" data-mw='{"name":"ref","attrs":{"name":"B134"},"body":{"id":"mw-reference-text-cite_note-B134"}}'><a href="#cite_note-B134"><span class="mw-reflink-text">[134]</span></a></sup>] described the typical change in microcirculation that occurs in diabetic patients after liver surgery. The ischaemic period and liver perfusion recovery are important factors related to hepatocellular damage because microcirculatory collapse is followed by a pronounced reduction of tissue oxygenation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B135" data-mw='{"name":"ref","attrs":{"name":"B135"},"body":{"id":"mw-reference-text-cite_note-B135"}}'><a href="#cite_note-B135"><span class="mw-reflink-text">[135]</span></a></sup>], which might result in degeneration and necrosis of hepatocytes and consequent liver dysfunction [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B136" data-mw='{"name":"ref","attrs":{"name":"B136"},"body":{"id":"mw-reference-text-cite_note-B136"}}'><a href="#cite_note-B136"><span class="mw-reflink-text">[136]</span></a></sup>]. Experimental models of I/R injury have offered evidence that insufficient hepatic microcirculatory perfusion, inflammatory cell activation, and consequent generation of ROS, cytokines, and chemokines can be considered essential in I/R syndrome [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B137" data-mw='{"name":"ref","attrs":{"name":"B137"},"body":{"id":"mw-reference-text-cite_note-B137"}}'><a href="#cite_note-B137"><span class="mw-reflink-text">[137]</span></a></sup>]. Although the authors [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B133" data-mw='{"name":"ref","attrs":{"name":"B133"},"body":{"id":"mw-reference-text-cite_note-B133"}}'><a href="#cite_note-B133"><span class="mw-reflink-text">[133]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B134" data-mw='{"name":"ref","attrs":{"name":"B134"},"body":{"id":"mw-reference-text-cite_note-B134"}}'><a href="#cite_note-B134"><span class="mw-reflink-text">[134]</span></a></sup>] did not report the relationship between diabetic liver failure after liver surgery and microcirculation collapse, we take this opportunity to raise this question for the development of future studies.</p>
<p>The alterations of hepatic haemodynamics are also related to hepatic steatosis, and a decrease in portal vein haemodynamics is observed in patients with a fatty liver disease [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B138" data-mw='{"name":"ref","attrs":{"name":"B138"},"body":{"id":"mw-reference-text-cite_note-B138"}}'><a href="#cite_note-B138"><span class="mw-reflink-text">[138]</span></a></sup>, <sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B139" data-mw='{"name":"ref","attrs":{"name":"B139"},"body":{"id":"mw-reference-text-cite_note-B139"}}'><a href="#cite_note-B139"><span class="mw-reflink-text">[139]</span></a></sup>]. Moreover, experimental animals with steatosis present decreased parenchymal microcirculation [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B140" data-mw='{"name":"ref","attrs":{"name":"B140"},"body":{"id":"mw-reference-text-cite_note-B140"}}'><a href="#cite_note-B140"><span class="mw-reflink-text">[140]</span></a></sup>]. Hepatic steatosis has long been reported in type 1 [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B141" data-mw='{"name":"ref","attrs":{"name":"B141"},"body":{"id":"mw-reference-text-cite_note-B141"}}'><a href="#cite_note-B141"><span class="mw-reflink-text">[141]</span></a></sup>] and type 2 DM [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B142" data-mw='{"name":"ref","attrs":{"name":"B142"},"body":{"id":"mw-reference-text-cite_note-B142"}}'><a href="#cite_note-B142"><span class="mw-reflink-text">[142]</span></a></sup>]. Steatosis is common in diabetic patients (36% incidence) [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B143" data-mw='{"name":"ref","attrs":{"name":"B143"},"body":{"id":"mw-reference-text-cite_note-B143"}}'><a href="#cite_note-B143"><span class="mw-reflink-text">[143]</span></a></sup>], and increased steatosis raises the sensibility of the liver parenchyma to I/R injury [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B144" data-mw='{"name":"ref","attrs":{"name":"B144"},"body":{"id":"mw-reference-text-cite_note-B144"}}'><a href="#cite_note-B144"><span class="mw-reflink-text">[144]</span></a></sup>]. In steatotic livers, the parenchymal regeneration ability is impaired, particularly after a surgical procedure [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B115" data-mw='{"name":"ref","attrs":{"name":"B115"},"body":{"id":"mw-reference-text-cite_note-B115"}}'><a href="#cite_note-B115"><span class="mw-reflink-text">[115]</span></a></sup>], which may partially explain the incapacity of some diabetic patients to resist liver surgery. The high mortality observed in diabetic patients is absent in nondiabetic patients with steatosis [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B143" data-mw='{"name":"ref","attrs":{"name":"B143"},"body":{"id":"mw-reference-text-cite_note-B143"}}'><a href="#cite_note-B143"><span class="mw-reflink-text">[143]</span></a></sup>]. In hepatocytes, increased accumulation of fatty acids induces OS arising from mitochondria, peroxisomes, or microsomes. ROS and lipid peroxidation products can influence KCs and stimulate NF-<i>κ</i>B activation, which in turn stimulates the production of TNF-<i>α</i> and several proinflammatory cytokines, such as IL-6 [<sup class="mw-ref" rel="dc:references" typeof="mw:Extension/ref" id="cite_ref-B143" data-mw='{"name":"ref","attrs":{"name":"B143"},"body":{"id":"mw-reference-text-cite_note-B143"}}'><a href="#cite_note-B143"><span class="mw-reflink-text">[143]</span></a></sup>], which are presented in this review as factors involved in decreased regeneration and increased liver damage.</p></section><section><h3 id="5._Conclusion">5. Conclusion</h3>
<p>The purpose of this review was to discuss the literature addressing the damaging effect of DM on liver recovery after a surgical procedure and, especially, to highlight the need to expand knowledge of this issue to benefit patients with DM subjected to surgical procedures, which are increasing in clinical practice. Extensive work is still necessary to assess the differences between the diabetic and nondiabetic liver after a surgical procedure. Exploring this subject will enable the development of new treatments that will improve the success of diabetic liver recovery after surgery.</p></section><section><h2 id="Acknowledgements">Acknowledgements</h2>
<h3 id="Acknowledgments">Acknowledgments</h3>
<p>The authors apologize to the many researchers whose work they have not been able to discuss in this limited review. The authors are supported by Grants 2016/24992-0 and 2017/11540-7 from the São Paulo Research Foundation (FAPESP), Grant 301617/2016-3 from the National Counsel of Technological and Scientific Development (CNPq, PQ-1D), and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).</p></section><section><h2 id="References">References</h2>
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{{articlefooter
| pmcid = 5964489
| license = Creative Commons Attribution 4.0 International
| main_subject = experimental diabetes mellitus
| batch_date = 2019-04-16
}}