2009
DOI: 10.1016/s0168-8278(09)60163-x
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161 Hepatoprotective Effect of Citrulline Against Ischemia-Reperfusion Injury in Rat

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Cited by 5 publications
(5 citation statements)
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“…Finally, Cit is involved in the regulation of protein and energy metabolism (16) because it activates muscle protein synthesis (17) and improves insulin sensitivity. Moreover, Cit also displays antioxidative properties, as previously shown by our group in a model of in vivo ischemia-reperfusion of the liver (18). Therefore, Cit may be able to restore hepatic energy metabolism, which plays a major role in the development of NAFLD.…”
Section: Introductionsupporting
confidence: 61%
“…Finally, Cit is involved in the regulation of protein and energy metabolism (16) because it activates muscle protein synthesis (17) and improves insulin sensitivity. Moreover, Cit also displays antioxidative properties, as previously shown by our group in a model of in vivo ischemia-reperfusion of the liver (18). Therefore, Cit may be able to restore hepatic energy metabolism, which plays a major role in the development of NAFLD.…”
Section: Introductionsupporting
confidence: 61%
“…Moussaoui et al did not utilize GGT as part of their liver integrity assessment. However, they found that CIT significantly reduced elevations of all serum biomarkers, in which the present study failed to demonstrate [15]. Jegatheesan et al used alkaline phosphatase (ALP), a marker of hepatobiliary injury similar to GGT; however, they also found that CIT only caused insignificant attenuation of ALP elevation [16].…”
Section: Discussioncontrasting
confidence: 81%
“…This finding is in agreement with those of other studies evaluating CIT hepatoprotective ability. Moussaoui et al reported on rats with modeled ischemia/reperfusion injury and found that CIT treatment significantly reduced elevations of ALT and AST (p<0.05), along with lactate dehydrogenase, arginase, and intrahepatic myeloperoxidase activity [15]. In addition, Jegatheesan et al identified a significant decrease of plasma ALT levels due to CIT in rats with fructose-induced liver steatosis.…”
Section: Discussionmentioning
confidence: 98%
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“…As a consequence, Cit significantly decreased liver weight compared with the WD group. The effect of Cit on lipid metabolism may be the result of decreased de novo lipogenesis, but also to a better VLDL-TAG release given the improved peripheral TAG oxidation previously demonstrated ( 29 ) .…”
Section: Discussionmentioning
confidence: 96%