Protective effects of rosiglitazone on hepatic ischemia reperfusion injury in rats.
10.11817/j.issn.1672-7347.2018.07.006
- Author:
Jisong CHEN
1
;
Haiwei LIU
2
;
Xianlin ZHANG
2
Author Information
1. Department of General Surgery, Affiliated Renhe Hospital of China Three Gorges University, Yichang Hubai 443001, China doctorcjs@163.com.
2. Department of General Surgery, Affiliated Renhe Hospital of China Three Gorges University, Yichang Hubai 443001, China.
- Publication Type:Journal Article
- MeSH:
Alanine Transaminase;
blood;
Animals;
Aspartate Aminotransferases;
blood;
Catalase;
blood;
Disease Models, Animal;
Glutathione Peroxidase;
blood;
L-Lactate Dehydrogenase;
blood;
Ligation;
Liver;
blood supply;
metabolism;
Malondialdehyde;
blood;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Reperfusion Injury;
blood;
etiology;
prevention & control;
Rosiglitazone;
Superoxide Dismutase;
blood;
Thiazolidinediones;
therapeutic use
- From:
Journal of Central South University(Medical Sciences)
2018;43(7):732-737
- CountryChina
- Language:Chinese
-
Abstract:
To explore the protective effect of rosiglitazone (RGZ) on hepatic ischemia reperfusion injury (HIRI) and the underlying mechanisms.
Methods: A rat model of ischemia-reperfusion injury was established by clamping the left and middle lobe of liver with noninvasive vascular clamp. A total of 30 Sprague-Dawley rats were randomly divided into a sham group, an HIRI group, and a RGZ group (10 rats in each group). Two hours after reperfusion, serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities, lactate dehydrogenase (LDH) level, malondialdehyde (MDA) content and catalase (CAT), glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities were examined. HE staining was used to observe liver pathological morphology. The liver peroxisome proliferators-activated receptor γ (PPAR-γ), p-PPAR-γ, nuclear factor related factor 2 (Nrf-2), antioxidant response element (ARE), heme oxygenase 1 (HO-1) and quinone oxidoreductase-1 (NQO-1) were detected by Western blot.
Results: Compared with the HIRI group, the levels of ALT, AST, LDH and MDA in the RGZ group were significantly decreased (all P<0.05), while the levels of Nrf-2, ARE, HO-1 and NQO-1 in the RGZ group were significantly increased. The hepatic swelling, necrosis and pathological damage were decreased (all P<0.05). In addition, there was no difference in the level of PPAR-γ between the 2 groups (P>0.05).
Conclusion: PPAR-γ agonist RGZ can attenuate HIRI, which may be related to activating Nrf2/ARE signaling pathway and enhancement of antioxidant ability.
