Protective effects of resveratrol on hepatic ischemia reperfusion injury in streptozotocin-induced diabetic rats

被引:21
作者
Aktas, Hanife Serife [1 ]
Ozel, Yahya [2 ]
Ahmad, Sarfraz [3 ]
Pence, Halime Hanim [4 ]
Ayaz-Adakul, Betul [5 ]
Kudas, Ilyas [2 ]
Tetik, Sermin [6 ]
Sekerler, Turgut [6 ]
Canbey-Goret, Ceren [7 ]
Kabasakal, Levent [5 ]
Elcioglu, Hatice Kubra [5 ]
机构
[1] Umraniye Res & Training Hosp, Internal Med Clin, Istanbul, Turkey
[2] Umraniye Res & Training Hosp, Gen Surg Clin, Istanbul, Turkey
[3] AdventHlth Med Ctr, 2501 N Orange Ave,Suite 786, Orlando, FL 32804 USA
[4] Hlth Sci Univ, Fac Med, Dept Biochem, Istanbul, Turkey
[5] Marmara Univ, Pharm Fac, Dept Pharmacol, Istanbul, Turkey
[6] Marmara Univ, Pharm Fac, Dept Biochem, Istanbul, Turkey
[7] Prof Dr Ilhan Varank Sancaktepe Res & Training Ho, Dept Pathol, Istanbul, Turkey
关键词
Resveratrol; Diabetes; Ischemia reperfusion injury; Inflammation; Experimental rats; ALPHA-LIPOIC ACID; OXIDATIVE STRESS; ISCHEMIA/REPERFUSION INJURY; CEREBRAL-ISCHEMIA; SIGNALING PATHWAY; LIVER; INFLAMMATION; MICE;
D O I
10.1007/s11010-019-03582-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Resveratrol (RSV) is a natural polyphenolic compound having antioxidant effects. This study was designed to investigate the protective effects of resveratrol against oxidative stress in hepatic ischemia-reperfusion (I/R) injury in streptozotocin (STZ)-induced diabetic rats. STZ was injected intraperitonally (i.p.) to 18 Sprague-Dawley albino rats, which were divided into three groups, each having six rats. First group was non-treated diabetic group (D), second diabetic group was subjected to 30 min of hepatic ischemia followed by a 45-min reperfusion period (D + I/R), and third diabetic group was subjected to 30 min of hepatic ischemia followed by a 45-min reperfusion period and treated with 20 mg/kg/day oral RSV before 30 min I/R injury (D + I/R + RSV). At the end of the experimental period, animals were decapitated, and blood samples were collected to determine tissue tumor necrosis factor-alpha (TNF-alpha) levels. Liver and lung tissue samples were obtained for the evaluation of biochemical parameters including malondialdehyde (MDA) and glutathione (GSH) levels and histopathological examinations. Compared to control, I/R injury resulted in decreases in GSH levels and increases in MDA levels. Tissue TNF-alpha levels were also increased in the D + I/R group compared to D group. Treatment with RSV prevented the alterations on biochemical parameters and histopathological changes induced by I/R. We demonstrate that in diabetic rats, hepatic I/R injury is associated with an augmented inflammatory response and oxidative stress, while RSV pre-treatment significantly decreased these responses. Larger clinical studies are desirable to determine the exact role(s) of RSV on hepatic I/R injury among diabetic subjects.
引用
收藏
页码:217 / 224
页数:8
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