Effect of Adrenomedullin and Omega-3 Polyunsaturated Fatty Acids on Celecoxib - Induced Acute Hepatic Injury in Experimental Rats

A. Elgendy, Wael M Elsaed, H. A. Elaziz, Amr E Ahmed
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Abstract

Celecoxib as a nonsteroidal anti-inflammatory agent has hepatotoxicity, increase both oxidative stress and proinflammatory cytokines. The present study investigated the effect of adrenomedullin and omega-3 polyunsaturated fatty acids in celecoxib - induced acute hepatic injury in experimental rats. Fifty Sprague-Dawley rats were divided into five groups; control, celecoxib treated group, celebrex and adrenomedullin treated group, celebrex and omega – 3 treated group, celebrex, adrenomedullin and omega – 3 treated group. Liver functions tests, hepatic oxidants and antioxidants parameters, plasma nitric oxide levels, serum proinflammatory cytokines, plasma PGE2 and adrenomedullin were measured and also histopathological examination was done. Celebrex significantly impaired liver functions, increase hepatic oxidants, decrease hepatic antioxidants, increase proinflammatory cytokines, decrease PGE2 and increase adrenomedullin ,moreover showing necrosis in histopathology. Adrenomedullin and omega-3 PUFAs improved liver functions, decrease oxidative stress, decrease cytokines and PGE2 but nitric oxide level was significantly increased by adrenomedullin whereas decreased by omega-3 PUFAs. There was insignificant change in serum albumin in all groups. Histopathological examination revealed that most of the hepatocytes appeared with normal colored esinophilic cytoplasm and vesicular basophilic nuclei. It could be concluded that celecoxib had an oxidant stress effect in addition to increase proinflammatory cytokines and consequent acute hepatic insult. The development of hepatic injury was celecoxib – dose dependent. Adrenomedullin and omega-3 polyunsaturated fatty acids could alleviate the acute hepatic injury, oxidative stress, decrease proinflammatory cytokines and by turn recovery of hepatic morphology and functions.
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肾上腺髓质素和Omega-3多不饱和脂肪酸对塞来昔布致大鼠急性肝损伤的影响
塞来昔布作为一种非甾体抗炎药具有肝毒性,增加氧化应激和促炎细胞因子。本研究探讨肾上腺髓质素和omega-3多不饱和脂肪酸在塞来昔布诱导的大鼠急性肝损伤中的作用。50只Sprague-Dawley大鼠分为5组;对照组、塞来昔布治疗组、西乐葆与肾上腺髓质素治疗组、西乐葆与omega - 3治疗组、西乐葆与肾上腺髓质素及omega - 3治疗组。测定肝功能、肝氧化剂和抗氧化剂参数、血浆一氧化氮水平、血清促炎细胞因子、血浆PGE2和肾上腺髓质素,并进行组织病理学检查。西乐brex显著损害肝功能,增加肝脏氧化剂,降低肝脏抗氧化剂,增加促炎细胞因子,降低PGE2,增加肾上腺髓质素,并在组织病理学上表现为坏死。肾上腺髓质素和omega-3 PUFAs可改善肝功能,减少氧化应激,降低细胞因子和PGE2,但一氧化氮水平显著升高,omega-3 PUFAs则显著降低。各组血清白蛋白变化不显著。组织病理学检查显示,大部分肝细胞呈现正常颜色的嗜酸性细胞质和泡状嗜碱性细胞核。由此可见,塞来昔布除了增加促炎细胞因子外,还具有氧化应激作用,从而导致急性肝损伤。肝损伤的发展是塞来昔布剂量依赖性的。肾上腺髓质素和omega-3多不饱和脂肪酸可减轻急性肝损伤和氧化应激,降低促炎因子,从而恢复肝脏形态和功能。
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