丝素蛋白对乙醇性胃溃疡的潜在保护作用

A. Aykaç, Buse Karanlik, A. Sehirli
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引用次数: 2

摘要

摘要:酒精引起的溃疡是常见的问题。本研究旨在探讨丝素蛋白对乙醇性溃疡模型大鼠促凋亡和抗凋亡蛋白表达水平的保护作用。给大鼠连续3天口服丝素或生理盐水。第4天,实验前24 h不给食物,自由饮水。对照组只给予生理盐水治疗,溃疡组给予生理盐水或丝素素口服治疗。两组均灌胃无水乙醇1 ml诱导溃疡。首先,在EtOH或生理盐水给药60分钟时取心内血,立即将动物斩首。在血液样本中,分析TNF-,IL-1β的量,而在胃组织中,测定MDA, GSH和MPO活性水平以及bcl-2, Bax, caspase-3和-9的表达水平。溃疡组TNF-、IL-1β、MDA、MPO、caspase-3、caspase-9含量显著高于对照组,而GSH、Bcl-2/Bax含量显著低于对照组(p < 0.005)。在治疗组中,观察到丝素蛋白恢复了TNF-、IL 1-β、MDA、MPO、GSH、caspase-3、caspase-9和Bcl2/Bax的量。综上所述,SF被认为是治疗胃溃疡非常有效的治疗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential protective effects of silk fibroin against ethanol induced gastric ulcer
ABSTRACT: Ulcers that develop due to alcohol consumption are frequently confronted. The aim of this study was to investigate the protective effects of silk fibroin on the pro-apoptotic and anti-apoptotic protein expression levels on ethanol induced-ulcer models in rats. For three consecutive days, orogastrically either silk fibroin or saline were given to rats. On the 4th day, animals were deprived of food but allowed free access to water for 24 h before the experiment. While control groups were treated with only physiological saline, the ulcer groups were treated orally either with saline or silk fibroin groups. For ulcer induction, 1 ml of absolute ethanol by gavage were given to both group. Firstly, intracardiac blood was taken at 60 min of EtOH or saline administration and immediately animals were decapitated. In blood samples, the amount of TNF-, IL-1β were analysed whereas in stomach tissues, the levels of MDA, GSH, and MPO activity and the expression levels of bcl-2, Bax, caspase-3 and -9 were determined. In ulcer groups, the amount of TNF- , IL-1β, MDA, MPO, caspase-3 and caspase-9 were found to be significantly higher compared to control groups whereas in GSH, Bcl-2/Bax were found to be lower (p < 0.005). In treatment groups it is observed that silk fibroin recovers the amount of TNF-, IL 1-β, MDA, MPO, GSH, caspase-3, caspase-9, and Bcl2/Bax. In conclusion, for the treatment of the gastric ulcer SF thought to be very efficient therapeutic agent.
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