海藻糖通过Il-6途径抑制老年小鼠肝损伤的作用

Rabiatul Aminah, A. Santoso, M. Cangara, Marhaen Hardjo, A. Aminuddin, Endy Adnan
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引用次数: 0

摘要

海藻糖是由1-1糖苷键连接的两个葡萄糖分子组成的非还原性双糖。海藻糖可发挥器官解毒、抗氧化酶活性、减少脂质过氧化和减少炎症因子TNF-、IL-1β、Il-6分泌的作用,从而抑制肝损伤。鉴于海藻糖的作用,本研究采用实验后测设计和对照组设计,旨在通过IL-6表达途径确定海藻糖给药对肝损伤的影响。本研究以老龄大鼠,即Wistar大鼠(Rattus novergicus)为研究对象。使用的老龄大鼠为雄性21种,分为3组,分别为老龄对照组、给予蔗糖的老龄大鼠组和给予海藻糖的老龄大鼠组。然后观察8周,即2021年3月至5月在望加锡哈萨丁大学医学院。三组实验结果显示,在老年小鼠中给予海藻糖具有降低炎症因子IL-6的作用,因为海藻糖可以激活巨噬细胞的自噬,从而减少细胞因子的产生和血管炎症,从而使所有衰老小鼠恢复到与年轻小鼠相似的水平。衰老大鼠肝脏以内质网UPR激活和炎症信号传导为特征,烟酰胺和udp - n -乙酰-己糖胺减少,蛋白酶体活性降低。因此,海藻糖可能是一种有效的治疗策略,对抗肝脏中与年龄相关的蛋白质停滞症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Trehalose in Inhibiting Liver Damage via The Il-6 Pathway in Old Mice
Trehalose is a non-reducing disaccharide consisting of two glucose molecules linked by a 1–1 glycosidic bond. Trehalose can play a role in organ detoxification, antioxidant enzyme activity, reducing lipid peroxidation and reducing the secretion of inflammatory factors TNF-, IL-1β, Il-6, thereby inhibiting liver damage. Because of its role, this study aims to determine the effect of trehalose administration on liver damage through the IL-6 expression pathway with experimental post-test design with control group design. This research was conducted using samples of old rats, namely Wistar rats (Rattus novergicus). The old rats used were 21 male species which were then divided into 3 groups, namely the old control group, the old rat group that was given sucrose, and the old rat group that was given trehalose. Then observed for 8 weeks, namely in March - May 2021 at the Faculty of Medicine, Hasanuddin University Makassar. The results obtained from the 3 groups showed a significant value that the administration of trehalose sugar in elderly mice had an effect on reducing the inflammatory factor IL-6 because it activated autophagy in macrophages thereby reducing cytokine production and vascular inflammation so as to be able to restore all aging mice to a level like observed in young mice. It is also known that aged rat liver, which is characterized by ER UPR activation and inflammatory signaling, decreases nicotinamide and UDP-N-acetyl-hexosamines, and reduces proteasome activity. Therefore, trehalose can be an effective therapeutic strategy against age-related disorders of proteostasis in the liver.
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