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Tauroursodeoxycholic acid attenuates endoplasmic reticulum stress and protects the liver from chronic intermittent hypoxia induced injury

机译:Tauroursodoxcholic酸衰减内质网胁迫并保护肝脏免受慢性间歇性缺氧诱导损伤的影响

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摘要

Obstructive sleep apnea that characterized by chronic intermittent hypoxia (CIH) has been reported to associate with chronic liver injury. Tauroursodeoxycholic acid (TUDCA) exerts liver-protective effects in various liver diseases. The purpose of this study was to test the hypothesis that TUDCA could protect liver against CIH injury. C57BL/6 mice were subjected to intermittent hypoxia for eight weeks and applied with TUDCA by intraperitoneal injection. The effect of TUDCA on liver histological changes, liver function, oxidative stress, inflammatory response, hepatocyte apoptosis and endoplasmic reticulum (ER) stress were investigated. The results showed that administration of TUDCA attenuated liver pathological changes, reduced serum alanine aminotransferase and aspartate aminotransferase level, suppressed reactive oxygen species activity, decreased tumor necrosis factor-alpha and interleukin-1 beta level and inhibited hepatocyte apoptosis induced by CIH. TUDCA also inhibited CIH-induced ER stress in liver as evidenced by decreased expression of ER chaperone 78 kDa glucose-related protein, unfolded protein response transducers and ER proapoptotic proteins. Altogether, the present study described a liver-protective effect of TUDCA in CIH mice model, and this effect seems at least partly through the inhibition of ER stress.
机译:据报道,表征慢性间歇性缺氧(CIH)的阻塞性睡眠呼吸暂停与慢性肝损伤相关联。 Tauroursodoxcholic酸(Tudca)对各种肝病施加肝脏保护作用。本研究的目的是测试TUDCA可以保护肝脏免受CIH损伤的假设。将C57BL / 6小鼠进行间歇性缺氧8周,并通过腹膜内注射用Tudca施用。研究了TUDCA对肝脏组织学变化,肝功能,氧化应激,炎症反应,肝细胞凋亡和内质网(ER)应激的影响。结果表明,Tudca衰减肝脏病理变化,减少血清丙氨酸氨基转移酶和天冬氨酸氨基转移酶水平,抑制反应性氧物质活性,降低肿瘤坏死因子-α和白细胞介素-1β水平,抑制CIH诱导的肝细胞凋亡。 Tudca还抑制了CIH诱导的肝脏的ER应激,通过ER伴侣78 kda葡萄糖相关蛋白,展开蛋白响应传感器和ER凋亡蛋白表达下降。同时,本研究描述了Tudca在CIH小鼠模型中的肝脏保护作用,并且这种效果似乎至少部分地通过抑制ER应力。

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