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昆仑雪菊多糖对乙酰氨基酚诱导的氧化应激、炎症和细胞凋亡的动物模型实验研究

Effects of the Kunlun snow chrysanthemum polysaccharides on acetaminophen-induced oxidative stress, inflammation and apoptosis using animal model.

作者信息

Zhao Wenhui, Zeng Cheng, Jia Qiqi, Yang Xiaoyi

机构信息

Central Laboratory, Xinjiang Medical University, Urumqi, PR China.

Central Laboratory, Xinjiang Medical University, Urumqi, PR China / Xinjiang Institute of Materia Medica, Urumqi, PR China.

出版信息

Pak J Pharm Sci. 2018 May;31(3(Supplementary)):985-990.

Abstract

To investigate the preventive effect of Kunlun snow chrysanthemum polysaccharides (KSCP) on acetaminophen (AP) induced liver damage and its possible mechanism. Mice acute liver injury model was established via intraperitoneal injection of AP (300 mg/kg). The biochemical indicators of plasma and liver tissue were tested. The effects of KSCP on the liver index were examined. The liver pathological changes were investigated. The expressions of related protein were detected via Western blotting. In our study, compared with model group, the concentrations and contents of ALT, AST, TNF-α, IL-1β and MDA were reduced and activities of SOD were increase in H-KSCP (1.2mg/10 g)-pretreated mice (P<0.01). The liver index was significantly reduced in H-KSCP-pretreated mice compared with model group (4.89±0.22 vs 7.4±0.66, P<0.01). Liver cellular swelling, degeneration and necrosis relieved, and pathological injury had been improved. Western blotting results showed that the caspase-3 protein level in H-KSCP group was significantly decreased, expression of Bcl-2 protein and Bcl-2/Bax ratio was increased, whereas which of Bax protein was decreased (P<0.01). KSCP-pretreated at middle and high doses can prevent against the liver injury, its action mechanism may be related to its anti-inflammatory effects and regulation of apoptosis related proteins expression. Overall, our results showed that KSCP may be an effective preventive agent in preventing acute liver injury.

摘要

探讨昆仑雪菊多糖(KSCP)对乙酰氨基酚(AP)所致肝损伤的预防作用及其可能机制。通过腹腔注射AP(300mg/kg)建立小鼠急性肝损伤模型。检测血浆和肝组织的生化指标,考察KSCP对肝脏指数的影响,观察肝脏病理变化,采用蛋白质印迹法检测相关蛋白表达。本研究中,与模型组相比,H-KSCP(1.2mg/10g)预处理小鼠的ALT、AST、TNF-α、IL-1β和MDA浓度及含量降低,SOD活性升高(P<0.01)。H-KSCP预处理小鼠的肝脏指数较模型组显著降低(4.89±0.22 vs 7.4±0.66,P<0.01)。肝细胞肿胀、变性及坏死减轻,病理损伤得到改善。蛋白质印迹结果显示,H-KSCP组caspase-3蛋白水平显著降低,Bcl-2蛋白表达及Bcl-2/Bax比值升高,而Bax蛋白表达降低(P<0.01)。中、高剂量KSCP预处理可预防肝损伤,其作用机制可能与其抗炎作用及调节凋亡相关蛋白表达有关。总体而言,本研究结果表明KSCP可能是预防急性肝损伤的有效药物。

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