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酸枣仁皂苷 A 通过抑制氧化应激、细胞凋亡和增强自噬来改善高脂饮食和链脲佐菌素诱导的糖尿病肾病。

Jujuboside A ameliorates high fat diet and streptozotocin induced diabetic nephropathy via suppressing oxidative stress, apoptosis, and enhancing autophagy.

机构信息

College of Food Science and Engineering, Northwest A&F University, Yangling, Shaanxi, 712100, China.

College of Food Science and Engineering, Northwest A&F University, Yangling, Shaanxi, 712100, China.

出版信息

Food Chem Toxicol. 2022 Jan;159:112697. doi: 10.1016/j.fct.2021.112697. Epub 2021 Nov 23.

Abstract

Jujuboside A (JuA) is a triterpenoid saponins isolated from the seed of jujube (semen Ziziphi spinosae) with anti-oxidant, anti-inflammation and anti-apoptosis properties. The present study aimed to investigate the reno-protective effects of JuA on type II diabetes. JuA (20 mg/kg) and Metformin (Met, 300 mg/kg) were administrated to diabetic Sprague Dawley rat for 8 weeks daily. Our results showed that JuA reduced blood glucose and kidney function markers including 24 h urinary protein, urinary β-NAG/urinary creatinine, serum urea nitrogen, serum uric acid and serum creatinine, and relieved renal pathological changes. In addition, JuA decreased O and HO level, enhanced SOD, CAT and GPx activities, decreased NOX4 expression and improved mitochondrial respiratory chain function through regulating respiratory chain complex expression. Moreover, JuA downregulated the expressions of mitochondrial apoptosis proteins: Bax, CytC, Apaf-1 and caspase 9. Apoptosis mediated by ER stress also been inhibited by JuA via downregulating p-PERK, p-IRE1, XBP1s, ATF4, p-CHOP and caspase 12 expressions. JuA also enhanced autophagy and mitophagy via regulating CaMKK2-AMPK-p-mTOR and PINK1/Parkin pathways. Collectively, these results indicated that JuA protected against type II diabetic nephropathy through inhibiting oxidative stress and apoptosis mediated by mitochondria and ER stress. In addition, autophagy and mitophagy was enhanced by JuA.

摘要

酸枣仁皂苷 A(JuA)是从枣(酸枣仁)种子中分离得到的一种三萜皂苷,具有抗氧化、抗炎和抗细胞凋亡作用。本研究旨在探讨 JuA 对 2 型糖尿病的肾脏保护作用。每日给予 20mg/kg JuA 和 300mg/kg 二甲双胍(Met)治疗 8 周。结果表明,JuA 降低了血糖和肾功能标志物,包括 24 小时尿蛋白、尿β-NAG/尿肌酐、血清尿素氮、血清尿酸和血清肌酐,并缓解了肾脏病理变化。此外,JuA 通过调节呼吸链复合物表达降低了 O 和 HO 水平,增强了 SOD、CAT 和 GPx 活性,降低了 NOX4 表达,改善了线粒体呼吸链功能。此外,JuA 通过下调 Bax、CytC、Apaf-1 和 caspase 9 等线粒体凋亡蛋白的表达,抑制了由 ER 应激引起的细胞凋亡。JuA 还通过下调 p-PERK、p-IRE1、XBP1s、ATF4、p-CHOP 和 caspase 12 的表达,抑制了 ER 应激介导的细胞凋亡。JuA 还通过调节 CaMKK2-AMPK-p-mTOR 和 PINK1/Parkin 通路增强自噬和线粒体自噬。综上所述,这些结果表明 JuA 通过抑制氧化应激和由线粒体和 ER 应激介导的细胞凋亡来保护 2 型糖尿病肾病,此外,JuA 还增强了自噬和线粒体自噬。

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