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健脾益肾方通过激活 SIRT3、调节线粒体动力学和抗氧化作用增强了培哚普利抑制慢性肾脏病进展的作用。

Jian-Pi-Yi-Shen formula enhances perindopril inhibition of chronic kidney disease progression by activation of SIRT3, modulation of mitochondrial dynamics, and antioxidant effects.

机构信息

Department of Nephrology, Shenzhen Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, Guangdong, China.

Shenzhen Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Shenzhen, Guangdong, China.

出版信息

Biosci Rep. 2021 Oct 29;41(10). doi: 10.1042/BSR20211598.

Abstract

Chronic kidney disease (CKD) is a global public health problem. Renin-angiotensin system (RAS) blockade is the mainstay of CKD therapy with limitations. Jian-Pi-Yi-Shen formula (JPYSF) is a traditional herbal decoction and has been used for treating CKD for decades. The purpose of the present study was to investigate the intervention effects of combined used of perindopril erbumine (PE) and JPYSF on CKD progression and explore their underlying mechanisms. CKD rat model was induced by feeding a diet containing 0.75% w/w adenine for 3 weeks. CKD rats were treated with PE or JPYSF or PE+JPYSF from the induction of CKD and lasted 4 weeks. Renal function was evaluated by serum creatinine (Scr) and blood urea nitrogen (BUN). Pathological lesions were observed by Periodic acid-Schiff (PAS) and Masson's trichrome staining. The protein expression was tested by Western blot and immunohistochemistry analysis. The morphology of mitochondria was observed by transmission electron microscope. The results showed that combined used of PE and JPYSF could better improve renal function and pathological lesions and ameliorate renal fibrosis in CKD rats. Administration of PE and JPYSF enhanced sirtuin 3 (SIRT3) expression, inhibited mitochondrial fission, promoted mitochondrial fusion, and suppressed oxidative stress in the kidney of CKD rats. In conclusion, combined use of PE and JPYSF protected against CKD more effectively than either alone. The underlying mechanism may be associated with activation of SIRT3, modulation of mitochondrial dynamics, and antioxidant effects.

摘要

慢性肾脏病(CKD)是一个全球性的公共卫生问题。肾素-血管紧张素系统(RAS)阻断是 CKD 治疗的主要方法,但存在局限性。健脾益肾方(JPYSF)是一种传统的中草药方剂,几十年来一直用于治疗 CKD。本研究旨在探讨培哚普利联合 JPYSF 对 CKD 进展的干预作用,并探讨其潜在机制。通过给予含 0.75%w/w 腺嘌呤的饮食 3 周来诱导 CKD 大鼠模型。在 CKD 诱导后,CKD 大鼠用培哚普利、JPYSF 或培哚普利联合 JPYSF 治疗 4 周。通过血清肌酐(Scr)和血尿素氮(BUN)评估肾功能。通过过碘酸希夫(PAS)和 Masson 三色染色观察病理损伤。通过 Western blot 和免疫组化分析检测蛋白表达。通过透射电子显微镜观察线粒体形态。结果表明,培哚普利联合 JPYSF 能更好地改善 CKD 大鼠的肾功能和病理损伤,减轻肾纤维化。培哚普利和 JPYSF 的联合应用增强了沉默信息调节因子 3(SIRT3)的表达,抑制了线粒体分裂,促进了线粒体融合,并抑制了 CKD 大鼠肾脏的氧化应激。总之,培哚普利联合 JPYSF 的疗效优于单独使用。其潜在机制可能与 SIRT3 的激活、线粒体动力学的调节和抗氧化作用有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22ce/8536834/ad3b6e815104/bsr-41-bsr20211598-g1.jpg

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