Huaiqihuang (HQH) protects podocytes from high glucose-induced apoptosis and inflammation response by regulating PI3K/AKT/mTOR pathway.

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Archives of Physiology and Biochemistry Pub Date : 2024-09-27 DOI:10.1080/13813455.2024.2407552
Peipei Zhang, Zhilong Liu, Guiqiao Ma, Junwei Wang, Jing Shao, Chaojing Ma, Liping Wang, Chanjuan Ma
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Abstract

Diabetic kidney disease (DKD) is one of the common microvascular complications of diabetes, and there are still lack of effective treatments. Huaiqihuang (HQH) is a kind of traditional Chinese medicine mixed preparation, which is mainly made of Trametes robiniophila Murr, Fructus Lycii, and Polygonatum sibiricumhas. It has been shown to be effective in the treatment of DKD, but the specific mechanism has not been fully elucidated. Our results showed that HQH increased the protein expressions of synaptopodin, podocin, WT-1, and Bcl-2, decreased the protein expressions of Bax and cleaved-casepase-3, and activated the NF-ĸB and PI3K/AKT/mTOR pathway in MPC5 cells exposed to high-glucose (HG). Real-time PCR results showed that HQH reduced the mRNA expression of TNF-α, IL-1β, MCP-1, and IL-6. In conclusion, our results showed that HQH may attenuate podocyte injury by inhibiting MPC5 cell apoptosis induced by HG and NF-κB-mediated inflammation response through activation of the PI3K/AKT/mTOR pathway.

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怀其黄(HQH)通过调节 PI3K/AKT/mTOR 通路,保护荚膜细胞免受高糖诱导的细胞凋亡和炎症反应的影响。
糖尿病肾病(DKD)是糖尿病常见的微血管并发症之一,目前仍缺乏有效的治疗方法。怀其黄是一种中药复方制剂,主要由罗汉果、枸杞子和何首乌组成。它对治疗 DKD 有一定疗效,但具体机制尚未完全阐明。我们的研究结果表明,在暴露于高葡萄糖(HG)的MPC5细胞中,HQH可增加突触素、荚膜素、WT-1和Bcl-2的蛋白表达,降低Bax和裂解酶-3的蛋白表达,并激活NF-ĸB和PI3K/AKT/mTOR通路。实时 PCR 结果显示,HQH 可降低 TNF-α、IL-1β、MCP-1 和 IL-6 的 mRNA 表达。总之,我们的研究结果表明,HQH 可通过激活 PI3K/AKT/mTOR 通路,抑制 HG 诱导的 MPC5 细胞凋亡和 NF-κB 介导的炎症反应,从而减轻荚膜损伤。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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