黄芪甲苷通过调节TXNIP/NLRP3/GSDMD信号通路减轻糖尿病肾病足细胞凋亡。

IF 3.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Zhibo Hu, Yu Zhou, Cailing Gao, Junfen Liu, Congqing Pan, Jun Guo
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引用次数: 0

摘要

目的:持续性炎症引起的糖尿病并发症包括糖尿病肾病(DKD)。炎症反应程序性细胞死亡的一个基本方法是炭疽热。糖尿病肾病在高血糖环境下进展的主要原因之一是肾常驻细胞的溶解。方法:探讨黄芪甲苷(AS-IV)的抗焦亡作用是否对肾脏具有保护作用。12周后,db/db小鼠经胃灌胃给予40 mg/kg AS-IV。为了验证可能的体外机制,培养小鼠足细胞进行进一步的实验。结果:AS-IV能显著降低db/db小鼠血尿素氮(BUN)、尿蛋白/肌酐比(UACR)、血清肌酐(CREA)和高血糖,减轻肾脏病理改变。此外,AS-IV干预后,NLR家族pyrin结构域pyrin domain containing 3 (NLRP3)、cleaved-caspase-1、gasdermin D (GSDMD)、IL-18和IL-1β下调表达,足细胞标志物podocin和nphs1上调。通过沉默GSDMD,我们在体外证明hg刺激的足细胞发生焦亡。我们还发现AS-IV可以减轻这种焦亡。为了证实AS-IV能够阻止NLRP3炎性体的激活,我们使用了NLRP3抑制剂CY-09。我们还发现as - iv可以抑制TXNIP和NLRP3的表达及其相互作用。TXNIP- sirna处理后,GSDMD表达显著下调,而TXNIP过表达细胞中GSDMD表达上调;这种上调可以用AS-IV来解除。结论:AS-IV通过TXNIP-NLRP3-GSDMD轴抗焦亡作用可改善db/db小鼠的肾功能和足细胞损伤,延缓DKD的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Astragaloside IV attenuates podocyte apoptosis via regulating TXNIP/NLRP3/GSDMD signaling pathway in diabetic nephropathy.

Objectives: Among all the diabetes complications brought on by persistent inflammation is diabetic kidney disease (DKD). One essential method of the inflammatory response's programmed cell death is anthrax. One of the main causes of diabetic renal disease progression in a high-glycemic environment is the lysis of renal resident cells.

Method: This investigation sought to determine whether Astragaloside IV (AS-IV)'s anti-pyroptosis action provides a protective function for the kidneys. For 12 weeks, db/db mice received 40 mg/kg of AS-IV by transgastric gavage. To validate the possible in vitro mechanism, mouse podocytes were cultivated for additional experiments.

Results: In vitro, AS-IV led to a significant reduction in blood urea nitrogen (BUN), urine albumen-to-creatinine ratio (UACR), serum creatinine (CREA), and hyperglycemia in db/db mice and lessen the pathological alterations in the kidney. Moreover, pyrin structural domain of the NLR family pyrin domain containing 3 (NLRP3), cleaved-caspase-1, gasdermin D (GSDMD), IL-18, and IL-1β were down-expressed and podocyte markers podocin and nphs1 were up-regulated following AS-IV intervention. By silencing GSDMD, we demonstrated in vitro that HG-stimulated podocytes undergo pyroptosis. We also discovered that AS-IV can mitigate this pyroptosis. To confirm that AS-IV prevented the NLRP3 inflammasome from activating, the NLRP3 inhibitor CY-09 was employed. It was also discovered that AS-IV prevents the expression of TXNIP and NLRP3 as well as their interaction. GSDMD expression was significantly downregulated following TXNIP-siRNA treatment, whereas GSDMD expression was upregulated in TXNIP overexpression cells; this upregulation could be undone with AS-IV.

Conclusions: The anti-pyroptosis effect of AS-IV via the TXNIP-NLRP3-GSDMD axis improves the renal function and podocyte damage of db/db mice and delays the onset of DKD, according to in vivo and in vitro experimental data.

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来源期刊
Diabetology & Metabolic Syndrome
Diabetology & Metabolic Syndrome ENDOCRINOLOGY & METABOLISM-
CiteScore
6.20
自引率
0.00%
发文量
170
审稿时长
7.5 months
期刊介绍: Diabetology & Metabolic Syndrome publishes articles on all aspects of the pathophysiology of diabetes and metabolic syndrome. By publishing original material exploring any area of laboratory, animal or clinical research into diabetes and metabolic syndrome, the journal offers a high-visibility forum for new insights and discussions into the issues of importance to the relevant community.
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