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黄芪甲苷IV通过调节糖尿病肾病中TXNIP/NLRP3/GSDMD信号通路减轻足细胞凋亡。

Astragaloside IV attenuates podocyte apoptosis via regulating TXNIP/NLRP3/GSDMD signaling pathway in diabetic nephropathy.

作者信息

Hu Zhibo, Zhou Yu, Gao Cailing, Liu Junfen, Pan Congqing, Guo Jun

机构信息

NHC Key Laboratory of Hormones and Development (Tianjin Medical University), Tianjin Key Laboratory of Metabolic Diseases, Tianjin Medical University Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin, 300134, China.

出版信息

Diabetol Metab Syndr. 2024 Dec 18;16(1):296. doi: 10.1186/s13098-024-01546-y.

Abstract

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.

摘要

目的

持续性炎症引发的糖尿病并发症中包括糖尿病肾病(DKD)。焦亡是炎症反应中程序性细胞死亡的一种重要方式。肾固有细胞的裂解是高血糖环境下糖尿病肾病进展的主要原因之一。

方法

本研究旨在确定黄芪甲苷IV(AS-IV)的抗焦亡作用是否对肾脏具有保护作用。db/db小鼠通过灌胃给予40mg/kg的AS-IV,持续12周。为验证可能的体外机制,培养小鼠足细胞进行进一步实验。

结果

在体外,AS-IV可使db/db小鼠的血尿素氮(BUN)、尿白蛋白与肌酐比值(UACR)、血清肌酐(CREA)显著降低,并减轻高血糖,减轻肾脏的病理改变。此外,AS-IV干预后,含NLR家族pyrin结构域蛋白3(NLRP3)、裂解的半胱天冬酶-1、gasdermin D(GSDMD)、IL-18和IL-1β表达下调,足细胞标志物足突蛋白和NPHS1表达上调。通过沉默GSDMD,我们在体外证明高糖刺激的足细胞发生焦亡。我们还发现AS-IV可减轻这种焦亡。为证实AS-IV可防止NLRP3炎性小体激活,使用了NLRP3抑制剂CY-09。还发现AS-IV可抑制硫氧还蛋白互作蛋白(TXNIP)和NLRP3的表达及其相互作用。TXNIP-siRNA处理后GSDMD表达显著下调,而在TXNIP过表达细胞中GSDMD表达上调;AS-IV可逆转这种上调。

结论

体内和体外实验数据表明,AS-IV通过TXNIP-NLRP3-GSDMD轴的抗焦亡作用改善了db/db小鼠的肾功能和足细胞损伤,延缓了DKD的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8544/11656976/02547e029f21/13098_2024_1546_Fig1_HTML.jpg

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