Tanshinone IIA reduces tubulointerstitial fibrosis by suppressing GSDMD-mediated pyroptosis.

IF 3.9 3区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Pharmaceutical Biology Pub Date : 2025-12-01 Epub Date: 2025-05-07 DOI:10.1080/13880209.2025.2498166
Xueling Yang, Qinglin Luo, Zhifen Wu, Chunxuan Wang, Yuanjing Yang, Luquan Zheng, Ke Li, Lei Zhao, Yang Jurong
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引用次数: 0

Abstract

Context: Tanshinone IIA (Tan IIA), a bioactive compound derived from the traditional Chinese herb Salvia miltiorrhiza (Family Lamiaceae, Authority Bunge), is well-known for its protective effects in various kidney diseases. However, its role in obstructive nephropathy has not been thoroughly investigated.

Objective: This study aimed to explore the protective effects of Tan IIA in a mouse model of unilateral ureteral obstruction (UUO) and to elucidate the cellular and molecular mechanisms underlying these effects.

Materials and methods: Gasdermin D (GSDMD) knockout mice and their wild-type (WT) littermates underwent UUO surgery, with Tan IIA treatment administered 24 h prior. Human proximal tubular cells (HK-2 cells) were treated with TGF-β1 to induce fibrosis (50 ng/mL for 24 h), followed by Tan IIA treatment (5 μM) for an additional 3 h.

Results: Tan IIA significantly reduced the expression of extracellular matrix (ECM) components, including collagen I, α-smooth muscle actin (α-SMA), vimentin and fibronectin, in UUO mice. Tan IIA attenuated GSDMD-mediated pyroptosis. However, in GSDMD knockout mice subjected to UUO, the protective effects of Tan IIA on ECM gene expression and collagen deposition in the tubular interstitium were reduced. In vitro studies showed that Tan IIA reduced GSDMD activation and fibronectin protein expression in HK-2 cells.

Discussion and conclusions: Tan IIA may mitigate GSDMD-mediated pyroptosis in renal tubular epithelial cells (RTECs) and reduce kidney fibrosis, highlighting its potential as a therapeutic strategy to prevent the progression of kidney disease after ureteral obstruction.

丹参酮IIA通过抑制gsdmd介导的焦亡来减少小管间质纤维化。
背景:丹参酮IIA (Tan IIA)是一种从中药丹参(丹参科,丹参科)中提取的生物活性化合物,因其对多种肾脏疾病的保护作用而闻名。然而,其在阻塞性肾病中的作用尚未被彻底研究。目的:探讨坦IIA对小鼠单侧输尿管梗阻(UUO)模型的保护作用,并探讨其细胞和分子机制。材料和方法:GSDMD基因敲除小鼠及其野生型(WT)仔鼠进行UUO手术,并在手术前24 h给予Tan IIA治疗。用TGF-β1 (50 ng/mL)诱导人近端小管细胞(HK-2细胞)纤维化24 h,再用5 μM的Tan IIA处理3 h。结果:Tan IIA显著降低UUO小鼠细胞外基质(ECM)成分,包括I型胶原、α-平滑肌肌动蛋白(α-SMA)、vimentin和纤维连接蛋白的表达。Tan IIA可减弱gsdmd介导的焦亡。然而,在UUO作用下的GSDMD基因敲除小鼠中,Tan IIA对ECM基因表达和小管间质胶原沉积的保护作用减弱。体外研究表明,Tan IIA可降低HK-2细胞中GSDMD的活化和纤维连接蛋白的表达。讨论和结论:Tan IIA可能减轻gsdmd介导的肾小管上皮细胞(RTECs)焦亡,减少肾纤维化,突出其作为预防输尿管梗阻后肾脏疾病进展的治疗策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutical Biology
Pharmaceutical Biology 医学-药学
CiteScore
6.70
自引率
2.60%
发文量
191
审稿时长
1 months
期刊介绍: Pharmaceutical Biology will publish manuscripts describing the discovery, methods for discovery, description, analysis characterization, and production/isolation (including sources and surveys) of biologically-active chemicals or other substances, drugs, pharmaceutical products, or preparations utilized in systems of traditional medicine. Topics may generally encompass any facet of natural product research related to pharmaceutical biology. Papers dealing with agents or topics related to natural product drugs are also appropriate (e.g., semi-synthetic derivatives). Manuscripts will be published as reviews, perspectives, regular research articles, and short communications. The primary criteria for acceptance and publication are scientific rigor and potential to advance the field.
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