You Wu, Yixiao Han, Jiahui Wang, Lijing Du, Younes Zaid, Zhengchun Wang, Xiaomeng Lin, Xudong Cai, Xin Peng
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引用次数: 0
Abstract
Ethnopharmacological relevance: Wenyang Xiaozheng Decoction (WXD) is traditionally prescribed for chronic kidney disease based on the principle of warming yang and resolving blood stasis. However, whether its anti-fibrotic effects involve inflammation-associated pyroptosis remains unclear.
Aim of the study: To evaluate the effects of WXD on renal fibrosis and associated changes in NF-κB- and pyroptosis-related signaling.
Materials and methods: Thirty-six male C57BL/6 mice were allocated to six groups and subjected to sham surgery or unilateral ureteral obstruction (UUO) with or without valsartan or graded doses of WXD. The effects of WXD were further evaluated in TGF-β1/TNF-α-stimulated HK-2 cells. Kidney transcriptomics was integrated with serum pharmacochemistry-based network pharmacology restricted to blood-absorbed constituents. Pharmacological perturbations using necrosulfonamide (NSA) and lipopolysaccharide (LPS) were performed in HK-2 cells.
Results: High-dose WXD reduced serum BUN, renal fibrotic area, and GSDMD-N expression by 24.7%, 27.6%, and 29.1%, respectively, compared with UUO mice (all P < 0.05). Transcriptomic analysis showed that WXD reversed UUO-induced activation of NF-κB, TNF, and NOD-like receptor signaling. Integration with serum pharmacochemistry identified 36 blood-absorbed constituents and yielded inflammation-related target and pathway profiles consistent with the transcriptomic findings. WXD reduced the abundance of phosphorylated p65, cleaved caspase-1, and GSDMD-N in vivo and in vitro. NSA partially reproduced, whereas LPS partially counteracted, the protective effects of WXD.
Conclusions: WXD attenuates renal fibrosis in association with reduced NF-κB- and pyroptosis-associated signaling. Integrating transcriptomics with network pharmacology based on blood-absorbed constituents provides a biologically relevant strategy for investigating multi-component traditional Chinese medicine formulas.
民族药理学相关性:温阳消正汤是治疗慢性肾脏病的传统方药,以温阳化瘀为原则。然而,其抗纤维化作用是否涉及炎症相关的焦亡尚不清楚。研究目的:探讨水解方对大鼠肾纤维化的影响及相关NF-κ b -和热释相关信号通路的改变。材料与方法:雄性C57BL/6小鼠36只,随机分为6组,分别给予或不给予缬沙坦或分级剂量的白化丹进行假手术或单侧输尿管梗阻。在TGF-β1/TNF-α-刺激的HK-2细胞中进一步评估WXD的作用。肾脏转录组学与基于血液吸收成分的血清药物化学网络药理学相结合。在HK-2细胞中使用necrosulfonamide (NSA)和脂多糖(LPS)进行药理学扰动。结果:与UUO小鼠相比,高剂量WXD使血清BUN、肾纤维化面积、GSDMD-N表达分别降低24.7%、27.6%、29.1%(均P < 0.05)。转录组学分析显示,WXD逆转了uuo诱导的NF-κB、TNF和nod样受体信号的激活。结合血清药物化学鉴定了36种血液吸收成分,并得出了与炎症相关的靶标和途径谱,与转录组学结果一致。WXD在体内和体外均降低了磷酸化p65、裂解caspase-1和GSDMD-N的丰度。NSA部分再现了WXD的保护作用,而LPS部分抵消了WXD的保护作用。结论:WXD减轻肾纤维化与NF-κ b -和焦热相关信号的减少有关。将转录组学与基于血液吸收成分的网络药理学相结合,为研究多组分中药方剂提供了一种与生物学相关的策略。
期刊介绍:
The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.