Comprehensive Evaluation of Triptolide’s Therapeutic Mechanisms in Diabetic Kidney Disease via Meta-Analysis, Network Pharmacology, Molecular Docking, and Mendelian Randomization

雷公藤甲素 孟德尔随机化 药理学 疾病 对接(动物) 医学 计算生物学 生物信息学 生物 内科学 遗传学 基因 基因型 护理部 细胞凋亡 遗传变异
作者
Jing Ni,Siyuan Song,Yi Wei,Qiling Zhang,Wei Li,Jiangyi Yu
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:32 (10): 791-810
标识
DOI:10.2174/0113816128367671250714100708
摘要

INTRODUCTION: Diabetic kidney disease (DKD) is a devastating complication of diabetes for which there are few potent treatments.Triptolide (TP), an active compound from Tripterygium wilfordii, has shown potential in early studies, but its therapeutic mechanisms in DKD are not fully understood. This study aims to systematically evaluate TP's efficacy and mechanisms using meta-analysis, network pharmacology, molecular docking, and Mendelian randomization (MR). METHODS: A comprehensive search across Chinese and English databases identified animal randomized controlled trials (RCTs) assessing the effects of TP on DKD. A total of 27 studies were incorporated, and a metaanalysis was conducted via Review Manager. TP's drug and disease targets were identified through network pharmacology and molecular docking, while bioinformatics methods were employed to explore the mechanisms. MR analysis was performed to assess potential causal relationships between TP and DKD-related targets. RESULTS: Meta-analysis showed that TP significantly reduced urinary protein, blood lipids, and glucose levels, while improving renal function, renal weight, and renal index (all p < 0.05). Seven core targets-IFNG, CXCL8, TNF, TGFB1, IL2, IL4, and RELA-were identified via network pharmacology, involving key pathways such as lipid-atherosclerosis, AGE-RAGE, and IL-17 signaling. Molecular docking demonstrated strong binding affinities between TP and these targets, with binding energies below -7.00 kJ/mol. Although MR analysis did not establish direct causal relationships between these core genes and DKD, a significant negative correlation between TNF, IL4, and GFR was observed, suggesting their involvement in DKD progression. DISCUSSION: . CONCLUSION: TP exerts therapeutic effects on DKD through multi-target and multi-pathway mechanisms, primarily involving immunomodulation, anti-inflammation, anti-oxidation, and anti-fibrosis processes.
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