Huperzine A as a potential therapeutic drug for diabetic nephropathy: Insights from transcriptome, metabolome, microbiome, and network pharmacology analysis

IF 9.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
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Abstract

Aims

Diabetic nephropathy (DN) is a major complication of diabetes mellitus (DM) without curative interventions currently. Huperzine A (Hup A), a natural alkaloid, has demonstrated significant hypoglycemic and anti-inflammatory effects. We aim to investigate the protective effects of Hup A on DN and explore the underlying mechanisms

Methods

We applied STZ induced diabetic rats as DN model and leveraged combination analysis of the transcriptome, metabolome, microbiome, and network pharmacology (NP). The total effect of Hup A on DN was detected (i.e. urine protein, renal tissue structure) and the differential genes were further verified at the level of diabetic patients, db/db mice and cells. Clinical data and small interfering RNA (siRNA)-Apoe were adopted.

Results

Hup A alleviated kidney injury in DN rats. Transcriptomics data and Western blot indicated that the improvement in DN was primarily associated with Apoe and Apoc2. Additionally, metabolomics data demonstrated that DN-induced lipid metabolism disruption was regulated by Hup A, potentially involving sphingosine. Hup A also enriched microbial diversity and ameliorated DN-induced microbiota imbalance. Spearman's correlation analysis demonstrated significant associations among the transcriptome, metabolome, and microbiome. Apoe level was positively correlated with clinical biomarkers in DN patients. Si-Apoe also played protective role in podocytes. NP analysis also suggested that Hup A may treat DN by modulating lipid metabolism, microbial homeostasis, and apoptosis, further validating our findings.

Conclusions

Collectively, we provide the first evidence of the therapeutic effect of Hup A on DN, indicating that Hup A is a potential drug for the prevention and treatment of DN.

作为糖尿病肾病潜在治疗药物的 Huperzine A:转录组、代谢组、微生物组和网络药理学分析的启示。
目的:糖尿病肾病(DN)是糖尿病(DM)的主要并发症之一,目前尚无治疗方法。胡朴素 A(Hup A)是一种天然生物碱,具有显著的降血糖和抗炎作用。方法:我们以 STZ 诱导的糖尿病大鼠为 DN 模型,利用转录组、代谢组、微生物组和网络药理学(NP)的组合分析。检测了 Hup A 对 DN 的总体影响(即尿蛋白、肾组织结构),并在糖尿病患者、db/db 小鼠和细胞水平上进一步验证了差异基因。研究采用了临床数据和小干扰 RNA(siRNA)-Apoe:结果:Hup A 可减轻 DN 大鼠的肾损伤。转录组学数据和 Western 印迹表明,DN 的改善主要与 Apoe 和 Apoc2 有关。此外,代谢组学数据表明,Hup A 可调节 DN 诱导的脂质代谢紊乱,其中可能涉及鞘磷脂。Hup A还丰富了微生物多样性,改善了DN诱导的微生物群失衡。斯皮尔曼相关分析表明,转录组、代谢组和微生物组之间存在显著的关联。载脂蛋白水平与 DN 患者的临床生物标志物呈正相关。Si-载脂蛋白还对荚膜细胞起到保护作用。NP 分析还表明,Hup A 可通过调节脂质代谢、微生物平衡和细胞凋亡来治疗 DN,这进一步验证了我们的研究结果:总之,我们首次提供了 Hup A 对 DN 有治疗作用的证据,表明 Hup A 是一种预防和治疗 DN 的潜在药物。
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来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
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