Palmatine reverse aristolochic acid-induced heart failure through activating EGFR pathway via upregulating IKBKB

马兜铃酸 巴马汀 医学 化学 生物 药理学 小檗碱 遗传学
作者
Ying Hu,Lixin Chen,Yulin Wu,Jilei Zhang,Z. M. Sheng,Ziyi Zhou,Youmei Xie,GY Tian,Jifeng Wan,X. B. Zhang,Na Cai,Yatong Zhou,Cao Yi,Tao Yang,Xiaomei Chen,Dalong Liao,Yurui Ge,Bo Cheng,Keyuan Zhong,Erli Tian,Lü Jin,Huiqiang Lu,Yan Zhao,Wei Yuan
出处
期刊:Ecotoxicology and Environmental Safety [Elsevier]
卷期号:285: 117100-117100
标识
DOI:10.1016/j.ecoenv.2024.117100
摘要

Aristolochic acid (AA) is renowned for engendering nephrotoxicity and teratogenicity. Previous literature has reported that AA treatment resulted in heart failure (HF) via inflammatory pathways. Yet, its implications in HF remain comparatively uncharted territory, particularly with respect to underlying mechanisms. In our study, the zebrafish model was employed to delineate the cardiotoxicity of AA exposure and the restorative capacity of a phytogenic alkaloid palmatine (PAL). PAL restored morphology and blood supply in AA-damaged hearts by o-dianisidine staining, fluorescence imaging, and Hematoxylin and Eosin staining. Furthermore, PAL attenuated the detrimental effects of AA on ATPase activity, implying myocardial energy metabolism recovery. PAL decreased the co-localization of neutrophils with cardiomyocytes, implying an attenuation of the inflammatory response induced by AA. A combination of network pharmacological analysis and qPCR validation shed light on the therapeutic mechanism of PAL against AA-induced heart failure via upregulation of the epidermal growth factor receptor (EGFR) signaling pathway. Subsequent evaluations using a transcriptological testing, inhibitor model, and molecular docking assay corroborated PAL as an IKBKB enzyme activator. The study underscores the possible exploitation of the EGFR pathway as a potential therapeutic target for PAL against AA-induced HF, thus furthering the continued investigation of the toxicology and advancement of protective pharmaceuticals for AA.

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