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四氢巴马汀通过调节精氨酸生物合成触发血管生成。

Tetrahydropalmatine triggers angiogenesis via regulation of arginine biosynthesis.

机构信息

School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, PR China.

Waters Technology Co.,Ltd, Beijing, PR China.

出版信息

Pharmacol Res. 2021 Jan;163:105242. doi: 10.1016/j.phrs.2020.105242. Epub 2020 Oct 16.

DOI:10.1016/j.phrs.2020.105242
PMID:33075491
Abstract

Over a short span of two decades, the central role of angiogenesis in the treatment of wound healing, diverse cancers, nerve defect, vascular injury and several ophthalmic diseases has become evident. Tetrahydropalmatine, as the index component of Corydalis yanhusuo W. T. Wang, is inseparable from protecting cardiovascular system, yet its role in angiogenesis has been poorly characterized. We have demonstrated the binding potential of THP and VEGFR2 using molecular docking based on the clinical experience of traditional Chinese medicine in the pretest study. Here, we identified tetrahydropalmatine (THP) as one proangiogenic trigger via regulation of arginine biosynthesis by pharmacological assays and DESI-MSI/GC-MS based metabolomics. First, the proangiogenic effects of THP were evaluated by quail chorioallantoic membrane test in vivo and multiple models of endothelial cells in vitro. According to virtual screening, the main mechanisms of THP (2/5 of the top terms with smaller p-value) were metabolic pathways. Hence, metabolomics was applied for the main mechanisms of THP and results showed the considerable metabolite difference in arginine biosynthesis (p < 0.05) altered by THP. Finally, correlated indicators were deteced using targeted metabolomics and pharmacological assays for validation, and results suggested the efficacy of THP on citrulline to arginine flux, arginine biosynthesis, and endothelial VEGFR2 expression sequentially, leading to the promotion of angiogenesis. Overall, this manuscript identified THP as the proangiogenic trigger with the potential to develop as pharmacological agents for unmet clinical needs.

摘要

在短短二十年的时间里,血管生成在治疗伤口愈合、各种癌症、神经缺损、血管损伤和几种眼科疾病中的核心作用已经变得显而易见。延胡索乙素作为延胡索的指标成分,与保护心血管系统密不可分,但它在血管生成中的作用尚未得到充分描述。我们在预试验研究中基于中药的临床经验,使用分子对接证明了 THP 与 VEGFR2 的结合潜力。在这里,我们通过药理学测定和基于 DESI-MSI/GC-MS 的代谢组学鉴定了延胡索乙素(THP)作为一种通过调节精氨酸生物合成促进血管生成的触发因子。首先,通过体内鹌鹑鸡胚绒毛尿囊膜试验和多种体外内皮细胞模型评估了 THP 的促血管生成作用。根据虚拟筛选,THP 的主要作用机制(前 5 个术语中有 2 个,p 值较小)是代谢途径。因此,应用代谢组学研究 THP 的主要作用机制,结果显示 THP 可显著改变精氨酸生物合成中的代谢物差异(p < 0.05)。最后,通过靶向代谢组学和药理学测定检测相关指标进行验证,结果表明 THP 对瓜氨酸到精氨酸通量、精氨酸生物合成和内皮 VEGFR2 表达的功效依次促进了血管生成。总的来说,本研究确定了 THP 作为一种促血管生成的触发因子,具有开发成满足未满足的临床需求的药理学药物的潜力。

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