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Tetrahydropalmatine triggers angiogenesis via regulation of arginine biosynthesis

机译:四氢丙氨酸通过调节精氨酸生物合成来触发血管生成

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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.
机译:在短短20年的时间里,血管生成在伤口愈合、多种癌症、神经缺损、血管损伤和几种眼科疾病的治疗中的核心作用已变得明显。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,但其在血管生成中的作用尚不清楚。在预试验研究中,我们基于中医临床经验,利用分子对接技术证明了THP和VEGFR2的结合潜力。在这里,我们通过药理学分析和基于DESI-MSI/GC-MS的代谢组学研究,确定延胡索乙素(THP)是一种促血管生成触发器,通过调节精氨酸生物合成。首先,通过活体鹌鹑绒毛尿囊膜试验和体外多种内皮细胞模型评估THP的促血管生成作用。根据虚拟筛选,THP的主要机制(2/5的顶部术语具有较小的p值)是代谢途径。因此,代谢组学被应用于THP的主要机制,结果表明,THP改变了精氨酸生物合成中相当大的代谢物差异(p<0.05)。最后,使用靶向代谢组学和药理学分析检测相关指标进行验证,结果表明THP对瓜氨酸-精氨酸通量、精氨酸生物合成和内皮VEGFR2表达的影响依次进行,从而促进血管生成。总的来说,这篇手稿确定THP是促血管生成的触发因子,有可能发展成为未满足临床需求的药理制剂。

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