Ma Xiurui, Yang Jinjing, Yang Guanrui, Li Lei, Hao Xiaojun, Wang Guoqin, An Jian, Wang Fei
Department of Cardiology, Shanxi Cardiovascular Hospital, Taiyuan, China.
Front Cardiovasc Med. 2022 Jun 2;9:910323. doi: 10.3389/fcvm.2022.910323. eCollection 2022.
Diabetes mellitus (DM) is accompanied by a series of macrovascular and microvascular injuries. Critical limb ischemia is the most severe manifestation of peripheral artery disease (PAD) caused by DM and is almost incurable. Therapeutic modulation of angiogenesis holds promise for the prevention of limb ischemia in diabetic patients with PAD. However, no small-molecule drugs are capable of promoting diabetic angiogenesis. An endogenous tryptophan metabolite, indole-3-aldehyde (3-IAld), has been found to have proangiogenic activity in endothelial cells. Nevertheless, the role of 3-IAld in diabetic angiogenesis remains unknown. Here, we found that 3-IAld ameliorated high glucose-induced mitochondrial dysfunction, decreasing oxidative stress and apoptosis and thus improving neovascularization.
糖尿病(DM)伴有一系列大血管和微血管损伤。严重肢体缺血是糖尿病引起的外周动脉疾病(PAD)最严重的表现,几乎无法治愈。血管生成的治疗性调节有望预防患有PAD的糖尿病患者的肢体缺血。然而,目前尚无能够促进糖尿病血管生成的小分子药物。一种内源性色氨酸代谢产物,吲哚 - 3 - 醛(3 - IAld),已被发现在内皮细胞中具有促血管生成活性。然而,3 - IAld在糖尿病血管生成中的作用仍然未知。在此,我们发现3 - IAld改善了高糖诱导的线粒体功能障碍,降低了氧化应激和细胞凋亡,从而改善了新生血管形成。