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肾上腺髓质素:一种用于散发性和遗传性血管性认知障碍的血管活性药物。

Adrenomedullin: A vasoactive agent for sporadic and hereditary vascular cognitive impairment.

作者信息

Ihara Masafumi, Washida Kazuo, Yoshimoto Takeshi, Saito Satoshi

机构信息

Department of Neurology, National Cerebral and Cardiovascular Center, 6-1 Kishibe Shimmachi, Suita, Osaka 564-8565 Japan.

出版信息

Cereb Circ Cogn Behav. 2021 Mar 4;2:100007. doi: 10.1016/j.cccb.2021.100007. eCollection 2021.

Abstract

Adrenomedullin (AM) is an endogenous peptide mainly secreted from endothelial cells, which has multiple physiological actions such as anti-inflammation, vasodilation, vascular permeability regulation and angiogenesis. Blood AM levels are upregulated in a variety of pathological states including sepsis, severe COVID-19, acute ischemic stroke and vascular cognitive impairment with white matter changes, likely serving as a compensatory biological defense response against infection and ischemia. AM is currently being tested in clinical trials for ulcerative colitis, Crohn's disease, severe COVID-19 for its anti-inflammatory properties and in ischemic stroke for its additional angiogenic action. AM has been proposed as a therapeutic option for vascular cognitive impairment as its arteriogenic and angiogenic properties are thought to contribute to a slowing of cognitive decline in mice after chronic cerebral hypoperfusion. As AM promotes differentiation of oligodendrocyte precursor cells into mature oligodendrocytes under hypoxic conditions, AM could also be used in the treatment of CADASIL, where reduced oxygen delivery is thought to lead to the death of hypoxia-prone oligodendrocytes. AM therefore holds potential as an innovative therapeutic drug, which may regenerate blood vessels, while controlling inflammation in cerebrovascular diseases.

摘要

肾上腺髓质素(AM)是一种主要由内皮细胞分泌的内源性肽,具有多种生理作用,如抗炎、血管舒张、调节血管通透性和血管生成。在包括脓毒症、重症新型冠状病毒肺炎、急性缺血性卒中和伴有白质改变的血管性认知障碍在内的多种病理状态下,血液中的AM水平会升高,这可能是机体针对感染和缺血的一种代偿性生物防御反应。目前,AM正在进行溃疡性结肠炎、克罗恩病、重症新型冠状病毒肺炎的抗炎特性以及缺血性卒中的促血管生成作用的临床试验。由于AM的促动脉生成和促血管生成特性被认为有助于减缓慢性脑灌注不足小鼠的认知衰退,因此它已被提议作为血管性认知障碍的一种治疗选择。由于AM在缺氧条件下可促进少突胶质前体细胞分化为成熟的少突胶质细胞,因此AM也可用于治疗伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL),该病中氧输送减少被认为会导致易缺氧的少突胶质细胞死亡。因此,AM作为一种创新治疗药物具有潜力,它可能在控制脑血管疾病炎症的同时实现血管再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c63/9616331/2481451be874/gr1.jpg

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