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Platelet Endothelial Cell Adhesion Molecule-1 and Oligodendrogenesis: Significance in Alcohol Use Disorders

机译:血小板内皮细胞粘附分子-1和少突胶质生成:在酒精使用障碍中的意义。

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摘要

Alcoholism is a chronic relapsing disorder with few therapeutic strategies that address the core pathophysiology. Brain tissue loss and oxidative damage are key components of alcoholism, such that reversal of these phenomena may help break the addictive cycle in alcohol use disorder (AUD). The current review focuses on platelet endothelial cell adhesion molecule 1 (PECAM-1), a key modulator of the cerebral endothelial integrity and neuroinflammation, and a targetable transmembrane protein whose interaction within AUD has not been well explored. The current review will elaborate on the function of PECAM-1 in physiology and pathology and infer its contribution in AUD neuropathology. Recent research reveals that oligodendrocytes, whose primary function is myelination of neurons in the brain, are a key component in new learning and adaptation to environmental challenges. The current review briefly introduces the role of oligodendrocytes in healthy physiology and neuropathology. Importantly, we will highlight the recent evidence of dysregulation of oligodendrocytes in the context of AUD and then discuss their potential interaction with PECAM-1 on the cerebral endothelium.
机译:酒精中毒是一种慢性复发性疾病,几乎没有针对核心病理生理的治疗策略。脑组织损失和氧化损伤是酒精中毒的关键因素,因此这些现象的逆转可能有助于打破酒精使用障碍(AUD)的成瘾周期。目前的审查集中在血小板内皮细胞粘附分子1(PECAM-1),脑内皮完整性和神经炎症的关键调节器,和可靶向跨膜蛋白,其在AUD内的相互作用尚未得到很好的研究。当前的审查将详述PECAM-1在生理和病理学中的功能,并推断其在AUD神经病理学中的作用。最近的研究表明,少突胶质细胞的主要功能是大脑神经元的髓鞘形成,是新学习和适应环境挑战的关键组成部分。本综述简要介绍了少突胶质细胞在健康生理学和神经病理学中的作用。重要的是,我们将重点介绍AUD背景下少突胶质细胞失调的最新证据,然后讨论它们与PECAM-1在脑内皮上的潜在相互作用。

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