β3-肾上腺素能受体:结构、疾病的生理病理和新出现的治疗潜力。

IF 2.1 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI:10.1155/2024/2005589
Julius T Dongdem, Axandrah E Etornam, Solomon Beletaa, Issah Alidu, Hassan Kotey, Cletus A Wezena
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引用次数: 0

摘要

β-肾上腺素能受体信号级联的发现和表征使得有效靶向受体进行药物开发成为可能。β-肾上腺素能受体是一类a类视紫红质型的G蛋白偶联受体(gpcr),主要受儿茶酚胺的刺激,因此介导副交感神经系统的多种作用,引发“战斗或逃跑”型反应。在几种人体组织中可以检测到它们,它们控制着过多的生理过程,因此有助于几种疾病的发病机制。鉴于β-肾上腺素能受体作为许多病理条件的分子靶点的相关性,本文旨在对β-肾上腺素能受体的最新研究进展进行深入探讨。更重要的是,我们深入研究了β3-肾上腺素能受体在各种临床领域作为治疗靶点的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The β3-Adrenergic Receptor: Structure, Physiopathology of Disease, and Emerging Therapeutic Potential.

The discovery and characterization of the signal cascades of the β-adrenergic receptors have made it possible to effectively target the receptors for drug development. β-Adrenergic receptors are a class A rhodopsin type of G protein-coupled receptors (GPCRs) that are stimulated mainly by catecholamines and therefore mediate diverse effects of the parasympathetic nervous system in eliciting "fight or flight" type responses. They are detectable in several human tissues where they control a plethora of physiological processes and therefore contribute to the pathogenesis of several disease conditions. Given the relevance of the β-adrenergic receptor as a molecular target for many pathological conditions, this comprehensive review aims at providing an in-depth exploration of the recent advancements in β3-adrenergic receptor research. More importantly, we delve into the prospects of the β3-adrenergic receptor as a therapeutic target across a variety of clinical domains.

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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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