黑素皮质素受体:治疗色素沉着、炎症、应激、体重失调和性功能障碍的新靶点。

IF 3 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Miteshkumar Maurya, Renuka Munshi, Sachin Zambre
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引用次数: 1

摘要

黑素皮质素是由原黑素皮质素翻译后裂解形成的微小蛋白质分子。这些是生物活性肽,负责人类和低等动物的色素沉着模式,能量稳态和性功能调节。这些肽通过在中枢神经系统和外周组织中产生来调节许多生理功能。根据最近的研究,黑素皮质激素通过与单独的G蛋白家族、两种主要的蛋白水解酶——前转化酶1和前转化酶2结合,产生各种生物效应。这些突破为研究黑素皮质素、拮抗剂和受体在许多生理活动中的作用开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Melanocortin Receptors: Emerging Targets for the Treatment of Pigmentation, Inflammation, Stress, Weight Disorders and Sexual Dysfunction.

Melanocortins are tiny protein molecules formed by the post-translational cleavage of proopiomelanocortin. These are bioactive peptides that are responsible for human and lower animal pigmentation patterns, energy homeostasis, and sexual function modulation. These peptides regulate numerous physiological functions by being generated in the central nervous system and peripheral tissues. Melanocortins elicit their varied biological effects by binding to a separate family of G protein, two primary proteolytic enzymes, proconvertases 1 and 2, according to recent research. These breakthroughs have opened up new avenues for research into the role of melanocortins, antagonists, and receptors in a number of physiological activities.

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来源期刊
Current drug targets
Current drug targets 医学-药学
CiteScore
6.20
自引率
0.00%
发文量
127
审稿时长
3-8 weeks
期刊介绍: Current Drug Targets aims to cover the latest and most outstanding developments on the medicinal chemistry and pharmacology of molecular drug targets e.g. disease specific proteins, receptors, enzymes, genes. Current Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of drug targets. The journal also accepts for publication mini- & full-length review articles and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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