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钙敏感受体:关于其在钙稳态中的作用及治疗意义的全面综述

The calcium-sensing receptor: a comprehensive review on its role in calcium homeostasis and therapeutic implications.

作者信息

Yuan Ming, Ma Tianrui, Fan Zhiran, Li Jing, Zhang Shenglan

机构信息

Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory) Guangzhou 510005, Guangdong, China.

Cellular Signaling Laboratory, International Research Center for Sensory Biology and Technology of MOST, Key Laboratory of Molecular Biophysics of MOE, College of Life Science and Technology, Huazhong University of Science and Technology Wuhan 430074, Hubei, China.

出版信息

Am J Transl Res. 2025 Mar 15;17(3):2322-2338. doi: 10.62347/QGTS5711. eCollection 2025.

Abstract

The calcium-sensing receptor (CaSR), a key member of the family C G protein-coupled receptors (GPCRs), plays a crucial role in regulating calcium homeostasis and parathyroid hormone (PTH) secretion. It responds to various physiological ligands, including calcium ions and amino acids, activating multiple signaling pathways through interactions with different G proteins and β-arrestin. This review focuses on the structural features of CaSR, emphasizing recent advances in understanding its activation mechanisms via agonists and allosteric modulators. CaSR holds significant therapeutic potential, particularly in treating calcitropic disorders such as hyperparathyroidism and hypoparathyroidism. Current pharmacological agents, including calcimimetics such as cinacalcet and etelcalcetide, have proven effective in managing secondary hyperparathyroidism (SHPT); however, they are associated with side effects such as hypocalcemia. Emerging investigational drugs, including palopegteriparatide and other small molecules, show promise in addressing various calcium-related conditions. Despite challenges that have led to the discontinuation of some drug developments, ongoing research is focused on refining CaSR-targeted therapies to improve efficacy, reduce adverse effects, and enhance patient outcomes.

摘要

钙敏感受体(CaSR)是C类G蛋白偶联受体(GPCR)家族的关键成员,在调节钙稳态和甲状旁腺激素(PTH)分泌中起关键作用。它对包括钙离子和氨基酸在内的各种生理配体作出反应,通过与不同的G蛋白和β-抑制蛋白相互作用激活多种信号通路。本综述重点关注CaSR的结构特征,强调在理解其通过激动剂和变构调节剂激活机制方面的最新进展。CaSR具有显著的治疗潜力,特别是在治疗诸如甲状旁腺功能亢进和甲状旁腺功能减退等钙调节紊乱方面。目前的药物制剂,包括西那卡塞和依特卡肽等拟钙剂,已被证明对治疗继发性甲状旁腺功能亢进(SHPT)有效;然而,它们与诸如低钙血症等副作用相关。新兴的研究药物,包括帕罗培特立帕肽和其他小分子药物,在解决各种与钙相关的病症方面显示出前景。尽管存在导致一些药物研发中断的挑战,但正在进行的研究集中于优化以CaSR为靶点的疗法,以提高疗效、减少不良反应并改善患者预后。

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本文引用的文献

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Nature. 2024 May;629(8011):481-488. doi: 10.1038/s41586-024-07331-1. Epub 2024 Apr 17.
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Allosteric modulation and G-protein selectivity of the Ca-sensing receptor.钙敏感受体的变构调节和 G 蛋白选择性。
Nature. 2024 Feb;626(8001):1141-1148. doi: 10.1038/s41586-024-07055-2. Epub 2024 Feb 7.
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Nanobodies as negative allosteric modulators for human calcium sensing receptor.纳米抗体作为人钙敏感受体的负变构调节剂。
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