Molecular pharmacology of the calcitonin receptor.

B. Purdue, N. Tilakaratne, P. Sexton
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引用次数: 97

Abstract

The peptide hormone calcitonin is widely used therapeutically in the treatment of bone disorders such as Paget's disease, osteoporosis, and the hypercalcemia of some malignancies. However, emerging evidence suggests the actions of calcitonin via its G protein-coupled receptor, the calcitonin receptor, may not be limited to bone. Calcitonin receptors have also been identified in the central nervous system, testes, skeletal muscle, lymphocytes, and the placenta. We are now becoming aware that the complexity of the calcitonin response mediated by the calcitonin receptor can be influenced by accessory proteins, receptor isoforms, genetic polymorphisms, developmental and/or transcriptional regulation, feedback inhibition, and the specific cellular or tissue background. This article discusses what is known about the molecular and pharmacological actions of the calcitonin receptor and highlights areas of current research.
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降钙素受体的分子药理学。
肽激素降钙素被广泛用于治疗骨疾病,如佩吉特病、骨质疏松症和一些恶性肿瘤的高钙血症。然而,新出现的证据表明,降钙素通过其G蛋白偶联受体(降钙素受体)的作用可能并不局限于骨骼。降钙素受体也在中枢神经系统、睾丸、骨骼肌、淋巴细胞和胎盘中被发现。我们现在意识到,降钙素受体介导的降钙素反应的复杂性可受辅助蛋白、受体同种异构体、遗传多态性、发育和/或转录调控、反馈抑制以及特定的细胞或组织背景的影响。本文讨论了已知的降钙素受体的分子和药理作用,并强调了当前研究的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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