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鉴定一种可口服的小分子 PTHR1 激动剂,用于治疗甲状旁腺功能减退症。

Identification of an orally active small-molecule PTHR1 agonist for the treatment of hypoparathyroidism.

机构信息

Research Division, Chugai Pharmaceutical Co., Ltd., 1-135, Komakado, Gotemba, Shizuoka 412-8513, Japan.

出版信息

Nat Commun. 2016 Nov 18;7:13384. doi: 10.1038/ncomms13384.

Abstract

Parathyroid hormone (PTH) is essential for calcium homeostasis and its action is mediated by the PTH type 1 receptor (PTHR1), a class B G-protein-coupled receptor. Hypoparathyroidism and osteoporosis can be treated with PTH injections; however, no orally effective PTH analogue is available. Here we show that PCO371 is a novel, orally active small molecule that acts as a full agonist of PTHR1. PCO371 does not affect the PTH type 2 receptor (PTHR2), and analysis using PTHR1-PTHR2 chimeric receptors indicated that Proline 415 of PTHR1 is critical for PCO371-mediated PTHR1 activation. Oral administration of PCO371 to osteopenic rats provokes a significant increase in bone turnover with limited increase in bone mass. In hypocalcemic rats, PCO371 restores serum calcium levels without increasing urinary calcium, and with stronger and longer-lasting effects than PTH injections. These results strongly suggest that PCO371 can provide a new treatment option for PTH-related disorders, including hypoparathyroidism.

摘要

甲状旁腺激素(PTH)对钙稳态至关重要,其作用是通过甲状旁腺激素 1 型受体(PTHR1)介导的,PTHR1 是一种 B 类 G 蛋白偶联受体。甲状旁腺功能减退症和骨质疏松症可以用 PTH 注射治疗;然而,目前还没有有效的口服 PTH 类似物。本文研究表明,PCO371 是一种新型的、具有口服活性的小分子,作为 PTHR1 的完全激动剂。PCO371 不影响甲状旁腺激素 2 型受体(PTHR2),使用 PTHR1-PTHR2 嵌合受体分析表明,PTHR1 中的脯氨酸 415 对 PCO371 介导的 PTHR1 激活至关重要。给予骨质疏松大鼠口服 PCO371 可显著增加骨转换,而骨量增加有限。在低钙血症大鼠中,PCO371 可恢复血清钙水平而不增加尿钙,且作用比 PTH 注射更强、更持久。这些结果强烈表明,PCO371 可为包括甲状旁腺功能减退症在内的 PTH 相关疾病提供新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3792/5120204/bf37bb615dc5/ncomms13384-f1.jpg

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