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

被引:47
|
作者
Tamura, Tatsuya [1 ]
Noda, Hiroshi [1 ]
Joyashiki, Eri [1 ]
Hoshino, Maiko [1 ]
Watanabe, Tomoyuki [1 ]
Kinosaki, Masahiko [1 ]
Nishimura, Yoshikazu [1 ]
Esaki, Tohru [1 ]
Ogawa, Kotaro [1 ]
Miyake, Taiji [1 ]
Arai, Shinichi [1 ]
Shimizu, Masaru [1 ]
Kitamura, Hidetomo [1 ]
Sato, Haruhiko [1 ]
Kawabe, Yoshiki [1 ]
机构
[1] Chugai Pharmaceut Co Ltd, Div Res, 1-135 Komakado, Gotemba, Shizuoka 4128513, Japan
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
关键词
PARATHYROID-HORMONE RECEPTOR; CLASS-B GPCRS; PROTEIN-KINASE; REPLACEMENT THERAPY; PTH/PTHRP RECEPTOR; FOLLOW-UP; SELECTIVITY; ACTIVATION; DISCOVERY; EFFICACY;
D O I
10.1038/ncomms13384
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:14
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