Pharmacological inhibition of gut-derived serotonin synthesis is a potential bone anabolic treatment for osteoporosis

被引:0
|
作者
Vijay K Yadav
Santhanam Balaji
Padmanaban S Suresh
X Sherry Liu
Xin Lu
Zhishan Li
X Edward Guo
J John Mann
Anil K Balapure
Michael D Gershon
Rudraiah Medhamurthy
Marc Vidal
Gerard Karsenty
Patricia Ducy
机构
[1] Columbia University Medical Center,Department of Genetics and Development
[2] Harvard Medical School,Department of Genetics
[3] and Center for Cancer Systems Biology and Dana-Farber Cancer Institute,Department of Molecular Reproduction
[4] Development and Genetics,Department of Biomedical Engineering
[5] Indian Institute of Science,Department of Pathology and Cell Biology
[6] Columbia University,Department of Psychiatry
[7] Columbia University,undefined
[8] Columbia University,undefined
[9] Tissue and Cell Culture Unit,undefined
[10] Central Drug Research Institute,undefined
来源
Nature Medicine | 2010年 / 16卷
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摘要
Osteoporosis results from misregulation of bone catabolism and bone anabolism, resulting in severe bone loss. Most current therapies act by decreasing bone catabolism, but targeting bone anabolism is more desired, because once bone is lost, it is difficult to replace. In a new report by Gerard Karsenty and his colleagues, they show that orally delivered pharmacological targeting of serotonin synthesis in the gut is sufficient to increase bone anabolism and thus restore lost bone in rat and mouse models of well-established osteoporosis (pages 264–265).
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页码:308 / 312
页数:4
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