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


Autoria(s): Yadav, Vijay K; Balaji, Santhanam; Suresh, Padmanaban S; Liu, X Sherry; Lu, Xin; Li, Zhishan; Guo, X Edward; Mann, J John; Balapure, Anil K; Gershon, Michael D; Medhamurthy, Rudraiah; Vidal, Marc; Karsenty, Gerard; Ducy, Patricia
Data(s)

01/03/2010

Resumo

Osteoporosis is a disease of low bone mass most often caused by an increase in bone resorption that is not sufficiently compensated for by a corresponding increase in bone formation(1). As gut-derived serotonin (GDS) inhibits bone formation(2), we asked whether hampering its biosynthesis could treat osteoporosis through an anabolic mechanism (that is, by increasing bone formation). We synthesized and used LP533401, a small molecule inhibitor of tryptophan hydroxylase-1 (Tph-1), the initial enzyme in GDS biosynthesis. Oral administration of this small molecule once daily for up to six weeks acts prophylactically or therapeutically, in a dose-dependent manner, to treat osteoporosis in ovariectomized rodents because of an isolated increase in bone formation. These results provide a proof of principle that inhibiting GDS biosynthesis could become a new anabolic treatment for osteoporosis.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/26389/1/nm.2098.pdf

Yadav, Vijay K and Balaji, Santhanam and Suresh, Padmanaban S and Liu, X Sherry and Lu, Xin and Li, Zhishan and Guo, X Edward and Mann, J John and Balapure, Anil K and Gershon, Michael D and Medhamurthy, Rudraiah and Vidal, Marc and Karsenty, Gerard and Ducy, Patricia (2010) Pharmacological inhibition of gut-derived serotonin synthesis is a potential bone anabolic treatment for osteoporosis. In: Nature Medicine, 16 (3). 308-U103.

Publicador

Nature Publishing Group.

Relação

http://www.nature.com/nm/journal/v16/n3/abs/nm.2098.html

http://eprints.iisc.ernet.in/26389/

Palavras-Chave #Molecular Reproduction, Development & Genetics (formed by the merger of DBGL and CRBME)
Tipo

Journal Article

PeerReviewed