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Regulation of bone mass in mice by the lipoxygenase gene Alox15.
Klein, Robert F; Allard, John; Avnur, Zafrira; Nikolcheva, Tania; Rotstein, David; Carlos, Amy S; Shea, Marie; Waters, Ruth V; Belknap, John K; Peltz, Gary; Orwoll, Eric S.
Afiliação
  • Klein RF; Bone and Mineral Research Unit, Department of Medicine, School of Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97239, USA. kleinro@ohsu.edu
Science ; 303(5655): 229-32, 2004 Jan 09.
Article em En | MEDLINE | ID: mdl-14716014
The development of osteoporosis involves the interaction of multiple environmental and genetic factors. Through combined genetic and genomic approaches, we identified the lipoxygenase gene Alox15 as a negative regulator of peak bone mineral density in mice. Crossbreeding experiments with Alox15 knockout mice confirmed that 12/15-lipoxygenase plays a role in skeletal development. Pharmacologic inhibitors of this enzyme improved bone density and strength in two rodent models of osteoporosis. These results suggest that drugs targeting the 12/15-lipoxygenase pathway merit investigation as a therapy for osteoporosis.
Assuntos
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Base de dados: MEDLINE Assunto principal: Araquidonato 12-Lipoxigenase / Araquidonato 15-Lipoxigenase / Densidade Óssea Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2004 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Araquidonato 12-Lipoxigenase / Araquidonato 15-Lipoxigenase / Densidade Óssea Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2004 Tipo de documento: Article