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Indirect regulation of PTH by estrogens may require FGF23.
Carrillo-López, Natalia; Román-García, Pablo; Rodríguez-Rebollar, Ana; Fernández-Martín, José Luis; Naves-Díaz, Manuel; Cannata-Andía, Jorge B.
Afiliação
  • Carrillo-López N; Bone and Mineral Research Unit, Instituto Reina Sofía de Investigación, Hospital Universitario Central de Asturias, REDinREN del ISCIII, Universidad de Oviedo, Oviedo, Asturias, Spain.
J Am Soc Nephrol ; 20(9): 2009-17, 2009 Sep.
Article em En | MEDLINE | ID: mdl-19628670
ABSTRACT
The mechanisms by which estrogens modulate PTH are controversial, including whether or not estrogen receptors (ERs) are present in the parathyroid glands. To explore these mechanisms, we combined a rat model of CKD with ovariectomy and exogenous administration of estrogens. We found that estrogen treatment significantly decreased PTH mRNA and serum levels. We did not observe ERalpha or ERbeta mRNA or protein in the parathyroids, suggesting an indirect action of estrogens on PTH regulation. Estrogen treatment significantly decreased serum 1,25(OH)(2) vitamin D(3) and phosphorus levels. In addition, estrogens significantly increased fibroblast growth factor 23 (FGF23) mRNA and serum levels. In vitro, estrogens led to transcriptional and translational upregulation of FGF23 in osteoblast-like cells in a time- and concentration-dependent manner. These results suggest that estrogens regulate PTH indirectly, possibly through FGF23.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hormônio Paratireóideo / Glândulas Paratireoides / Estradiol / Insuficiência Renal Crônica / Fatores de Crescimento de Fibroblastos / Hiperparatireoidismo Secundário Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hormônio Paratireóideo / Glândulas Paratireoides / Estradiol / Insuficiência Renal Crônica / Fatores de Crescimento de Fibroblastos / Hiperparatireoidismo Secundário Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2009 Tipo de documento: Article