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2-Hydroxyestradiol enhances binge onset in female rats and reduces prefrontal cortical dopamine in male rats.
Babbs, R K; Unger, E L; Corwin, R L W.
Afiliação
  • Babbs RK; Pennsylvania State University, IGDP Physiology, 110 Chandlee Laboratory, University Park, PA 16802, USA. rkb145@psu.edu
Horm Behav ; 63(1): 88-96, 2013 Jan.
Article em En | MEDLINE | ID: mdl-23116652
ABSTRACT
Women are more likely to suffer from a bingeing-related eating disorder, which is surprising, since estradiol reduces meal size and is associated with reduced binge frequency. This apparent contradiction may involve the estradiol metabolite, 2-hydroxyestradiol. We previously reported that female rats had faster escalations in shortening intake during the development of bingeing than did males, but acute administration of 2-hydroxyestradiol increased the intake of vegetable shortening to a greater extent in male rats once bingeing was established. Here, we report two separate studies that follow up these previous findings. In the first, we hypothesized that chronic exposure to 2-hydroxyestradiol would promote escalation of bingeing during binge development in ovariectomized female rats. In the second, we hypothesized that acute exposure to 2-hydroxyestradiol would enhance dopamine signaling in the prefrontal cortex after bingeing was established in male rats. In study 1, non-food-deprived female rats were separated into 3 groups ovariectomized (OVX) with chronic 2-hydroxyestradiol supplementation (E), OVX with vehicle supplementation (O), and intact with vehicle (I). Each group was given access to an optional source of dietary fat (shortening) on Mon, Wed, and Fri for 4 weeks. 2-hydroxyestradiol supplementation prevented OVX-induced weight gain and enhanced escalation of shortening intake over the four-week period (ps<0.05). Additionally, in week 4, rats in the E group ate significantly more shortening than I controls, less chow than either the O or I group, and had a higher shortening to chow ratio than O or I (ps<0.05). Study 2 indicated that acute injection of 2-hydroxyestradiol abolished shortening-evoked dopamine efflux in the prefrontal cortex of bingeing male rats (p<0.05). Together, these studies indicate that 2-hydroxyestradiol can exacerbate bingeing as it develops and can suppress dopamine signaling in the prefrontal cortex once bingeing is established.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dopamina / Bulimia / Córtex Pré-Frontal / Ingestão de Alimentos / Estradiol / Comportamento Alimentar Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Horm Behav Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dopamina / Bulimia / Córtex Pré-Frontal / Ingestão de Alimentos / Estradiol / Comportamento Alimentar Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Horm Behav Ano de publicação: 2013 Tipo de documento: Article