3.9 Article

Effects of orexins A and B on expression of orexin receptors and progesterone release in luteal and granulosa ovarian cells

Journal

REGULATORY PEPTIDES
Volume 178, Issue 1-3, Pages 56-63

Publisher

ELSEVIER
DOI: 10.1016/j.regpep.2012.06.008

Keywords

Orexins; Hypocretins; OX1 receptor; OX2 receptor; Progesterone; Ovary

Funding

  1. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [PIP 00363]
  2. Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT) [PICT 2007-01050]
  3. Universidad de Buenos Aires [M 043]

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Orexin-A and orexin-B are neuropeptides controlling sleep-wakefulness, feeding and neuroendocrine functions via their G protein-coupled receptors, orexin-1R and orexin-2R. They are synthesized in the lateral hypothalamus and project throughout the brain. Orexins and orexin receptors have also been described outside the brain. Previously we demonstrated the presence of both receptors in the ovary, their increased expression during proestrous afternoon and the dependence on the gonadotropins. Here we studied the effects of orexins on the mRNA expression of both receptors, by quantitative real-time PCR, on luteal cells from superovulated rat ovaries and granulosa cells from diethylstilbestrol-treated rat ovaries. Effects on progesterone secretion were also measured. In luteal cells, 1 nM of either orexin-A or orexin-B decreased progesterone secretion. Orexin-A treatment increased expression of both orexin-1R and orexin-2R mRNA. The effect on orexin-1R mRNA expression was abolished by an orexin-1R selective receptor antagonist SB-334867 and the effect on orexin-2R mRNA expression was abolished by a selective orexin-2R antagonist JNJ-10397049. Orexin-B did not modify orexin-1R mRNA expression, but increased orexin-2R mRNA expression. The effect of orexin-B on orexin-2R was abolished by a selective orexin-2R antagonist. Neither the expression of orexin receptors nor progesterone secretions by granulosa cells were affected by orexins. FSH, as positive control, increased both steroid hormones secretion, but did not induce the expression of OX receptors in granulosa cells isolated from late preantral/early antral follicles. Finally in ovaries obtained immediately after sacrifice, the expression of orexin-1R and orexin-2R was higher in superovulated rat ovaries compared to control or diethylstilbestrol treated rat ovaries. A selective presence and function of both orexinergic receptors in luteal and granulosa cells is described, suggesting that the orexinergic system may have a functional role in the ovary. (C) 2012 Elsevier B.V. All rights reserved.

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