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Published-Ahead-of-Print December 8, 2005, DOI:10.2164/jandrol.05144
Journal of Andrology, Vol. 27, No. 3, May/June 2006
Copyright © American Society of Andrology
DOI: 10.2164/jandrol.05144

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Role of Metastin in the Release of Gonadotropin-Releasing Hormone From the Hypothalamus of the Male Rat

STANLEY J. NAZIAN

From the Department of Physiology and Biophysics, College of Medicine, and The Neuroscience Program, Health Science Center, University of South Florida, Tampa, Florida.

Correspondence to: Stanley J. Nazian, Department of Physiology and Biophysics, MDC 08, University of South Florida College of Medicine, 12901 Bruce B. Downs Blvd, Tampa, FL 33625 (e-mail: snazian{at}hsc.usf.edu).


Recent genetic analysis has suggested that the expression of the orphan receptor GPR54 is essential for the onset of puberty in both rodents and humans. Indirect evidence has suggested that this action is via gonadotropin-releasing hormone induction of luteinizing hormone release. The experiments described here were intended to provide direct evidence that metastin, the naturally occurring ligand for GPR54, was capable of stimulating GnRH secretion by examining GnRH release from an immortalized hypothalamic cell line (GT1-7) and from male rat hypothalamic explants. GT1-7 cells were treated for 21/2 hours and overnight with the biologically active fragment of metastin, metastin(45-54), in amounts ranging from 0.1 nM to 1 µM. Hypothalamic fragments were obtained from infantile male rats and exposed to progressively increasing concentrations of metastin(45-54) (0.1 nM to 1 µM) for 1-hour periods. In both experiments, GnRH release was measured by radioimmunoassay (RIA). The release of metastin from hypothalami obtained from infantile and adult male rats was also determined. Explants were incubated for 6 hours, and the release of metastin into the media was determined by RIA. The results support the hypothesis that metastin stimulates GnRH secretion from the hypothalamus. The data indicate that an increase in the secretion of metastin, rather than the appearance of the receptor, is required for puberty onset. The results also suggest that metastin influences the GnRH-secreting neurons indirectly via an interneuron rather than acting directly on the GnRH-secreting neurons.

     Key words: Puberty, sexual maturation, kisspeptin




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