Female pheromones stimulate release of luteinizing hormone and testosterone without altering GnRH mRNA in adult male Syrian hamsters ( Mesocricetus auratus)

• Published in: General and comparative endocrinology 2004-09, Vol.138 (3), p.211-217
• Main Authors: Richardson, Heather N., Nelson, Aaron L.A., Ahmed, Eman I., Parfitt, David B., Romeo, Russell D., Sisk, Cheryl L.
• Format: Article
• Language: English
• Subjects: Animals; Brain - cytology; Brain - metabolism; Chemosensory; Cricetinae; Female; GnRH; Gonadotropin-Releasing Hormone - genetics; Gonadotropin-Releasing Hormone - metabolism; Hamster; Hypothalamo-Hypophyseal System - cytology; Hypothalamo-Hypophyseal System - metabolism; LHRH; Luteinizing Hormone - blood; Male; Mesocricetus; Mesocricetus auratus; mRNA; Neurons - metabolism; Pheromones; Pheromones - physiology; Reproduction - physiology; RNA, Messenger - analysis; Sex Factors; Smell - physiology; Testosterone - blood
• ISSN: 0016-6480; 1095-6840
• DOI: 10.1016/j.ygcen.2004.06.008

In many species chemosensory stimuli function as important signals that influence reproductive status. Neurons synthesizing the peptide gonadotropin-releasing hormone (GnRH) are critical mediators of reproductive function via their regulation of the hypothalamic–pituitary–gonadal (HPG) axis, and they are thought to be responsive to chemosensory information. In the present study, we sought to elucidate the effects of female chemosensory stimuli on the HPG axis in sexually naive adult male Syrian hamsters. In Experiment 1, serial blood samples were collected from catheterized male hamsters following exposure to female pheromones in order to characterize the luteinizing hormone (LH) response to this chemosensory stimulus. In Experiment 2, brains and terminal blood samples were collected from animals 0, 60, and 120 min following pheromone exposure. GnRH mRNA was measured in brain tissue sections using in situ hybridization, and plasma concentrations of LH and testosterone were measured using radioimmunoassay. Data from Experiment 1 indicated that female pheromones elicited a rapid rise in plasma LH that peaked at 15 min and returned to baseline 45 min after exposure. In Experiment 2, testosterone was elevated in terminal blood samples obtained 60 min, but not 120 min, after exposure to pheromones. LH levels were unaffected at both of these time points. The chemosensory-induced increases in LH and testosterone release were not accompanied by subsequent changes in GnRH mRNA over the time course studied. These data suggest that while activation of the male HPG axis by female pheromones involves release of GnRH, it does not involve increases in GnRH mRNA 1–2 h after pheromonal stimulation as a mechanism for replenishment of released peptide.