Effects of delta-9-tetrahydrocannabinol on the hypothalamic-pituitary control of luteinizing hormone and follicle-stimulating hormone secretion in adult male rats

• Published in: Neuroendocrinology Vol. 46; no. 6; p. 488
• Main Authors: Wenger, T, Rettori, V, Snyder, G D, Dalterio, S, McCann, S M
• Format: Journal Article
• Language: English
• Published: Switzerland 01-12-1987
• Subjects: Animals; Cells, Cultured; Dronabinol - administration & dosage; Dronabinol - pharmacology; Follicle Stimulating Hormone - blood; Follicle Stimulating Hormone - secretion; Gonadotropin-Releasing Hormone - metabolism; Hypothalamo-Hypophyseal System - drug effects; Hypothalamo-Hypophyseal System - physiology; Hypothalamus - metabolism; Injections, Intraventricular; Luteinizing Hormone - blood; Luteinizing Hormone - secretion; Male; Pituitary Gland, Anterior - drug effects; Pituitary Gland, Anterior - secretion; Rats; Rats, Inbred Strains
• ISSN: 0028-3835
• DOI: 10.1159/000124870

The main psychoactive component of marihuana, delta-9-tetrahydrocannabinol (THC) was injected into the 3rd cerebral ventricle. A single dose of THC (2 microliter of 10(-6) M) decreased serum LH temporarily but did not alter serum follicle-stimulating hormone (FSH) levels. The mediobasal hypothalamic (MBH) luteinizing hormone-releasing hormone (LHRH) content was elevated by 30 min after the injection. The elevation persisted for 1 h. Then, the LHRH content returned towards the preinjection level. In contrast, the LHRH in the organum vasculosum of the lamina terminalis did not change after a single dose of THC. The results indicate that THC alters pituitary LH release by inhibiting the release of LHRH which then increases in the MBH by continued synthesis or transport from rostral areas. In addition, the data support the existence of an FSH releasing factor, the release of which is not suppressed by this dose of THC. THC did not alter the release, storage or responsiveness to LHRH of cultured anterior pituitary cells, which further supports the view that its principal site of action is on the hypothalamus.