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Effects of drugs which modify catecholamine activity on amplification of LH release induced by locus coeruleus
1Department of Physiology, School of Medicine, University of Maryland, Baltimore 21201.
Abstract:
Norepinephrine may be the neurotransmitter responsible for triggering the surge release of luteinizing hormone (LH) in proestrous and steroid-treated ovariectomized rats. In a previous study, we electrically stimulated (ES) the locus coeruleus (LC), a norepinephrine cell body region from which some axons project to the hypothalamus. These studies were performed in estradiol-treated rats in which the medial preoptic nucleus (MPN) initially had been electrochemically stimulated (ECS) to partially depolarize luteinizing hormone-releasing hormone (LH-RH) neurons. We observed that LC-ES markedly amplified the amount of LH released after preoptic-ECS. The purpose of the present study was to determine if these amplifying effects of LC-ES were due to the release of a catecholamine and if so which neurotransmitter was involved in this response. All rats in this study were ovariectomized and 7 days later (day 0) they were treated with estradiol for 2 days (day 2). On day 2, all animals were anesthetized with chloral hydrate. In control rats, the MPN was electrochemically stimulated (100 microA/60 s DC) and 30 min later the LC was electrically stimulated for 15 min. MPN-ECS significantly increased plasma concentrations of LH and LC-ES markedly amplified these plasma LH levels. Thereafter, 3 studies were performed and the following drugs were given: (1) alpha-methyl-p-tyrosine (MPT, 300 mg/kg i.p.); (2) phenoxybenzamine (PX, 15 mg/kg i.p.) and (3) propranolol (PROP, 15 mg/kg i.p.). MPT and PROP were administered 15 min prior to MPN-ECS and PX was given 90 min before MPN-ECS. None of these drugs affected the amount of LH released after preoptic stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)