» Articles » PMID: 4945749

Stimulation of Tubero-infundibular Dopamine Neurones and Gonadotrophin Secretion

Overview
Journal J Physiol
Specialty Physiology
Date 1971 Dec 1
PMID 4945749
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

1. In ovariectomized rats pre-treated with oestrogen and progesterone, the intensity of the catecholamine fluorescence was determined by micro-fluorimetry in the cell bodies of the tubero-infundibular dopamine neurones (situated in the arcuate and periventricular hypothalamic nuclei). The concentrations of follicle-stimulating (FSH) and luteinizing hormone (LH) in serum and pituitary were estimated by bio-assay.2. The characteristic changes in fluorescence intensity of the tuberal catecholamine-containing nerve cell group that are induced by unilateral intermittent electrical stimulation of the arcuate nucleus or of the medial preoptic area during 5-60 min, were accompanied by a marked rise in serum LH concentration. With arcuate stimulation, the rise in serum LH paralleled the increase in the fluorescence intensity of the nerve cell bodies, whereas with preoptic stimulation, the initial increase in cellular fluorescence intensity preceded the rise in serum LH. Preoptic stimulation also caused a moderate fall in pituitary LH which was simultaneous with the increase in fluorescence intensity. No systematic changes in FSH concentration were observed during the time interval studied.3. Pre-treatment with the tyrosine hydroxylase inhibitor alpha-methyltyrosine completely blocked the increase in fluorescence intensity caused by electrical stimulation of the arcuate nucleus but did not prevent the rise in serum LH.4. It is concluded that the tubero-infundibular dopamine neurones serve as an intermediary between the medial preoptic area (and possibly other forebrain structures) and neurones containing releasing factors. Under the present experimental conditions, stimulation of the tuberoinfundibular dopamine neurones increased the release of LH, probably by promoting the release of LH-releasing factor.

Citing Articles

Monoamine-containing structures in the hypothalamo-hypophyseal system in the human fetus.

Partanen S, Hervonen A Z Anat Entwicklungsgesch. 1973; 140(1):53-60.

PMID: 4749132 DOI: 10.1007/BF00520717.


Transformations of hypothalamic arcuate neurons. I. Changes associated with stages of the estrous cycle.

King J, Williams T, GERALL A Cell Tissue Res. 1974; 153(4):497-515.

PMID: 4474918 DOI: 10.1007/BF00231543.


Electrophysiological identification of cell bodies of the tubero-infundibular neurones in the rat.

Sawaki Y, Yagi K J Physiol. 1973; 230(1):75-85.

PMID: 4349809 PMC: 1350386. DOI: 10.1113/jphysiol.1973.sp010175.


Inhibition and facilitation of antidromically identified tubero-infundibular neurones following stimulation of the median eminence in the rat.

Sawaki Y, Yagi K J Physiol. 1976; 260(2):447-60.

PMID: 978540 PMC: 1309100. DOI: 10.1113/jphysiol.1976.sp011524.

References
1.
EVERETT J . OVULATION IN RATS FROM PREOPTIC STIMULATION THROUGH PLATINUM ELECTRODES. IMPORTANCE OF DURATION AND SPREAD OF STIMULUS. Endocrinology. 1965; 76:1195-201. DOI: 10.1210/endo-76-6-1195. View

2.
ANTON-TAY F, Pelham R, Wurtman R . Increased turnover of 3H-norepinephrine in rat brain following castration or treatment with ovine follicle-stimulating hormone. Endocrinology. 1969; 84(6):1489-92. DOI: 10.1210/endo-84-6-1489. View

3.
Kordon C, Glowinski J . Selective inhibition of superovulation by blockade of dopamine synthesis during the "critical period" in the immature rat. Endocrinology. 1969; 85(5):924-31. DOI: 10.1210/endo-85-5-924. View

4.
Borth R, DICZFALUSY E, HEINRICHS H . [Principles of statistical interpretation of bioassay]. Arch Gynakol. 1957; 188(6):497-538. DOI: 10.1007/BF00985483. View

5.
Tejasen T, EVERETT J . Surgical analysis of the preoptico-tuberal pathway controlling ovulatory release of gonadotropins in the rat. Endocrinology. 1967; 81(6):1387-96. DOI: 10.1210/endo-81-6-1387. View