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Quantitative radioautographic light and electron microscopic analysis of the localization of monoamines in the median eminence of the rat
Authors:Dr. Michael A. Belenky  Vladimir K. Chetverukhin  Andrey L. Polenov
Affiliation:(1) Laboratory of Neuroendocrinology, Sechenov Institute of Evolutionary Physiology and Biochemistry of the USSR Academy of Sciences, Leningrad, USSR;(2) Sechenov Institute, 194223, K-223 Leningrad, USSR
Abstract:Summary Serotonin containing structures in the median eminence of the rat have been studied by quantitative light and electron microscopic radioautography following intraventricular infusion of tritiated 5-hydroxytryptophan. One hour after injection of the tracer the highest density of silver grains was recorded in the ependymal and external zones, especially in the lateral palisade zone. The proportion of labelled neurosecretory terminals was also larger in the lateral palisade zone (29%) as compared with the medial palisade zone (13%), although the mean number of developed silver grains per one terminal was higher in the latter. On the average, 16% of neurosecretory terminals sequestered radiolabelled 5-hydroxytryptophan in the external zone of the rat median eminence. It is suggested that serotonin, like catecholamines, is discharged from neurosecretory terminals localized in the external zone and via the portal circulation affects the function of the anterior pituitary. The sites of origin of serotoninergic structures of the median eminence as well as the possible role of monoamine (catecholamine and indolamine) neurohormones in a dual peptidergic and monoaminergic control of anterior pituitary functions are discussed.This work was presented at the joint session of the Society of Anatomists, Histologists and Embryologists, the Society of Physiologists, and the Society of Neuroendocrinologists dedicated to the memory of Professor Wolfgang Bargmann, held in Leningrad, January 17, 1979
Keywords:Median eminence  Rat  Serotonin  Quantitative light and electron microscopic radioautography
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