Pharmacologic Evidence that a D2 Receptor Subtype Mediates Dopaminergic Stimulation of Prolactin Secretion from the Anterior Pituitary Gland

1991 ◽  
Vol 54 (2) ◽  
pp. 175-183 ◽  
Author(s):  
Thomas P. Burris ◽  
Clarence Stringer ◽  
Marc E. Freeman
Keyword(s):  
Pituitary Gland ◽  
Anterior Pituitary ◽  
D2 Receptor ◽  
Prolactin Secretion ◽  
Anterior Pituitary Gland ◽  
Receptor Subtype ◽  
Dopaminergic Stimulation ◽  
Stimulation Of

OESTRADIOL RECEPTORS IN THE RAT ANTERIOR PITUITARY GLAND DURING THE OESTROUS CYCLE: QUANTITATION OF RECEPTOR ACTIVITY IN RELATION TO GONADOTROPHIN RELEASING HORMONE-MEDIATED LUTEINIZING HORMONE RELEASE

1978 ◽  
Vol 76 (2) ◽  
pp. 211-218 ◽  
Author(s):  
K. K. SEN ◽  
K. M. J. MENON
Keyword(s):  
Pituitary Gland ◽  
Binding Sites ◽  
Anterior Pituitary ◽  
Anterior Pituitary Gland ◽  
Oestrous Cycle ◽  
Hormone Release ◽  
Releasing Hormone ◽  
Lh Release ◽  
Gonadotrophin Releasing Hormone ◽  
Stimulation Of

Specific oestradiol binding to a receptor in nuclear and cytosol fractions of the rat anterior pituitary gland and pituitary responsiveness to gonadotrophin releasing hormone (GnRH) during the oestrous cycle have been studied. To accomplish this, both unoccupied and occupied oestradiol-binding sites in the cytosol and oestradiol-binding sites in the nucleus and total cell were measured during the oestrous cycle. The concentration of unoccupied and occupied sites and total oestradiol binding in the cytosol fluctuated during the cycle. At pro-oestrus, the concentration of cytosol receptor was diminished by about 40% and replenishment occurred during oestrus. On the other hand, a profound increase in concentrations of cellular and nuclear receptors occurred at pro-oestrus. Administration of GnRH significantly stimulated LH release at all stages of the cycle. The maximum stimulation of LH release by GnRH was observed at 13.00 h of pro-oestrus. From these studies, it is concluded that pituitary responsiveness to exogenous GnRH during pro-oestrus parallels the changes in the content of oestrogen receptors in the cytosol and nucleus.

POSSIBLE PRIMING EFFECT OF LUTEINIZING HORMONE RELEASING HORMONE ON THE ANTERIOR PITUITARY GLAND IN THE JAPANESE QUAIL AND THE STIMULATION OF SECRETION OF FOLLICLE-STIMULATING HORMONE

1979 ◽  
Vol 82 (1) ◽  
pp. 71-75 ◽  
Author(s):  
D. T. DAVIES ◽  
J. COLLINS
Keyword(s):  
Pituitary Gland ◽  
Japanese Quail ◽  
Anterior Pituitary ◽  
Follicle Stimulating Hormone ◽  
Anterior Pituitary Gland ◽  
Luteinizing Hormone Releasing Hormone ◽  
Releasing Hormone ◽  
Lh Rh ◽  
Lh Releasing Hormone ◽  
Stimulation Of

SUMMARY After the i.m. injection of 10 μg synthetic LH releasing hormone (LH-RH) into Japanese quail the levels of LH and FSH in plasma rose significantly within 2 min. The increased level of LH declined rapidly but that of FSH was maintained for the duration of the experiment. To determine whether the anterior pituitary gland is primed by LH-RH a double injection schedule was adopted. It would appear that, while endogenous LH-RH may prime the avian pituitary gland slightly, synthetic LH-RH is ineffective.

scholarly journals Intermedin/Adrenomedullin-2 Inhibits Growth Hormone Release from Cultured, Primary Anterior Pituitary Cells

Endocrinology ◽  
2006 ◽  
Vol 147 (2) ◽  
pp. 859-864 ◽  
Author(s):  
Meghan M. Taylor ◽  
Sara L. Bagley ◽  
Willis K. Samson
Keyword(s):  
Pituitary Gland ◽  
Anterior Pituitary ◽  
Hormone Secretion ◽  
Prolactin Secretion ◽  
Anterior Pituitary Gland ◽  
Male Rats ◽  
Pituitary Cells ◽  
Anterior Pituitary Cells ◽  
Peptide Family

Intermedin (IMD), a novel member of the adrenomedullin (AM), calcitonin gene-related peptide (CGRP), amylin (AMY) peptide family, has been reported to act promiscuously at all the known receptors for these peptides. Like AM and CGRP, IMD acts in the circulation to decrease blood pressure and in the brain to inhibit food intake, effects that could be explained by activation of the known CGRP, AM, or AMY receptors. Because AM, CGRP, and AMY have been reported to affect hormone secretion from the anterior pituitary gland, we examined the effects of IMD on GH, ACTH, and prolactin secretion from dispersed anterior pituitary cells harvested from adult male rats. IMD, in log molar concentrations ranging from 1.0 pm to 100 nm, failed to significantly alter basal release of the three hormones. Similarly, IMD failed to significantly alter CRH-stimulated ACTH or TRH-stimulated prolactin secretion in vitro. However, IMD concentration-dependently inhibited GHRH-stimulated GH release from these cell cultures. The effects of IMD, although requiring higher concentrations, were as efficacious as those of somatostatin and, like somatostatin, may be mediated, at least in part, by decreasing cAMP accumulation. These actions of IMD were not shared by other members of the AM-CGRP-AMY family of peptides, suggesting the presence of a novel, unique IMD receptor in the anterior pituitary gland and a potential neuroendocrine action of IMD to interact with the hypothalamic mechanisms controlling growth and metabolism.

GONADOTROPHIN SECRETION AFTER ELECTRICAL STIMULATION OF THE PREOPTIC AREA DURING THE OESTROUS CYCLE OF THE RAT

1974 ◽  
Vol 62 (3) ◽  
pp. 589-604 ◽  
Author(s):  
G. FINK ◽  
M. S. AIYER
Keyword(s):  
Electrical Stimulation ◽  
Luteinizing Hormone ◽  
Pituitary Gland ◽  
Anterior Pituitary ◽  
Preoptic Area ◽  
Medial Preoptic Area ◽  
Anterior Pituitary Gland ◽  
Oestrous Cycle ◽  
Early Afternoon ◽  
Stimulation Of

SUMMARY The responsiveness of the hypothalamo-hypophysial axis to electrical stimulation of the medial preoptic area was tested at various times during the oestrous cycle of the rat. Animals were anaesthetized with sodium pentobarbitone, and glass-insulated bipolar platinum electrodes were stereotaxically implanted in the medial preoptic area. The stimulus consisted of accurately balanced biphasic rectangular pulses, height 500 μA, duration 2 ms and frequency 60 Hz, applied in trains of 30 s intervals. The concentration of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in blood samples withdrawn from the external jugular vein immediately before and at frequent intervals up to 1 h after application of the stimulus was determined by radioimmunoassay. In all animals the stimulus was applied for a period of 15 min, for it was found that under these conditions the profiles of LH and FSH produced in individual animals were similar to those which followed the i.v. injection of 50 ng synthetic luteinizing hormone releasing factor (LH-RF)/100 g body wt, the minimal ovulatory dose of LH-RF in our laboratory. Both for LH and FSH, the profiles of responsiveness of the hypothalamo-hypophysial axis to electrical stimulation through the oestrous cycle resembled closely the profile of responsiveness of the anterior pituitary gland to LH-RF administered intravenously. There was a relatively gradual increase in pituitary sensitivity, in terms of the mean maximal increments, between the early afternoon of dioestrus and pro-oestrus, followed by an abrupt and marked rise which reached a peak at 18.00 and 21.00 h of pro-oestrus for LH and FSH, respectively. Sensitivity of the hypothalamo-hypophysial axis declined through oestrus and metoestrus reaching a nadir at 13.30 h of dioestrus. While these results do not exclude a change in sensitivity of the neural component of the hypothalamo-hypophysial axis during the oestrus cycle, they do indicate that the timing and magnitude of changes in sensitivity of the anterior pituitary gland to both endogenous and exogenous LH-RF are similar. This raises the possibility that a marked increase in the secretion of LH-RF during the afternoon of pro-oestrus may not be necessary for the occurrence of the surge of LH and FSH, for conceivably the latter could depend on a change in sensitivity of pituitary gonadotrophs to constant or only slightly increased levels of LH-RF in hypophysial portal blood. Our findings are compared with those of workers who have employed electrochemical stimulation of the preoptic area.

In-vitro evidence for the autoregulation of prolactin secretion at the level of the pituitary gland in the rat

1987 ◽  
Vol 115 (1) ◽  
pp. 13-18 ◽  
Author(s):  
A. M. Bentley ◽  
M. Wallis
Keyword(s):  
Monoamine Oxidase ◽  
Pituitary Gland ◽  
Anterior Pituitary ◽  
Prolactin Secretion ◽  
Anterior Pituitary Gland ◽  
Physiological Significance ◽  
Secretory Product ◽  
Secretory Products ◽  
Male Tissue

ABSTRACT The autoregulation of rat prolactin secretion at the level of the pituitary gland was investigated, using a static incubation system. The rate of prolactin secretion from the female anterior pituitary gland in vitro was found to be constant when the medium was changed at 20-min intervals. However, when the medium was left unchanged and secretory products were allowed to accumulate, prolactin secretion began to decline within 60 min. This effect was not observed with the male tissue, where the level of accumulated prolactin did not reach that at which the inhibition occurred using female tissue. The nature of the putative secretory product causing the inhibition of prolactin secretion was investigated. Exogenous bovine prolactin (1–4 mg/l) caused an inhibition of endogenous rat prolactin secretion. Inclusion of monoamine oxidase in unchanged medium, to prevent dopamine accumulation in the medium (a possible consequence of co-storage and cosecretion with prolactin granules), did not prevent the inhibition observed in the control incubation. We therefore conclude that in-vitro autoregulation of prolactin secretion can occur at the level of the pituitary gland, probably due to the accumulated prolactin having a feedback action on the lactotroph. This might be of physiological significance if localized concentrations of the hormone within the gland are high. J. Endocr. (1987) 115, 13–18

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