2001
DOI: 10.1016/s0006-8993(00)03139-5
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Melatonin inhibits Arg–vasopressin release via MT2 receptor in the suprachiasmatic nucleus-slice culture of rats

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Cited by 20 publications
(12 citation statements)
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“…However, whether melatonin is able to suppress pituitary-adrenal activity in a similarly direct manner, i.e. independent from sleep, is presently unclear as are the pineal-hypothalamic links that, perhaps via an action on releasing factors such as CRH and vasopressin, mediate such inhibition (32,41,42). Also, we emphasize here that a pharmacological dose of melatonin was used; this dose induced clearly supraphysiological blood concentrations and, thus, precludes any speculations concerning the physiological role of endogenous melatonin for pituitary-adrenal function and sleep.…”
Section: Discussionmentioning
confidence: 99%
“…However, whether melatonin is able to suppress pituitary-adrenal activity in a similarly direct manner, i.e. independent from sleep, is presently unclear as are the pineal-hypothalamic links that, perhaps via an action on releasing factors such as CRH and vasopressin, mediate such inhibition (32,41,42). Also, we emphasize here that a pharmacological dose of melatonin was used; this dose induced clearly supraphysiological blood concentrations and, thus, precludes any speculations concerning the physiological role of endogenous melatonin for pituitary-adrenal function and sleep.…”
Section: Discussionmentioning
confidence: 99%
“…The PT is an endocrine structure characterized by a very high density of MT 1 receptors in all mammals except humans. The MT 2 receptor is present in the retina and possibly in the brain and SCN as well Isobe et al, 2001). In the SCN, MT 1 receptors would mediate the inhibitory effect on electrical activity, whereas the MT 2 receptor would mediate the phase-shifting effect of MEL.…”
Section: Sites and Mechanisms Of Action Of Melatoninmentioning
confidence: 99%
“…The possible mechanism by which melatonin can modify the vasopressinergic and oxytocinergic neurones activity includes specific G protein-coupled membrane receptors, called MT 1 and MT 2 , activation of which inhibits the synthesis of cAMP [21,24]. These receptors are situated mainly in the pars tuberalis of the pituitary [25] and in the hypothalamic suprachiasmatic (SCN) [15,[26][27][28] as well as magnocellular SON and PVN nuclei [29]. It has been found that AVP-containing cells in the SCN express both MT 1 [27] and MT 2 [28] melatonin receptors and melatonin inhibits AVP release from cultured SCN neurones [15,28].…”
Section: Discussionmentioning
confidence: 99%
“…These receptors are situated mainly in the pars tuberalis of the pituitary [25] and in the hypothalamic suprachiasmatic (SCN) [15,[26][27][28] as well as magnocellular SON and PVN nuclei [29]. It has been found that AVP-containing cells in the SCN express both MT 1 [27] and MT 2 [28] melatonin receptors and melatonin inhibits AVP release from cultured SCN neurones [15,28]. Moreover, it has been found that the cAMP-dependent pathways are involved in an increase in AVP gene expression in the SCN [30].…”
Section: Discussionmentioning
confidence: 99%