Central serotonergic control of cardiovascular reflexes

Central serotonergic neurones control reflex parasympathetic outflow to the heart, airways and bladder in a number of species, and different 5-HT receptor subtypes are involved in this effect. 5-HTiA and 5-HT3 receptors in the brainstem facilitate these reflexes, whilst 5-HTiB/id, 5-HT2 and 5-HT4 re...

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Main Author: Kellett, Daniel Otto
Published: University College London (University of London) 2005
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413551
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spelling ndltd-bl.uk-oai-ethos.bl.uk-4135512016-06-21T03:19:15ZCentral serotonergic control of cardiovascular reflexesKellett, Daniel Otto2005Central serotonergic neurones control reflex parasympathetic outflow to the heart, airways and bladder in a number of species, and different 5-HT receptor subtypes are involved in this effect. 5-HTiA and 5-HT3 receptors in the brainstem facilitate these reflexes, whilst 5-HTiB/id, 5-HT2 and 5-HT4 receptors inhibit them. Recently, central 5-HT7 receptors have been implicated in bladder reflexes. Experiments on anaesthetised rats showed that the selective 5-HT7 receptor antagonists SB-269970 and SB-656104, given intracisternally (i.e.), attenuated cardiopulmonary, baroreflex and chemoreflex bradycardias. Similarly, the selective 5-HTia receptor antagonist WAY-100635 attenuated cardiopulmonary and chemoreflex (but not baroreflex) bradycardia, whilst robalzotan and (-)-pindolol (antagonists at 5-HTiA receptors) had no effect on cardiopulmonary and baroreflex bradycardias respectively. Chemical stimulation of presumed serotonergic cell bodies in raphe magnus/pallidus evoked a bradycardia that could not be attenuated either by 5-HT receptor antagonists (given i.v.) or by prior 5-HT depletion. The latter did, however, significantly attenuate cardiovascular reflex sensitivity. Activation of nucleus tractus solitarius (NTS) neurones by the vagus was inhibited by the iontophoretic AMP A receptor antagonist DNQX or by topical SB-269970. Subsequent histology suggested that 5-HT containing terminals do not make close appositions with these neurones. Preliminary data demonstrate that SB-269970 (given i.e.) effectively attenuates the cardiopulmonary reflex in awake rats, but has variable effects on the chemoreflex. The data suggest that 5-HT7 receptors in the NTS are crucially involved in the central transmission of reflex bradycardias, at least in rats. The role of the 5-HTia receptor is less clear-cut than in the rabbit, and may reveal a species difference. The origin of 5-HT activating these receptors is unlikely to be the medullary raphe neurones, but may be primary afferents terminating in the NTS. Since recent ultrastructural evidence shows 5-HT terminals and NTS cardiovascular neurones are often separated by astroglial leaflets, astrocytes may be involved in serotonergic-glutamatergic signalling.612.89University College London (University of London)http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413551http://discovery.ucl.ac.uk/1446450/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 612.89
spellingShingle 612.89
Kellett, Daniel Otto
Central serotonergic control of cardiovascular reflexes
description Central serotonergic neurones control reflex parasympathetic outflow to the heart, airways and bladder in a number of species, and different 5-HT receptor subtypes are involved in this effect. 5-HTiA and 5-HT3 receptors in the brainstem facilitate these reflexes, whilst 5-HTiB/id, 5-HT2 and 5-HT4 receptors inhibit them. Recently, central 5-HT7 receptors have been implicated in bladder reflexes. Experiments on anaesthetised rats showed that the selective 5-HT7 receptor antagonists SB-269970 and SB-656104, given intracisternally (i.e.), attenuated cardiopulmonary, baroreflex and chemoreflex bradycardias. Similarly, the selective 5-HTia receptor antagonist WAY-100635 attenuated cardiopulmonary and chemoreflex (but not baroreflex) bradycardia, whilst robalzotan and (-)-pindolol (antagonists at 5-HTiA receptors) had no effect on cardiopulmonary and baroreflex bradycardias respectively. Chemical stimulation of presumed serotonergic cell bodies in raphe magnus/pallidus evoked a bradycardia that could not be attenuated either by 5-HT receptor antagonists (given i.v.) or by prior 5-HT depletion. The latter did, however, significantly attenuate cardiovascular reflex sensitivity. Activation of nucleus tractus solitarius (NTS) neurones by the vagus was inhibited by the iontophoretic AMP A receptor antagonist DNQX or by topical SB-269970. Subsequent histology suggested that 5-HT containing terminals do not make close appositions with these neurones. Preliminary data demonstrate that SB-269970 (given i.e.) effectively attenuates the cardiopulmonary reflex in awake rats, but has variable effects on the chemoreflex. The data suggest that 5-HT7 receptors in the NTS are crucially involved in the central transmission of reflex bradycardias, at least in rats. The role of the 5-HTia receptor is less clear-cut than in the rabbit, and may reveal a species difference. The origin of 5-HT activating these receptors is unlikely to be the medullary raphe neurones, but may be primary afferents terminating in the NTS. Since recent ultrastructural evidence shows 5-HT terminals and NTS cardiovascular neurones are often separated by astroglial leaflets, astrocytes may be involved in serotonergic-glutamatergic signalling.
author Kellett, Daniel Otto
author_facet Kellett, Daniel Otto
author_sort Kellett, Daniel Otto
title Central serotonergic control of cardiovascular reflexes
title_short Central serotonergic control of cardiovascular reflexes
title_full Central serotonergic control of cardiovascular reflexes
title_fullStr Central serotonergic control of cardiovascular reflexes
title_full_unstemmed Central serotonergic control of cardiovascular reflexes
title_sort central serotonergic control of cardiovascular reflexes
publisher University College London (University of London)
publishDate 2005
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413551
work_keys_str_mv AT kellettdanielotto centralserotonergiccontrolofcardiovascularreflexes
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