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dc.contributor.authorCallaghan, B
dc.contributor.authorHunne, B
dc.contributor.authorHirayama, H
dc.contributor.authorSartor, DM
dc.contributor.authorNguyen, TV
dc.contributor.authorAbogadie, FC
dc.contributor.authorFerens, D
dc.contributor.authorMcIntyre, P
dc.contributor.authorBan, K
dc.contributor.authorBaell, J
dc.contributor.authorFurness, JB
dc.contributor.authorBrock, JA
dc.identifierpii: ajpheart.00418.2012
dc.identifier.citationCallaghan, B., Hunne, B., Hirayama, H., Sartor, D. M., Nguyen, T. V., Abogadie, F. C., Ferens, D., McIntyre, P., Ban, K., Baell, J., Furness, J. B. & Brock, J. A. (2012). Sites of action of ghrelin receptor ligands in cardiovascular control. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 303 (8), pp.H1011-H1021.
dc.descriptionC1 - Journal Articles Refereed
dc.description.abstractCirculating ghrelin reduces blood pressure, but the mechanism for this action is unknown. This study investigated whether ghrelin has direct vasodilator effects mediated through the growth hormone secretagogue receptor 1a (GHSR1a) and whether ghrelin reduces sympathetic nerve activity. Mice expressing enhanced green fluorescent protein under control of the promoter for growth hormone secretagogue receptor (GHSR) and RT-PCR were used to locate sites of receptor expression. Effects of ghrelin and the nonpeptide GHSR1a agonist capromorelin on rat arteries and on transmission in sympathetic ganglia were measured in vitro. In addition, rat blood pressure and sympathetic nerve activity responses to ghrelin were determined in vivo. In reporter mice, expression of GHSR was revealed at sites where it has been previously demonstrated (hypothalamic neurons, renal tubules, sympathetic preganglionic neurons) but not in any artery studied, including mesenteric, cerebral, and coronary arteries. In rat, RT-PCR detected GHSR1a mRNA expression in spinal cord and kidney but not in the aorta or in mesenteric arteries. Moreover, the aorta and mesenteric arteries from rats were not dilated by ghrelin or capromorelin at concentrations >100 times their EC(50) determined in cells transfected with human or rat GHSR1a. These agonists did not affect transmission from preganglionic sympathetic neurons that express GHSR1a. Intravenous application of ghrelin lowered blood pressure and decreased splanchnic nerve activity. It is concluded that the blood pressure reduction to ghrelin occurs concomitantly with a decrease in sympathetic nerve activity and is not caused by direct actions on blood vessels or by inhibition of transmission in sympathetic ganglia.
dc.subjectAnimal Physiology - Systems; Cardiovascular System and Diseases
dc.titleSites of action of ghrelin receptor ligands in cardiovascular control
dc.typeJournal Article
melbourne.peerreviewPeer Reviewed
melbourne.affiliationThe University of Melbourne
melbourne.affiliation.departmentAnatomy And Neuroscience
melbourne.source.titleAmerican Journal of Physiology: Heart and Circulatory Physiology
melbourne.contributor.authorFurness, John
melbourne.contributor.authorBrock, James
melbourne.contributor.authorNguyen, Trung
melbourne.contributor.authorMcIntyre, Peter
melbourne.contributor.authorHIRAYAMA, HARUKO
melbourne.contributor.authorFERENS, DOROTA
melbourne.contributor.authorAbogadie, Fe
melbourne.contributor.authorSARTOR, DANIELA
melbourne.contributor.authorHunne, Billie-Lea
melbourne.contributor.authorCallaghan, Brid
melbourne.contributor.authorBAN, KUNG
melbourne.identifier.fundernameidNHMRC, 1005811
melbourne.accessrightsThis item is currently not available from this repository

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