Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1997-1-7
pubmed:abstractText
Human adrenomedullin, a novel hypotensive peptide, contains a six-member ring structure similar to that found in calcitonin gene-related peptide and pancreatic amylin. Unlike the full-sequence peptide, human adrenomedullin-(15-22) [hADM-(15-22)], which contains the ring structure, increases systemic arterial pressure in the rat but not the cat. We undertook the present study to investigate the mechanism by which hADM-(15-22) increases systemic arterial pressure in the rat. Injection of hADM-(15-22) in doses of 10 to 300 nmol/kg i.v. increased systemic arterial pressure in a dose-dependent manner and was threefold less potent than norepinephrine when doses were compared on a nanomole basis. However, the ring structures of human calcitonin gene-related peptide and human amylin, human calcitonin gene-related peptide-(1-8) and human amylin-(1-8), respectively, had no significant effect on systemic arterial pressure in the rat. Pressor responses to hADM-(15-22) were reduced significantly after administration of phentolamine or reserpine. Responses to hADM-(15-22) were not altered by the angiotensin type 1 blocking agent DuP 753 or the endothelin-A/endothelin-B receptor blocking agent bosentan, and responses to hADM-(15-22) and the nicotinic agonist 1,1-dimethyl-4-phenylpiperazinium (DMPP) were reduced after bilateral adrenalectomy. Pressor responses to DMPP were reduced by hexamethonium, whereas the nicotinic blocking agent had no effect on the pressor response to hADM-(15-22). These data suggest that increases in systemic arterial pressure in response to hADM-(15-22) in the rat are mediated by the activation of alpha-adrenergic receptors by catecholamines released from the adrenal medulla. The present data suggest that hADM-(15-22) releases catecholamines from the adrenal medulla by a noncholinergic mechanism.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0194-911X
pubmed:author
pubmed:issnType
Print
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1041-6
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8952594-Adrenalectomy, pubmed-meshheading:8952594-Adrenomedullin, pubmed-meshheading:8952594-Animals, pubmed-meshheading:8952594-Antihypertensive Agents, pubmed-meshheading:8952594-Blood Pressure, pubmed-meshheading:8952594-Calcitonin Gene-Related Peptide, pubmed-meshheading:8952594-Catecholamines, pubmed-meshheading:8952594-Cats, pubmed-meshheading:8952594-Dose-Response Relationship, Drug, pubmed-meshheading:8952594-Female, pubmed-meshheading:8952594-Humans, pubmed-meshheading:8952594-Injections, Intravenous, pubmed-meshheading:8952594-Male, pubmed-meshheading:8952594-Peptide Fragments, pubmed-meshheading:8952594-Peptides, pubmed-meshheading:8952594-Pressoreceptors, pubmed-meshheading:8952594-Rats, pubmed-meshheading:8952594-Rats, Sprague-Dawley, pubmed-meshheading:8952594-Structure-Activity Relationship
pubmed:year
1996
pubmed:articleTitle
Catecholamine release mediates pressor effects of adrenomedullin-(15-22) in the rat.
pubmed:affiliation
Department of Pharmacology, Tulane University School of Medicine, New Orleans, La 70112, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't