Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2 Pt 1
pubmed:dateCreated
1990-3-28
pubmed:abstractText
The present study uses various kinin agonists and antagonists to examine the cellular mechanisms of bradykinin's actions on intracellular calcium, prostaglandins, and adenosine 3',5'-cyclic monophosphate (cAMP) accumulation in cultured arterial smooth muscle cells (casmc) obtained from rat mesenteric arteries. Exposure to bradykinin produced a rapid release of calcium (peak less than or equal to 20 s) from intracellular stores and an increase in prostaglandin (PG) E2 and cAMP production in casmc. Compared with bradykinin, the bradykinin B1-agonist [des-Arg9]BK produced only a small increase in intracellular calcium. The bradykinin-mediated increase in intracellular calcium was competitively blocked by the B2 receptor antagonist [D-Arg-O-Hyp3-Thi5,8-D-Phe7]BK (B4307) but not the B1-antagonist ([des-Arg9-Leu8]BK). In addition, the similarity of the dose-response curves for the bradykinin-mediated increase in Ca2+, PGE2, and cAMP (half-maximal stimulation of 12, 11, and 13 nM, respectively) and the ability of the B2-antagonist (B4307) to block each of these effects of bradykinin suggest that all three effects are mediated by the same bradykinin (B2) receptor. Further studies revealed that increases in intracellular calcium are necessary for the bradykinin-mediated increase in PGE2 formation and the subsequent PGE2-dependent formation of cAMP. Taken together, these results suggest that bradykinin acts via a B2-receptor on arterial smooth muscle cells to release calcium from intracellular stores, leading to increases in PGE2 production and the PGE2-dependent activation of adenylate cyclase.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/6-Ketoprostaglandin F1 alpha, http://linkedlifedata.com/resource/pubmed/chemical/8-(N,N-diethylamino)octyl-3,4,5-trim..., http://linkedlifedata.com/resource/pubmed/chemical/Actins, http://linkedlifedata.com/resource/pubmed/chemical/Bradykinin, http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP, http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone, http://linkedlifedata.com/resource/pubmed/chemical/Gallic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Triphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Indomethacin, http://linkedlifedata.com/resource/pubmed/chemical/Isoproterenol
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0002-9513
pubmed:author
pubmed:issnType
Print
pubmed:volume
258
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
C299-308
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:2154931-6-Ketoprostaglandin F1 alpha, pubmed-meshheading:2154931-Actins, pubmed-meshheading:2154931-Animals, pubmed-meshheading:2154931-Bradykinin, pubmed-meshheading:2154931-Calcium, pubmed-meshheading:2154931-Calcium Channel Blockers, pubmed-meshheading:2154931-Cells, Cultured, pubmed-meshheading:2154931-Cyclic AMP, pubmed-meshheading:2154931-Dinoprostone, pubmed-meshheading:2154931-Fluorescent Antibody Technique, pubmed-meshheading:2154931-Gallic Acid, pubmed-meshheading:2154931-Guanosine Triphosphate, pubmed-meshheading:2154931-Indomethacin, pubmed-meshheading:2154931-Isoproterenol, pubmed-meshheading:2154931-Kinetics, pubmed-meshheading:2154931-Mesenteric Arteries, pubmed-meshheading:2154931-Muscle, Smooth, Vascular, pubmed-meshheading:2154931-Rats, pubmed-meshheading:2154931-Rats, Inbred Strains, pubmed-meshheading:2154931-Structure-Activity Relationship
pubmed:year
1990
pubmed:articleTitle
Effects of kinins on cultured arterial smooth muscle.
pubmed:affiliation
Department of Medicine, Veterans Administration Medical Center, University of Colorado Health Sciences Center, Denver.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't