Source:http://linkedlifedata.com/resource/pubmed/id/11742831
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2001-12-14
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pubmed:abstractText |
Recently, we reported that, whereas in cerebral arteries of the adult a majority of norepinephrine (NE)-induced increase in intracellular Ca2+ concentration ([Ca2+]i) comes from release of the sarcoplasmic reticulum (SR) Ca2+ stores, in the fetus the SR Ca2+ stores are relatively small, and NE-induced increase in [Ca2+]i results mainly from activation of plasma membrane L-type Ca2+ channels (20). In an effort to establish further the role of L-type Ca2+ channels in the developing cerebral arteries, we tested the hypothesis that, in the fetus, increased reliance on plasmalemmal L-type Ca2+ channels is mediated, in part, by increased L-type Ca2+ channel density. We used 3H-labeled (+)isopropyl-4-(2,1,3-benzoxadiazol-4-y1)-1,4-dihydro-(2,6-dimethyl-5-methoxycarbonyl)pyridine-3-carboxylate (PN200-110, isradipine) to measure L-type Ca2+ channel density (Bmax) in the cerebral arteries, common carotid artery (CCA), and descending aortae of fetal (approximately 140 gestation days), newborn (7-10 days), and adult sheep. In the cerebral and common carotid arteries, B(max) values (fmol/mg protein) of fetuses and newborns were significantly greater than those of adults. Western immunoblotting assay also revealed that the density of L-type Ca2+ channel protein in the cerebral arteries and CCA was about twofold greater in the fetus than the adult. Finally, compared with the adult, fetal cerebral arteries demonstrated a significantly greater maximum tension and [Ca2+]i in response to stimulation with the L-type Ca2+ channel agonist Bay K 8644. In addition, Bay K 8644-stimulated fetal vessels demonstrated a maximal tension and [Ca2+]i similar to that observed in response to stimulation with 10(-4) NE. These results support the idea that fetal cerebrovascular smooth muscle relies more on extracellular Ca2+ and L-type Ca2+ channels for contraction than does the adult and that this increased reliance is mediated, in part, by greater L-type Ca2+ channel density. This may have important implications in the regulation of cerebral blood flow in the developing organism.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/3-Pyridinecarboxylic acid...,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, L-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Isradipine,
http://linkedlifedata.com/resource/pubmed/chemical/Norepinephrine,
http://linkedlifedata.com/resource/pubmed/chemical/Tritium,
http://linkedlifedata.com/resource/pubmed/chemical/Vasoconstrictor Agents
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0363-6119
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
R131-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11742831-3-Pyridinecarboxylic acid...,
pubmed-meshheading:11742831-Age Factors,
pubmed-meshheading:11742831-Animals,
pubmed-meshheading:11742831-Animals, Newborn,
pubmed-meshheading:11742831-Aorta,
pubmed-meshheading:11742831-Calcium,
pubmed-meshheading:11742831-Calcium Channel Agonists,
pubmed-meshheading:11742831-Calcium Channel Blockers,
pubmed-meshheading:11742831-Calcium Channels, L-Type,
pubmed-meshheading:11742831-Cerebral Arteries,
pubmed-meshheading:11742831-Cerebrovascular Circulation,
pubmed-meshheading:11742831-Immunoblotting,
pubmed-meshheading:11742831-Isradipine,
pubmed-meshheading:11742831-Muscle, Smooth, Vascular,
pubmed-meshheading:11742831-Norepinephrine,
pubmed-meshheading:11742831-Radioligand Assay,
pubmed-meshheading:11742831-Sheep,
pubmed-meshheading:11742831-Tritium,
pubmed-meshheading:11742831-Vasoconstriction,
pubmed-meshheading:11742831-Vasoconstrictor Agents
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pubmed:year |
2002
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pubmed:articleTitle |
L-type Ca2+ channels in fetal and adult ovine cerebral arteries.
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pubmed:affiliation |
Center for Perinatal Biology, Department of Physiology/Pharmacology, School of Medicine, Loma Linda University, Loma Linda, California 92350, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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