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Norepinephrine stimulates arachidonic acid release from vascular smooth muscle via activation of cPLA2

Norepinephrine stimulates arachidonic acid release from vascular smooth muscle via activation of... Abstract The mechanism of agonist-activated arachidonate release was studied in segments of rat tail artery. Tail artery segments were prelabeled with 3 Harachidonate and then stimulated with norepinephrine (NE), and the radioactivity of the extracellular medium was determined. NE stimulated arachidonate release from the tissue without increasing arachidonic acid levels within cellular cytosol or crude membranes. About 90% of the extracellular radioactivity was shown to be unmetabolized arachidonate by TLC. Arachidonic acid release was not inhibited by the removal of the endothelium from the artery. NE exerted a half-maximal effect at a concentration of 0.2 μM. NE-stimulated arachidonate release was not inhibited by blockers of phospholipase C (U-73122), diacylglycerol lipase (RHC-80267), secretory phospholipase A 2 (manoalide), calcium-insensitive phospholipase A 2 (HELSS), or β-adrenergic receptors (propranolol). NE-stimulated arachidonic acid release was inhibited by blockers of cytosolic phospholipase A 2 (cPLA 2 ) (AACOCF 3 ), α 1 -adrenergic receptors (prazosin), and specific G proteins (pertussis toxin). This indicated that NE stimulated arachidonate release from vascular smooth muscle via activation of α-adrenergic receptors, either G i or G o , and cPLA 2 . NE-activated arachidonic acid release from vascular smooth muscle may play a role in force generation by the tissue. Perhaps arachidonic acid extends the effect of NE on one specific smooth muscle cell to its nearby neighbor cells. rat tail artery calcium force regulation phospholipase C cytosolic phospholipase A 2 Footnotes Address for reprint requests: E. F. LaBelle, Dept. of Physiology, Allegheny Univ. of the Health Sciences, 2900 Queen La., Philadelphia, PA 19129. Copyright © 1998 the American Physiological Society http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png AJP - Cell Physiology The American Physiological Society

Norepinephrine stimulates arachidonic acid release from vascular smooth muscle via activation of cPLA2

AJP - Cell Physiology , Volume 274 (4): C1129 – Apr 1, 1998

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Publisher
The American Physiological Society
Copyright
Copyright © 2010 the American Physiological Society
ISSN
0363-6143
eISSN
1522-1563
Publisher site
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Abstract

Abstract The mechanism of agonist-activated arachidonate release was studied in segments of rat tail artery. Tail artery segments were prelabeled with 3 Harachidonate and then stimulated with norepinephrine (NE), and the radioactivity of the extracellular medium was determined. NE stimulated arachidonate release from the tissue without increasing arachidonic acid levels within cellular cytosol or crude membranes. About 90% of the extracellular radioactivity was shown to be unmetabolized arachidonate by TLC. Arachidonic acid release was not inhibited by the removal of the endothelium from the artery. NE exerted a half-maximal effect at a concentration of 0.2 μM. NE-stimulated arachidonate release was not inhibited by blockers of phospholipase C (U-73122), diacylglycerol lipase (RHC-80267), secretory phospholipase A 2 (manoalide), calcium-insensitive phospholipase A 2 (HELSS), or β-adrenergic receptors (propranolol). NE-stimulated arachidonic acid release was inhibited by blockers of cytosolic phospholipase A 2 (cPLA 2 ) (AACOCF 3 ), α 1 -adrenergic receptors (prazosin), and specific G proteins (pertussis toxin). This indicated that NE stimulated arachidonate release from vascular smooth muscle via activation of α-adrenergic receptors, either G i or G o , and cPLA 2 . NE-activated arachidonic acid release from vascular smooth muscle may play a role in force generation by the tissue. Perhaps arachidonic acid extends the effect of NE on one specific smooth muscle cell to its nearby neighbor cells. rat tail artery calcium force regulation phospholipase C cytosolic phospholipase A 2 Footnotes Address for reprint requests: E. F. LaBelle, Dept. of Physiology, Allegheny Univ. of the Health Sciences, 2900 Queen La., Philadelphia, PA 19129. Copyright © 1998 the American Physiological Society

Journal

AJP - Cell PhysiologyThe American Physiological Society

Published: Apr 1, 1998

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