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Article: Anoxia and endothelium-dependent reactivity of the canine femoral artery

TitleAnoxia and endothelium-dependent reactivity of the canine femoral artery
Authors
Issue Date1983
PublisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0022-3751
Citation
Journal Of Physiology, 1983, v. Vol. 335, p. 65-74 How to Cite?
AbstractExperiments were designed to determine the role of the endothelium in the responsiveness of the arterial wall to anoxia. Paired rings of canine femoral arteries were mounted for isometric tension recording in organ chambers filled with aerated Krebs-Ringer bicarbonate solution (37°C). One ring served as control; in the other the intimal layer was removed mechanically. Anoxia was induced by gassing the organ chamber with 95% N2/5% CO2. In control rings anoxia augmented contractile responses to noradrenaline, KCl and BaCl2. On return to O2 the contractile responses were transiently depressed. Removal of the endothelium reduced the anoxic augmentation, but did not affect the post-anoxic inhibition. Indomethacin did not affect the response to anoxia. Anoxia abolished the endothelium-dependent inhibitory effect of acetylcholine and thrombin, reduced that of adenosine triphosphate, but augmented that of arachidonic acid. These experiments indicate that endothelial cells may contribute to anoxic facilitation of the responsiveness of the canine arterial wall.
Persistent Identifierhttp://hdl.handle.net/10722/170699
ISSN
2023 Impact Factor: 4.7
2023 SCImago Journal Rankings: 1.708
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDe Mey, JGen_US
dc.contributor.authorVanhoutte, PMVen_US
dc.date.accessioned2012-10-30T06:10:30Z-
dc.date.available2012-10-30T06:10:30Z-
dc.date.issued1983en_US
dc.identifier.citationJournal Of Physiology, 1983, v. Vol. 335, p. 65-74en_US
dc.identifier.issn0022-3751en_US
dc.identifier.urihttp://hdl.handle.net/10722/170699-
dc.description.abstractExperiments were designed to determine the role of the endothelium in the responsiveness of the arterial wall to anoxia. Paired rings of canine femoral arteries were mounted for isometric tension recording in organ chambers filled with aerated Krebs-Ringer bicarbonate solution (37°C). One ring served as control; in the other the intimal layer was removed mechanically. Anoxia was induced by gassing the organ chamber with 95% N2/5% CO2. In control rings anoxia augmented contractile responses to noradrenaline, KCl and BaCl2. On return to O2 the contractile responses were transiently depressed. Removal of the endothelium reduced the anoxic augmentation, but did not affect the post-anoxic inhibition. Indomethacin did not affect the response to anoxia. Anoxia abolished the endothelium-dependent inhibitory effect of acetylcholine and thrombin, reduced that of adenosine triphosphate, but augmented that of arachidonic acid. These experiments indicate that endothelial cells may contribute to anoxic facilitation of the responsiveness of the canine arterial wall.en_US
dc.languageengen_US
dc.publisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0022-3751en_US
dc.relation.ispartofJournal of Physiologyen_US
dc.subject.meshAnimalsen_US
dc.subject.meshBarium - Pharmacologyen_US
dc.subject.meshDogsen_US
dc.subject.meshEndothelium - Physiologyen_US
dc.subject.meshFemoral Artery - Physiologyen_US
dc.subject.meshGlucose - Pharmacologyen_US
dc.subject.meshIndomethacin - Pharmacologyen_US
dc.subject.meshMuscle Contraction - Drug Effectsen_US
dc.subject.meshMuscle, Smooth, Vascular - Physiologyen_US
dc.subject.meshNorepinephrine - Pharmacologyen_US
dc.subject.meshOxygen - Pharmacology - Physiologyen_US
dc.subject.meshPotassium - Pharmacologyen_US
dc.titleAnoxia and endothelium-dependent reactivity of the canine femoral arteryen_US
dc.typeArticleen_US
dc.identifier.emailVanhoutte, PMV:vanhoutt@hku.hken_US
dc.identifier.authorityVanhoutte, PMV=rp00238en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1113/jphysiol.1983.sp014519-
dc.identifier.pmid6875896-
dc.identifier.scopuseid_2-s2.0-0020647593en_US
dc.identifier.volumeVol. 335en_US
dc.identifier.spage65en_US
dc.identifier.epage74en_US
dc.identifier.isiWOS:A1983QE88200006-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridDe Mey, JG=7101918486en_US
dc.identifier.scopusauthoridVanhoutte, PMV=7202304247en_US
dc.identifier.issnl0022-3751-

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