Linked Life Data

8048595

Source:http://linkedlifedata.com/resource/pubmed/id/8048595

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1 Pt 2
pubmed:dateCreated
1994-9-1
pubmed:abstractText
Myogenic activation of isolated small arteries (200-500 microns) of the dog kidney was evaluated by measuring vessel diameters during stepwise elevations of transmural pressure before and after removal of the endothelium by mechanical rubbing or air perfusion. Myogenic activation was unaffected by mechanical rubbing, but air perfusion caused the arteries to constrict and attenuated the myogenic response; i.e., vessel diameters increased as transmural pressure was elevated. However, air-perfused arteries still constricted in response to norepinephrine and dilated during superfusion with Ca(2+)-free solution, demonstrating that loss of the myogenic response did not result from an inability of the vessel to contract. Intact arteries contracted with 1 microM norepinephrine exhibited normal myogenic responses, demonstrating that loss of myogenic activation in the air-perfused vessels was not a nonspecific effect secondary to constriction of the artery. These results suggest that myogenic activation of small renal arteries is independent of the endothelium and that the method of endothelial removal may affect conclusions regarding the role of the endothelium in mediating the myogenic response.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0002-9513
pubmed:author
pubmed:issnType
Print
pubmed:volume
267
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
H302-7
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1994
pubmed:articleTitle
Myogenic activation of canine small renal arteries after nonchemical removal of the endothelium.
pubmed:affiliation
Department of Physiology, Medical College of Wisconsin, Milwaukee 53226.
pubmed:publicationType
Journal Article, In Vitro, Research Support, U.S. Gov't, P.H.S.