Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1989-9-21
pubmed:abstractText
1. The postjunctional alpha-adrenoceptors mediating contractions in the isolated vascular bed of the perfused rat tail have been investigated, in the presence and absence of an increase in perfusion pressure by arginine vasopressin (AVP). 2. In the absence of AVP, bolus doses of noradrenaline (NA) and phenylephrine produced pressor responses of similar time course, while UK-14,304 was practically inactive. Responses to noradrenaline were inhibited more by 0.05 microM prazosin than by 1 microM rauwolscine, suggesting the presence of alpha1-adrenoceptors. 3. Following a sustained elevation in perfusion pressure by AVP, both UK-14,304 and NA (the latter in the presence of 0.05 microM prazosin to inhibit alpha 1-adrenoceptors) elicited dose-dependent pressor responses. The maximum response to UK-14,304 under these conditions was approximately 30% of the maximum response to NA in the absence of prazosin and AVP. Responses to phenylephrine were not affected by the AVP-induced increase in vascular tone. 4. In the presence of AVP, pressor responses to UK-14,304 were resistant to 0.05 microM prazosin and susceptible to antagonism by 1 microM rauwolscine (-log Kb 7.65 +/- 0.15). Similarly, responses to NA in the presence of 0.05 microM prazosin and AVP were inhibited by 1 microM rauwolscine. This represents the first demonstration of prazosin-resistant, rauwolscine-sensitive alpha 2-adrenoceptor-mediated responses in the vasculature of the rat tail. 5. These results suggest that in isolated vascular preparations, functional populations of postjunctional alpha 2-adrenoceptors may be 'uncovered' by the presence of AVP.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-228207, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2436929, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2441781, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2876766, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2886504, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2893852, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2901046, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2905911, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2906557, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-2991496, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-3014118, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-3015687, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-3031281, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-3038576, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-4093454, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-4312931, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6105621, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6134815, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6138712, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6140057, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6144048, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6144792, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6145472, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6196037, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6203480, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6250857, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6279105, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-6327971, http://linkedlifedata.com/resource/pubmed/commentcorrection/2547477-744021
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0007-1188
pubmed:author
pubmed:issnType
Print
pubmed:volume
97
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
563-71
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
Evidence for prazosin-resistant, rauwolscine-sensitive alpha-adrenoceptors mediating contractions in the isolated vascular bed of the rat tail.
pubmed:affiliation
Institute of Physiology, University of Glasgow, Scotland.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't