Document Detail


Stress susceptibility as a determinant of the response to adrenergic stimuli in mesenteric resistance arteries of the rat.
MedLine Citation:
PMID:  12409976     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Characterized by the behavioral response to apomorphine, two outbred lines of Wistar rats can be recognized with constitutionally determined high (apomorphine susceptible, APO-SUS) or low (apomorphine unsusceptible, APO-UNSUS) adrenal responses to similar environmental stress. Within the accumbens nucleus, the APO-SUS and APO-UNSUS rats differ in alpha -adrenergic receptor responsiveness. This study explored whether these differences in adrenergic receptor sensitivity also exist in mesenteric resistance arteries. A Mulvany myograph was used to study the vasomotor responses of isolated mesenteric resistance arteries to adrenergic receptor stimulation. Phenylephrine (alpha1-agonist)-induced vasoconstriction did not differ between the two lines (pEC : 5.8 +/- 0.05 microM versus 5.8 +/- 0.04 microM and Emax: 36 +/- 2 kPa versus 33 +/- 1 kPa for APO-SUS, n = 9, and APO-UNSUS, n = 11, respectively, p > 0.1). After precontraction with phenylephrine, salbutamol (beta -agonist)-induced relaxation was less in APO-SUS rats (pEC50 4.9 +/- 0.06 versus 5.3 +/- 0.06M for APO-SUS, n = 9, and APO-UNSUS, n = 7, respectively, p < 0.001). Likewise, clonidine (alpha2-agonist)-induced relaxation was reduced in APO-SUS rats (pEC50: 6.7 +/- 0.07 versus 7.0 +/- 0.04, for APO-SUS, n = 9, and APO-UNSUS, n = 8, respectively; p < 0.01). In conclusion, constitutionally determined high susceptibility to stress is accompanied by an impaired vasorelaxation to adrenergic stimuli whereas vasoconstriction is unaffected. An unopposed vasoconstrictor action of norepinephrine may place the APO-SUS rats at increased risk for the development of hypertension, insulin resistance, and atherosclerosis.
Authors:
Bart W Smits; Helene L M Siero; Bart A Ellenbroek; Niels P Riksen; Alexander R Cools; Joop M P M Borggreven; Gerard A Rongen; Frans G M Russel; Paul Smits
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of cardiovascular pharmacology     Volume:  40     ISSN:  0160-2446     ISO Abbreviation:  J. Cardiovasc. Pharmacol.     Publication Date:  2002 Nov 
Date Detail:
Created Date:  2002-10-31     Completed Date:  2003-03-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7902492     Medline TA:  J Cardiovasc Pharmacol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  678-83     Citation Subset:  IM    
Affiliation:
Department of Pharmacology-Toxicology, University Medical Center Nijmegen, Nijmegen, the Netherlands.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apomorphine / administration & dosage,  pharmacology*
Dopamine Agonists / administration & dosage,  pharmacology*
Dose-Response Relationship, Drug
Drug Interactions
Male
Mesenteric Arteries / drug effects
Phenylephrine / pharmacology
Rats
Receptors, Adrenergic / drug effects*
Vasoconstriction / drug effects*
Vasoconstrictor Agents / pharmacology
Vasodilation / drug effects
Chemical
Reg. No./Substance:
0/Dopamine Agonists; 0/Receptors, Adrenergic; 0/Vasoconstrictor Agents; 58-00-4/Apomorphine; 59-42-7/Phenylephrine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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