Alpha-adrenoceptor activation induces rhythmic contractile activity in carotid arteries from young, not adult, rats. Acta Physiol Scand 1997 Feb;159(2):123-9
Date
02/01/1997Pubmed ID
9055939DOI
10.1046/j.1365-201X.1997.579338000.xScopus ID
2-s2.0-0031030704 (requires institutional sign-in at Scopus site) 6 CitationsAbstract
Rhythmic contractions are produced by small arteries, arterioles and veins in several vascular beds, but they are often absent in large arteries. However, under certain conditions, and in certain disease states large arteries may produce rhythmic contractions. For this reason, the present study was undertaken to test the hypothesis that rhythmic contractions may be a 'normal' response in large arteries at some stage in development. We investigated this hypothesis by examining contractions of carotid arteries in male and female rats aged 15, 25 and 30 days and in adult rats. Rhythmic contractions were produced by exposure to, or during washout of alpha-adrenoceptor agonists in young, but not adult, rats. In particular, rhythmic activity was identified in 40, 95 and 50% of the arteries from, respectively, 15, 25 and 30-day-old rats. No differences were found in rhythmic activity between female and male rats. Furthermore, the rhythmic activity was not inhibited by the K+ channel blocker TEA (20 mM) or the Na+/K(+)-ATPase inhibitor, ouabain (32 microM). Nor was it inhibited by endothelial denudation. However, the Ca2+ channel blocker, nifedipine (0.1 microM), completely eliminated rhythmic contraction. These results suggest that receptor-induced rhythmic contractile activity is a 'normal' characteristic at approximately 25 days of development in carotid arteries of rats, but that this activity declines with age until it is completely absent by adulthood. We proposed that this difference was due to unfused and fused Ca2+ channel activities in, respectively, young and adult rat arteries, to differential expression of Ca2+ channel isotypes, or to differences in receptor-mediated signal transduction mechanisms 'upstream' from Ca2+ channels.
Author List
Eddinger TJ, Ratz PHAuthor
Thomas Eddinger PhD Bioological Sciences in the Biology department at Marquette UniversityMESH terms used to index this publication - Major topics in bold
AgingAnimals
Animals, Newborn
Calcium Channel Blockers
Carotid Arteries
Enzyme Inhibitors
Female
Male
Nifedipine
Ouabain
Periodicity
Potassium Channel Blockers
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, alpha
Sodium-Potassium-Exchanging ATPase
Tetraethylammonium
Tetraethylammonium Compounds
Vasoconstriction