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Differences in adrenergic nerve and receptor function in dog internal thoracic, coronary and mesenteric arteries
- Source :
- Japanese journal of pharmacology. 66(4)
- Publication Year :
- 1994
-
Abstract
- Isolated dog internal thoracic arteries (ITA) responded to norepinephrine and phenylephrine with concentration-related contractions, which were suppressed by prazosin, but not by yohimbine. Clonidine did not contract ITA. In coronary arterial strips, norepinephrine produced a relaxation. Isoproterenol relaxed coronary arterial strips contracted with serotonin but did not alter the tone of ITA. Forskolin and beraprost, an analog of prostaglandin I2, relaxed coronary and ITA strips to a similar extent. The beta-adrenoceptor density, assayed by [3H]dihydroalprenolol binding, was markedly less in ITA than in coronary arteries. Nicotine and transmural electrical stimulation did not alter the tension of ITA. Immunohistochemical study indicated that nerve fibers containing tyrosine hydroxylase immunoreactivity were markedly less in ITA than in coronary and mesenteric arteries. These results indicate that beta-adrenoceptor function and adrenergic innervation are considerably reduced in dog ITA. Norepinephrine-induced vasocontraction appears to be mediated by alpha 1-adrenoceptors in the arteries.
- Subjects :
- Male
medicine.medical_specialty
Sympathetic Nervous System
Tyrosine 3-Monooxygenase
Muscle Relaxation
Adrenergic
In Vitro Techniques
Muscle, Smooth, Vascular
Norepinephrine (medication)
Radioligand Assay
Dogs
Thoracic Arteries
Internal medicine
medicine.artery
Isometric Contraction
Receptors, Adrenergic, beta
Prazosin
medicine
Thoracic aorta
Animals
Phenylephrine
Mesenteric arteries
Pharmacology
business.industry
Coronary Vessels
Immunohistochemistry
Electric Stimulation
Mesenteric Arteries
Receptors, Adrenergic
Coronary arteries
medicine.anatomical_structure
Endocrinology
Circulatory system
Female
business
medicine.drug
Muscle Contraction
Subjects
Details
- ISSN :
- 00215198
- Volume :
- 66
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Japanese journal of pharmacology
- Accession number :
- edsair.doi.dedup.....a5b40edbb264c4b5838f2620ebc2f5f1