The effects of alpha- or beta-adrenergic receptor agonists and antagonists and calcium entry blockers on the spontaneous vasomotion
- PMID: 6150420
- DOI: 10.1016/0026-2862(84)90014-1
The effects of alpha- or beta-adrenergic receptor agonists and antagonists and calcium entry blockers on the spontaneous vasomotion
Abstract
The effects of systemic injections of vasoactive substances were studied in the micro-circulation of the hamster skin fold window preparation, which can be observed without anesthesia, exposure, and acute surgical procedures. The effects were characterized by the continuous measurement of the diameter of the arterial microvessels ranging from 100 to 8 micron. Power spectrum analysis was utilized to determine the frequency and the amplitude of the fundamental component of spontaneous diameter changes. Epinephrine and norepinephrine increased the frequency of vasomotion and reduced mean diameter at low dosages. Phentolamine reduced the frequency of vasomotion and increased mean diameter. Propranolol increased the frequency of vasomotion and did not significantly change mean diameter. Adenosine and verapamil suppressed vasomotion and increased mean diameter. These results are explained by postulating that low-dosage alpha-adrenergic receptor stimulation facilitates the spontaneous discharge of smooth muscle cells; beta-adrenergic receptor stimulation has the opposite effect, whereas beta-adrenergic receptor inhibition also enhances the vasomotor effect. Calcium entry blockers abolish the rhythmic discharge. This explanation of the activity of the various substances supports the hypothesis that the spontaneous vasomotion of the arterial microvessels is related to the intrinsic property of smooth muscle cells.
Similar articles
-
Effects of a calcium antagonist and of the adrenergic system on spontaneous vasomotion and mean arteriolar diameter in the hamster cheek pouch: influence of buflomedil.Int J Microcirc Clin Exp. 1997 Jul-Aug;17(4):164-74. doi: 10.1159/000179225. Int J Microcirc Clin Exp. 1997. PMID: 9378566
-
Systemic and topical drug administration in the pig ureter: effect of phosphodiesterase inhibitors alpha1, beta and beta2-adrenergic receptor agonists and antagonists on the frequency and amplitude of ureteral contractions.J Urol. 2001 Aug;166(2):714-20. doi: 10.1016/s0022-5347(05)66049-1. J Urol. 2001. PMID: 11458123
-
Cerebrovascular smooth muscle culture. II. Characterization of adrenergic receptors linked to adenylate cyclase.Life Sci. 1984 Feb 20;34(8):783-91. doi: 10.1016/0024-3205(84)90386-2. Life Sci. 1984. PMID: 6142395
-
Impact of exercise-induced coronary vasomotion on anti-ischemic therapy.Coron Artery Dis. 2000 Jun;11(4):363-9. doi: 10.1097/00019501-200006000-00011. Coron Artery Dis. 2000. PMID: 10860181 Review.
-
Adrenoceptors in airway smooth muscle.Pharmacol Ther. 1990;48(3):295-322. doi: 10.1016/0163-7258(90)90051-3. Pharmacol Ther. 1990. PMID: 1982179 Review.
Cited by
-
Ca2+ signalling in rat vascular smooth muscle cells: a role for protein kinase C at physiological vasoconstrictor concentrations of vasopressin.J Physiol. 2000 May 1;524 Pt 3(Pt 3):821-31. doi: 10.1111/j.1469-7793.2000.00821.x. J Physiol. 2000. PMID: 10790161 Free PMC article.
-
Relationship between gastric mucosal hemodynamics and gastric motility.Gastroenterol Jpn. 1990 Jun;25(3):299-305. doi: 10.1007/BF02779442. Gastroenterol Jpn. 1990. PMID: 2358162
-
Vasomotion and neurovascular coupling in the visual thalamus in vivo.PLoS One. 2011;6(12):e28746. doi: 10.1371/journal.pone.0028746. Epub 2011 Dec 9. PLoS One. 2011. PMID: 22174886 Free PMC article.
-
Central angiotensin II stimulates arteriolar vasomotion in conscious hamsters.J Comp Physiol B. 1989;159(5):577-82. doi: 10.1007/BF00694382. J Comp Physiol B. 1989. PMID: 2575095
-
The impact of vasomotion on analysis of rodent fMRI data.Front Neurosci. 2023 Feb 24;17:1064000. doi: 10.3389/fnins.2023.1064000. eCollection 2023. Front Neurosci. 2023. PMID: 36908777 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources