Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11304
Title: Effect of verapamil withdrawal on cardiac beta 1-adrenoceptor density.
Authors: Nayler, W G;Dillon, J S
Affiliation: Department of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australia.
Issue Date: 16-May-1990
Citation: European Journal of Clinical Pharmacology; 39 Suppl 1(): S13-6
Abstract: Ischaemia imposes a progression of damage on the myocardium, starting with a loss of adenosine triphosphate, creatine phosphate, potassium and active tension-generating capacity. These changes progress until the tissue is incapable of maintaining ionic homeostasis, is depleted of purine precursors and shows evidence of structural disorganization. Upon reperfusion the ischaemia-induced damage is exaggerated, primarily because of the accompanying uncontrolled gain in calcium, increasing tissue osmolarity and release of endogenous noradrenaline. When used prophylactically, calcium antagonists attenuate many of the deleterious effects of ischaemia and reperfusion. We have previously shown that long-term administration of verapamil to rats (50 mg/kg daily, orally) depletes their cardiac stores of noradrenaline (NA) (3.9 +/- 0.3 micrograms/g dry wt in controls vs 0.9 +/- 0.1 micrograms/g dry wt NA after 6 weeks of therapy). This loss of NA was not accompanied by a change in beta 1-adrenoceptor density (35.5 +/- 1.9 fmol/mg protein for controls vs 31.2 +/- 2.3 fmol/mg protein after 6 weeks of therapy). Verapamil withdrawal after 6 weeks of therapy resulted in a restoration of ventricular NA levels; within 2 days they had recovered to 75% of their original values. The density of the beta 1-adrenoceptor was unaltered. Withdrawal of verapamil results in rapid repletion of cardiac NA, with an initial but transient reduction in beta 1-adrenoceptor density. The absence of beta 1-adrenoceptor "up-regulation" under these conditions probably contributes to the absence of withdrawal problems upon cessation of verapamil therapy.
Internal ID Number: 2175707
URI: http://ahro.austin.org.au/austinjspui/handle/1/11304
URL: http://www.ncbi.nlm.nih.gov/pubmed/2175707
Type: Journal Article
Subjects: Animals
Ischemia.etiology
Kinetics
Male
Norepinephrine.metabolism
Rats
Receptor Aggregation.drug effects
Receptors, Adrenergic, beta.metabolism
Time Factors
Verapamil.administration & dosage.pharmacology
Appears in Collections:Journal articles

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