The porphyrogenic effects of calcium channel blocking drugs
- 1 November 1985
- journal article
- research article
- Published by Portland Press Ltd. in Clinical Science
- Vol. 69 (5) , 581-586
- https://doi.org/10.1042/cs0690581
Abstract
Treatment of monolayers of chick embryo hepatocytes with the calcium channel blocking drugs nifedipine and verapamil resulted in a decrease in the activity of uroporphyrinogen decarboxylase, an increase in the activity of .delta.-aminolaevulinate synthase and accumulation of porphyrins with uroporphyrin and heptacarboxylic porphyrin predominating. Diltiazem, another calcium channel blocking drug did not affect uroporphyrinogen decarboxylase activity and had a slight effect only on the accumulation of porphyrins. Experiments with nifedipine and verapamil in the presence of various concentrations of calcium indicate that the porphyrogenic effect is apparently not related to blocking of calcium channels.This publication has 3 references indexed in Scilit:
- The effects of succinylacetone (4,6-dioxoheptanoic acid) on δ-aminolevulinate synthase activity and the content of heme in monolayers of chick embryo liver cellsBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1982
- Intravenous Verapamil for Termination of Re-Entrant Supraventricular TachycardiasAnnals of Internal Medicine, 1980
- INDUCTION IN VITRO OF SYNTHESIS OF DELTA-AMINOLEVULINIC ACID SYNTHETASE IN CHEMICAL PORPHYRIA - A RESPONSE TO CERTAIN DRUGS SEX HORMONES AND FOREIGN CHEMICALS1966