AI Article Synopsis

  • The study examined how calcium channel blockers affect halothane metabolism in guinea pig liver microsomes.
  • The experiment used a mix of liver microsomes, NADPH, calcium channel blockers (verapamil, diltiazem, nicardipine, nifedipine), and halothane.
  • Verapamil, diltiazem, and nicardipine were found to competitively inhibit the metabolism of halothane, suggesting they prevent the formation of harmful radicals during this process.

Article Abstract

The effect of calcium channel blocking agents on the reductive metabolism of halothane in liver microsomes of guinea pigs was investigated. The reaction mixture for the measurement of the end products consisted of microsomal suspension, 5 mM NADPH, calcium channel blocking agents (verapamil, diltiazem, nicardipine and nifedipine) and halothane in 0.1 M phosphate buffer (pH 7.4). The reductive metabolism of halothane was inhibited competitively by verapamil, diltiazem and nicardipine. The binding spectra for the interaction of these three drugs with cytochrome P-450 in microsomes were investigated. Verapamil caused the reverse type I difference spectrum and diltiazem caused the type I difference spectrum. However, the change caused by nicardipine was not observed by the presence of its specific spectra. NADPH-cytochrome P-450 reductase activity in microsomes did not change by the addition of these three drugs. These results suggest that these three calcium channel blocking agents inhibit the production of radical intermediates during the reductive metabolism of halothane.

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Source
http://dx.doi.org/10.1002/jat.2550110106DOI Listing

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