Literature DB >> 7105084

Sensitivity of cat papillary muscles to verapamil and nifedipine: enhanced effect in acidosis.

M G Briscoe, H J Smith.   

Abstract

The effects of acidosis on the myocardial sensitivity to verapamil and nifedipine were examined by measuring the changes in tension in cat papillary muscles perfused in oxygenated physiological saline. Calcium concentration was altered over a range of 2 to 12 mmol . litre-1 and pH adjusted to 7.4, 6.8 or 6.0. Addition of verapamil or nifedipine moved the calcium dose response to the right. At pH 7.4 a Schild plot confirmed competitive interaction between verapamil and calcium, with a calculated dissociation constant (KB) for verapamil of 4.6 +/- 0.2 micrograms . cm-3. At pH 6.0 the slope was less than 1.0 (not significant, P = 0.2) but KB was significantly lower (P less than 0.01) at 0.62 +/- 0.4 microgram . cm-3. Similar enhancement of sensitivity by lowered pH was found for nifedipine. It is proposed that partial inhibition of the slow channel by acidosis increases the sensitivity to calcium entry blockers. This might create a differential effect between normal and diseased tissue in vivo.

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Year:  1982        PMID: 7105084     DOI: 10.1093/cvr/16.4.173

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  5 in total

1.  Calcium channel antagonists: pharmacological considerations.

Authors:  D Rampe; C M Su; F Yousif; D J Triggle
Journal:  Br J Clin Pharmacol       Date:  1985       Impact factor: 4.335

2.  Effects of hypoxia, elevated K+ and acidosis on the potency of verapamil, diltiazem and nifedipine in the guinea-pig isolated papillary muscle.

Authors:  M J Robertson; P Lumley
Journal:  Br J Pharmacol       Date:  1989-11       Impact factor: 8.739

3.  The mechanism of action of calcium antagonists on arrhythmias in early myocardial ischaemia: studies with nifedipine and DHM9.

Authors:  M J Curtis; M J Walker
Journal:  Br J Pharmacol       Date:  1988-08       Impact factor: 8.739

4.  Actions of the verapamil analogues, anipamil and ronipamil, against ischaemia-induced arrhythmias in conscious rats.

Authors:  M J Curtis; M J Walker; T Yuswack
Journal:  Br J Pharmacol       Date:  1986-06       Impact factor: 8.739

5.  The structurally novel Ca2+ channel blocker Ro 40-5967, which binds to the [3H] desmethoxyverapamil receptor, is devoid of the negative inotropic effects of verapamil in normal and failing rat hearts.

Authors:  J P Clozel; M Véniant; W Osterrieder
Journal:  Cardiovasc Drugs Ther       Date:  1990-06       Impact factor: 3.727

  5 in total

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