Literature DB >> 1003699

Simultaneous assessment of effects of coronary vasodilators on the coronary blood flow and the myocardial contractility by using the blood-perfused canine papillary muscle.

N Himori, H Ono, N Taira.   

Abstract

Effects of 6 coronary vasodilators on the coronary blood flow and the contractile force of the ventricular muscle were examined simultaneously by injecting these drugs to the arterially blood-perfused canine papillary muscle preparation. All compounds produced a dose-dependent increase in blood flow rate, and relative potencies determined on the basis of doses producing a 100% increase in blood flow rate, ED100, were in the descending order : nifedipine greater than verapamil greater than diltiazem greater than dilazep greater than dipyridamole greater than carbochromen, and approximately 1 : 1/12 : 1/26 : 1/100 : 1/300 : 1/500. All drugs except for dipyridamole caused a dose-dependent decrease in the developed tension of the papillary muscle, although nifedipine and diltiazem in low doses produced a slight increase. Relative potencies determined on the basis of doses producing a 50% decrease in developed tension, ID50, were as follows: nifedipine (1), verapamil (1/13), diltiazem (1/40), dilazep (1/100), and carbochromen (1/270). Ratios of the ID50 to ED100 were as follows: diltiazem (5.2), nifedipine (3.5), verapamil (3.5), dilazep (2.5), and carbochromen (1.8). The higher the value the more predominant on the coronary vascular bed or the less depressant on the myocardial contractility were their actions.

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Year:  1976        PMID: 1003699     DOI: 10.1254/jjp.26.427

Source DB:  PubMed          Journal:  Jpn J Pharmacol        ISSN: 0021-5198


  17 in total

1.  Negative chronotropic and inotropic effects of class I antiarrhythmic drugs assessed in isolated canine blood-perfused sinoatrial node and papillary muscle preparations.

Authors:  A Sugiyama; S Takehana; R Kimura; K Hashimoto
Journal:  Heart Vessels       Date:  1999       Impact factor: 2.037

2.  Voltage-dependent effects of YC-170, a dihydropyridine calcium channel modulator, in cardiovascular tissues.

Authors:  H Nakaya; Y Hattori; N Tohse; M Kanno
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1986-08       Impact factor: 3.000

3.  Positive inotropic effects of calcium channel antagonists are not necessarily caused by partial calcium channel agonism.

Authors:  N C Punt; F T van Amsterdam; M M Goddijn; M Haas; J Zaagsma
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1988-08       Impact factor: 3.000

Review 4.  Calcium channel antagonists, Part I: Fundamental properties: mechanisms, classification, sites of action.

Authors:  L H Opie
Journal:  Cardiovasc Drugs Ther       Date:  1987-12       Impact factor: 3.727

5.  Differential potentiation by depolarization of the effects of calcium antagonists on contraction and Ca2+ current in guinea-pig heart.

Authors:  R Okuyama; S Adachi-Akahane; T Nagao
Journal:  Br J Pharmacol       Date:  1994-10       Impact factor: 8.739

6.  Calcium channel activation: a different type of drug action.

Authors:  S B Freedman; R J Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1984-09       Impact factor: 11.205

7.  Electrophysiological effects of diltiazem, nifedipine and Ni2+ on the subepicardial muscle cells of canine heart under the condition of combined hypoxia, hyperkalemia and acidosis.

Authors:  S Kimura; H Nakaya; M Kanno
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1983-11       Impact factor: 3.000

Review 8.  Diltiazem. A review of its pharmacological properties and therapeutic efficacy.

Authors:  M Chaffman; R N Brogden
Journal:  Drugs       Date:  1985-05       Impact factor: 9.546

9.  Alternatives to beta-blockade in therapy of hypertension with angina pectoris: role of nifedipine or of labetalol.

Authors:  L H Opie; D White; J Lee; W F Lubbe
Journal:  Br J Clin Pharmacol       Date:  1982-06       Impact factor: 4.335

10.  Positive inotropic and negative chronotropic effects of (-)-cis-diltiazem in rat isolated atria.

Authors:  Y Nasa; K Ichihara; R Yoshida; Y Abiko
Journal:  Br J Pharmacol       Date:  1992-03       Impact factor: 8.739

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