Inotropic and Chronotropic Effects of 4-(4′-n-Butylaniline)-7,8-dimethoxy-5H-pyrimido[5,4–b]indole in Guinea-pig Atria

Author:

Castiella E1,Frechilla D2,Lasheras B2,Cenarruzabeitia E2,Martínez De Irujo J J1,Alberdi E1,Santiago E1,Monge A3,Villanueva A3,Martinez F J3,Font M3

Affiliation:

1. Department of Biochemistry, Centro de Investigacion en Farmacobiologia Aplicada, Universidad de Navarra, 31080 Pamplona, Spain

2. Department of Pharmacology, Centro de Investigacion en Farmacobiologia Aplicada, Universidad de Navarra, 31080 Pamplona, Spain

3. Department of Medicinal Chemistry, Centro de Investigacion en Farmacobiologia Aplicada, Universidad de Navarra, 31080 Pamplona, Spain

Abstract

Abstract Cardiotonic effect of 4-(4′-n-butylaniline)-7,8-dimethoxy-5H-pyrimido[5,4-b)]indole (B11) was investigated in isolated cardiac tissue preparations. The action of this agent on force of contraction, beating frequency and cyclic nucleotide phosphodiesterase (PDE) activity was studied. Amrinone was used for comparison. B11 produced concentration-dependent (5 × 10−6-1 × 10−4m) positive inotropic and positive chronotropic responses in guinea-pig atrial tissues. The potency of B11 was greater than that of amrinone. The cardiotonic effects of B11 were not modified by β-adrenoceptor blockade. Carbachol inhibited the positive inotropic effect of B11. The activity of B11 was increased in desensitized left atrial tissues. B11 inhibited the activities of PDE isoenzymes (type I, II, IV and V) from dog heart ventricle and PDE type IV from guinea-pig heart ventricle nonselectively. It is concluded that B11 possesses potent positive inotropic activity in guinea-pig atria, and the effect is probably mediated by a non-selective inhibition of PDE activity.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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