Literature DB >> 7018149

Modulation by verapamil of insulin and glucagon secretion in man.

D Giugliano, S Gentile, M Verza, N Passariello, G Giannetti, M Varricchio.   

Abstract

The present investigation was designed to evaluate the effect of acute and protracted verapamil administration on insulin and glucagon secretion in man. For this purpose, 14 normal subjects received two consecutive glucose pulses (5 g.i.v. in less than 20 sec or 20 g.i.v. in less than 1 min, 7 subjects for each group), 70 or 90 min apart, before and during an infusion of verapamil (160 microgram/min). Seven additional normal subjects received two consecutive arginine pulses (5 g i.v.), 70 min apart. In 14 inpatients with coronary heart disease, we investigated the effect of protracted verapamil administration. Seven of these subjects underwent two oral glucose tolerance tests (100 g) and the other 7 two arginine tests (30 g) before and after a 10-day treatment with verapamil, 240 mg/die p.o. divided into three doses; the last dose, 80 mg, was given orally 1 h before the performance of the post-treatment test. Verapamil significantly inhibited the acute insulin response (AIR, mean change from 3-10 min) to glucose (5 g), as well as the AIR and AGR (acute glucagon response) to arginine (5 g). By contrast, verapamil failed to alter significantly the AIR to the higher glucose pulse. There was no significant change of oral glucose tolerance after verapamil, nor was there a change in insulin response to oral glucose. By contrast, insulin and glucagon responses to arginine infusion were significantly reduced by the drug.

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Year:  1981        PMID: 7018149     DOI: 10.1007/bf02099002

Source DB:  PubMed          Journal:  Acta Diabetol Lat        ISSN: 0001-5563


  12 in total

1.  [BAY a 1040--a highly potent Ca ++ -antagonistic inhibitor of electro-mechanical coupling processes in mammalian myocardium].

Authors:  A Fleckenstein; H Tritthart; H J Döring; K Y Byon
Journal:  Arzneimittelforschung       Date:  1972-01

2.  Requirement for calcium ion in insulin secretion by the perfused rat pancreas.

Authors:  D L Curry; L L Bennett; G M Grodsky
Journal:  Am J Physiol       Date:  1968-01

3.  Calcium antagonists and islet function. I. Inhibition of insulin release by verapamil.

Authors:  G Devis; G Somers; E Van Obberghen; W J Malaisse
Journal:  Diabetes       Date:  1975-06       Impact factor: 9.461

4.  Effect of furosemide on insulin and glucagon responses to arginine in normal subjects.

Authors:  D Giugliano; R Torella; S Sgambato; F D'Onofrio
Journal:  Diabetologia       Date:  1980-04       Impact factor: 10.122

5.  Effect of Verapamil on pancreatic glucagon release from the isolated, perfused canine pancreas.

Authors:  K Hermansen; J Iversen
Journal:  Scand J Clin Lab Invest       Date:  1977-04       Impact factor: 1.713

6.  Cation requirements for insulin secretion in the isolated perfused pancreas.

Authors:  G M Grodsky; L L Bennett
Journal:  Diabetes       Date:  1966-12       Impact factor: 9.461

7.  Effect of verapamil on insulin response to alcohol hypoglycemia in patients with primary hyperparathyroidism.

Authors:  S Röjdmark
Journal:  Diabetes       Date:  1979-01       Impact factor: 9.461

Review 8.  Glucoreceptor mechanisms and the control of insulin release and biosynthesis.

Authors:  S J Ashcroft
Journal:  Diabetologia       Date:  1980-01       Impact factor: 10.122

9.  Impairment of insulin secretion in man by nifedipine.

Authors:  D Giugliano; R Torella; F Cacciapuoti; S Gentile; M Verza; M Varricchio
Journal:  Eur J Clin Pharmacol       Date:  1980-11       Impact factor: 2.953

10.  [Uterus relaxation by highly potent Ca plus,plus-antagonistic inhibitors of electro-mechanical coupling such as Isoptin (verapamil, iproveratril), compound D 600 and Segontin (prenylamine). Experiments on the isolated virgin rat uterus].

Authors:  A Fleckenstein; G Grün; H Tritthart; K Byon
Journal:  Klin Wochenschr       Date:  1971-01
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  1 in total

1.  Nicardipine does not cause deterioration of glucose homoeostasis in man: a placebo controlled study in elderly hypertensives with and without diabetes mellitus.

Authors:  D Giugliano; F Saccomanno; G Paolisso; A Ceriello; R Torella; M Varricchio; F D'Onofrio
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

  1 in total

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