Diabetic rat aorta responsiveness to D600 and nifedipine

Clin Exp Pharmacol Physiol. 1993 Feb;20(2):77-81. doi: 10.1111/j.1440-1681.1993.tb00578.x.

Abstract

1. The responsiveness of aortic rings from 4 and 12 week streptozotocin-induced diabetic rats to D600 (Gallopamil) and nifedipine was studied. 2. The sensitivity and responsiveness to D600 were significantly enhanced (P < 0.05; 5-test, ANOVA; 9 d.f.) only in the 4 week diabetic preparations precontracted with noradrenaline. 3. Nifedipine-induced relaxations were significantly enhanced (P < 0.05-0.01; t-test, ANOVA; 8-12 d.f.) in all the diabetic (4 and 12 weeks) aortic preparations precontracted with both noradrenaline (10(-7) mol/L) and KCl (40 mmol/L) when compared with controls. 4. D600, unlike nifedipine, did not produce significant relaxation of diabetic aortic preparations precontracted with KCl (40 mmol/L) at both week 4 and 12 of the disease when compared with controls. 5. These results suggest that there is differential responsiveness of streptozotocin diabetic rat aorta to D600 and nifedipine.

MeSH terms

  • Animals
  • Aorta / drug effects*
  • Diabetes Mellitus, Experimental / physiopathology*
  • Gallopamil / pharmacology*
  • In Vitro Techniques
  • Male
  • Nifedipine / pharmacology*
  • Norepinephrine / pharmacology
  • Potassium Chloride / pharmacology
  • Rats
  • Rats, Wistar
  • Time Factors
  • Vasodilation / drug effects

Substances

  • Gallopamil
  • Potassium Chloride
  • Nifedipine
  • Norepinephrine