EFFECTS OF STREPTOZOTOCIN-INDUCED DIABETES ON VASCULAR REACTIVITY IN GENETICALLY HYPERINSULINEMIC OBESE ZUCKER RATS

Authors
Citation
Nc. Turner et P. White, EFFECTS OF STREPTOZOTOCIN-INDUCED DIABETES ON VASCULAR REACTIVITY IN GENETICALLY HYPERINSULINEMIC OBESE ZUCKER RATS, Journal of cardiovascular pharmacology, 27(6), 1996, pp. 884-890
Citations number
43
Categorie Soggetti
Cardiac & Cardiovascular System","Respiratory System","Pharmacology & Pharmacy
ISSN journal
01602446
Volume
27
Issue
6
Year of publication
1996
Pages
884 - 890
Database
ISI
SICI code
0160-2446(1996)27:6<884:EOSDOV>2.0.ZU;2-I
Abstract
Although the fa/fa Zucker rat shows many of the features of type II di abetes, the absence of consistent cardiovascular complications in this model may be due to the absence of significant hyperglycaemia. We stu died the consequences of streptozotocin (STZ)-induced insulin deficien cy and hyperglycaemia on vascular reactivity in the fa/fa Zucker rat. Hyperinsulinaemic obese Zucker rats were rendered diabetic by injectio n of STZ (50-60 mg/kg intraperitoneally, i.p.), and vascular tissue wa s removed for study 10-12 weeks later. In isolated aorta, there was no difference in the phenylephrine (PE) concentration-response relation between lean and obese control animals, but the concentration-response curve was shifted to the left in diabetic animals, (pD(2) 7.56 +/- 0. 04 in STZ diabetic animals, n = 8; 7.4 +/- 0.04 in obese control, n = 9, p < 0.05); The maximum response was also enhanced in both aorta and perfused mesentery of STZ-treated animals. In contrast, the potency o f serotonin (5-HT) in inducing contractions of isolated aorta were enh anced in tissues from obese as compared with lean animals (pD(2) 6.63 +/- 0.06, n = 9; 6.17 +/- 0.07, n = 7 respectively; p < 0.01) and was attenuated in animals with STZ-induced diabetes (pD(2) 6.31 +/- 0.09, n = 8, p = 0.05). The differential effects of hyperglycaemia on PE and 5-HT-induced vasoconstriction suggest that the long-lasting modulatio n of vasoconstrictor responses induced by increases in blood glucose l evel may be specific for some agonists.