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
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.