D. Cameronsmith et al., REDUCTION IN HYPERGLYCEMIA BY MILD FOOD RESTRICTION IN STREPTOZOTOCIN-INDUCED DIABETIC RATS IMPROVES INSULIN SENSITIVITY, Hormone and Metabolic Research, 26(7), 1994, pp. 316-321
Hyperglycemia has been shown to contribute to the development and main
tenance of insulin resistance in diabetic subjects and animal models o
f diabetes. Normalisation of circulating glucose levels is effective i
n restoring insulin action. The aim of the current study was to invest
igate the effects of mild food restriction on hyperglycemia in strepto
zotocin (STZ) treated (50 mg/kg) diabetic rats and to determine if the
reductions in glycemia following food restriction were sufficient to
alter insulin sensitivity. Food restriction was achieved in STZ diabet
ic and normal rats by limiting food access to two one-hourly meals dai
ly and further in normal rats by restricting the feeding period to a s
ingle two-hour meal daily. Food intake was lowered by 39.7% (p < 0.01)
in the food restricted STZ rats, without significant alteration in we
ight gain over 4 weeks. Similarly in the normal rats once and twice da
ily meals lowered food intake by 37.6% and 21.6% when compared to the
ad-libitum fed group, respectively. After 3 weeks food restriction in
the STZ diabetic rats mean plasma glucose levels over a 12 hour period
were reduced by 13.9%, glucose levels after a 6 hr fast were reduced
by 33% (p < 0.05). Plasma insulin levels remained unaltered by food re
striction. After 4 weeks food restriction in STZ diabetic rats basal g
lucose turnover was reduced (p < 0.05) and the metabolic clearance rat
e of glucose (MCR) increased (p < 0.05). During the hyperinsulinemic c
lamp hepatic glucose output (HGO) was suppressed and MCR elevated more
effectively in the food restricted STZ than the ad-libitum STZ rats.
In normal rats food restriction resulted in increased basal and insuli
n-stimulated glucose disposal (MCR). We conclude that food restriction
is effective in lowering plasma glucose levels and increases insulin
sensitivity in STZ diabetic rats.