D. Hugi et al., INSULIN-DEPENDENT GLUCOSE-UTILIZATION IN INTENSIVELY MILK-FED VEAL CALVES IS MODULATED BY SUPPLEMENTAL LACTOSE IN AN AGE-DEPENDENT MANNER, The Journal of nutrition, 128(6), 1998, pp. 1023-1030
Postprandial insulin resistance with excessive hyperinsulinemia, hyper
glycemia and glucosuria develops with increasing age in Veal calves in
tensively fed milk replacers. We tested the age dependency of insulin
resistance, modulated by high lactose intake, glucose oxidation and in
sulin receptor number and affinity after an overnight period without f
ood. Male carves were fed a milk replacer containing 290 or 423 g lact
ose and 310 and 541 g total sugar/kg from 69-195 kg body weight. At me
an body weights of 95 and 170 kg, insulin-dependent glucose metabolism
was studied in euglycemic-hyperinsulinemic glucose clamps (EGC), and
glucose-dependent insulin responses were tested in hyperglycemic clamp
s (HGC). EGC were combined with infusions of [C-13(6)]glucose to measu
re glucose kinetics and glucose oxidation by determination of (CO2)-C-
13 exhalation. During EGC and HGC, insulin concentrations were similar
in both groups, indicating comparable insulin secretion and metabolic
clearance rates. On the basis of glucose infusion rates required to m
aintain eu-or hyperglycemia in EGC and HGC, respectively, insulin-depe
ndent glucose utilization was not age dependent. However, in calves re
ceiving a high lactose intake, insulin-dependent glucose utilization w
as enhanced in the early phases, but was reduced in the late stages of
the growth trial, insulin-dependent glucose utilization behaved inver
sely with atom % excess of [C-13(6)]glucose, but changed in a manner s
imilar to that of the rate of glucose appearance. inhibition of endoge
nous glucose output, exhalation of (CO2)-C-13 and amounts of oxidized
glucose exhibited no group differences. More glucose was therefore sto
red in lactose-supplemented calves. A reduced insulin receptor number
in skeletal muscle in calves fed high amounts of lactose likely contri
buted to low insulin-dependent glucose utilization.