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J. Biol. Chem., Vol. 266, Issue 6, 3675-3681, Feb, 1991
CJ Field, R Chayoth, M Montambault and EB Marliss
Glucose metabolism in splenocytes from the BB rat was studied for the
presence of abnormalities in [14C] 2-deoxy-D-glucose (2-dGlc) uptake,
[U-14C]glucose conversion to 14CO2, and the production of lactate and
pyruvate. Cells were studied freshly isolated ("resting"), and following
culture both unstimulated (control) and stimulated with concanavalin A
(ConA) or phorbol myristate acetate (PMA) + ionomycin. Both resting and
control cells from diabetic (BBd) and diabetes-prone (BBdp) rats
transported more (p less than 0.05) 2-dGlc than did cells from
nondiabetes-prone (BBn) rats. Consistent with prior in vivo activation,
sustained in vitro, lactate production was higher (p less than 0.05) under
control conditions in BBd and BBdp than in BBn cells. Lactate production
increased less with ConA and PMA + ionomycin in both BBd and BBdp than in
BBn cells. PMA + ionomycin increased 2-dGlc uptake as much in BBd and BBdp
cells as in BBn cells. Elevated rates of pyruvate production were observed
in BBd cells under resting, control, and (especially) ConA conditions,
suggesting an abnormality in pyruvate conversion to lactate. Few changes
were observed in 14CO2 production. The presence of similar abnormalities in
BBdp cells to those of the BBd cells suggests that the diabetic state is
not causal, and the absence of an in vitro effect of 15 mmol/liter glucose
in BBn cells further tends to exclude hyperglycemia as a cause of these
alterations.
Enhanced 2-deoxy-D-glucose uptake and metabolism in splenocytes from diabetic and diabetes-prone BB rats. Further evidence to support prior in vivo activation
McGill Nutrition and Food Science Centre, The Royal Victoria Hospital, Montreal, Quebec, Canada.
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