K L Cottrill | PubMed Health

PubMed1992

Phlorizin enhancement of memory in rats and mice.

Glucose administration near the time of training or testing elevates blood glucose levels and enhances memory in rodents and humans. The magnitude of increases in circulating glucose levels predicts later retention performance in these and several other situations. Thus, circulating glucose levels appear to contribute to the regulation of memory storage processes. Phlorizin is an inhibitor of glucose transport, which, in view of the effects of glucose on memory, should impair memory. However, rats and mice injected with phlorizin before training in an inhibitory (passive) avoidance task demonstrated significantly enhanced memory performance compared to that of control animals. The effective dose of phlorizin did not significantly change regional brain-relative 3H-2-deoxyglucose uptake or plasma glucose levels. To summarize, phlorizin is a potent memory-enhancing drug. While the mechanism of this enhancement is unknown, it does not appear to include changes in blood glucose levels or brain glucose uptake.

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PubMed1988

Blood glucose and brain function: interactions with CNS cholinergic systems.

We recently found that glucose injections attenuate amnesia and hyperactivity produced by scopolamine, a muscarinic antagonist. The present study examined whether glucose would augment behavioral effects produced by a muscarinic agonist, physostigmine. In experiment I, doses were first determined for which neither glucose (10 mg/kg) nor physostigmine (0.05 mg/kg) altered scopolamine-induced hyperactivity. However, combined glucose-physostigmine injections significantly reduced scopolamine hyperactivity. Experiment II evaluated the effects of glucose on physostigmine-induced tremors. Glucose (10, 100, and 250 mg/kg) or saline injections were given 20 min before physostigmine injections (0.4 or 0.05 mg/kg). Observations of glucose effects on the severity of physostigmine-induced tremors were then obtained at 5-min intervals for 25 min after physostigmine injections. Glucose (100 mg/kg) significantly facilitated the onset of tremors when injected before either dose of physostigmine, and augmented (at 100 and 250 mg/kg) tremor severity when injected before the lower dose of physostigmine. These findings indicate that glucose can facilitate the actions of a cholinergic agonist on two behaviors, locomotor activity and tremors, adding support to the view that circulating glucose levels can modulate central cholinergic function. More generally, the results provide additional evidence that circulating glucose levels can influence brain function.

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