S. Nagamatsu et al., GENE-EXPRESSION OF GLUT3 GLUCOSE-TRANSPORTER REGULATED BY GLUCOSE IN-VIVO IN MOUSE-BRAIN AND IN-VITRO IN NEURONAL CELL-CULTURES FROM RAT EMBRYOS, Biochemical journal, 300, 1994, pp. 125-131
This study was designed to determine whether glucose regulates the gen
e expression of glucose transporter GLUT3 in neurons. We examined the
regulation of GLUT3 mRNA by glucose in vivo in mouse brain and in vitr
o by using neuronal cultures from rat embryos. Hypoglycaemia (< 30 mg/
dl), produced by 72 h of starvation, increased GLUT3 mRNA in mouse bra
in by 2-fold. Hybridization studies in situ demonstrated that hypoglyc
aemia-induced increases in GLUT3 mRNA expression were observed selecti
vely in brain regions including the hippocampus, dentate gyrus, cerebr
al cortex and piriform cortex, but not the cerebellum. Primary neurona
l cultures from rat embryos deprived of glucose for 48 h also showed a
n increase (4-fold over control) in GLUT3 mRNA, indicating that glucos
e can directly regulate expression of GLUT3 mRNA. In contrast with hyp
oglycaemia, hyperglycaemia produced by streptozotocin did not alter th
e expression of GLUT3 mRNA. We also confirmed previous findings that h
ypoglycaemia increases GLUT1 mRNA expression in brain. The increase in
GLUT1 expression was probably limited to the blood-brain barrier in v
ivo, since GLUT1 mRNA could not be detected in neurons of the mouse ce
rebrum. Thus we conclude that up-regulation of neuronal GLUT3 in respo
nse to glucose starvation represents a protective mechanism against en
ergy depletion in neurons.