In brains of the rabbit, pig, and human, expression of the high-affini
ty Na+-D-glucose cotransporter SGLT1 and of the protein RS1, which alt
ers the activity of SGLT1, was demonstrated. In situ hybridization sho
wed that SGLT1 and RSI are transcribed in pyramidal cells of brain cor
tex and hippocampus and in Purkinje cells of cerebellum. In neurons of
pig brain SGLT1 protein was demonstrated by western blotting with syn
aptosomal membranes and by immunohistochemistry, which showed SGLT1 in
pyramidal and Purkinje cells. To test whether SGLT1 in neurons may be
activated during increased D-glucose consumption, an epileptic seizur
e was induced in rat brain, and the uptake of specific nonmetabolized
substrates of SGLT1 {[C-14] methyl-alpha-D-glucopyranoside ([C-14]AMG)
} and of Na+-independent transporters {2-deoxy-D-[C-14] glucose ([C-14
]2-DG)} was analyzed by autoradiography. During the seizure the uptake
of AMG and 2-DG was increased in the focus. Within two hours after th
e seizure 2-DG uptake in the focus returned to normal. In contrast, th
e AMG uptake in the focus area was still increased 1 day later. The da
ta show that the high-affinity Na+-D-glucose cotransporter SGLT1 is ex
pressed in neurons and can be up-regulated.