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Vol. 303, Issue 3, 1014-1020, December 2002
Department of Experimental Biology "Bernardo Loddo," University
of Cagliari (F.B., L.M., S.C., P.L.C., G.G., A.M., C.M., P.F., G.B.),
and Consiglio Nazionale delle Ricerche Institute of Neuroscience,
Section of Neuropsychopharmacology (M.P.M., G.B.), Cagliari, Italy; and
Department of Neuropharmacology (R.H.P.), the Scripps Research
Institute, La Jolla, California
The effects of ganaxolone, a synthetic analog of the endogenous
neuroactive steroid allopregnanolone, on the function and expression of
GABAA receptors were determined. Electrophysiological recordings demonstrated that ganaxolone potentiated with a potency and
efficacy similar to those of allopregnanolone the Cl
currents evoked by GABA at recombinant human GABAA
receptors (comprising
1
2
2L or
2
2
2L subunit
assemblies) expressed in Xenopus oocytes. Exposure of
cultured rat cerebellar granule cells to 1 µM ganaxolone for 5 days
had no effect on the abundance of mRNAs encoding the
1,
2,
3,
4,
5,
2L, or
2S subunits of the GABAA receptor.
Withdrawal of ganaxolone after such long-term treatment, however,
induced an increase in the abundance of
2,
4, and
5 subunit
mRNAs and a decrease in the amounts of
1,
2L, and
2S subunit
mRNAs. These changes were maximal 3 to 6 h after drug withdrawal
and were reversible, being no longer apparent after 24 h. These
results suggest that long-term exposure of cerebellar granule cells to
ganaxolone does not affect the sensitivity of the GABAA
receptor to several positive modulators. Nevertheless, the reduction in
the amounts of the
1 and
2 subunit mRNAs together with the
increase in the abundance of the
4 subunit mRNA induced by abrupt
discontinuation of long-term treatment with ganaxolone suggest that
withdrawal of this drug might result in a reduced response to classic benzodiazepines.
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