Abstract / Description of output
The expression of c-fos mRNA in rat brain was induced by intraperitoneal administration of pentylenetetrazole (PTZ) and picrotoxin, which act on the picrotoxin binding site of the gamma-aminobutyric acid-benzodiazepine (GABA-BZ) receptor complex, by N-methyl-D-aspartate (NMDA) and kainic acid, agonists of different classes of glutamate receptors and by caffeine, an antagonist of adenosine receptors. The actions of PTZ and picrotoxin but not that of NMDA were blocked by ethanol and the NMDA-receptor antagonist, MK-801. Ro 15-4513 partially reversed the inhibitory effect of ethanol on PTZ-induced c-fos mRNA synthesis. Acute ethanol administration blocked the actions of PTZ and NMDA without affecting the response to kainic acid or caffeine. Taken together, these data suggest that ethanol blocks c-fos gene activation by noncompetitive antagonists of the GABA-BZ receptor via actions on both the NMDA and GABA receptors.
Original language | English |
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Pages (from-to) | 1309-15 |
Number of pages | 7 |
Journal | Journal of Neurochemistry |
Volume | 59 |
Issue number | 4 |
DOIs | |
Publication status | Published - Oct 1992 |
Keywords / Materials (for Non-textual outputs)
- Animals
- Azides
- Benzodiazepines
- Brain
- Ethanol
- Male
- N-Methylaspartate
- Pentylenetetrazole
- Picrotoxin
- Proto-Oncogene Proteins c-fos
- RNA, Messenger
- Rats
- Rats, Wistar
- Receptors, GABA-A
- Receptors, N-Methyl-D-Aspartate