Abstract:
:Single electrode voltage-clamp recording from CA3 neurons in guinea pig hippocampal slices was applied to study effects of a new GABAB antagonist, CGP 55845A, on (-)baclofen (IBac)- or gamma-aminobutyric acid (IGABA)-induced potassium (K)-currents and on inhibitory postsynaptic K-currents (K-IPSCs) recorded in the presence of blockers for fast synaptic transmission. K-IPSCs were induced by bath application of 4-amino-pyridine (4-AP). CGP 55845A, in 10(-8) to 10(-7) M concentrations, blocked all these K-currents and was more potent than all GABAB antagonists known to date. However, onset of the CGP 55845A effect and recovery were slow. We conclude that a potent and selective GABAB antagonist is now available to study the physiological role of GABAB receptors in the mammalian brain.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Jarolimek W,Demmelhuber J,Bijak M,Misgeld Udoi
10.1016/0304-3940(93)90164-gsubject
Has Abstractpub_date
1993-05-14 00:00:00pages
31-4issue
1-2eissn
0304-3940issn
1872-7972pii
0304-3940(93)90164-Gjournal_volume
154pub_type
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