Abstract:
:The depression of the amplitude of extracellularly recorded monosynaptic excitatory field potentials in the lumbar spinal cord of pentobarbitone anaesthetised rats and cats by three thienyl derivatives of GABA: 4-amino-3-(2-thienyl)-butanoic acid; 4-amino-3-(2-thienyl-5-methyl)-butanoic acid and 4-amino-3-(2-thienyl-5-chloro)-butanoic acid was reversibly blocked by the (-)-baclofen antagonist 3-aminopropyl-diethoxymethyl-phosphinic acid (CGP 35348). These compounds, of which the most potent, the 5-chloro derivative, was weaker than (-)-baclofen, thus activate baclofen receptors in the cat and rat spinal cord.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Lacey G,Berthelot P,Vaccher C,Flouquet N,Vaccher MP,Debaert M,Curtis DRdoi
10.1016/0304-3940(93)90799-qsubject
Has Abstractpub_date
1993-09-03 00:00:00pages
64-6issue
1-2eissn
0304-3940issn
1872-7972pii
0304-3940(93)90799-Qjournal_volume
159pub_type
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