Thienyl-GABA derivatives as specific baclofen agonists in the rat and cat spinal cord in vivo.

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 Lett

journal_title

Neuroscience letters

authors

Lacey G,Berthelot P,Vaccher C,Flouquet N,Vaccher MP,Debaert M,Curtis DR

doi

10.1016/0304-3940(93)90799-q

subject

Has Abstract

pub_date

1993-09-03 00:00:00

pages

64-6

issue

1-2

eissn

0304-3940

issn

1872-7972

pii

0304-3940(93)90799-Q

journal_volume

159

pub_type

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