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Acta Physiologica Sinica ; (6): 374-378, 2004.
Article in English | WPRIM | ID: wpr-352765

ABSTRACT

Experiments were performed on Sprague Dawley rats with multibarrel microelectrode technique. The effects of acoustic response of A I cortex neurons produced by electrical stimulation of lateral amygdaloid nucleus (LA) and the influence of GABA were observed. Experimental results showed that iontophoretic administration of GABA caused a pronounced inhibition of the electrical activity of A-I neurons. Blockade of GABA(A) with bicuculline (BIC) facilitated the acoustic response. The acoustic response of A-I neurons was inhibited when the LA was stimulated. Iontophoretic application of GABA resulted in a similar inhibitory effect as that of LA stimulation. Blockade of GABA(A) with bicuculline reversed the inhibitory effect of LA stimulation on the acoustic response of A-I neurons. In contrast, application of strychnine, a glycine receptor antagonist, could not reverse the inhibitory effect of LA. Baclofen, a GABA(B) agonist, did not affect the acoustic response of the auditory neurons. These results indicate that GABA is the ultimate transmitter which mediates the LA stimulation-induced inhibition of the acoustic response of A-I neurons in rats, possibly via the GABA(A) receptor.


Subject(s)
Animals , Male , Rats , Acoustic Stimulation , Amygdala , Physiology , Baclofen , Pharmacology , Bicuculline , Pharmacology , Cerebral Cortex , Physiology , Electric Stimulation , Evoked Potentials, Auditory , Physiology , GABA Agonists , Pharmacology , GABA Antagonists , Pharmacology , Iontophoresis , Methods , Microelectrodes , Neurons , Physiology , Rats, Sprague-Dawley , Receptors, GABA-A , Physiology , gamma-Aminobutyric Acid , Physiology
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