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Alpha‐adrenoreceptor activation modulates swimming via glycinergic and GABAergic inhibitory pathways in Xenopus laevis tadpoles
Author(s) -
Merrywest Simon D.,
Fischer Hanno,
Sillar Keith T.
Publication year - 2002
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.0953-816x.2001.01865.x
Subject(s) - glycine receptor , strychnine , gabaa receptor , xenopus , inhibitory postsynaptic potential , bicuculline , gabaergic , receptor , biology , gaba receptor antagonist , neuroscience , glycine , biochemistry , amino acid , gene
This study focuses upon the network pathways underlying the adrenoreceptor‐mediated modulation of fictive swimming in the immobilized Xenopus laevis tadpole. As shown recently, noradrenaline (NA) increases cycle periods while simultaneously reducing the rostrocaudal delay in head‐to‐tail firing and the duration of swimming episodes. Furthermore, both swimming frequency and duration are reduced by selective pharmacological activation of α 1 ‐ and/or α 2 ‐adrenoreceptors, while α 1 ‐receptor activation also reduces rostrocaudal delays. We show that NA could still modulate aspects of swimming after blocking either glycine or GABA A receptors with strychnine and bicuculline, respectively. Furthermore, after prior application of NA, strychnine could counteract noradrenergic effects on cycle periods and rostrocaudal delays, while bicuculline could counteract effects on cycle periods, suggesting that these two fast inhibitory pathways are both involved in the NA modulation of swimming. In addition, blocking glycine receptors reduced the effects of α 1 ‐receptors on cycle periods and delays, while blocking GABA A receptors had no effect. Blocking either glycine or GABA A receptors, however, lessened the reduction in swimming frequency by α 2 ‐receptors. In addition, pre‐application of bicuculline prevented a reduction in episode durations by NA, α 1 ‐ and α 2 ‐receptors. Our findings suggest that the noradrenergic modulation of Xenopus swimming is mediated via α‐adrenoreceptors interacting with both glycinergic and GABAergic inhibitory pathways. Both α 1 ‐ and α 2 ‐receptor activation influences the GABAergic pathway controlling the duration of swimming episodes and is involved in the glycinergic modulation of the swimming rhythm and its longitudinal co‐ordination, with α 2 ‐receptors additionally affecting swimming frequency through GABAergic pathways.