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AMPA/kainate and NMDA‐like glutamate receptors at the chromatophore neuromuscular junction of the squid: role in synaptic transmission and skin patterning
Author(s) -
Lima Pedro A.,
Nardi Giovanna,
Brown Euan R.
Publication year - 2003
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.1460-9568.2003.02477.x
Subject(s) - kainate receptor , ampa receptor , cnqx , nmda receptor , neurotransmission , glutamate receptor , dnqx , biophysics , biology , excitatory postsynaptic potential , neuroscience , chemistry , receptor , biochemistry , inhibitory postsynaptic potential
Abstract Glutamate receptor types were examined at the chromatophore synapses of the squids Alloteuthis subulata and Loligo vulgaris , where nerve‐induced muscle contraction causes chromatophore expansion. Immunoblotting with antibody raised against a squid AMPA receptor (sGluR) demonstrated that AMPA/kainate receptors are present in squid skin. Application of l ‐glutamate evoked chromatophore muscle contractions in both ventral and dorsal skins, while NMDA was only active on a subpopulation of dorsal chromatophores. In dorsal skin, neurotransmission was partly blocked by either AMPA/kainate receptor antagonists (CNQX and DNQX) or NMDA receptor antagonists (AP‐5 and MK‐801) or completely blocked by simultaneous application of both classes of antagonists. In isolated muscle fibres, ionophoretic application of l ‐glutamate evoked fast inward CNQX‐ and DNQX‐sensitive currents with reversal potentials around +14 mV and a high conductance to Na + . In fibres from dorsal skin only, a slower outward glutamate‐sensitive current appeared at positive holding potentials. At negative potentials, currents were potentiated by glycine or by removing external Mg 2+ and were blocked by AP‐5 and MK‐801. Glutamate caused a fast, followed by a slow, transient increase in cytoplasmic Ca 2+ . The slow component was increased in amplitude and duration by glycine or by lowering external Mg 2+ and decreased by AP‐5 and MK‐801. In cells from ventral skin, no ‘NMDA‐like responses’ were detected. Thus, while AMPA/kainate receptors mediated fast excitatory synaptic transmission and rapid colour change over the whole skin, activation of both AMPA/kainate and NMDA‐like receptors in a subpopulation of dorsal chromatophores prolonged the postsynaptically evoked Ca 2+ elevation causing temporally extended colour displays with behavioural significance.