Journal of Neuroscience, Vol 9, 3218-3229, Copyright © 1989 by Society for Neuroscience
Modulation of ionic currents in Aplysia motor neuron B15 by serotonin, neuropeptides, and second messengers
R Taussig, A Sweet-Cordero and RH Scheller
Department of Biological Sciences, Stanford University, California 94305.
Both 5-HT and the 9 amino acid neuropeptide SCPb modulate 3 ionic currents
in B15, enhancing a voltage-dependent inward sodium current, decreasing an
outward potassium current and increasing an inward rectifying potassium
current. In contrast, FMRFamide decreases a voltage-dependent inward sodium
current and increases an outward potassium current. We have also
investigated the roles of several second-messenger systems that may be
mediating the effects of these modulators. Bath application of membrane
permeable analogs of cAMP enhance the voltage-dependent inward sodium
current and both 5-HT and SCPb increase cAMP levels in B15, suggesting that
cAMP may be mediating part of the observed effects of these transmitters on
B15. Experiments with phorbol ester, a protein kinase inhibitor, and a
phospholipase inhibitor suggest that the phospholipase C/protein kinase C
cascade may decrease an outward potassium current. Thus, 5-HT and SCPb may
activate multiple second-messenger systems to modulate 3 ionic currents in
B15. Additional studies suggest that a cascade involving arachidonic acid
may be involved in mediating part of the FMRFamide responses in B15. These
studies are beginning to define molecular mechanisms whereby a neuron
differentially modulates multiple ionic currents in response to distinct
chemical messengers.