Abstract
Nicotinic acetylcholine (ACh) receptors, such as α7, α3β4 and α4β2 receptors in the hippocampus, are suggested to modulate neurotransmitter release. 8-[2-(2-Pentyl-cyclopropyl-methyl)-cyclopropyl]- octanoic acid (DCP-LA) (100 nM), a linoleic acid derivative, potentiated responses of α7, α3β4 and α4β2 ACh receptors expressed in Xenopus oocytes that are blocked by 3-(1-[dimethylaminopropyl] indol-3-yl)-4-[indol-3-yl] maleimide (GF109203X), a selective inhibitor of protein kinase C (PKC), except for α3β4 ACh receptors. DCP-LA enhanced the nicotine-triggered release of GABA from rat hippocampal slices in the presence of tetrodotoxin in a bell-shaped dose-dependent manner at concentrations ranging from 10 nM to 10 μM, although DCP-LA by itself had no effect on GABA release. The DCP-LA action was inhibited by GF109203X or α-bungarotoxin, an inhibitor of α7 ACh receptors, but not by mecamylamine or dihydro-β-erithroidine, an inhibitor of α3β4 and α4β2 ACh receptors. A similar effect on GABA release was obtained with 12-O-tetradecanoylphorbol 13-acetate, a PKC activator. DCP-LA (100 nM) also enhanced GABA release triggered by choline, an agonist of α7 ACh receptors, but not 3-[2(s)-azetidinylmethoxy] pyridine, an agonist of α4β2 ACh receptors. In addition, DCP-LA (100 nM) increased the rate of nicotine-triggered GABAA receptor-mediated miniature inhibitory post-synaptic currents, monitored from CA1 pyramidal neurons of rat hippocampal slices, and the effect was also inhibited by GF109203X or α-bungarotoxin but not by mecamylamine. Thus, the results of the present study indicate that DCP-LA stimulates GABA release by enhancing activity of pre-synaptic α7 ACh receptors present on the GABAergic terminals of interneurons that transmit to CA1 pyramidal neurons via a PKC pathway. © 2005 International Society for Neurochemistry.
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Kanno, T., Yaguchi, T., Yamamoto, S., Yamamoto, H., Fujikawa, H., Nagata, T., … Nishizaki, T. (2005). 8-[2-(2-Pentyl-cyclopropylmethyl)-cyclopropyl]-octanoic acid stimulates GABA release from interneurons projecting to CA1 pyramidal neurons in the rat hippocampus via pre-synaptic α7 acetylcholine receptors. Journal of Neurochemistry, 95(3), 695–702. https://doi.org/10.1111/j.1471-4159.2005.03398.x
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