Literature DB >> 16472927

Presynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors modulate release of inhibitory amino acids in rat spinal cord dorsal horn.

H S Engelman1, R L Anderson, C Daniele, A B Macdermott.   

Abstract

Local inhibition within the spinal cord dorsal horn is mediated by the neurotransmitters GABA and glycine and strongly influences nociceptive and temperature signaling. Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors are expressed by inhibitory interneurons and have been shown to modulate GABA release in other regions of the CNS. In the spinal cord, there is morphological evidence for presynaptic AMPA receptor subunits in GABAergic dorsal horn neurons, but functional data are lacking. To determine if AMPA receptors are indeed functional at presynaptic terminals of inhibitory neurons, we recorded evoked and miniature inhibitory postsynaptic currents (mIPSPs) in the superficial dorsal horn of the rat spinal cord. We show that AMPA receptor activation enhances spontaneous release of inhibitory amino acids in the presence of tetrodotoxin onto both lamina II neurons and NK1 receptor-expressing (NK1R+) lamina I neurons. This effect is sensitive to the concentration of extracellular Ca2+, yet is not fully blocked in most neurons in the presence of Cd2+, suggesting possible Ca2+ entry through AMPA receptors. Postsynaptic Ca2+ elevation is not required for these changes. AMPA-induced increases in mIPSP frequency are also seen in more mature dorsal horn neurons, indicating that these receptors may play a role in nociceptive processing in the adult. In addition, we have observed AMPA-induced depression of evoked release of GABA and glycine onto lamina I NK1R+ neurons. Taken together these data support a role for presynaptic AMPA receptors in modulating release of GABA and glycine in the superficial dorsal horn. Because inhibition in the dorsal horn is important for controlling pain signaling, presynaptic AMPA receptors acting to modulate the inhibitory inputs onto dorsal horn neurons would be expected to impact upon pain signaling in the spinal cord dorsal horn.

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Year:  2006        PMID: 16472927     DOI: 10.1016/j.neuroscience.2005.12.038

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  6 in total

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Journal:  Mol Neurobiol       Date:  2009-10-31       Impact factor: 5.590

2.  Intrathecal midazolam regulates spinal AMPA receptor expression and function after nerve injury in rats.

Authors:  Jeongae Lim; Grewo Lim; Backil Sung; Shuxing Wang; Jianren Mao
Journal:  Brain Res       Date:  2006-10-17       Impact factor: 3.252

3.  A Cooperative Mechanism Involving Ca2+-Permeable AMPA Receptors and Retrograde Activation of GABAB Receptors in Interpeduncular Nucleus Plasticity.

Authors:  Peter Koppensteiner; Riccardo Melani; Ipe Ninan
Journal:  Cell Rep       Date:  2017-08-01       Impact factor: 9.423

4.  Role of presynaptic glutamate receptors in pain transmission at the spinal cord level.

Authors:  Rita Bardoni
Journal:  Curr Neuropharmacol       Date:  2013-09       Impact factor: 7.363

5.  Characterization of sensory neuron subpopulations selectively expressing green fluorescent protein in phosphodiesterase 1C BAC transgenic mice.

Authors:  Carole Torsney; Rebecca L Anderson; Kerry-Anne G Ryce-Paul; Amy B MacDermott
Journal:  Mol Pain       Date:  2006-05-08       Impact factor: 3.395

6.  Prolonged Use of NMDAR Antagonist Develops Analgesic Tolerance in Neuropathic Pain via Nitric Oxide Reduction-Induced GABAergic Disinhibition.

Authors:  Jun Li; Lin Zhang; Chu Xu; Yu-Hui Lin; Yu Zhang; Hai-Yin Wu; Lei Chang; Ying-Dong Zhang; Chun-Xia Luo; Fei Li; Dong-Ya Zhu
Journal:  Neurotherapeutics       Date:  2020-07       Impact factor: 6.088

  6 in total

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