Characterization of spinal amino acid release and touch-evoked allodynia produced by spinal glycine or GABA A receptor antagonist

• Published in: Neuroscience Vol. 95; no. 3; pp. 781 - 786
• Main Authors: Ishikawa, T, Marsala, M, Sakabe, T, Yaksh, T.L
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.12.1999
• Subjects: bicuculline; excitatory amino acid release; modulatory receptor systems; strychnine; tactile stimulation; touch-evoked agitation; GLU, glutamate; modulatory receptor systems; excitatory amino acid release; strychnine; touch-evoked agitation; ACSF, artificial cerebrospinal fluid; SER, serine; STR, strychnine; bicuculline; GLY, glycine; BIC, bicuculline; TEA, touch-evoked agitation; tactile stimulation; NMDA, N-methyl- d-aspartate; TAU, taurine
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/S0306-4522(99)00461-3

Intrathecal strychnine (glycine antagonist) or bicuculline (GABA A antagonist) yields a touch-evoked agitation that is blocked by N-methyl- d-aspartate receptor antagonism. We examined the effects of intrathecal strychnine and bicuculline on touch-evoked agitation and the spinal release of amino acids. Fifty-two Sprague–Dawley rats were prepared under halothane anesthesia with a lumbar intrathecal catheter and a loop dialysis catheter. Four days after implantation, rats were randomized to receive an intrathecal injection of N-methyl- d-aspartate (3 μg), strychnine (3 μg) or bicuculline (10 μg), or a combination of N-methyl- d-aspartate with bicuculline or strychnine. The agitation produced by brief light tactile stroking of the flank (tactile allodynia), and the spontaneous spinal release of glutamate, taurine and serine was measured. Intrathecal N-methyl- d-aspartate, strychnine and bicuculline produced similar touch-evoked allodynia. Intrathecal bicuculline and N-methyl- d-aspartate alone evoked a transient spinal release of glutamate and taurine, but not serine, in the 0–10 min sample, while strychnine did not affect spinal transmitter release at any time. As GABA A but not glycine receptor inhibition at equi-allodynic doses increases glutamate release, while the allodynia of both is blocked by N-methyl- d-aspartate receptor antagonism, we hypothesize that GABA A sites regulate presynaptic glutamate release, while glycine regulates the excitability of neurons postsynaptic to glutamatergic terminals.