Abstract

Songorine, a diterpenoid alkaloid isolated from the genus Aconitum, was recently found to enhance the excitatory synaptic transmission in rat hippocampus. The mechanism underlying the effects was examined in the present study. The alkaloid at 0.1–300 μM inhibited the specific binding of [ 3H]muscimol to Triton-treated synaptic membranes of rat brain in a concentration-dependent manner ( IC 50=7.06 μM; 95% confidence limits: 3.28–10.84 μM). Scatchard analysis and Lineweaver–Burk double reciprocal plot of [ 3H]muscimol saturation binding data indicate a non-competitive inhibition of the alkaloid on the γ-aminobutyric acid A (GABA A) receptor. In acutely dissociated rat hippocampal neurons the alkaloid did not elicit current response, but markedly inhibited the GABA-induced inward current ( IC 50=19.6 μM). The results suggest that songorine is a novel non-competitive antagonist at the GABA A receptor in rat brain.

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