Fig. 2. Effects of nonhalogenated alkanes cyclopropane and butane on recombinant GABAAand glycine receptors. (A ) Cyclopropane (1, 2, and 5 minimum alveolar concentration [MAC]) significantly enhanced the current responses of α1glycine receptors to an EC5of agonists. On α1(S267C) mutant receptor, the enhancing effect of cyclopropane (5 MAC) was completely eliminated. On the other hand, GABAAreceptors required 5 MAC of cyclopropane for a small, but significant, potentiation. Cyclopropane showed similar effects on α2β1GABAAreceptors. (B ) Butane (1 MAC) significantly enhanced the α1glycine and the α2β1GABAAreceptors with much higher potentiation of the glycine receptors than the GABAAreceptors. Error bars represent SEM; n = 6–13 oocytes.

Fig. 2. Effects of nonhalogenated alkanes cyclopropane and butane on recombinant GABAAand glycine receptors. (A ) Cyclopropane (1, 2, and 5 minimum alveolar concentration [MAC]) significantly enhanced the current responses of α1glycine receptors to an EC5of agonists. On α1(S267C) mutant receptor, the enhancing effect of cyclopropane (5 MAC) was completely eliminated. On the other hand, GABAAreceptors required 5 MAC of cyclopropane for a small, but significant, potentiation. Cyclopropane showed similar effects on α2β1GABAAreceptors. (B ) Butane (1 MAC) significantly enhanced the α1glycine and the α2β1GABAAreceptors with much higher potentiation of the glycine receptors than the GABAAreceptors. Error bars represent SEM; n = 6–13 oocytes.

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