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Fig. 2 | BMC Anesthesiology

Fig. 2

From: Trichloroethanol, an active metabolite of chloral hydrate, modulates tetrodotoxin-resistant Na+ channels in rat nociceptive neurons

Fig. 2

Effect of TCE on the voltage-dependence of TTX-R Na+ channels. (A) A schematic illustration of voltage step pulses to examine the voltage-activation relationship of TTX-R Na+ channels. The TTX-R INa was induced by 50 ms depolarization pulses from − 80 to + 20 mV in 10 mV increments at a VH of − 80 mV. (B) Typical traces of TTX-R INa elicited by voltage step pulses in the absence (left) and presence (right) of 3 mM TCE. (C) a, The conductance-voltage relationship of TTX-R Na+ channels in the absence (black circles) and presence (red circles) of 3 mM TCE. Continuous lines represent the best fit of the Boltzmann function. Each point represents the mean and SEM from seven experiments. b, TCE-induced changes in the midpoint voltage for the activation (V50, activation) of TTX-R Na+ channels. Each column represents the mean and SEM from seven experiments for 1, 3, and 10 mM TCE. **; p < 0.01, n.s; not significant. (D) A schematic illustration of voltage step pulses to examine the voltage-steady state fast inactivation relationship of TTX-R Na+ channels. The TTX-R INa was induced by 50 ms depolarization pulses to − 10 mV after 300 ms prepulse from − 120 to − 20 mV in 10 mV increments. (E) Typical traces of TTX-R INa elicited by voltage step pulses in the absence (left) and presence (right) of 3 mM TCE. (F) a, The voltage-inactivation relationship of TTX-R Na+ channels in the absence (black circles) and presence (red circles) of 3 mM TCE. Continuous lines represent the best fit of the Boltzmann function. Each point represents the mean and SEM from seven experiments. b, TCE-induced changes in the midpoint voltage for the inactivation (V50, inactivation) of TTX-R Na+ channels. Each column represents the mean and SEM from seven experiments for 1, 3, and 10 mM TCE. **; p < 0.01

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