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Fig. 5 | BMC Anesthesiology

Fig. 5

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

Fig. 5

Effect of TCE on the recovery from inactivation of TTX-R Na+ channels. (A) A schematic illustration of the two-pulse protocol for determining recovery kinetics. The TTX-R INa was induced by initial conditioning pulses (P1: − 10 mV depolarization, 100 ms duration), followed by test pulses (P2: − 10 mV depolarization, 50 ms duration). The second TTX-R INa was recovered with various interpulse intervals of 1–5000 ms at − 80 mV. (B) Typical traces of TTX-R INa elicited by test pulses (P2) in the two-pulse protocol in the absence (left) and presence (right) of 3 mM TCE. The dotted lines represent the amplitude elicited by conditioning pulses (P1). (C) The P2/P1 ratio of TTX-R INa against the duration of conditioning pulses in the absence (black circles) and presence (red circles) of 3 mM TCE. Continuous lines represent the best fit of the double exponential function. Each point represents the mean and SEM from seven experiments. (D) TCE (3 mM)-induced changes in kinetic parameters [a: fast time constant (τfast), b: intermediate time constant (τintermediate), c: slow time constant (τslow), d: amplitude fraction of fast time constant (Afast), amplitude fraction of intermediate time constant (Aintermediate), f: amplitude fraction of slow time constant (Aslow). Each column represents the mean and SEM from seven experiments. **; p < 0.01, n.s; not significant. (E) TCE (1, 3, and 10 mM)-induced changes in weighted time constant (τweighted) of the P2/P1 ratio of TTX-R INa. The τweighted was normalized to the respective control (dotted line). Each column represents the mean and SEM from seven experiments for 1, 3, and 10 mM TCE. *; p < 0.05, **; p < 0.01, n.s; not significant

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