Key result
Low extracellular pH (6.0) produced isoform-specific effects, decreasing maximum availability in neuronal NaV1.2 channels while enhancing availability in cardiac NaV1.5 channels, with minimal effects on skeletal muscle NaV1.4 channels.
Why the study?
Does low extracellular pH (acidosis) differentially modulate the biophysical properties of NaV1.2, NaV1.4, and NaV1.5 channels?
Does low extracellular pH (acidosis) differentially modulate the biophysical properties of NaV1.2, NaV1.4, and NaV1.5 channels?
Acidosis modulates voltage-gated sodium channels in an isoform-specific manner, with profound effects on gating in NaV1.2 and NaV1.5, which may impact neuronal and cardiac excitability during ischemic or acidic conditions.
Acidosis may alter neuronal and cardiac excitability via NaV isoforms; leaves open translation to human ischemia.
Na(V) channels play a crucial role in neuronal and muscle excitability. Using whole-cell recordings we studied effects of low extracellular pH on the biophysical properties of Na(V)1.2, Na(V)1.4, and Na(V)1.5, expressed in cultured mammalian cells. Low pH produced different effects on different channel subtypes. Whereas Na(V)1.4 exhibited very low sensitivity to acidosis, primarily limited to partial block of macroscopic currents, the effects of low pH on gating in Na(V)1.2 and Na(V)1.5 were profound. In Na(V)1.2 low pH reduced apparent valence of steady-state fast inactivation, shifted the τ(V) to depolarizing potentials and decreased channels availability during onset to slow and use-dependent inactivation (UDI). In contrast, low pH delayed open-state inactivation in Na(V)1.5, right-shifted the voltage-dependence of window current, and increased channel availability during onset to slow and UDI. These results suggest that protons affect channel availability in an isoform-specific manner. A computer model incorporating these results demonstrates their effects on membrane excitability.
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Vilin et al. (2012) studied Sodium channel electrophysiology. Low extracellular pH (pH 6.0) vs. Normal physiological pH (pH 7.4) was evaluated on Channel availability and gating properties (fast, slow, and use-dependent inactivation). Low extracellular pH (6.0) produced isoform-specific effects, decreasing maximum availability in neuronal NaV1.2 channels while enhancing availability in cardiac NaV1.5 channels, with minimal effects on skeletal muscle NaV1.4 channels.
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