Key result
Hydrogen peroxide at 100 micromol/L gradually slowed the time-course of inactivation of the transient outward current in rabbit atrial myocytes and increased the peak by 9%.
Why the study?
Does hydrogen peroxide alter the transient outward current in rabbit atrial myocytes?
Does hydrogen peroxide alter the transient outward current in rabbit atrial myocytes?
Hydrogen peroxide alters the transient outward current in rabbit atrial myocytes via a protein kinase C-modulated mechanism, which may be relevant during ischemia/reperfusion.
In the present study, we investigated the effects of hydrogen peroxide (H2O2) on the 4-aminopyridine-sensitive transient outward current (I(TO)) in rabbit atrial myocytes using the amphotericin B-perforated patch voltage-clamp method. 2. Superfusion of myocytes with H2O2 at 100 micromol/L gradually slowed the time-course of inactivation of I(TO) and increased the peak by 9% (n = 9). The H2O2-induced slowing of I(TO) inactivation was concentration dependent (over the concentration range 10 micromol/L to 1 mmol/L). These effects were hardly reversed by washout of H2O2, but were quickly abolished by dithiothreitol (2 mmol/L). 3. Bisindolylmaleimide (100 nmol/L), an inhibitor of protein kinase C, significantly attenuated the H2O2-induced effects on I(TO). 4. These results suggest that rabbit atrial I(TO) is susceptible to oxidation by H2O2 at concentrations relevant to those encountered during ischaemia/reperfusion and that protein kinase C modulates the effects of H2O2.
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Tanaka et al. (2001) studied this question. Hydrogen peroxide (H2O2) was evaluated on 4-aminopyridine-sensitive transient outward current (I(TO)). Hydrogen peroxide at 100 micromol/L gradually slowed the time-course of inactivation of the transient outward current in rabbit atrial myocytes and increased the peak by 9%.
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