Key result
Insulin exposure in vitro caused a voltage-dependent increase of approximately 70% in Na+-K+ pump current in rabbit ventricular myocytes at near physiological diastolic potentials.
Why the study?
Does insulin exposure regulate Na+-K+ pump function in rabbit ventricular myocytes?
Does insulin exposure regulate Na+-K+ pump function in rabbit ventricular myocytes?
Insulin stimulates the Na+-K+ pump in rabbit ventricular myocytes via a voltage-dependent mechanism involving tyrosine kinase, PI3K, and PP1 pathways.
Does not support clinical changes in insulin use; leaves open translation of voltage-dependent pump effects to human myocytes.
Insulin enhances Na(+)-K(+) pump activity in various noncardiac tissues. We examined whether insulin exposure in vitro regulates Na(+)-K(+) pump function in rabbit ventricular myocytes. Pump current (I(p)) was measured using the whole-cell patch-clamp technique at test potentials (V(m)s) from -100 to +60 mV. When the Na(+) concentration in the patch pipette ([Na](pip)) was 10 mM, insulin caused a V(m)-dependent increase in I(p). The increase was approximately 70% when V(m) was at near physiological diastolic potentials. This effect persisted after elimination of extracellular voltage-dependent steps and when K(+) and K(+)-congeners were excluded from the patch pipettes. When [Na](pip) was 80 mM, causing near-maximal pump stimulation, insulin had no effect, suggesting that it did not cause an increase in membrane pump density. Effects of tyrphostin A25, wortmannin, okadaic acid, or bisindolylmaleimide I in pipette solutions suggested that the insulin-induced increase in I(p) involved activation of tyrosine kinase, phosphatidylinositol 3-kinase, and protein phosphatase 1, whereas protein phosphatase 2A and protein kinase C were not involved.
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Hansen et al. (2000) studied this question. Insulin was evaluated on Pump current (Ip). Insulin exposure in vitro caused a voltage-dependent increase of approximately 70% in Na+-K+ pump current in rabbit ventricular myocytes at near physiological diastolic potentials.
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