Epidermal growth factor increases i(f) in rabbit SA node cells by activating a tyrosine kinase

Biochim Biophys Acta. 2000 Jan 15;1463(1):15-9. doi: 10.1016/s0005-2736(99)00233-3.

Abstract

Our previous results have demonstrated that tyrosine kinase inhibition reduces i(f) in rabbit SA node myocytes, suggesting that tyrosine kinases regulate i(f). One receptor tyrosine kinase the EGF receptor kinase is known to increase heart rate. To determine if this action is mediated through changes in i(f), we examined the effect of epidermal growth factor (EGF) on i(f) with the permeabilized patch-clamp technique. 0.1 microM EGF increased i(f) amplitude in response to single-step hyperpolarizations in the diastolic range of potentials. This increase was 20+/-3%, n=11 at -75 mV. This effect is caused by activating a tyrosine kinase because 50 microM genistein, a tyrosine kinase inhibitor, eliminated this EGF action. A two-step pulse protocol showed that maximal i(f) conductance was increased by EGF. We further examined this conductance change by constructing the activation curve. The maximal i(f) conductance was increased by 23% with no change in midpoint, V(1/2), control=-74+/-2 mV, V(1/2) EGF=-74+/-1 mV. Thus EGF acts via a tyrosine kinase to increase maximal i(f) conductance with no change in the voltage dependence of activation. These results suggest that EGF effects on i(f) contribute to the positive chronotropic effect of EGF on SA node.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Epidermal Growth Factor / pharmacology*
  • Genistein / pharmacology
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • In Vitro Techniques
  • Ion Channels / drug effects*
  • Ion Channels / metabolism*
  • Membrane Potentials
  • Patch-Clamp Techniques
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism*
  • Rabbits
  • Sinoatrial Node / cytology
  • Sinoatrial Node / drug effects*
  • Sinoatrial Node / metabolism*

Substances

  • Enzyme Inhibitors
  • Ion Channels
  • Epidermal Growth Factor
  • Genistein
  • Protein-Tyrosine Kinases