AIM: To study the mechanism of calcium overload induced by melittin in myoc
ytes. METHODS: Whole-cell patch-clamp technique was applied for recording t
he currents. RESULTS: Mel 0.05, 0.1 mu mol/L increased the peak amplitude o
f I-Na(nA) from -2.1+/-0.8 to -3.2+/-1.0 (n = 7, P < 0.05) and -3.1+/-1.5 (
n = 7, P < 0.05) respectively at testing potential of -40 mV. Mel 0.05, 0.1
, 0.2 mu mol/L had no significant effect on I-Ca, but enhanced INa-Ca(pA) f
rom 53 +/- 21 to 427+/-256 (n = 5, P < 0.05), 349 +/- 147 (n = 5, P < 0.01)
and 320 +/- 91 (n = 5, P < 0.05) respectively at a testing potential of 50 mV. CONCLUSION: The stimulating effect of Mel on INa-Ca rather than the
effect on Ica contributes to the calcium overload of myocytes.