MECHANISM OF ANTIARRHYTHMIC EFFECT OF THE ANTIMALARIAL ARTEMISININ
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Abstract
AIM: To determine the ionic basis of antiarrhythmic action of artemisinin. METHODS: The effects of artemisinin on the inward rectifier K current (Ik1) in isolated rabbit myocytes were studied using whole cell voltage clamp technique, and its effects on the cloned inward rectifier K channels (Kir2.1) expressed in xenopus oocytes were investigated by two microelectrode voltage clamp technique. RESULTS: In rabbit myocytes, artemisinin significantly decreased Ik1 in a concentration-dependent manner. Artemisinin (50 μmol.L-1) decreased Ik1 from -2.36±0.39 nA to -1.43±0.31 nA (P<0.05, n=6) at -100 mV. Artemisinin reduced the current of Kir2.1 channel in xenopus oocytes in a dose-dependent and voltage-dependent manner when artemisinin was perfused with different concentration after Kir2.1 cRNA was injected. The blockade effect of artemisinin on Kir2.1 channel was revertible. CONCLUSION: Artemisinin inhibited effectively Ik1 in isolated rabbit myocytes. The mechanism of antiarrhythmic action of artemisinin may be related to its inhibition on Ik1 and blockade of Kir2.1 channel current.
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