Anticholinergic effects of artemisinin, an antimalarial drug, in isolated guinea pig heart preparations
2007
Hara, Y.(Kitasato Univ., Towada, Aomori (Japan). School of Veterinary Medicine and Animal Sciences) | Yamawaki, H. | Shimada, M. | Okada, K. | Tanai, T. | Ichikawa, D. | Miyake, K. | Kizaki, K.
Concern has been growing about the cardiac toxicity of antimalarial drugs. Artemisinin, a unique type of antimalarial drug originating from a Chinese medicinal plant, has minimal adverse effects, but it has been reported to inhibit delayed rectifier potassium current, a voltage-gated potassium current. However, no studies have been published concerning the effect of artemisinin on ligand-gated potassium currents. Therefore, in the present study, we examined the influence of artemisinin on the acetylcholine receptor-operated potassium current (Isub(K.ACh)), a ligand-gated potassium current, in guinea pig atrial myocytes using a patch clamp technique. Artemisinin (1 to 300 microM) inhibited Isub(K.ACh) induced by extracellular application of both carbachol (1 microM) and adenosine (10 microM) and that induced by intracellular loading of GTPgammaS (100 microM) in a concentration-dependent manner. Artemisinin inhibited carbachol-induced, adenosine-induced, and GTPgammaS-activated Isub(K.ACh) within almost the same concentration range. In left atria, artemisinin (1 to 100 microM) partially reversed the shortening of action potential duration induced by carbachol in a concentration-dependent manner. Carbachol-induced negative inotropic action in left atria was also inhibited by artemisinin (10 to 300 microM). In conclusion, we suggest that the anticholinergic action of artemisinin is mediated through inhibition of Isub(K.ACh) via inhibition of the muscarinic potassium channel and/or associated GTP-binding proteins.
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