ANTIMALARIAL-DRUGS INHIBIT CALCIUM-DEPENDENT BACKWARD SWIMMING AND CALCIUM CURRENTS IN PARAMECIUM-CALKINSI

被引:14
作者
BARRY, SR
BERNAL, J
机构
[1] UNIV AUTONOMA AGUASCALIENTES,DEPT FISIOL & FARMACOL,AGUASCALIENTES 20100,MEXICO
[2] MARINE BIOL LAB,WOODS HOLE,MA 02543
关键词
PARAMECIUM; ANTIMALARIAL DRUGS; CALCIUM CURRENTS; QUINACRINE; CALCIUM CHANNEL BLOCKERS;
D O I
10.1007/BF00213527
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The antimalarial drugs, quinacrine, chloroquine, quinine, primaquine, and mefloquine, share structural similarities with W-7, a compound that inhibits calcium-dependent backward swimming and calcium currents in Paramecium. Therefore, we tested whether antimalarial drugs also inhibit backward swimming and calcium currents in P. calkinsi. When the Paramecium is depolarized in high potassium medium, voltage-dependent calcium channels in the ciliary membrane open causing the cell to swim backward for 30 to 70 s. Application of calcium channel inhibitors, such as W-7, reduce the duration of backward swimming. In 0.05 mM calcium, quinacrine, mefloquine, quinine, chloroquine, primaquine and W-7 all reduced the duration of backward swimming. These effects were seen in sodium-containing and sodium-free high potassium solutions as well as sodium-free depolarizing solutions containing potassium channel blockers. In these low calcium solutions, backward swimming was inhibited by 50% at concentrations ranging from 100 nM to 30 muM. At higher calcium concentrations (1 mM or 15 mM), the effects of the antimalarials and W-7 were reduced. The effects of quinacrine and W-7 were tested directly on calcium currents using the two microelectrode voltage clamp technique. In 15 mM calcium, 100 muM quinacrine and 100 muM W-7 reduced the peak calcium current by 51% and 42%, respectively. Thus, antimalarial drugs reduce calcium currents in Paramecium calkinsi.
引用
收藏
页码:457 / 466
页数:10
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