Shen M R, Chen S S
Department of Physiology, Kaohsiung Medical College, Taiwan, Republic of China.
Gaoxiong Yi Xue Ke Xue Za Zhi. 1990 Jun;6(6):295-301.
The in-vitro effects of four anticonvulsant drugs (phenytoin, phenobarbitone, carbamazepine and valproate) on human sperm motility were studied with a trans-membrane migration method. Sperm motility was measured either immediately after semen had been mixed with the drug or after a 2-hour pre-incubation at 37 degrees C. When the drug effect was evaluated after the semen-drug mixture had been pre-incubated for 2 hours, the concentration of phenytoin, carbamazepine and valproate that inhibited sperm motility to 50% of control (EC50) was 1.59, 4.23, and 5.00 mM, respectively. If sperm motility was immediately measured without preincubation, the EC50 was increased to 8.47 and 100.00 mM for carbamazepine and valproate, respectively, whereas phenytoin could not inhibit sperm motility to less than 50% of the control at the tested concentrations. Both with and without pre-incubation, phenobarbitone, even up to 12.92 mM, could not inhibit sperm motility to less than 50% of the control. The result was compatible with previous findings that drugs with a membrane stabilizing effect may inhibit human sperm motility. This study provided further information regarding the application of human sperm motility as a cellular model for future pharmacological research.
采用跨膜迁移法研究了四种抗惊厥药物(苯妥英、苯巴比妥、卡马西平和丙戊酸盐)对人类精子活力的体外影响。在精液与药物混合后立即或在37℃预孵育2小时后测量精子活力。当精液-药物混合物预孵育2小时后评估药物效果时,抑制精子活力至对照值50%(半数有效浓度[EC50])的苯妥英、卡马西平和丙戊酸盐浓度分别为1.59、4.23和5.00 mM。如果不进行预孵育直接测量精子活力,卡马西平和丙戊酸盐的EC50分别增至8.47和100.00 mM,而在测试浓度下苯妥英无法将精子活力抑制至对照值的50%以下。无论有无预孵育,苯巴比妥即使浓度高达12.92 mM,也无法将精子活力抑制至对照值的50%以下。该结果与之前关于具有膜稳定作用的药物可能抑制人类精子活力的研究结果相符。本研究为将人类精子活力作为未来药理学研究的细胞模型的应用提供了进一步信息。