Finnegan K T, Calder L, Clikeman J, Wei S, Karler R
Psychiatry Service, Veterans Administration Medical Center, Salt Lake City, UT 84148.
Brain Res. 1993 Feb 12;603(1):134-8. doi: 10.1016/0006-8993(93)91310-o.
The calcium channel antagonists verapamil nifedipine and flunarizine all increased the threshold for convulsions induced by N-methyl-D-aspartate in rats. By contrast, only flunarizine blocked the long-term serotonin-depleting effects of 3,4-methylenedioxymethamphetamine. Flunarizine was also the only drug that antagonized methamphetamine-induced stereotypy. These findings suggest that calcium influx through L-type channels does not participate in the neurotoxic mechanism of MDMA, and that the neuroprotective actions of flunarizine are probably related to its anti-dopaminergic activity.
钙通道拮抗剂维拉帕米、硝苯地平和氟桂利嗪均提高了大鼠由N-甲基-D-天冬氨酸诱导惊厥的阈值。相比之下,只有氟桂利嗪能阻断3,4-亚甲基二氧甲基苯丙胺长期耗竭血清素的作用。氟桂利嗪也是唯一能拮抗甲基苯丙胺诱导的刻板行为的药物。这些发现表明,通过L型通道的钙内流不参与摇头丸的神经毒性机制,并且氟桂利嗪的神经保护作用可能与其抗多巴胺能活性有关。