EFFECTS OF L-TYPE CALCIUM-CHANNEL ANTAGONISTS ON THE SEROTONIN-DEPLETING ACTIONS OF MDMA IN RATS

被引:5
作者
FINNEGAN, KT
CALDER, L
CLIKEMAN, J
WEI, SH
KARLER, R
机构
[1] UNIV UTAH,SCH MED,VET ADM MED CTR,DEPT PSYCHIAT,PSYCHIAT SERV,SALT LAKE CITY,UT 84132
[2] UNIV UTAH,COLL PHARM,DEPT PHARMACOL & TOXICOL,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,SCH MED,DEPT PHARMACOL,SALT LAKE CITY,UT 84132
关键词
CALCIUM; NEUROTOXICITY; AMPHETAMINE; GLUTAMATE; ANTICONVULSANT; VOLTAGE-SENSITIVE CHANNEL;
D O I
10.1016/0006-8993(93)91310-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:134 / 138
页数:5
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