Johnson M, Hanson G R, Gibb J W
Department of Pharmacology and Toxicology, University of Utah, Salt Lake City 84112.
Biochem Pharmacol. 1987 Dec 1;36(23):4085-93. doi: 10.1016/0006-2952(87)90565-x.
The influence of N-ethyl-3,4-methylenedioxyamphetamine (MDE) on the central serotonergic and dopaminergic systems of the rat after a single or multiple injections was studied. MDE (10 mg/kg) produced a significant decrease in the concentration of 5-hydroxytryptamine (5-HT) 1 hr later in the frontal cortex and the hippocampus without affecting the concentration of 5-hydroxyindoleacetic acid (5-HIAA) or tryptophan hydroxylase (TPH) activity. Hypothalamic and neostriatal concentrations of 5-HT, 5-HIAA, dopamine (DA), dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) remained unaffected, as well as the neostriatal TPH and tyrosine hydroxylase (TH) activities. However, 3 hr after the MDE injection, the serotonergic variables including TPH activity were decreased in most of the brain areas examined. The dopaminergic system remained unaffected, except for a significant reduction in neostriatal DOPAC concentrations. The changes in transmitter concentrations after a single injection were dose dependent; the maximum depletion in TPH activity was reached with a 10 mg/kg dose. The administration of multiple doses of MDE caused greater decreases in TPH activity and 5-HT concentrations 3 hr after the treatment than did a single injection; in addition, a partial recovery from multiple administrations occurred by 18 hr. The effects of MDE on DA and its metabolites were transient, and neostriatal TH activity was not altered. This study demonstrates that MDE primarily affects the central serotonergic system, as reported for its congeners 3,4-methylenedioxyamphetamine and 3,4-methylenedioxymethamphetamine. It does, however, produce less neurotoxicity as judged by its lower potency on the dopaminergic and the serotonergic systems as well as the recovery occurring in these systems.
研究了单次或多次注射N-乙基-3,4-亚甲基二氧苯丙胺(MDE)对大鼠中枢5-羟色胺能和多巴胺能系统的影响。注射MDE(10mg/kg)1小时后,额叶皮质和海马体中5-羟色胺(5-HT)的浓度显著降低,而5-羟吲哚乙酸(5-HIAA)的浓度或色氨酸羟化酶(TPH)的活性未受影响。下丘脑和新纹状体中5-HT、5-HIAA、多巴胺(DA)、二羟基苯乙酸(DOPAC)和高香草酸(HVA)的浓度以及新纹状体中TPH和酪氨酸羟化酶(TH)的活性均未受影响。然而,在注射MDE 3小时后,所检测的大多数脑区中包括TPH活性在内的5-羟色胺能变量均降低。除新纹状体中DOPAC浓度显著降低外,多巴胺能系统未受影响。单次注射后递质浓度的变化呈剂量依赖性;10mg/kg剂量时TPH活性达到最大耗竭。多次注射MDE后,治疗3小时后TPH活性和5-HT浓度的降低程度比单次注射更大;此外,多次给药后18小时出现部分恢复。MDE对DA及其代谢产物的影响是短暂的,新纹状体TH活性未改变。本研究表明,MDE主要影响中枢5-羟色胺能系统,这与其同系物3,4-亚甲基二氧苯丙胺和3,4-亚甲基二氧甲基苯丙胺的情况相同。然而,从其对多巴胺能和5-羟色胺能系统的较低效力以及这些系统中出现的恢复情况判断,它产生的神经毒性较小。