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亚甲基二氧甲基苯丙胺与大鼠脑片单胺递质释放机制的相互作用。

Interactions of methylenedioxymethamphetamine with monoamine transmitter release mechanisms in rat brain slices.

作者信息

Fitzgerald J L, Reid J J

机构信息

Department of Pharmacology, University of Melbourne, Victoria, Australia.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1993 Mar;347(3):313-23. doi: 10.1007/BF00167451.

Abstract

This study investigates the effects of methylenedioxymethamphetamine (MDMA) and amphetamine on monoamine release from rat superfused brain slices in both the presence and absence of vesicular stores of transmitter. MDMA caused the release of radioactivity from slices incubated with [3H]5-hydroxytryptamine, [3H]noradrenaline or [3H]dopamine with EC50 values of 1.9 mumol/l (95% confidence limits 1.5-2.3 mumol/l), 4.5 mumol/l (2.3-8.7 mumol/l), and greater than 30 mumol/l, respectively. In contrast, amphetamine (0.1-300 mumol/l) was more effective in releasing radioactivity from slices incubated with [3H]dopamine than [3H]noradrenaline or [3H]5-hydroxytryptamine. When Ca2+ was excluded from the superfusion fluid, the MDMA-induced release of radioactivity from slices incubated with [3H]dopamine was unaltered, but that from slices incubated with [3H]noradrenaline or [3H]5-hydroxytryptamine was enhanced. MDMA (10 mumol/l) facilitated the stimulation-induced (5 Hz, 1 min) outflow of radioactivity from slices incubated with [3H]noradrenaline or [3H]5-hydroxytryptamine to 7.5-fold and 2.1-fold of control values, respectively, but had no effect on that from slices incubated with [3H]dopamine. Amphetamine (1 mumol/l) increased the stimulation-induced outflow from slices incubated with [3H]noradrenaline, but not that from slices incubated with [3H]5-hydroxytryptamine or [3H]dopamine. Inhibition of monoamine oxidase by a 30-min incubation with pargyline (100 mumol/l) enhanced the releasing action of MDMA on all three monoamines. Pargyline (100 mumol/l) also enhanced the facilitation caused by MDMA, of the stimulation-induced outflow of radioactivity from slices incubated with [3H]noradrenaline, [3H]5-hydroxytryptamine or [3H]dopamine. In some experiments, slices were obtained from reserpinised rats (2.5 mg/kg s.c. 24 h prior) and pre-exposed for 30 min to the monoamine oxidase inhibitor parglyine (100 mumol/l). Under these conditions, electrical stimulation evoked a small residual stimulation-induced outflow of radioactivity from slices incubated with [3H]noradrenaline, and failed to evoke an outflow of radioactivity from slices incubated with [3H]5-hydroxytryptamine or [3H]dopamine. However, a Ca(2+)-dependent stimulation-induced outflow of radioactivity was evoked in the presence of either MDMA (10 mumol/l) or amphetamine (1 mumol/l) from slices incubated with either [3H]dopamine or [3H]noradrenaline, but not from slices incubated with [3H]5-hydroxytryptamine. The stimulation-induced outflow of radioactivity from slices incubated with [3H]noradrenaline was enhanced in the presence of desipramine (1 mumol/l), however this enhancement was less than that caused by 10 mumol/l MDMA or 1 mumol/l amphetamine. The Ca(2+)-dependent response to electrical stimulation in the presence of MDMA from slices incubated with [3H]noradrenaline was greatly reduced when rats were pretreated with a higher dose of reserpine (10 mg/kg s.c.).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本研究调查了亚甲基二氧甲基苯丙胺(摇头丸)和苯丙胺在存在和不存在递质囊泡储存的情况下,对大鼠脑片单胺释放的影响。摇头丸导致与[3H]5-羟色胺、[3H]去甲肾上腺素或[3H]多巴胺一起孵育的脑片释放放射性,其半数有效浓度(EC50)值分别为1.9 μmol/L(95%置信限1.5 - 2.3 μmol/L)、4.5 μmol/L(2.3 - 8.7 μmol/L)和大于30 μmol/L。相比之下,苯丙胺(0.1 - 300 μmol/L)在使与[3H]多巴胺孵育的脑片释放放射性方面,比使与[3H]去甲肾上腺素或[3H]5-羟色胺孵育的脑片更有效。当灌注液中不含Ca2+时,摇头丸诱导的与[3H]多巴胺孵育的脑片放射性释放未改变,但与[3H]去甲肾上腺素或[3H]5-羟色胺孵育的脑片的放射性释放增强。摇头丸(10 μmol/L)使与[3H]去甲肾上腺素或[3H]5-羟色胺孵育的脑片刺激诱导(5 Hz,1分钟)的放射性流出分别增加到对照值的7.5倍和2.1倍,但对与[3H]多巴胺孵育的脑片无影响。苯丙胺(1 μmol/L)增加了与[3H]去甲肾上腺素孵育的脑片刺激诱导的流出,但对与[3H]5-羟色胺或[3H]多巴胺孵育的脑片无影响。用帕吉林(100 μmol/L)孵育30分钟抑制单胺氧化酶,增强了摇头丸对所有三种单胺的释放作用。帕吉林(100 μmol/L)也增强了摇头丸对与[3H]去甲肾上腺素、[3H]5-羟色胺或[3H]多巴胺孵育的脑片刺激诱导的放射性流出的促进作用。在一些实验中,脑片取自利血平化大鼠(24小时前皮下注射2.5 mg/kg),并预先暴露于单胺氧化酶抑制剂帕吉林(100 μmol/L)30分钟。在这些条件下,电刺激引起与[3H]去甲肾上腺素孵育的脑片有少量残余的刺激诱导放射性流出,而未能引起与[3H]5-羟色胺或[3H]多巴胺孵育的脑片放射性流出。然而,在存在摇头丸(10 μmol/L)或苯丙胺(1 μmol/L)的情况下,与[3H]多巴胺或[3H]去甲肾上腺素孵育的脑片会诱发Ca(2+)依赖性刺激诱导的放射性流出,但与[3H]5-羟色胺孵育的脑片则不会。在存在地昔帕明(1 μmol/L)的情况下,与[3H]去甲肾上腺素孵育的脑片刺激诱导的放射性流出增强,然而这种增强小于10 μmol/L摇头丸或1 μmol/L苯丙胺引起的增强。当大鼠用更高剂量的利血平(10 mg/kg皮下注射)预处理时,在存在摇头丸的情况下,与[3H]去甲肾上腺素孵育的脑片对电刺激的Ca(2+)依赖性反应大大降低。(摘要截断于400字)

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