Invernizzi R, Fracasso C, Caccia S, Di Clemente A, Garattini S, Samanin R
Istituto di Ricerche Farmacologiche, Mario Negri, Milan, Italy.
Eur J Pharmacol. 1989 Apr 12;163(1):77-83. doi: 10.1016/0014-2999(89)90397-x.
The effect of L-cysteine on the depletion of serotonin and 5-hydroxyindoleacetic acid concentrations caused by p-chloroamphetamine and d-fenfluramine was studied in various brain regions one week after drug injection. p-Chloroamphetamine (2.5 and 5 mg/kg i.p.) and d-fenfluramine (13.4 mg/kg i.p.) significantly reduced serotonin and 5-hydroxyindoleacetic acid levels in the striatum, hippocampus and cortex, particularly in the latter areas. L-cysteine (500 mg/kg i.p.), administered 30 min before and 5 h after p-chloroamphetamine or d-fenfluramine, significantly reduced the effect of either drug on the concentrations of both indoles without causing any effect by itself. In another experiment, the rats were treated as above and were killed at various times after p-chloroamphetamine or d-fenfluramine injection to determine, in parallel, the indole levels in the whole brain and the concentration of p-chloroamphetamine, d-fenfluramine and its metabolite d-norfenfluramine in the plasma and brain. p-Chloroamphetamine and d-fenfluramine markedly lowered both indoles, particularly 16 and 24 h after injection. L-cysteine had no effect on the indole concentrations but significantly reduced the effect of p-chloroamphetamine, d-fenfluramine 16 and 24 h after injection. At these times, the brain concentrations of p-chloroamphetamine, d-fenfluramine and d-norfenfluramine were markedly lower in the L-cysteine-treated than in the control rats. Analysis of the blood concentration of p-chloroamphetamine, d-fenfluramine and d-norfenfluramine showed that the rats treated with L-cysteine eliminated the drugs studied more rapidly than the control animals.(ABSTRACT TRUNCATED AT 250 WORDS)
在注射药物一周后,研究了L-半胱氨酸对由对氯苯丙胺和右旋芬氟拉明引起的血清素和5-羟吲哚乙酸浓度降低的影响。对氯苯丙胺(2.5和5mg/kg腹腔注射)和右旋芬氟拉明(13.4mg/kg腹腔注射)显著降低纹状体、海马体和皮质中的血清素和5-羟吲哚乙酸水平,尤其是在后两个区域。在对氯苯丙胺或右旋芬氟拉明注射前30分钟和注射后5小时给予L-半胱氨酸(500mg/kg腹腔注射),可显著降低两种药物对两种吲哚浓度的影响,且其本身无任何作用。在另一项实验中,大鼠按上述方法处理,并在注射对氯苯丙胺或右旋芬氟拉明后的不同时间处死,以同时测定全脑中的吲哚水平以及血浆和脑中对氯苯丙胺、右旋芬氟拉明及其代谢物去甲右旋芬氟拉明的浓度。对氯苯丙胺和右旋芬氟拉明显著降低两种吲哚水平,尤其是在注射后16和24小时。L-半胱氨酸对吲哚浓度无影响,但在注射后16和24小时显著降低对氯苯丙胺、右旋芬氟拉明的作用。在这些时间点,L-半胱氨酸处理组大鼠脑中对氯苯丙胺、右旋芬氟拉明和去甲右旋芬氟拉明的浓度明显低于对照组大鼠。对对氯苯丙胺、右旋芬氟拉明和去甲右旋芬氟拉明血药浓度的分析表明,L-半胱氨酸处理的大鼠比对照动物更快地清除所研究的药物。(摘要截短于250字)