Wolf W A, Youdim M B, Kuhn D M
Eur J Pharmacol. 1985 Mar 12;109(3):381-7. doi: 10.1016/0014-2999(85)90399-1.
The question of whether serotonin is deaminated by MAO before it can be released or after release has occurred was investigated by studying the 5-HT behavioral syndrome in acutely reserpinized rats. The release of serotonin from vesicles by reserpine does not produce the serotonin behavioral syndrome which is an in vivo index of serotonin release and receptor activation. However, if rats are first pretreated with a nonselective monoamine oxidase inhibitor (e.g., tranylcypromine), the injection of reserpine is followed by symptoms which are characteristic of the behavioral syndrome including forepaw treading, hindlimb abduction and head weaving. Neither selective MAO-A or -B inhibition with clorgyline or deprenyl, respectively, nor inhibition of serotonin reuptake with fluoxetine prior to reserpine produced the serotonin behavioral syndrome. However, the combination of clorgyline and deprenyl followed by reserpine does so. These behavioral data along with neurochemical analyses of serotonin and 5-hydroxyindoleacetic acid levels lead to the conclusion that serotonin does not have to be released before it is metabolized to 5-hydroxyindoleacetic acid. Consequently, the levels of 5-hydroxyindoleacetic acid in brain reflect MAO activity and not serotonin release or utilization.
通过研究急性利血平化大鼠的5-羟色胺行为综合征,对5-羟色胺在释放前还是释放后被单胺氧化酶脱氨基的问题进行了研究。利血平使5-羟色胺从囊泡中释放出来,但不会产生5-羟色胺行为综合征,该综合征是5-羟色胺释放和受体激活的体内指标。然而,如果大鼠先用非选择性单胺氧化酶抑制剂(如反苯环丙胺)预处理,再注射利血平,随后就会出现行为综合征的特征性症状,包括前爪踩踏、后肢外展和头部摆动。分别用氯吉兰或司来吉兰选择性抑制MAO-A或MAO-B,或在注射利血平前用氟西汀抑制5-羟色胺再摄取,均未产生5-羟色胺行为综合征。然而,氯吉兰和司来吉兰联合使用后再注射利血平则会产生该综合征。这些行为学数据以及对5-羟色胺和5-羟吲哚乙酸水平的神经化学分析得出结论,5-羟色胺在代谢为5-羟吲哚乙酸之前不必被释放。因此,脑中5-羟吲哚乙酸的水平反映的是单胺氧化酶的活性,而不是5-羟色胺的释放或利用情况。