Matos F F, Rollema H, Basbaum A I
Department of Anatomy, University of California San Francisco 94143.
Brain Res. 1990 Sep 24;528(1):39-47. doi: 10.1016/0006-8993(90)90192-e.
Extracellular levels of serotonin (5-HT), dopamine (DA) and their major metabolites 5-hydroxyindoleacetic acid (5-HIAA), 3,4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA), were measured in the lateral hypothalamus of awake, freely moving rats using microdialysis combined with HPLC and electrochemical detection. To characterize the factors which control 5-HT release, the effects of various drugs were assessed. TTX had a reversible inhibitory effect on the basal levels of 5-HT, 5-HIAA, DOPAC and HVA. Infusion of K+ concomitantly increased 5-HT and DA and decreased 5-HIAA and HVA. Imipramine increased extracellular levels of 5-HT and DA and decreased 5-HIAA levels; this effect was TTX-sensitive. Systemic pargyline increased extracellular 5-HT and markedly decreased the metabolic levels. Pargyline pretreatment in the presence of imipramine, infused through the dialysis probe, slowly increased 5-HT levels above that produced by the reuptake blocker alone. Infusion with AMPH produced a dramatic, TTX-insensitive, increase in 5-HT and DA and a decrease in the metabolic levels. These results provide evidence that (1) basal release of 5-HT in the lateral hypothalamus results from neuronal activity, (2) the metabolites in the extracellular fluid derive primarily from intracellular monoamine oxidase (MAO) activity, (3) 5-HT is mainly removed from the extracellular space by a reuptake mechanism, with minimal contribution of an extracellular MAO, and (4) the AMPH-evoked release of 5-HT and DA is a Na+ channel-independent process.
采用微透析结合高效液相色谱和电化学检测法,测定清醒、自由活动大鼠外侧下丘脑细胞外5-羟色胺(5-HT)、多巴胺(DA)及其主要代谢产物5-羟吲哚乙酸(5-HIAA)、3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)的水平。为了确定控制5-HT释放的因素,评估了各种药物的作用。河豚毒素(TTX)对5-HT、5-HIAA、DOPAC和HVA的基础水平有可逆的抑制作用。同时注入钾离子会使5-HT和DA增加,5-HIAA和HVA减少。丙咪嗪可增加细胞外5-HT和DA的水平,并降低5-HIAA的水平;这种作用对TTX敏感。全身性给予帕吉林可增加细胞外5-HT水平,并显著降低代谢水平。在丙咪嗪存在的情况下,通过透析探针进行帕吉林预处理,可使5-HT水平缓慢升高至高于单独使用再摄取阻滞剂所产生的水平。注入苯丙胺(AMPH)会使5-HT和DA急剧增加且对TTX不敏感,并使代谢水平降低。这些结果证明:(1)外侧下丘脑5-HT的基础释放源于神经元活动;(2)细胞外液中的代谢产物主要来自细胞内单胺氧化酶(MAO)的活性;(3)5-HT主要通过再摄取机制从细胞外空间清除,细胞外MAO的作用最小;(4)AMPH诱发的5-HT和DA释放是一个不依赖钠离子通道的过程。