Arai R, Kimura H, Nagatsu I, Maeda T
Department of Anatomy, Fujita Health University, School of Medicine, Aichi, Japan.
Brain Res. 1997 Jan 16;745(1-2):352-6. doi: 10.1016/s0006-8993(96)01239-5.
Using enzyme histochemistry for monoamine oxidase (MAO) activity, we have examined whether MAO type A or type B or both are localized in neurons of the locus coeruleus (LC) and dorsal raphe nucleus (DR) of the rat. After pretreatment with various concentrations of the MAO type A inhibitor clorgyline or the type B inhibitor deprenyl, non-fixed frozen sections of the brain were histochemically stained for MAO activity with tyramine as a common substrate for the two types. MAO activity of the stained neuron was determined by measuring optical density of the staining. Percentage inhibition of the control MAO activity was plotted against increasing concentrations of the inhibitors. MAO activity of LC neurons was inhibited by low concentrations of clorgyline with a monophasic dose-response curve but not with a biphasic curve. Higher concentrations of deprenyl were needed to inhibit of LC neurons. MAO activity of DR neurons was inhibited by low concentrations of deprenyl with a monophasic dose-response curve. Clorgyline inhibited the MAO activity of DR neurons at only higher concentrations. When the sections without inhibitor pretreatment were incubated with the type A preferential substrate serotonin, the MAO activity was strongly stained in LC neurons but very weakly in DR neurons. With the type B preferential substrate beta-phenylethylamine, the staining was intense in DR neurons while very faint in LC neurons. These findings suggest that (i) almost all the MAO activity in LC neurons is of type A, and (ii) the MAO activity in DR neurons is predominantly of type B.
我们运用单胺氧化酶(MAO)活性的酶组织化学方法,研究了MAO A型或B型,或两者是否定位于大鼠蓝斑(LC)和中缝背核(DR)的神经元中。在用不同浓度的MAO A型抑制剂氯吉兰或B型抑制剂司来吉兰进行预处理后,对脑的未固定冰冻切片用酪胺作为这两种类型的共同底物进行MAO活性的组织化学染色。通过测量染色的光密度来测定染色神经元的MAO活性。将对照MAO活性的抑制百分比相对于抑制剂浓度的增加进行作图。LC神经元的MAO活性被低浓度的氯吉兰以单相剂量反应曲线抑制,但不是双相曲线。需要更高浓度的司来吉兰才能抑制LC神经元。DR神经元的MAO活性被低浓度的司来吉兰以单相剂量反应曲线抑制。氯吉兰仅在较高浓度时抑制DR神经元的MAO活性。当未用抑制剂预处理的切片与A型优先底物5-羟色胺一起孵育时,MAO活性在LC神经元中强烈染色,但在DR神经元中非常微弱。用B型优先底物β-苯乙胺时,染色在DR神经元中强烈,而在LC神经元中非常微弱。这些发现表明:(i)LC神经元中几乎所有的MAO活性都是A型;(ii)DR神经元中的MAO活性主要是B型。