Budantsev A Y, Zharikova A D
Histochemistry. 1976 Sep 13;48(4):335-45. doi: 10.1007/BF00499250.
The method of Glenner et al. for the histochemical demonstration of MAO activity was studied by means of scanning microdensitometry and discrete measurement of optical density (lambda=590 nm) of the liver and brain tissues sections. The experiments indicated that: (1) The optimal time of incubation (the thickness of sections is 15 mum) is 60-90 min. (2) The histochemical reaction proceeds with the following substrates: dopamine, noradrenalin, serotonin, and tryptamine. (3) Iproniazid is the best inhibitor for preincubation whereas for simultaneous inhibition the substrate semicarbazide is better. (4) The incubation under the anaerobic conditions caused a considerable decrease of the stain intensity of the sections. We consider these data to indicate that both the aldehydes and acids formed under oxidation may take part in direct reduction of NBT to diformazan. (5) The histochemical reaction for MAO without substrates testifies to the presence of endogenous amines or other redox reactions leading to the reduction of NBT.
采用扫描显微密度测定法以及对肝脏和脑组织切片的光密度(波长=590nm)进行离散测量,对格伦纳等人用于单胺氧化酶(MAO)活性组织化学显示的方法进行了研究。实验表明:(1)孵育的最佳时间(切片厚度为15μm)为60 - 90分钟。(2)组织化学反应可使用以下底物进行:多巴胺、去甲肾上腺素、血清素和色胺。(3)异烟酰异丙肼是预孵育的最佳抑制剂,而对于同时抑制,氨基脲作为底物效果更好。(4)在厌氧条件下孵育会导致切片染色强度显著降低。我们认为这些数据表明氧化过程中形成的醛和酸可能都参与了将氮蓝四唑直接还原为双甲臜的过程。(5)无底物的MAO组织化学反应证明存在内源性胺或其他导致氮蓝四唑还原的氧化还原反应。