Dikow A, Gossrau R
Department of Cell Biology and Morphology, Bulgarian Academy of Sciences, Sofia.
Acta Histochem. 1990;88(2):167-74. doi: 10.1016/s0065-1281(11)80129-7.
Although many synthetic substrates and methods are available for the histochemical detection of non-specific esterases and non-specific acid phosphatase, there are still further possibilities to investigate these hydrolases histochemically. This was shown for menadiol diacetate and menadiol diphosphate using tetrazolium salt, simultaneous azo-dye as well as metal salt methods in many rat tissues. In comparison, the azo-dye procedure with various Fast salts or hexazonium Pararosaniline or New Fuchsin delivered less satisfactory results; precisely localized stain in sufficient amounts was obtained for non-specific esterases using nitro BT, tetranitro BT or benzothiazolystyrylphthalhydrazidyl tetrazolium (BSPT) and for non-specific acid phosphatase with BSPT in the tetrazolium salt method or using cerium ions for phosphate trapping in the diaminobenzidine-nickel-hydrogen peroxide procedure.
尽管有许多合成底物和方法可用于非特异性酯酶和非特异性酸性磷酸酶的组织化学检测,但仍有进一步通过组织化学研究这些水解酶的可能性。在许多大鼠组织中,使用四氮唑盐、同时偶氮染料以及金属盐方法对二醋酸甲萘醌和二磷酸甲萘醌进行研究,结果表明了这一点。相比之下,使用各种固蓝盐、六偶氮对苯二胺或新复红的偶氮染料程序得到的结果不太令人满意;在四氮唑盐法中,使用硝基BT、四硝基BT或苯并噻唑基苯乙烯基邻苯二甲酰肼四氮唑(BSPT)可获得足够量的、定位精确的非特异性酯酶染色,而在二氨基联苯胺-镍-过氧化氢程序中,使用BSPT或铈离子捕获磷酸盐可获得非特异性酸性磷酸酶的染色。