Meijer A E, de Vries G P
Histochemistry. 1975 Jun 5;43(3):225-36. doi: 10.1007/BF00499703.
Improved histochemical techniques for the demonstration of NADP+-specific isocitrate dehydrogenase and malate dehydrogenase in tissue sections are described. With these techniques a semipermeable membrane is interposed between the incubating solutions and the tissue sections preventing diffusion of enzymes into the medium during incubation. In the histochemical system the NADP+-dependent enzymes catalyze the electron transfer from threo-Ds-isocitrate or L-malate into NADP+. Phenazine methosulphate and menadione serve as intermediate electron acceptors between reduced coenzyme and nitro-BT. Sodium-azide and amytal are incorporated into the incubating-medium to block electron transfer to the cytochromes. For demonstrating enzyme activities in sections containing non-specific alkaline phosphatase, a phosphatase inhibitor is added into the incubation media. Problems involved in the histochemical demonstration of both enzymes are discussed.
本文描述了用于在组织切片中显示NADP⁺特异性异柠檬酸脱氢酶和苹果酸脱氢酶的改良组织化学技术。采用这些技术时,在孵育液和组织切片之间插入半透膜,以防止酶在孵育过程中扩散到培养基中。在组织化学系统中,依赖NADP⁺的酶催化电子从苏糖-Ds-异柠檬酸或L-苹果酸转移到NADP⁺。吩嗪硫酸甲酯和甲萘醌作为还原辅酶与硝基蓝四唑之间的中间电子受体。将叠氮化钠和戊巴比妥加入孵育培养基中以阻断电子向细胞色素的转移。为了在含有非特异性碱性磷酸酶的切片中显示酶活性,在孵育培养基中加入磷酸酶抑制剂。文中讨论了这两种酶组织化学显示中涉及的问题。