Tsuji S, Larabi Y
Histochemistry. 1983;78(3):317-23. doi: 10.1007/BF00496619.
In the original Karnovsky and Roots' method for the localization of acetylcholinesterase (AChE), thiocholine reduces the ferricyanide and cupric ions of this medium competitively, giving simultaneously cupric (Koelle's precipitate) as histochemical products. We modified the method in order to promote the true Karnovsky's reaction, and to slow down the secondary Koelle's reaction by increasing the concentration of the ferricyanide ion from 0.5 mM to 5.0 mM and by decreasing the concentration of the cupric ion from 3.0 mM to 2.5 mM. The cupric ion, complexed with 5 mM sodium citrate in the original method, was further stabilized by the use of 0.1 M citrate buffer in order to prevent the interaction of cupric ion with increased ferricyanide. In order to suppress completely the residual Koelle's precipitate, we used acetylthiocholine chloride as a substrate, instead of acetylthiocholine iodide. The chloride salt of cuprous thiocholine is soluble, contrary to the iodide salt. In addition, the pH of the medium was lowered from 6.0 to 5.0 to avoid artefactual nuclear staining, appearing at a pH beyond 5.5. In this modified medium, Karnovsky's cupric ferrocyanide becomes the sole precipitate at the enzymatic site and this provides fine localization of acetylcholinesterase activity.
在最初由卡诺夫斯基(Karnovsky)和鲁茨(Roots)提出的乙酰胆碱酯酶(AChE)定位方法中,硫代胆碱竞争性地还原该介质中的铁氰化物和铜离子,同时产生铜(科勒氏沉淀)作为组织化学产物。我们对该方法进行了改进,以促进真正的卡诺夫斯基反应,并通过将铁氰化物离子浓度从0.5 mM提高到5.0 mM以及将铜离子浓度从3.0 mM降低到2.5 mM来减缓继发性科勒反应。在原方法中与5 mM柠檬酸钠络合的铜离子,通过使用0.1 M柠檬酸盐缓冲液进一步稳定,以防止铜离子与增加的铁氰化物发生相互作用。为了完全抑制残留的科勒氏沉淀,我们使用氯化乙酰硫代胆碱作为底物,而不是碘化乙酰硫代胆碱。与碘化物盐相反,硫代胆碱亚铜的氯化物盐是可溶的。此外,将介质的pH从6.0降低到5.0,以避免在pH超过5.5时出现的人为核染色。在这种改良的介质中,卡诺夫斯基的亚铁氰化铜在酶位点成为唯一的沉淀,这为乙酰胆碱酯酶活性提供了良好的定位。