Muther T F
J Histochem Cytochem. 1977 Sep;25(9):1043-50. doi: 10.1177/25.9.71324.
Data are presented that support a nonenzymic mechanism for the staining obtained with the cobalt-bicarbonate method. The biochemically inactive apocarbonic anhydrase and Cu+2 apocarbonic anhydrase stain positively and this stain is inhibited by acetazolamide. The staining of the acetazolamide resistant carbonic anhydrase of male rat liver is inhibited by 10-6 M acetazolamide, at which concentration no biochemical inhibition is observed. There is no correlation between the biochemical and histochemical inhibitory potencies of a number of sulfonamides. The nonsulfonamide inhibitor, KCNO, does not inhibit staining. When incubations are performed in media exposed to atmospheres of increasing CO2 content, staining is not abolished until the atmospheric pCO2 approaches that generated by the medium itself. This finding renders the carbonic anhydrase catalyzed dehydration of HCO3- an improbable reaction for the staining. Studies with modified media show differences in staining patterns and in sensitivity to acetazolamide inhibition which question the specificity of the method for carbonic anhydrase.
所呈现的数据支持了用碳酸氢钴法染色的非酶机制。生化上无活性的脱辅基碳酸酐酶和铜离子脱辅基碳酸酐酶呈阳性染色,且这种染色被乙酰唑胺抑制。雄性大鼠肝脏中对乙酰唑胺耐药的碳酸酐酶的染色被10 - 6 M乙酰唑胺抑制,在此浓度下未观察到生化抑制作用。多种磺胺类药物的生化抑制效力与组织化学抑制效力之间没有相关性。非磺胺类抑制剂氰酸钾不抑制染色。当在暴露于二氧化碳含量不断增加的大气中的培养基中进行孵育时,直到大气中的pCO2接近培养基自身产生的pCO2时,染色才会消失。这一发现使得碳酸酐酶催化的HCO3 - 脱水反应不太可能是染色的反应。对改良培养基的研究表明,染色模式和对乙酰唑胺抑制的敏感性存在差异,这对该方法检测碳酸酐酶的特异性提出了质疑。