Butcher R G, Van Noorden C J
Histochem J. 1985 Sep;17(9):993-1008. doi: 10.1007/BF01417948.
The reaction rate of glucose-6-phosphate dehydrogenase activity in liver sections from fed and starved rats has been monitored by the continuous measurement at 37 degrees C of the reaction product as it is formed using scanning and integrating microdensitometry. Control media lacked either substrate or both substrate and coenzyme. All reactions were nonlinear; however, subtraction of either of the controls from the test response produced linearity. Differing responses in sections of livers from fed and fasted rats indicate that the appropriate control medium for use in the assay of this dehydrogenase is one lacking both substrate and coenzyme rather than a medium containing coenzyme. The reaction rate was the same with each of the final acceptors. Problems with the diffusion of the formazan of BPST and with the failure to precipitate the formazan of Neotetrazolium make Tetranitro BT and Nitro BT the tetrazolium salts of choice in quantitative dehydrogenase assays.
通过使用扫描和积分显微密度测定法在37℃连续测量喂食和饥饿大鼠肝脏切片中葡萄糖-6-磷酸脱氢酶活性的反应产物形成速率,对该反应速率进行了监测。对照培养基缺乏底物或同时缺乏底物和辅酶。所有反应均为非线性;然而,从测试反应中减去任何一种对照均可产生线性关系。喂食和禁食大鼠肝脏切片的不同反应表明,用于该脱氢酶测定的合适对照培养基是一种既缺乏底物又缺乏辅酶的培养基,而不是含有辅酶的培养基。与每种最终受体的反应速率相同。BPST的甲臜扩散问题以及新四氮唑甲臜沉淀失败使得四硝基BT和硝基BT成为定量脱氢酶测定中首选的四氮唑盐。