Lugoviĭ V I, Zolochevs'ka L I, Dziuba A M
Ukr Biokhim Zh. 1977 May-Jun;49(3):10-5.
Activity of hexokinase, phosphorylase, glucoso-6-phosphate dehydrogenase lactate-dehydrogenase was studied in liver slices, homogenate and supernatant fraction after freezing at a rate of 1 degree/min down to -30 degrees C. The enzyme activity in homogenate and supernatant fraction does not change after freezing. A significant reduction in the activity of most enzymes that is followed by an increase in their activity in the freezing medium was observed in the experiments. Cryoprotectant polyethylene glycol, mol. wt. 300 and 1,000 (PEG-300 and PEG-1,000), partially prevents the observed changes in the enzyme activity; PEG-1,000 is more effective than PEG-300. Experimental results show that the main reason for the reduction of the enzyme activity observed after freezing the tissue slices is a decrease in the volume of intracellular enzyme proteins due to their leakage from the injured cellular elements into the exocellular medium.
以每分钟1摄氏度的速率将肝脏切片、匀浆和上清液组分冷冻至-30摄氏度后,对己糖激酶、磷酸化酶、葡萄糖-6-磷酸脱氢酶和乳酸脱氢酶的活性进行了研究。冷冻后,匀浆和上清液组分中的酶活性没有变化。实验中观察到,大多数酶的活性显著降低,随后在冷冻介质中其活性又有所增加。分子量为300和1000的冷冻保护剂聚乙二醇(PEG - 300和PEG - 1000)可部分防止所观察到的酶活性变化;PEG - 1000比PEG - 300更有效。实验结果表明,组织切片冷冻后观察到酶活性降低的主要原因是细胞内酶蛋白因从受损细胞成分泄漏到细胞外介质中而导致其体积减小。