Kudriavtseva M V, Shalakhmetova T M, Kudriavtsev B N
Tsitologiia. 1977 Sep;19(9):978-84.
A cytofluorimetrical study was made of glycogen content on smears of isolated rat liver cells, obtained by perfusion of different solutions: 1/15 M phosphate buffer, the Locke solution, only the Locke solution plus sodium citrate, a calcium-free Locke solution, 0.25 M sucrose, physiological saline, Versene. No loss of glycogen occurred during any perfusion procedure, however, it took place during the smear preparation. The main cell injury is observed due to mechanical factors. An additional treatment of liver, after perfusion, by homogenization and centrigugation at mild conditions decreases the cell glycogen content by 30%. The least cell injury and the best glycogen retention was achieved when phosphate buffers were employed for cell isolation.
1/15 M磷酸缓冲液、洛克溶液、仅洛克溶液加柠檬酸钠、无钙洛克溶液、0.25 M蔗糖、生理盐水、维尔烯。在任何灌注过程中均未发生糖原损失,然而,在涂片制备过程中发生了糖原损失。主要观察到细胞损伤是由机械因素引起的。灌注后对肝脏进行温和条件下的匀浆和离心的额外处理会使细胞糖原含量降低30%。当使用磷酸缓冲液进行细胞分离时,细胞损伤最小且糖原保留最佳。