Hasselgren P O, Jennische E, Fornander J, Hellman A
Acta Chir Scand. 1982;148(7):601-7.
Hepatic cell membrane potential (HCMP) and protein synthesis were studied in rats during and after a period (60 min) of liver ischemia. ATP-MgCl2 (5 mumol . 100 g bw-1) or saline was administered slowly intravenously before or after the period of liver ischemia. No beneficial effect of ATP-MgCl2 on the impaired HCMP or protein synthesis was observed. On the contrary, the post-ischemic restitution of these cellular metabolic variables was slower in animals receiving ATP-MgCl2 after the period of liver ischemia as compared with saline-treated rats. At the end of the ischemic period, ATP, glucose and lactate in liver tissue were the same in animals receiving ATP-MgCl2 or saline before ischemia. These results suggest that the beneficial effects previously reported after administration of ATP-MgCl2 in conditions with reduced hepatic blood flow are not primarily due to an improved metabolic situation in the liver.
在大鼠肝脏缺血60分钟期间及之后,对其肝细胞膜电位(HCMP)和蛋白质合成进行了研究。在肝脏缺血期之前或之后,将ATP - MgCl₂(5 μmol·100 g体重⁻¹)或生理盐水缓慢静脉注射。未观察到ATP - MgCl₂对受损的HCMP或蛋白质合成有有益作用。相反,与生理盐水处理的大鼠相比,在肝脏缺血期后接受ATP - MgCl₂的动物中,这些细胞代谢变量的缺血后恢复较慢。在缺血期结束时,缺血前接受ATP - MgCl₂或生理盐水的动物肝脏组织中的ATP、葡萄糖和乳酸水平相同。这些结果表明,先前报道的在肝血流减少情况下给予ATP - MgCl₂后的有益作用,并非主要归因于肝脏代谢状况的改善。