Sharapov V I, Grek O R, Zykov A A
Vopr Med Khim. 1988 Jan-Feb;34(1):25-9.
Total ischemia of rat liver tissue within 30 min caused distinct alterations in lipid component of endoplasmic reticulum membranes, which occurred within three weeks of the postischemic period. During this period the rate of microsomal lipids saturation was elevated due to an increase in the relative content of saturated fatty acids. Two-step alterations were observed in the patterns of fluorescent probe binding (I-amino naphthalene-8-sulfonate) as well as in sensitivity of cytochrome P-450 to the impairment in vitro after induction of lipid peroxidation in microsomal membranes. Within 1-3 days after the ischemia affinity of the fluorescent probe to microsomes was decreased, while stability of cytochrome P-450 to impairment during lipid peroxidation induction was increased. Within 7-14 days affinity of the fluorescent probe to membranes was markedly elevated and stability of cytochrome P-450 to the impairment in vitro was lowered in the reactions of lipid peroxidation.
大鼠肝组织在30分钟内的完全缺血导致内质网膜脂质成分发生明显改变,这种改变发生在缺血后的三周内。在此期间,由于饱和脂肪酸相对含量增加,微粒体脂质饱和度升高。在微粒体膜脂质过氧化诱导后,荧光探针(1-氨基萘-8-磺酸盐)的结合模式以及细胞色素P-450对体外损伤的敏感性出现了两步变化。缺血后1-3天,荧光探针与微粒体的亲和力降低,而在脂质过氧化诱导过程中细胞色素P-450对损伤的稳定性增加。在7-14天内,荧光探针与膜的亲和力显著升高,并且在脂质过氧化反应中细胞色素P-450对体外损伤的稳定性降低。