[THE ROLE OF THE BLOOD OXYGEN IN PROTECTIVE MECHANISM OF ISCHEMIC PRECONDITIONING DURING HEPATIC ISCHEMIA-REPERFUSION].

M N Khodosovskii
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Abstract

The role of blood oxygen in the protective mechanism of ischemic preconditioning (IPC) was investigated in rabbits during hepatic ischemia-reperfusion (HIR). Animals were divided into 2 experimental groups: in the 1st group (n = 11) hepatic ischemia (30 min) was induced by Pringle maneuver, reperfusion was lasted 120 min; in the 2nd group (n = 8) the short period of vascular clamping (10 min) and reperfusion (10 min) were performed before HIR. The parameters of blood oxygen (рО2, p50, Hb), acid-base balance (рН, рСО2, TCO2, ABE, SBE, SBC and etc.), lipid peroxidation (Schiff bases, conjugated dienes), antioxidant system (catalase, α-tocopherol), plasma transaminases (ALT, AST) and nitrite/nitrate concentration (NOx) were measured. HIR in the 1st group leads to elevation of p50, lipid peroxidation, ALT and AST accompanied by reduction of рН, TCO2, ABE, SBE, SBC, catalase activity, α-tocopherol and NOx levels. IPC significantly reduces p50, lipid peroxidation, ALT and AST simultaneously improves рН, TCO2, ABE, SBC, catalase activity, α-tocopherol and NOx levels. These findings indicate that IPC prevents oxidative stress in liver trough increased blood hemoglobin-oxygen affinity and limitation of oxygen participation in free radical processes during reperfusion.

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[血氧在肝缺血再灌注缺血预处理保护机制中的作用]。
研究了血氧在兔肝缺血再灌注(HIR)过程中缺血预处理(IPC)保护机制中的作用。将动物分为2个实验组:第一组(n = 11)采用Pringle手法诱导肝缺血(30 min),再灌注持续120 min;第二组(n = 8)在HIR前进行短时间血管夹持(10 min)和再灌注(10 min)。测定血氧(рО2、p50、Hb)、酸碱平衡(рН、рСО2、TCO2、ABE、SBE、SBC等)、脂质过氧化(希夫碱、共轭二烯)、抗氧化系统(过氧化氢酶、α-生育酚)、血浆转氨酶(ALT、AST)、亚硝酸盐/硝酸盐浓度(NOx)等指标。第一组HIR导致p50、脂质过氧化、ALT和AST升高,同时рН、TCO2、ABE、SBE、SBC、过氧化氢酶活性、α-生育酚和NOx水平降低。IPC显著降低p50、脂质过氧化、ALT和AST,同时提高рН、TCO2、ABE、SBC、过氧化氢酶活性、α-生育酚和NOx水平。这些发现表明,IPC通过增加血液血红蛋白-氧亲和力和限制氧参与再灌注自由基过程来防止肝脏氧化应激。
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