Tamura M
First Department of Surgery, Asahikawa Medical College, Japan.
Jpn Circ J. 1992 Apr;56(4):366-75. doi: 10.1253/jcj.56.366.
The protective effects of the PGI2 analogue, OP-2507 against hypoxic tissue injury were investigated in a 60-70 min acute hemorrhagic shock model in 29 rats. To assess the metabolic recovery of mitochondria after tissue injury induced by hemorrhagic hypotension with a mean arterial pressure of 30 mmHg, we have non-invasively monitored changes in the brain tissue parameters of cyt. aa3 redox state, blood oxygenation and relative blood volume by spectrophotometry through the closed skull and intact skin. Pretreatment with 0.1 mg/Kg s.c. of OP-2507 at 30-40 min before induction of shock was performed on 14 rats (OP-treated group). The remaining 15 rats were used as a control (control group). There was a consistent prolongation of survival time and a significant improvement in survival rate after reinfusion of the shed blood in the OP-treated group. In this group there was a rapid and complete reoxidation of cyt. aa3 with a mean overshoot of 9 +/- 5.5% above the baseline value after reinfusion. On the other hand, in the control group the extent of reoxidation was significantly lower, with a minimal 11 +/- 3.2% below the base line. In order to evaluate the mechanisms involved 10 mg of NaCN i.v. was administered to the living rats at 60-70 min after reinfusion of the blood in both groups. In the OP-treated group, brain Hb saturation increased up to 20% above the pre-cyanide infusion level. However in the control group there was a non-significant increase in the Hb oxygenation level. These observation indicate that in the OP-treated group oxygen consumption by mitochondria is significantly higher than that in the control group. Thus, enhanced oxygen utilization could lead to the active restoration of injured tissue by promoting oxidative phosphorylation. Under these experimental conditions the oxidative response of cyt. aa3 is concluded to correlate closely with the prognosis of shock animals in both groups. These results indicate the potential usefulness of OP-2507 in protecting the brain and other organs from oxygen insufficiency as a result of tissue ischemia and anoxia.
在29只大鼠的60 - 70分钟急性失血性休克模型中,研究了前列环素(PGI2)类似物OP - 2507对缺氧组织损伤的保护作用。为了评估平均动脉压为30 mmHg的失血性低血压所致组织损伤后线粒体的代谢恢复情况,我们通过闭合的颅骨和完整的皮肤,采用分光光度法无创监测了细胞色素aa3氧化还原状态、血液氧合和相对血容量等脑组织参数的变化。在诱导休克前30 - 40分钟,对14只大鼠(OP治疗组)进行皮下注射0.1 mg/Kg的OP - 2507预处理。其余15只大鼠作为对照(对照组)。OP治疗组在回输 shed blood后,存活时间持续延长,存活率显著提高。在该组中,细胞色素aa3迅速且完全再氧化,回输后平均超调量比基线值高9±5.5%。另一方面,对照组的再氧化程度明显较低,比基线值最低低11±3.2%。为了评估其中涉及的机制,两组在回输血后60 - 70分钟,对存活大鼠静脉注射10 mg氰化钠。在OP治疗组,脑血红蛋白饱和度比注射氰化物前水平升高了20%。然而,在对照组中,血红蛋白氧合水平无显著升高。这些观察结果表明,OP治疗组中线粒体的氧消耗明显高于对照组。因此,增强的氧利用可能通过促进氧化磷酸化导致受损组织的积极恢复。在这些实验条件下,得出细胞色素aa3的氧化反应与两组休克动物的预后密切相关的结论。这些结果表明,OP - 2507在保护大脑和其他器官免受组织缺血和缺氧导致的氧不足方面具有潜在的有用性。