Role of xanthine oxidase inhibition in survival from hemorrhagic shock.

Circulatory shock Pub Date : 1994-01-01
D Mannion, G J Fitzpatrick, M Feeley
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Abstract

The irreversible loss of adenine nucleotides and the formation of free radicals have both been suggested as causes of irreversibility following prolonged hemorrhagic shock. This study was performed to assess the effect of xanthine oxidase inhibition (allopurinol 50 mg/kg/day), free radical scavenging (superoxide dismutase 15,000 u/kg, catalase 15,000 u/kg, dimethylsulfoxide 20 mg/kg, and alpha tocopherol 100 mg/kg/day) or both, on the 24-hr survival of dogs subjected to irreversible haemorrhagic shock. Twenty anesthetized dogs were bled to a mean arterial pressure of 30 mm Hg for 4 hr. The dogs were allocated to a control, an allopurinol pretreated, a free radical scavenger, or a combined treatment group. Both groups pretreated with allopurinol had significantly improved survival (P < 0.05) over that seen in the control group, but the free radical scavenger treated group was not significantly different from the control group. This study demonstrates the beneficial effect of xanthine oxidase inhibition on survival, and suggests that it may be due to preservation of adenine nucleotides rather than prevention of free radical formation.

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黄嘌呤氧化酶抑制在失血性休克存活中的作用。
腺嘌呤核苷酸的不可逆损失和自由基的形成都被认为是长时间失血性休克后不可逆性的原因。本研究旨在评估黄嘌呤氧化酶抑制(别嘌呤醇50 mg/kg/天)、自由基清除(超氧化物歧化酶15,000 u/kg、过氧化氢酶15,000 u/kg、二甲亚砜20 mg/kg和α生育酚100 mg/kg/天)或两者对不可逆失血性休克犬24小时存活的影响。20只麻醉犬在平均动脉压30 mm Hg下放血4小时。这些狗被分配到对照组、别嘌呤醇预处理组、自由基清除剂组或联合治疗组。别嘌呤醇预处理组与对照组相比,生存率均有显著提高(P < 0.05),但自由基清除剂预处理组与对照组比较差异无统计学意义。本研究证明了黄嘌呤氧化酶抑制对生存的有益作用,并表明这可能是由于保存腺嘌呤核苷酸而不是防止自由基的形成。
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Comparison of binding specificity and the function of two human IgM anti-lipid A monoclonal antibodies. Hypertonic saline/dextran versus lactated Ringer's treatment for hemorrhage in dehydrated swine. Lysozyme regulates LPS-induced interleukin-6 release in mice. Liver oxygen uptake dependence and mitochondrial function in septic rats. Efficacy of continuous arteriovenous hemofiltration in endotoxic shock.
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