Brannan T S, Maker H S, Bernstein M
J Neurochem. 1982 Aug;39(2):589-91. doi: 10.1111/j.1471-4159.1982.tb03988.x.
Glutathione peroxidase, glutathione reductase, and catalase activities were measured to 48 h after death in mouse brains held at temperatures replicating the cooling occurring in human cadaver brain. Glutathione peroxidase was stable for 48 h; catalase was stable for 24 h and then declined 20% in activity. Glutathione reductase was stable for 4 h and then decreased to 55% of its initial activity by 48 h. Perfusion of mouse brain with 0.9% (wt/vol) NaCl did not decrease enzyme activities, indicating that erythrocyte contamination has little effect on measured brain activities. The results suggest that glutathione peroxidase would not be affected by moderate time delays in obtaining human postmortem brains but catalase activity may be affected if brains are not promptly removed. Glutathione reductase is not stable and measurements would require controls carefully matched for postmortem conditions.
在模拟人类尸体大脑冷却温度的条件下,对小鼠大脑死后48小时内的谷胱甘肽过氧化物酶、谷胱甘肽还原酶和过氧化氢酶活性进行了测定。谷胱甘肽过氧化物酶在48小时内保持稳定;过氧化氢酶在24小时内保持稳定,之后活性下降20%。谷胱甘肽还原酶在4小时内保持稳定,然后到48小时时降至其初始活性的55%。用0.9%(重量/体积)的NaCl灌注小鼠大脑不会降低酶活性,这表明红细胞污染对所测大脑活性影响很小。结果表明,谷胱甘肽过氧化物酶不会受到获取人类死后大脑时适度时间延迟的影响,但如果大脑未及时取出,过氧化氢酶活性可能会受到影响。谷胱甘肽还原酶不稳定,测量时需要仔细匹配死后条件的对照。