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血清羟自由基清除能力的测定,采用无铁羟自由基源。

Serum hydroxyl radical scavenging capacity as quantified with iron-free hydroxyl radical source.

机构信息

The Wakasa Wan Energy Research Center, Tsuruga, Fukui 914-0192, Japan.

出版信息

J Clin Biochem Nutr. 2009 Sep;45(2):193-201. doi: 10.3164/jcbn.08-265. Epub 2009 Aug 28.

DOI:10.3164/jcbn.08-265
PMID:19794928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2735632/
Abstract

We have developed a simple ESR spin trapping based method for hydroxyl (OH) radical scavenging-capacity determination, using iron-free OH radical source. Instead of the widely used Fenton reaction, a short (typically 5 seconds) in situ UV-photolysis of a dilute hydrogen peroxide aqueous solution was employed to generate reproducible amounts of OH radicals. ESR spin trapping was applied to quantify OH radicals; the decrease in the OH radical level due to the specimen's scavenging activity was converted into the OH radical scavenging capacity (rate). The validity of the method was confirmed in pure antioxidants, and the agreement with the previous data was satisfactory. In the second half of this work, the new method was applied to the sera of chronic renal failure (CRF) patients. We show for the first time that after hemodialysis, OH radical scavenging capacity of the CRF serum was restored to the level of healthy control. This method is simple and rapid, and the low concentration hydrogen peroxide is the only chemical added to the system, that could eliminate the complexity of iron-involved Fenton reactions or the use of the pulse-radiolysis system.

摘要

我们开发了一种简单的基于 ESR 自旋捕获的方法,用于测定羟基(OH)自由基清除能力,使用无铁的 OH 自由基源。我们没有使用广泛使用的 Fenton 反应,而是采用短时间(通常为 5 秒)的原位紫外线光解稀过氧化氢水溶液的方法来产生可重复的 OH 自由基。我们应用 ESR 自旋捕获来定量 OH 自由基;由于标本的清除活性,OH 自由基水平的降低被转化为 OH 自由基清除能力(速率)。该方法在纯抗氧化剂中的有效性得到了验证,与先前数据的一致性令人满意。在这项工作的后半部分,我们将新方法应用于慢性肾衰竭(CRF)患者的血清中。我们首次表明,在血液透析后,CRF 血清的 OH 自由基清除能力恢复到健康对照的水平。这种方法简单快速,系统中只添加了低浓度的过氧化氢,这可以消除涉及铁的 Fenton 反应的复杂性或使用脉冲辐射分解系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/9b4c821d8cc7/jcbn08-265f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/54c846cc762d/jcbn08-265f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/1d34d68e5667/jcbn08-265f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/059d32911502/jcbn08-265f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/a377521177b9/jcbn08-265f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/9b4c821d8cc7/jcbn08-265f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/54c846cc762d/jcbn08-265f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/1d34d68e5667/jcbn08-265f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/059d32911502/jcbn08-265f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/a377521177b9/jcbn08-265f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1ab/2735632/9b4c821d8cc7/jcbn08-265f05.jpg

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