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抗氧化氮氧化物可保护肝细胞免受氧化应激诱导的细胞死亡。

Antioxidant nitroxides protect hepatic cells from oxidative stress-induced cell death.

作者信息

Shinto Saki, Matsuoka Yuta, Yamato Mayumi, Yamada Ken-Ichi

机构信息

Physical Chemistry for Life Science Laboratory, Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

J Clin Biochem Nutr. 2018 Mar;62(2):132-138. doi: 10.3164/jcbn.17-60. Epub 2018 Feb 7.

DOI:10.3164/jcbn.17-60
PMID:29610552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5874234/
Abstract

Oxidative stress causes cell death and induces many kinds of disease, including liver disease. Nitroxides are known to react catalytically with free radicals. In this study, the cell protective activities of nitroxides were compared with those of other antioxidants. Nitroxides showed much greater inhibition of hydrogen peroxide-induced cell death than other antioxidants in a hepatic cell line and in primary hepatocytes. The intracellular oxidative stress level at 24 h after hydrogen peroxide stimulation was significantly decreased by nitroxides, but not by other antioxidants. To clarify the mechanism of cell protection by nitroxides, we investigated whether nitroxides inhibited DNA damage and mitogen-activated protein kinase pathway activation. We found that nitroxides reduced caspase-3 activation and may have ultimately inhibited cell death. In conclusion, nitroxides are very useful for attenuating cell damage due to oxidative stress. Nitroxides are thus a potential therapeutic agent for oxidative stress-related diseases.

摘要

氧化应激会导致细胞死亡,并引发包括肝脏疾病在内的多种疾病。已知氮氧化物可与自由基发生催化反应。在本研究中,将氮氧化物的细胞保护活性与其他抗氧化剂的活性进行了比较。在肝细胞系和原代肝细胞中,氮氧化物对过氧化氢诱导的细胞死亡的抑制作用比其他抗氧化剂强得多。过氧化氢刺激后24小时,氮氧化物可显著降低细胞内氧化应激水平,而其他抗氧化剂则不能。为阐明氮氧化物的细胞保护机制,我们研究了氮氧化物是否能抑制DNA损伤和丝裂原活化蛋白激酶途径的激活。我们发现氮氧化物可降低半胱天冬酶-3的激活,最终可能抑制细胞死亡。总之,氮氧化物对于减轻氧化应激引起的细胞损伤非常有用。因此,氮氧化物是一种治疗氧化应激相关疾病的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/0b9c677ca768/jcbn17-60f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/b9207e5978ea/jcbn17-60f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/1775a6a18d08/jcbn17-60f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/8667e762ad7f/jcbn17-60f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/a81bc1cd8c8c/jcbn17-60f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/0b9c677ca768/jcbn17-60f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/b9207e5978ea/jcbn17-60f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/1775a6a18d08/jcbn17-60f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/8667e762ad7f/jcbn17-60f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/a81bc1cd8c8c/jcbn17-60f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7652/5874234/0b9c677ca768/jcbn17-60f05.jpg

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