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利用乳酸菌保护人类肠道上皮细胞免受汞引起的氧化应激影响。

Protection of human intestinal epithelial cells from oxidative stress caused by mercury using lactic acid bacteria.

作者信息

Kinoshita Hideki, Jumonji Mai, Yasuda Shin, Igoshi Keiji

机构信息

Department of Bioscience, School of Agriculture, Tokai University, 9-1-1 Toroku, Higashi-ku, Kumamoto-shi, Kumamoto, Japan.

Department of Food Management, School of Food, Agricultural and Environmental Sciences, Miyagi University, 2-2-1 Hatatate, Taihaku-ku, Sendai-shi, Miyagi, Japan.

出版信息

Biosci Microbiota Food Health. 2020;39(3):183-187. doi: 10.12938/bmfh.2019-049. Epub 2020 May 2.

DOI:10.12938/bmfh.2019-049
PMID:32775138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7392913/
Abstract

Heavy metals are harmful to human health. Therefore, we investigated the biosorption of heavy metals by lactic acid bacteria (LAB). Of all the tested heavy metals, biosorption by LAB was highest for mercury, followed by lead, cadmium, and finally arsenic. The viability of HCT-116 cells was reduced by half in the presence of 7.5 µg/mL mercury but recovered after the addition of selected LAB strains. HCT-116 cells showed increased superoxide dismutase and catalase activities, whereas glutathione peroxidase activities decreased significantly. Addition of TOKAI 57m recovered all antioxidant enzyme activities. Our results suggest that this strain can be used for cellular detoxification.

摘要

重金属对人体健康有害。因此,我们研究了乳酸菌(LAB)对重金属的生物吸附作用。在所有测试的重金属中,LAB对汞的生物吸附作用最高,其次是铅、镉,最后是砷。在存在7.5 µg/mL汞的情况下,HCT-116细胞的活力降低了一半,但在添加选定的LAB菌株后恢复。HCT-116细胞的超氧化物歧化酶和过氧化氢酶活性增加,而谷胱甘肽过氧化物酶活性显著降低。添加TOKAI 57m可恢复所有抗氧化酶活性。我们的结果表明,该菌株可用于细胞解毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/0eb2e1adb5d4/bmfh-39-183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/a32a6effc0b8/bmfh-39-183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/f4580a62b995/bmfh-39-183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/0eb2e1adb5d4/bmfh-39-183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/a32a6effc0b8/bmfh-39-183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/f4580a62b995/bmfh-39-183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd8/7392913/0eb2e1adb5d4/bmfh-39-183-g003.jpg

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本文引用的文献

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3
23017 Relieves Mercury Toxicity in the Colon by Modulation of Oxidative Stress and Inflammation Through the Interplay of MAPK and NF-κB Signaling Cascades.
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Front Microbiol. 2018 Oct 12;9:2425. doi: 10.3389/fmicb.2018.02425. eCollection 2018.
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