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喂食至饱足会在幼鼠大脑中引发轻度氧化/羰基应激。

Feeding to satiation induces mild oxidative/carbonyl stress in the brain of young mice.

作者信息

Kuzniak Oksana V, Sorochynska Oksana M, Bayliak Maria M, Klonovskyi Andrii Ya, Vasylyk Yulia V, Semchyshyn Halyna M, Storey Kenneth B, Garaschuk Olga, Lushchak Volodymyr I

机构信息

Department of Biochemistry and Biotechnology, Vasyl Stefanyk Precarpathian National University, 57 Shevchenko Str., Ivano-Frankivsk, 76018, Ukraine.

Institute of Biochemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario, K1S 5B6, Canada.

出版信息

EXCLI J. 2022 Jan 5;21:77-92. doi: 10.17179/excli2021-4347. eCollection 2022.

DOI:10.17179/excli2021-4347
PMID:35145367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8822308/
Abstract

Intermittent fasting as a dietary intervention can prevent overweight and obesity in adult organisms. Nevertheless, information regarding consequences of intermittent fasting for redox status and reactive metabolite-mediated processes that are crucial for the normal functioning of organisms is limited. Since the information on effects of intermittent fasting on parameters of oxidative/carbonyl stress in the brains of young mice was absent, the present study addressed these questions using an every-other-day fasting (EODF) protocol. The levels of carbonyl proteins were ~28 %, 22 % and 18 % lower in the cerebral cortex of EODF males and females and middle parts of the brain of EODF males, respectively, as compared to their fed counterparts. Lipid peroxides and α-dicarbonyl compounds were lower only in the cortex and medulla part of EODF male brain. The EODF regimen resulted in higher total non-specific antioxidant capacity in different parts of male brain and a tendency to be higher this parameter in females. At the same time, EODF regimen had no effect on the activities of the defensive antioxidant enzymes, namely superoxide dismutase, catalase, glutathione-S-transferase, glutathione peroxidase, glyoxylase 1 and glucose-6-phosphate dehydrogenase in the cortex of both sexes, but even decreased activities of these enzymes in medulla and middle part of the brain. In general, the results suggest that in the brain of young mice feeding induces mild oxidative/carbonyl stress which may be partially alleviated by the EODF regimen. The effect of EODF regimen is more pronounced in the medulla part than in the cortex.

摘要

间歇性禁食作为一种饮食干预手段,可以预防成年生物体超重和肥胖。然而,关于间歇性禁食对氧化还原状态以及对生物体正常功能至关重要的活性代谢物介导过程的影响的信息有限。由于缺乏关于间歇性禁食对幼鼠大脑氧化/羰基应激参数影响的信息,本研究采用隔日禁食(EODF)方案来解决这些问题。与正常进食的同龄鼠相比,EODF雄性和雌性小鼠大脑皮层以及EODF雄性小鼠大脑中部的羰基化蛋白质水平分别降低了约28%、22%和18%。脂质过氧化物和α-二羰基化合物仅在EODF雄性小鼠大脑的皮层和髓质部分含量较低。EODF方案使雄性小鼠大脑不同部位的总非特异性抗氧化能力提高,雌性小鼠该参数也有升高趋势。同时,EODF方案对两性大脑皮层中防御性抗氧化酶(即超氧化物歧化酶、过氧化氢酶、谷胱甘肽-S-转移酶、谷胱甘肽过氧化物酶、乙二醛酶1和葡萄糖-6-磷酸脱氢酶)的活性没有影响,但甚至降低了这些酶在髓质和大脑中部的活性。总体而言,结果表明在幼鼠大脑中,进食会引发轻度氧化/羰基应激,而EODF方案可能会部分缓解这种应激。EODF方案在髓质部分的效果比在皮层更明显。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/7fd2a582b127/EXCLI-21-77-g-005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/16d3ce563ec1/EXCLI-21-77-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/65c66c633be0/EXCLI-21-77-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/1a4f24822a02/EXCLI-21-77-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/36fda2718a71/EXCLI-21-77-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/feb95016cf31/EXCLI-21-77-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/6ca9df3c2ac0/EXCLI-21-77-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/7fd2a582b127/EXCLI-21-77-g-005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/16d3ce563ec1/EXCLI-21-77-t-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/65c66c633be0/EXCLI-21-77-t-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/1a4f24822a02/EXCLI-21-77-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/36fda2718a71/EXCLI-21-77-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/feb95016cf31/EXCLI-21-77-g-003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/6ca9df3c2ac0/EXCLI-21-77-g-004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b9/8822308/7fd2a582b127/EXCLI-21-77-g-005.jpg

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