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在高皮质醇背景下,硒通过Nrf2途径抑制脂多糖诱导的牛子宫内膜基质细胞氧化应激。

Selenium suppressed the LPS-induced oxidative stress of bovine endometrial stromal cells through Nrf2 pathway with high cortisol background.

作者信息

Cui Luying, Zheng Fangling, Zhang Min, Wang Zhihao, Meng Xia, Dong Junsheng, Liu Kangjun, Guo Long, Wang Heng, Li Jianji

机构信息

College of Veterinary Medicine, Yangzhou University, Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou, Jiangsu, PR China.

Joint International Research Laboratory of Agriculture and Agriproduct Safety of the Ministry of Education, Yangzhou, Jiangsu, PR China.

出版信息

J Anim Sci. 2024 Jan 3;102. doi: 10.1093/jas/skae260.

DOI:10.1093/jas/skae260
PMID:39219376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11445656/
Abstract

Stress and infection seriously threaten the reproductive performance and health of dairy cows. Various perinatal stresses increase plasma cortisol concentrations in cows, and chronically high cortisol levels may increase the incidence and severity of the uterine diseases. Selenium (Se) enhances antioxidant capacity of cows. The aim of this study was to explore how Se affects the oxidative stress of primary bovine endometrial stromal cells (BESC) with high cortisol background. The levels of reactive oxygen species (ROS) and other biomarkers of oxidative stress were measured using flow cytometry and assay kits. The changes in nuclear NF-E2-related factor 2 (Nrf2) pathway were detected by Western blot, qPCR, and immunofluorescence. The result showed that lipopolysaccharide (LPS) increased (P < 0.01) ROS and malondialdehyde (MDA) content and reduced (P < 0.01) superoxide dismutase (SOD) concentration, provoking BESC oxidative stress. The elevated levels of cortisol resulted in the accumulation (P < 0.05) of ROS and MDA and inhibition (P < 0.05) of SOD in unstimulated BESC but demonstrated an antioxidative effect in LPS-stimulated cells. Pretreatment with Se reduced (P < 0.01) the levels of ROS and MDA, while increasing (P < 0.05) the antioxidant capacities and the relative abundance of gene transcripts and proteins related to the Nrf2 pathway in BESC. This antioxidant effect was more pronounced in the presence of high cortisol level. In conclusion, cortisol alone induced the oxidative damage but provided an antioxidant protection in the presence of LPS. Se alleviated the LPS-induced cellular oxidative stress, which is probably achieved through activating Nrf2 pathway. At high cortisol levels, Se supplement has a more significant protective effect on BESC oxidative stress. This study provided evidence for the protective role of Se in bovine endometrial oxidative damage of stressed animals and suggested the potential regulatory mechanism in vitro.

摘要

应激和感染严重威胁奶牛的繁殖性能和健康。各种围产期应激会增加奶牛血浆皮质醇浓度,而长期高水平的皮质醇可能会增加子宫疾病的发病率和严重程度。硒(Se)可增强奶牛的抗氧化能力。本研究的目的是探讨硒如何影响高皮质醇背景下原代牛子宫内膜基质细胞(BESC)的氧化应激。使用流式细胞术和检测试剂盒测量活性氧(ROS)水平和其他氧化应激生物标志物。通过蛋白质免疫印迹、qPCR和免疫荧光检测核因子E2相关因子2(Nrf2)通路的变化。结果表明,脂多糖(LPS)增加了(P < 0.01)ROS和丙二醛(MDA)含量,降低了(P < 0.01)超氧化物歧化酶(SOD)浓度,引发了BESC氧化应激。皮质醇水平升高导致未受刺激的BESC中ROS和MDA积累(P < 0.05),SOD受到抑制(P < 0.05),但在LPS刺激的细胞中表现出抗氧化作用。硒预处理降低了(P < 0.01)ROS和MDA水平,同时增加了(P < 0.05)BESC的抗氧化能力以及与Nrf2通路相关的基因转录本和蛋白质的相对丰度。在高皮质醇水平下,这种抗氧化作用更为明显。总之,单独的皮质醇会诱导氧化损伤,但在LPS存在时提供抗氧化保护。硒减轻了LPS诱导的细胞氧化应激,这可能是通过激活Nrf2通路实现的。在高皮质醇水平下,补充硒对BESC氧化应激具有更显著的保护作用。本研究为硒在应激动物牛子宫内膜氧化损伤中的保护作用提供了证据,并提出了体外潜在的调节机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/e9045982ab9d/skae260_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/61b6056e3e58/skae260_iffig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/291c347e7bb4/skae260_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/4c5627cc8817/skae260_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/6088fc1e903f/skae260_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/bc12dd7ccabc/skae260_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/137351c684fd/skae260_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/732910863226/skae260_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/bccbf7f14d9a/skae260_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/e9045982ab9d/skae260_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/61b6056e3e58/skae260_iffig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/291c347e7bb4/skae260_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/4c5627cc8817/skae260_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/6088fc1e903f/skae260_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/bc12dd7ccabc/skae260_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/137351c684fd/skae260_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/732910863226/skae260_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/bccbf7f14d9a/skae260_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691c/11445656/e9045982ab9d/skae260_fig8.jpg

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