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Journal articles on the topic '158N murine oligodendrocytes'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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1

Zhou, Jie, Marcia R. Terluk, Lisa Basso, et al. "N-acetylcysteine Provides Cytoprotection in Murine Oligodendrocytes through Heme Oxygenase-1 Activity." Biomedicines 8, no. 8 (2020): 240. http://dx.doi.org/10.3390/biomedicines8080240.

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Oligodendrocytic injury by oxidative stress can lead to demyelination, contributing to neurodegeneration. We investigated the mechanisms by which an antioxidant, N-acetylcysteine (NAC), reduces oxidative stress in murine oligodendrocytes. We used normal 158N and mutant 158JP cells with endogenously high reactive oxygen species (ROS) levels. Oxidative stress was induced in 158N cells using hydrogen peroxide (H2O2, 500 μM), and both cells were treated with NAC (50 µM to 500 µM). ROS production, total glutathione (GSH) and cell survival were measured 24 h after treatment. In normal cells, H2O2 tr
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2

Nury, Thomas, Margaux Doria, Gérard Lizard, and Anne Vejux. "Docosahexaenoic Acid Attenuates Mitochondrial Alterations and Oxidative Stress Leading to Cell Death Induced by Very Long-Chain Fatty Acids in a Mouse Oligodendrocyte Model." International Journal of Molecular Sciences 21, no. 2 (2020): 641. http://dx.doi.org/10.3390/ijms21020641.

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In the case of neurodegenerative pathologies, the therapeutic arsenal available is often directed towards the consequences of the disease. The purpose of this study is, therefore, to evaluate the ability of docosahexaenoic acid (DHA), a molecule present in certain foods and considered to have health benefits, to inhibit the cytotoxic effects of very long-chain fatty acids (C24:0, C26:0), which can contribute to the development of some neurodegenerative diseases. The effect of DHA (50 µM) on very long-chain fatty acid-induced toxicity was studied by several complementary methods: phase contrast
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3

Kharroubi, Wafa, Thomas Nury, Samia Haj Ahmed, et al. "Induction by arsenate of cell-type-specific cytotoxic effects in nerve and hepatoma cells." Human & Experimental Toxicology 36, no. 12 (2017): 1256–69. http://dx.doi.org/10.1177/0960327116687893.

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The aim of the study was to compare the effect of sodium arsenate (AsV) on two different cell types: 158N murine oligodendrocytes and HepG2 human hepatoma cells. Exposure of 158N cells to AsV (0.1–400 µM; 48 h) induced a biphasic cytoxic effect defined as hormesis. Thus, low concentrations of AsV stimulate cell proliferation, as shown by phase-contrast microscopy, cell counting with trypan blue, and crystal violet assay, whereas high concentrations induce cell death associated with a loss of cell adhesion. These side effects were confirmed by staining with propidium iodide and cell cycle analy
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4

Ragot, Kévin, John J. Mackrill, Amira Zarrouk, et al. "Absence of correlation between oxysterol accumulation in lipid raft microdomains, calcium increase, and apoptosis induction on 158N murine oligodendrocytes." Biochemical Pharmacology 86, no. 1 (2013): 67–79. http://dx.doi.org/10.1016/j.bcp.2013.02.028.

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5

Meddeb, Wiem, Leila Rezig, Amira Zarrouk, et al. "Cytoprotective Activities of Milk Thistle Seed Oil Used in Traditional Tunisian Medicine on 7-Ketocholesterol and 24S-Hydroxycholesterol-Induced Toxicity on 158N Murine Oligodendrocytes." Antioxidants 7, no. 7 (2018): 95. http://dx.doi.org/10.3390/antiox7070095.

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The Asteraceae family is economically very important, because many of these plants are grown mainly for their food value, such as lettuce (Lactuca), chicory (Cichorium), and sunflower (Heliantus aminus). One of the typical properties of this family, which includes milk thistle (Sylibum marianum), is the richness of the oil in various compounds (flavonoids, alkaloids, tocopherols, and unsaturated fatty acids). Currently, and for the coming decades, age-related diseases, including neurodegenerative diseases, are a major public health problem. Preventing their appearance or opposing their evoluti
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6

Badreddine, Asmaa, Amira Zarrouk, El Mostafa Karym, et al. "Argan Oil-Mediated Attenuation of Organelle Dysfunction, Oxidative Stress and Cell Death Induced by 7-Ketocholesterol in Murine Oligodendrocytes 158N." International Journal of Molecular Sciences 18, no. 10 (2017): 2220. http://dx.doi.org/10.3390/ijms18102220.

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7

Sghaier, Randa, Amira Zarrouk, Thomas Nury та ін. "Biotin attenuation of oxidative stress, mitochondrial dysfunction, lipid metabolism alteration and 7β-hydroxycholesterol-induced cell death in 158N murine oligodendrocytes". Free Radical Research 53, № 5 (2019): 535–61. http://dx.doi.org/10.1080/10715762.2019.1612891.

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8

Sghaier, Randa, Thomas Nury, Valerio Leoni та ін. "Dimethyl fumarate and monomethyl fumarate attenuate oxidative stress and mitochondrial alterations leading to oxiapoptophagy in 158N murine oligodendrocytes treated with 7β-hydroxycholesterol". Journal of Steroid Biochemistry and Molecular Biology 194 (листопад 2019): 105432. http://dx.doi.org/10.1016/j.jsbmb.2019.105432.

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9

Ragot, Kévin, Dominique Delmas, Anne Athias, Thomas Nury, Mauhamad Baarine та Gérard Lizard. "α-Tocopherol impairs 7-ketocholesterol-induced caspase-3-dependent apoptosis involving GSK-3 activation and Mcl-1 degradation on 158N murine oligodendrocytes". Chemistry and Physics of Lipids 164, № 6 (2011): 469–78. http://dx.doi.org/10.1016/j.chemphyslip.2011.04.014.

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10

Bezine, Maryem, Meryam Debbabi, Thomas Nury, et al. "Evidence of K + homeostasis disruption in cellular dysfunction triggered by 7-ketocholesterol, 24S-hydroxycholesterol, and tetracosanoic acid (C24:0) in 158N murine oligodendrocytes." Chemistry and Physics of Lipids 207 (October 2017): 135–50. http://dx.doi.org/10.1016/j.chemphyslip.2017.03.006.

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11

Bezine, Maryem, Sonia Maatoug, Rym Ben Khalifa, et al. "Modulation of Kv3.1b potassium channel level and intracellular potassium concentration in 158N murine oligodendrocytes and BV-2 murine microglial cells treated with 7-ketocholesterol, 24S-hydroxycholesterol or tetracosanoic acid (C24:0)." Biochimie 153 (October 2018): 56–69. http://dx.doi.org/10.1016/j.biochi.2018.02.008.

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12

Nury, Thomas, Amira Zarrouk, Anne Vejux та ін. "Induction of oxiapoptophagy, a mixed mode of cell death associated with oxidative stress, apoptosis and autophagy, on 7-ketocholesterol-treated 158N murine oligodendrocytes: Impairment by α-tocopherol". Biochemical and Biophysical Research Communications 446, № 3 (2014): 714–19. http://dx.doi.org/10.1016/j.bbrc.2013.11.081.

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13

Nury, Thomas, Amira Zarrouk, John J. Mackrill та ін. "Induction of oxiapoptophagy on 158N murine oligodendrocytes treated by 7-ketocholesterol-, 7β-hydroxycholesterol-, or 24(S)-hydroxycholesterol: Protective effects of α-tocopherol and docosahexaenoic acid (DHA; C22:6 n-3)". Steroids 99 (липень 2015): 194–203. http://dx.doi.org/10.1016/j.steroids.2015.02.003.

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14

Baarine, Mauhamad, Kevin Ragot, Emmanuelle C. Genin, et al. "Peroxisomal and mitochondrial status of two murine oligodendrocytic cell lines (158N, 158JP): potential models for the study of peroxisomal disorders associated with dysmyelination processes." Journal of Neurochemistry 111, no. 1 (2009): 119–31. http://dx.doi.org/10.1111/j.1471-4159.2009.06311.x.

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15

Zarrouk, Amira, Thomas Nury, El-Mostafa Karym, et al. "Attenuation of 7-ketocholesterol-induced overproduction of reactive oxygen species, apoptosis, and autophagy by dimethyl fumarate on 158 N murine oligodendrocytes." Journal of Steroid Biochemistry and Molecular Biology 169 (May 2017): 29–38. http://dx.doi.org/10.1016/j.jsbmb.2016.02.024.

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