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Minocycline diminishes the rotenone induced neurotoxicity and glial activation via suppression of apoptosis, nitrite levels and oxidative stress

机译:米诺环素通过抑制细胞凋亡,亚硝酸盐水平和氧化应激来减少旋转酮诱导的神经毒性和胶质激活

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The study was conducted to evaluate the effect of minocycline against pesticide rotenone induced adverse effects in different rat brain regions. Assessment of oxidative stress, nitrite levels, degenerating neurons and level of cleaved caspase-3 was done in frontal cortex, mid brain, hippocampus and striatum regions of rat brain. In addition the expression profile of neuronal (MAP2), astrocytes (GFAP) and microglia (cd11b) markers was done after treatments. Rotenone induced DNA fragmentation was also assessed in all studied rat brain regions by utilizing comet assay. Rotenone administration caused significantly decreased level of glutathione along with increased level of nitrite and lipid peroxidation. Significant oxidative and nitrosative stress was also observed after rotenone administration which was considerably inhibited in minocycline treated rats in time dependent manner. Fluorojade staining and levels of cleaved caspase 3 showed the degeneration of neurons and apoptosis respectively in studied rat brain regions which were further inhibited with minocycline treatment. Rotenone administration caused significantly increased reactivity of astrocytes, microglia and altered neuronal morphology in rat brain regions which was also partially restored with minocycline treatment. In conclusion, present study showed that minocycline treatment attenuated the rotenone induced oxidative stress, nitrite level, degeneration of neurons, augmented glial reactivity and apoptosis. (C) 2018 Elsevier B.V. All rights reserved.
机译:进行该研究以评价米诺环素对农药旋转酮诱导不同大鼠脑区的不良影响的影响。氧化应激,亚硝酸盐水平,退化神经元和切割的Caspase-3水平的评估是在大鼠脑,中脑,海马和纹状体区域的颅脑中进行的。此外,在处理后,在处理后进行神经元(MAP2),星形胶质细胞(GFAP)和微胶质细胞(CD11b)标记的表达谱。还通过利用COMET测定,在所有研究的大鼠脑区域中也评估了RotenOne诱导的DNA碎片。旋转酮给药导致谷胱甘肽水平显着降低以及亚硝酸盐和脂质过氧化水平增加。在旋转酮给药后,还观察到显着的氧化和亚硝酸盐应激,其在米诺辛锌处理的大鼠中随时依赖性方式显着抑制。氟杂交染色和切割的caspase 3的水平分别显示了在研究大鼠脑区中的神经元和细胞凋亡的退化,这进一步抑制了米诺环素治疗。转炉给药在大鼠脑区中的星形细胞,微胶质细胞和改变的神经元形态产生显着提高,该大鼠脑区也有部分恢复了米诺环素治疗。总之,目前的研究表明,米诺环素治疗减弱了转炉诱导的氧化应激,亚硝酸盐水平,神经元变性,增强胶质反应性和细胞凋亡。 (c)2018 Elsevier B.v.保留所有权利。

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