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氟西汀对慢性持续光照诱导的 Wistar 大鼠昼夜节律分子标志物、认知障碍、氧化损伤和阿尔茨海默病样病理生物标志物的神经保护作用。

Neuroprotective Effects of Fluoxetine on Molecular Markers of Circadian Rhythm, Cognitive Deficits, Oxidative Damage, and Biomarkers of Alzheimer's Disease-Like Pathology Induced under Chronic Constant Light Regime in Wistar Rats.

机构信息

Neuropharmacology Laboratory, School of Pharmaceutical Sciences, Shoolini University, Post Box No. 9, Solan, Himachal Pradesh 173212, India.

School of Biotechnology and Applied Sciences, Shoolini University, Post Box No. 9, Solan, Himachal Pradesh 173212, India.

出版信息

ACS Chem Neurosci. 2021 Jun 16;12(12):2233-2246. doi: 10.1021/acschemneuro.1c00238. Epub 2021 May 24.

Abstract

There is mounting evidence of circadian rhythm disruption in Alzheimer's disease (AD); however, the cause-and-effect relationship between them is not understood. Chronic constant light exposure effectively disrupts circadian rhythm in rats. On the basis of previous publications, we hypothesized that chronic constant light exposure might contribute significantly to development of AD-like-phenotype in rats and that fluoxetine (Flx) treatment might protect the brain against it. Adult male rats were exposed to normal light-dark cycles, constant light (LL), constant dark, and LL+Flx (5 mg/kg/day, ZT5) for four months. The expression of molecular markers of circadian rhythm: transcripts; and protein expression of peroxiredoxin-1 (PRX1) and hyperoxidized peroxiredoxins (PRX-SO) were significantly dysregulated in the suprachiasmatic nuclei (SCN) of LL rats, which was prevented with concomitant fluoxetine administration. The levels of glutamate and γ-aminobutyric acid were dysregulated, and oxidative damage was observed in the SCN and hippocampi of LL rats. Fluoxetine treatment conferred protection against oxidative damage in LL rats. Constant light exposure also impaired rats' performance on Y-maze, Morris maze, and novel object recognition test, which was prevented with fluoxetine administration. A significant elevation in soluble Aβ levels, which strongly correlated with upregulation of and transcripts was observed in the hippocampus of LL rats. Further, the expression of antiaging gene was downregulated, and neuronal damage indicator was upregulated in hippocampus. Fluoxetine rescued Aβ upregulation and AD-related genes' dysregulation. Our findings show that circadian disruption by exposure to chronic constant light may contribute to progression of AD, which can be prevented with fluoxetine treatment.

摘要

越来越多的证据表明,阿尔茨海默病(AD)存在昼夜节律紊乱;然而,它们之间的因果关系尚不清楚。慢性持续光照能有效地扰乱大鼠的昼夜节律。基于之前的研究结果,我们假设慢性持续光照可能会显著促进大鼠出现类似 AD 的表型,而氟西汀(Flx)治疗可能会保护大脑免受其影响。成年雄性大鼠接受正常的明暗循环、持续光照(LL)、持续黑暗和 LL+Flx(5mg/kg/天,ZT5)处理四个月。分子节律标志物的表达:mRNA;以及过氧化物还原酶-1(PRX1)和过氧亚硝酸盐化过氧化物还原酶(PRX-SO)的蛋白表达在 LL 大鼠的视交叉上核(SCN)中明显失调,同时给予氟西汀可预防这种失调。谷氨酸和γ-氨基丁酸的水平失调,并且在 SCN 和海马体中观察到氧化损伤。氟西汀治疗可防止 LL 大鼠的氧化损伤。持续光照还损害了大鼠在 Y 迷宫、莫里斯迷宫和新物体识别测试中的表现,而氟西汀的给予则可以预防这种损害。在 LL 大鼠的海马体中观察到可溶性 Aβ水平显著升高,这与 和 转录本的上调密切相关。此外,在海马体中,抗衰老基因 的表达下调,神经元损伤标志物 的表达上调。氟西汀挽救了 Aβ的上调和与 AD 相关基因的失调。我们的研究结果表明,慢性持续光照引起的昼夜节律紊乱可能会促进 AD 的进展,而氟西汀治疗可以预防这种情况。

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