去氧黄质对d -半乳糖诱导衰老小鼠脑氧化损伤和肠道微生物群的保护作用。

IF 4.3 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-11-01 Epub Date: 2025-07-19 DOI:10.1007/s12035-025-05215-7
Huijuan Su, Yutao Li, Jiayi Wan, Jieyu Lin, Jiayao Wang, Rui Fan, Dingming Liu, Jing Wei, Hongbo Xin, Yuejin Hua, Shengjie Li
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引用次数: 0

摘要

去氧黄质(DX)是由耐辐射球菌合成的一种特殊的羟基化四萜类化合物,在体外和体内均表现出强大的抗氧化活性。体内过多的活性氧(ROS)和自由基的积累会引起大脑氧化损伤,从而促进衰老过程。给药DX是否能保护大脑免受衰老过程中的氧化损伤是人们非常感兴趣的。在这项研究中,我们探讨了DX对体内d -半乳糖(D-gal)诱导的衰老小鼠的潜在有益作用,特别是它对大脑抗氧化损伤的保护作用,以及它对衰老小鼠肠道微生物群的影响。我们发现,低剂量(25 mg/kg/day)和中剂量(50 mg/kg/day)的DX治疗可以有效缓解d -gal诱导的衰老小鼠的运动缺陷,减少海马的病理改变,抑制小胶质细胞和星形胶质细胞的激活,并减轻氧化应激。然而,高剂量的DX (100mg /kg/天)治疗似乎加剧了这些变化,表明过量的DX可能会加剧衰老小鼠的氧化损伤。此外,适当剂量的DX可以恢复衰老小鼠的肠道菌群,而高剂量的DX进一步加重了衰老小鼠肠道菌群的紊乱。总之,我们得出结论,适当服用DX可能有利于防止大脑氧化损伤和改善衰老小鼠的肠道微生物群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective Effects of Deinoxanthin on Brain Oxidative Damage and Gut Microbiota in the D-Galactose-Induced Aging Mice.

Deinoxanthin (DX), a special hydroxylated tetraterpenoid synthesized by Deinococcus radiodurans, exhibits robust antioxidative activities in vitro and in vivo. The accumulation of excessive reactive oxygen species (ROS) and free radicals in the body would induce brain oxidative damage, thereby contributing to the process of aging. Whether the administration of DX could protect the brain against oxidative damage in aging is of great interest. In this study, we explored the potential beneficial effects of DX on D-galactose (D-gal)-induced aging mice in vivo, particularly its protective effects on the brain against oxidative damage, and its impact on the gut microbiota of aging mice. We demonstrated that treatment with a low dose (25 mg/kg/day) and a middle dose (50 mg/kg/day) of DX could effectively alleviate motor deficits, reduce the hippocampal pathological changes, suppress microglia and astrocyte activation, and attenuate oxidative stress in D-gal-induced aging mice. However, the treatment with a high dose of DX (100 mg/kg/day) seemed to exacerbate these changes, indicating that excessive DX may exacerbate oxidative damage in aging mice. Furthermore, the administration of appropriate DX could restore the gut microbiota in aging mice, while the high dose of DX further aggravated the disturbance of the gut microbiota in aging mice. Collectively, we conclude that taking DX appropriately may be beneficial in preventing oxidative damage to the brain and improving the gut microbiota in aging mice.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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