Evidence map›Paper›PMID 40682717›Full record

ArticleMolecular neurobiology2025

Protective Effects of Deinoxanthin on Brain Oxidative Damage and Gut Microbiota in the D-Galactose-Induced Aging Mice.

Huijuan Su, Yutao Li, Jiayi Wan, Jieyu Lin, Jiayao Wang, Rui Fan, Dingming Liu, Jing Wei, Hongbo Xin, Yuejin Hua and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Food science & nutrition · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Huijuan SuSchool of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang, 330031, China.
Yutao LiNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Jiayi WanNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Jieyu LinSchool of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang, 330031, China.
Jiayao WangNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Rui FanNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Dingming LiuNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Jing WeiNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China.
Hongbo XinSchool of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang, 330031, China.
Yuejin HuaMOE Key Laboratory of Biosystems Homeostasis & Protection, Institute of Biophysics, College of Life Sciences, Zhejiang University, Hangzhou, China.
Shengjie LiNational Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Province Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Xuefu Avenue 1299, Honggutan New District, Nanchang, 330031, Jiangxi Province, China. lishengjie1104@ncu.edu.cn.

Funding

"Chunhui project" of Cooperative Research Foundation of Ministry of Education 202200648Jiangxi Natural Science Foundation of China 20224BAB206078National Natural Science Foundation of China 82260389
6 · The paper itself

Abstract

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.

Indexed as

AgingBrainGalactoseGastrointestinal MicrobiomeNeuroprotective AgentsOxidative StressAnimalsAstrocytesMaleMiceMice, Inbred C57BLMicrogliaGalactoseNeuroprotective AgentsAging miceAntioxidantDeinoxanthinGut microbiotaOxidative stress

Identifiers

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.