Evidence map›Paper›PMID 30030965›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

Lutein Suppresses Oxidative Stress and Inflammation by Nrf2 Activation in an Osteoporosis Rat Model.

Hongtao Li, Caihong Huang, Jun Zhu, Kehai Gao, Jun Fang, Huazhuang Li

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
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

39 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  3. Lute-GenAntioxidants (Basel, Switzerland) · 2026
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  7. Nrf2 signaling pathway: focus on oxidative stress in osteoporosis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
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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

6 authors at 1 institution in 1 country.

Hongtao LiDepartment of Spine Surgery, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Caihong HuangDepartment of Health Management, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Jun ZhuDepartment of Spine Surgery, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Kehai GaoDepartment of Spine Surgery, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Jun FangDepartment of Spine Surgery, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Huazhuang LiDepartment of Spine Surgery, Yidu Central Hospital of Weifang, Qingzhou, Shandong, China (mainland).
Yidu Central Hospital of Weifang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Osteoporosis is a major health risk for women worldwide. Osteoporosis is caused by an imbalance between bone resorption and formation. Hormonal imbalance and increased redox signaling cause bone deterioration. MATERIAL AND METHODS Oxidative stress was determined through assessment of ROS, lipid peroxide levels, and antioxidant activity. Inflammatory protein markers and Nrf2-related protein expressions were determined through Western blot analysis. Interleukin expressions were determined using ELSA. RESULTS In the present study, we showed that supplementation of lutein protects the ovariectomized (OVX) rats against oxidative stress through its antioxidant protection. OVX rats showed an increase in oxidative stress markers. Lutein treatment significantly decreased the lipid peroxidation levels and ROS in the OVX rats. OVX rats showed inflammatory responses through NF-κB activation and increased inflammatory cytokines (TNF-α, IL-6, IL-8). Further, there was significant upregulation in osteoclast-specific marker NFATc1 in OVX rats compared to sham rats. Lutein supplementation activated Nrf2 driven antioxidant gene expression (HO-1, NQO1) and protected OVX rats against inflammatory responses. CONCLUSIONS We showed the critical role of Lutein in protection against osteoporosis in OVX rats by downregulation of inflammation and osteoclast-specific marker (NFATc1) expression through Nrf2 activation.

Indexed as

AnimalsAntioxidantsDisease Models, AnimalFemaleInflammationLipid PeroxidationLuteinNF-E2-Related Factor 2OsteoclastsOsteoporosisOvariectomyOxidative StressRANK LigandRatsRats, Sprague-DawleyReactive Oxygen SpeciesAntioxidantsLuteinNFATC1 protein, ratNfe2l2 protein, ratNF-E2-Related Factor 2RANK LigandReactive Oxygen SpeciesTranscription Factors

Identifiers

PMID30030965
PMCPMC6067024
OpenAlexW2883099241

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.