Evidence map›Paper›PMID 38794681›Full record

ArticleNutrients2024

Lycopene Promotes Osteogenesis and Reduces Adipogenesis through Regulating FoxO1/PPARγ Signaling in Ovariectomized Rats and Bone Marrow Mesenchymal Stem Cells.

Bingke Xia, Xuan Dai, Hanfen Shi, Jiyuan Yin, Tianshu Xu, Tianyuan Liu, Gaiyue Yue, Haochen Guo, Ruiqiong Liang, Yage Liu and 7 more

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

17 authors.

Bingke XiaDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Xuan DaiDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Hanfen ShiDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Jiyuan YinDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Tianshu XuDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Tianyuan LiuDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Gaiyue YueDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Haochen GuoDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Ruiqiong LiangDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Yage LiuDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Junfeng GaoThe Scientific Research Center, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China.
Xinxiang WangThe Scientific Research Center, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China.
Xiaofei ChenDepartment of Pharmacology, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou 450003, China.
Jinfa TangDepartment of Pharmacology, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou 450003, China.
Lili WangDepartment of TCM Pharmacology, Chinese Material Medica School, Beijing University of Chinese Medicine, Beijing 102488, China.
Ruyuan ZhuInstitute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, China.ORCID 0000-0003-2907-3417
Dongwei ZhangDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.ORCID 0000-0002-7793-1482

Funding

National Natural Science Foundation of China 82074235, 81874373 and 82274335
6 · The paper itself

Abstract

Recent interest in preventing the development of osteoporosis has focused on the regulation of redox homeostasis. However, the action of lycopene (LYC), a strong natural antioxidant compound, on osteoporotic bone loss remains largely unknown. Here, we show that oral administration of LYC to OVX rats for 12 weeks reduced body weight gain, improved lipid metabolism, and preserved bone quality. In addition, LYC treatment inhibited ROS overgeneration in serum and bone marrow in OVX rats, and in BMSCs upon H

Indexed as

AdipogenesisLycopeneMesenchymal Stem CellsOsteogenesisSignal TransductionAnimalsAntioxidantsFemaleForkhead Box Protein O1OsteoporosisOvariectomyOxidative StressPPAR gammaRatsRats, Sprague-DawleyReactive Oxygen SpeciesAntioxidantsForkhead Box Protein O1Foxo1 protein, ratLycopenePPAR gammaPPAR gamma, ratReactive Oxygen SpeciesadipogenesisBMSCsFoxO1/PPARγ signalinglycopeneosteogenesisOVX rats

Identifiers

PMID38794681
PMCPMC11123960

What OpenQuestion holds

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LicenceCC BY
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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.