Evidence map›Paper›PMID 30577593›Full record

ArticleInternational journal of molecular sciences2018

Oxyresveratrol Increases Energy Expenditure through Foxo3a-Mediated Ucp1 Induction in High-Fat-Diet-Induced Obese Mice.

Jin Hee Choi, No-Joon Song, A Reum Lee, Dong Ho Lee, Min-Ju Seo, Suji Kim, Seo-Hyuk Chang, Dong Kwon Yang, Yu-Jin Hwang, Kyung-A Hwang and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

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  11. Protein clearance strategies for disease intervention.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Review
  12. Mechanism of interaction between autophagy and apoptosis in cancer.Apoptosis : an international journal on programmed cell death · 2021
    Review
  13. Review
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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

13 authors at 4 institutions in 1 country.

Jin Hee ChoiDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. theresa159@naver.com.
No-Joon SongDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. songnj413@naver.com.
A Reum LeeDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. areumy@icloud.com.
Dong Ho LeeDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. zestcoren@gmail.com.
Min-Ju SeoDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. smj713@naver.com.
Suji KimDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. suji_11@nate.com.
Seo-Hyuk ChangDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. adc153@naver.com.
Dong Kwon YangDepartment of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Chonbuk National University, Iksan, Jeollabuk-do 54596, Korea. dkyang0502@gmail.com.
Yu-Jin HwangDepartment of Agrofood Resources, National Institute of Agricultural Sciences, RDA, Wanju-Gun, Jeollabuk-do 55365, Korea. yjhwang1022@korea.kr.
Kyung-A HwangDepartment of Agrofood Resources, National Institute of Agricultural Sciences, RDA, Wanju-Gun, Jeollabuk-do 55365, Korea. kah366@korea.kr.
Tal Soo HaDepartment of Life Science, Deagu University, Gyeongsan, Gyeongsangbuk-do 38453, Korea. tal.ha@daegu.ac.kr.
Ui Jeong YunDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. yunc@skku.edu.
Kye Won ParkDepartment of Food Science and Biotechnology, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea. kwpark@skku.edu.ORCID 0000-0003-2771-249X
Sungkyunkwan University · KRNational Institute of Agricultural Science and Technology · KRDaegu University · KRJeonbuk National University · KR

Funding

National Research Foundation of Korea NRF-2017R1A2B4002005National Research Foundation of Korea NRF-2017R1A6A3A11029584
6 · The paper itself

Abstract

The phytochemical oxyresveratrol has been shown to exert diverse biological activities including prevention of obesity. However, the exact reason underlying the anti-obese effects of oxyresveratrol is not fully understood. Here, we investigated the effects and mechanism of oxyresveratrol in adipocytes and high-fat diet (HFD)-fed obese mice. Oxyresveratrol suppressed lipid accumulation and expression of adipocyte markers during the adipocyte differentiation of 3T3-L1 and C3H10T1/2 cells. Administration of oxyresveratrol in HFD-fed obese mice prevented body-weight gains, lowered adipose tissue weights, improved lipid profiles, and increased glucose tolerance. The anti-obese effects were linked to increases in energy expenditure and higher rectal temperatures without affecting food intake, fecal lipid content, and physical activity. The increased energy expenditure by oxyresveratrol was concordant with the induction of thermogenic genes including Ucp1, and the reduction of white adipocyte selective genes in adipose tissue. Furthermore, Foxo3a was identified as an oxyresveratrol-induced gene and it mimicked the effects of oxyresveratrol for induction of thermogenic genes and suppression of white adipocyte selective genes, suggesting the role of Foxo3a in oxyresveratrol-mediated anti-obese effects. Taken together, these data show that oxyresveratrol increases energy expenditure through the induction of thermogenic genes in adipose tissue and further implicates oxyresveratrol as an ingredient and Foxo3a as a molecular target for the development of functional foods in obesity and metabolic diseases.

Indexed as

3T3-L1 CellsAdipocytesAdipose TissueAnimalsCell DifferentiationCell LineCell SurvivalDiet, High-FatEnergy MetabolismForkhead Box Protein O3Gene Expression RegulationLipid MetabolismMaleMetabolomicsMiceObesityForkhead Box Protein O3FoxO3 protein, mousePlant Extractspuag-haadStilbenesUcp1 protein, mouseUncoupling Protein 1brown adipocyteenergy expenditureobesityoxyresveratrolUcp1

Identifiers

PMID30577593
PMCPMC6337118
OpenAlexW2903829256

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.