Evidence map›Paper›PMID 28578672›Full record

ArticleLipids in health and disease2017

Sake lees extract improves hepatic lipid accumulation in high fat diet-fed mice.

Hisako Kubo, Masato Hoshi, Takuya Matsumoto, Motoko Irie, Shin Oura, Hiroko Tsutsumi, Yoji Hata, Yasuko Yamamoto, Kuniaki Saito

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Hisako KuboHuman Health Sciences, Graduate School of Medicine and Faculty of Medicine, Kyoto University, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Masato HoshiDepartment of Biochemical and Analytical Sciences, Fujita Health University Graduate School of Health Sciences, 1-98 Dengakugakubo, Kutsukakecho, Toyoake, Aichi, 470-1192, Japan.
Takuya MatsumotoHuman Health Sciences, Graduate School of Medicine and Faculty of Medicine, Kyoto University, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Motoko IrieResearch Institute, Gekkeikan Sake Co. Ltd., 247 Minamihamcho, Fushimi, Kyoto, 612-8385, Japan.
Shin OuraResearch Institute, Gekkeikan Sake Co. Ltd., 247 Minamihamcho, Fushimi, Kyoto, 612-8385, Japan.
Hiroko TsutsumiResearch Institute, Gekkeikan Sake Co. Ltd., 247 Minamihamcho, Fushimi, Kyoto, 612-8385, Japan.
Yoji HataResearch Institute, Gekkeikan Sake Co. Ltd., 247 Minamihamcho, Fushimi, Kyoto, 612-8385, Japan.
Yasuko YamamotoDepartment of Disease Control and Prevention, Fujita Health University Graduate School of Health Sciences, 1-98 Dengakugakubo, Kutsukakecho, Toyoake, Aichi, 470-1192, Japan.
Kuniaki SaitoHuman Health Sciences, Graduate School of Medicine and Faculty of Medicine, Kyoto University, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan. saitok@fujita-hu.ac.jp.
KAN Research Institute · JPFujita Health University Hospital · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonalcoholic fatty liver disease (NAFLD) is increasing worldwide as one of the leading causes of chronic liver disease. Sake lees (SL) are secondary products of sake manufacturing and are considered to have beneficial effects on human health. To investigate these effects, we used high fat diet (HFD)-fed mice treated with or without the SL extract.

methodMice were the HFD ad libitum for 8 weeks and were administered 500 μL of distilled water with or without the SL extract (350 mg/mL) by a feeding needle daily for the last 4 weeks. Food intake, body weight, and liver weight were measured. Triacylglycerol content and the mRNA and protein expression levels of various lipid and glucose metabolism-related genes were determined in liver tissues. The levels of triglyceride, free fatty acids, glucose, insulin, and liver cell damage markers were determined in serum. Fatty acid-induced lipid accumulation in HepG2 cells was assessed in the presence or absence of the SL extract.

resultsMice fed a HFD and treated with the SL extract demonstrated a significant reduction in hepatic lipid accumulation and mRNA and protein levels of peroxidome proliferator-activated receptor γ (PPARγ), PPARα, CD36, and phosphoenolpyruvate carboxykinase 1 in the liver, while the SL extract did not affect body weight and food intake. Moreover, insulin resistance and hepatic inflammation in HFD-fed mice improved after administration of the SL extract. In HepG2 cells, the SL extract suppressed fatty acid-induced intracellular lipid accumulation.

conclusionsThese findings suggest that treatment with the SL extract could potentially reduce the risk of NAFLD development, and that the SL extract may be clinically useful for the treatment of NAFLD.

Indexed as

Alcoholic BeveragesAnimalsDiet, High-FatFatty AcidsGlucoseHep G2 CellsHumansInsulinInsulin ResistanceLipid MetabolismLipogenesisLiverMiceNon-alcoholic Fatty Liver DiseaseObesityPPAR alphaFatty AcidsGlucoseInsulinPPAR alphaTriglyceridesInsulin resistanceLipid accumulationNAFLDSake lees extract

Identifiers

PMID28578672
PMCPMC5457550
OpenAlexW2621355815

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Registered trials

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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.