Evidence map›Paper›PMID 40410568›Full record

ArticleScientific reports2025

Development of a silkworms-based evaluation system for the extracts and compounds for their obesity and lipid metabolism improving activity.

Yuki Murata, Hari Prasad Devkota, Mikiyo Wada

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Yuki MurataGraduate School of Pharmaceutical Sciences, Kumamoto University, 5 - 1 Oe-honmachi, Chuo- ku, Kumamoto, 862 0973, Japan.
Hari Prasad DevkotaGraduate School of Pharmaceutical Sciences, Kumamoto University, 5 - 1 Oe-honmachi, Chuo- ku, Kumamoto, 862 0973, Japan.
Mikiyo WadaGraduate School of Pharmaceutical Sciences, Kumamoto University, 5 - 1 Oe-honmachi, Chuo- ku, Kumamoto, 862 0973, Japan. wadayo@kumamoto-u.ac.jp.ORCID http://orcid.org/0000-0001-8126-6692

Funding

Japan Society for the Promotion of Science JP23804033
6 · The paper itself

Abstract

As lifestyle-related diseases like obesity, dyslipidemia, and non-alcoholic fatty liver disease are increasing globally, the demand for developing therapeutic agents and health foods remains high. However, there is a growing concern worldwide regarding the use of animals for biological testing. Herein, we developed a method using the silkworm, Bombyx mori, to evaluate the effects of compounds on improving obesity and lipid metabolism. A silkworm obesity and lipid metabolism disorder (SOLD) model, fed a 10% glucose diet for 72 h showed increased fat body weight and accumulation of neutral fat in the hemolymph and fat body. Administration of fenofibrate reduced neutral fat levels in the hemolymph, and epigallocatechin gallate reduced neutral fat levels in the hemolymph and fat body. Silkworms with improved lipid metabolism, exhibited activation of lipoprotein lipase in muscle tissue, and decreased activities of acetyl-CoA carboxylase, and activation of AMPK in the fat body. Furthermore, enhanced fatty acid beta-oxidation contributed to the promotion of lipolysis. These effects and mechanisms of action observed in silkworms are similar to those found in mammals. These results demonstrate the usefulness of the evaluation system in screening materials for their anti-obesity and lipid metabolism improvement effects using the SOLD model.

Indexed as

Anti-Obesity AgentsBombyxLipid MetabolismObesityAcetyl-CoA CarboxylaseAMP-Activated Protein KinasesAnimalsCatechinDisease Models, AnimalFat BodyHemolymphLipolysisAcetyl-CoA CarboxylaseAMP-Activated Protein KinasesAnti-Obesity AgentsCatechinepigallocatechin gallateAnimal modelsHyperlipidemiaLipid metabolismObesitySilkworm

Identifiers

PMID40410568
PMCPMC12102173

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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.