Evidence map›Paper›PMID 40967782›Full record

ArticleThe Journal of veterinary medical science2025

Potential inhibitory effect of Shigyakusan on gallstone formation in a mice model of cholesterol gallstone Disease.

Go Utsunomiya, Yuta Shinohara, Haruki Kurihara, Yishan Liu, Yusuke Ishihara, Minami Kobayashi, Mohamed Elbadawy, Amira Abugomaa, Tatsuya Usui, Kazuaki Sasaki

Abstract read
In one paragraph

Article in The Journal of veterinary medical science, 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

10 authors.

Go UtsunomiyaLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Yuta ShinoharaLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Haruki KuriharaLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Yishan LiuLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Yusuke IshiharaCAPITAL, Kanagawa, Japan.
Minami KobayashiLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Mohamed ElbadawyLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Amira AbugomaaLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Tatsuya UsuiLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Kazuaki SasakiLaboratory of Veterinary Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol gallstones (CGs) are formed in the biliary system due to cholesterol supersaturation in the bile and delayed bile excretion. The current treatments for CGs involve potentially severe complications, and novel therapeutic approaches are still required. Shigyakusan is a traditional Chinese medicine used for treating CG disease (CGD), but there are no reports on the action or efficacy of Shigyakusan in CGD. The present study was conducted to clarify the inhibitive effects of Shigyakusan on CGD. Mice were fed a normal or lithogenic diet for 8 weeks (to create a mouse model of CGD) and simultaneously treated with vehicle or Shigyakusan. Organs were removed after blood sampling to examine CG formation and perform pathological evaluations. Genetic analysis of the liver, gallbladder, and ileum tissues was also conducted. CGD was induced by feeding mice with a lithogenic diet. Specifically, gallstones were detected, and serum T-CHO and LDL-C were significantly elevated. Administration of Shigyakusan to CGD mice reduced the development of CGs and lowered the serum T-CHO and LDL-C levels. Additionally, Shigyakusan administration increased ABCG5/G8 and ABCB4 mRNA expression in the liver, AQP5 expression in the gallbladder, and ABCG5 expression in the ileum of CGD mice. Shigyakusan administration diminished the synthesis of CGs in mice by lowering serum cholesterol and improving bile flow. The results show that Shigyakusan may be a beneficial option for CGD treatment and prevention.

Indexed as

Drugs, Chinese HerbalGallstonesAnimalsDisease Models, AnimalGallbladderIleumLiverMaleMedicine, Chinese TraditionalMiceMice, Inbred C57BLDrugs, Chinese Herbalshigyaku-sancholesterol gallstonegallstone diseaseherbal therapyShigyakusantraditional Chinese medicine

Identifiers

PMID40967782
PMCPMC12614825

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LicenceCC BY-NC-ND
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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.