Evidence map›Paper›PMID 38498120›Full record

ArticleJournal of natural medicines2024

The protective effects of Ninjin'yoeito against liver steatosis/fibrosis in a non-alcoholic steatohepatitis model mouse.

Kyohei Takano, Marisa Kaneda, Yayoi Aoki, Nina Fujita, Shigeki Chiba, Seiwa Michihara, Li-Kun Han, Ryuji Takahashi

Open access · hybridAbstract read
In one paragraph

Article in Journal of natural medicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

8 authors at 1 institution in 1 country.

Kyohei TakanoKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan. takano_kyohei@kracie.co.jp.ORCID http://orcid.org/0009-0007-4051-5251
Marisa KanedaKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Yayoi AokiKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Nina FujitaKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Shigeki ChibaKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Seiwa MichiharaKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Li-Kun HanKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Ryuji TakahashiKampo Research Laboratory, Pharmaceutical Company, Kracie, Ltd., 3-1 Kanebo-Machi, Takaoka, Toyama, Japan.
Toyama Industrial Technology Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic steatohepatitis (NASH) is a progressive fibrotic form of non-alcoholic fatty liver disease. Liver fibrosis leads to liver cancer and cirrhosis, and drug therapy for NASH remains lacking. Ninjin'yoeito (NYT) has shown antifibrotic effects in a model of liver fibrosis without steatosis but has not been studied for NASH. Therefore, we evaluated the efficacy of NYT in mice fed a choline-deficient, L-amino acid-defined, high-fat diet (CDAHFD) as a NASH model. Compared with the normal diet group, mice fed CDAHFD showed decreased body weight and increased white adipose tissue, liver weight, and triglyceride content in the liver. Furthermore, a substantial increase in the hepatic concentration of hydroxyproline, expression of α-smooth muscle actin (α-SMA), and transforming growth factor-β was observed in CDAHFD-fed mice. Masson's trichrome and Picro-Sirius red staining revealed a remarkable increase in collagen fiber compared with the normal diet group. Compared with mice that received CDAHFD alone, those supplemented with NYT exhibited reduced hepatic triglyceride and hydroxyproline levels and α-SMA expression. Additionally, compared with the group fed CDAHFD alone, the stained liver tissues of NYT-treated mice exhibited a reduction in Masson's trichrome- and Picro-Sirius red-positive areas. Locomotor activity was significantly reduced in the CDAHFD-fed group compared with the normal diet group. In the NYT-treated group, the CDAHFD-induced decrease in locomotor activity was significantly suppressed. The findings indicate that NYT inhibited fatty and fibrotic changes in the livers of NASH mice and alleviated the decrease in locomotor activity. Therefore, NYT may serve as a novel therapeutic approach for NASH.

Indexed as

Diet, High-FatDisease Models, AnimalLiverLiver CirrhosisNon-alcoholic Fatty Liver DiseaseActinsAnimalsDrugs, Chinese HerbalHydroxyprolineMaleMiceMice, Inbred C57BLTransforming Growth Factor betaTriglyceridesActinsDrugs, Chinese HerbalHydroxyprolineTransforming Growth Factor betaTriglyceridesCholine-deficient L-amino acid-defined high-fat dietFibrosisNinjin’yoeitoNon-alcoholic steatohepatitisSteatosis

Identifiers

PMID38498120
PMCPMC11101552
OpenAlexW4392911066

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.