Evidence map›Paper›PMID 37240141›Full record

ArticleInternational journal of molecular sciences2023

Isoquercitrin Attenuates Steatohepatitis by Inhibition of the Activated NLRP3 Inflammasome through HSP90.

Ji Ma, Maoru Li, Tingting Yang, Yang Deng, Yadong Ding, Tiantian Guo, Jing Shang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Bioactive Components ofAntioxidants (Basel, Switzerland) · 2026
    Review
  6. Frontiers in pharmacology · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Targeting hepatic macrophages for non-alcoholic fatty liver disease therapy.Frontiers in cell and developmental biology · 2024
    Review
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

7 authors at 1 institution in 1 country.

Ji MaSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.ORCID 0000-0003-4608-3908
Maoru LiSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Tingting YangSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Yang DengSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Yadong DingSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Tiantian GuoSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Jing ShangSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
China Pharmaceutical University · CN

Funding

National Science Technology Major Project of China 2018ZX09301030-005
6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a chronic liver disease with a global prevalence of 25%. However, the medicines approved by the FDA or EMA are still not commercially available for the treatment of NAFLD. The NOD-like receptor thermal protein domain-associated protein 3 (NLRP3) inflammasome plays a crucial role in inflammatory responses, and the mechanisms related to steatohepatitis have been sufficiently clarified. NLRP3 has been widely evaluated as a potential target for multiple active agents in treating NAFLD. As a quercetin glycoside, isoquercitrin (IQ) has a broad inhibitory effect on oxidative stress, cancers, cardiovascular diseases, diabetes, and allergic reactions in vitro and in vivo. This study aimed to investigate the undercover mechanism of IQ in the treatment of NAFLD, particularly in anti-steatohepatitis, by suppressing the NLRP3 inflammasome. In this study, a methionine-choline-deficient induced steatohepatitis mice model was used to explore the effect of IQ on NAFLD treatment. Further mechanism exploration based on transcriptomics and molecular biology revealed that IQ inhibited the activated NLRP3 inflammasome by down-regulating the expression of heat shock protein 90 (HSP90) and suppressor of G-two allele of Skp1 (SGT1). In conclusion, IQ could alleviate NAFLD by inhibiting the activated NLRP3 inflammasome by suppressing the expression of HSP90.

Indexed as

InflammasomesNon-alcoholic Fatty Liver DiseaseAnimalsLiverMiceMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinQuercetinInflammasomesisoquercitrinNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseQuercetinheat shock protein 90isoquercitrinmetabolic-associated fatty liver diseaseNLRP3 inflammasome

Identifiers

PMID37240141
PMCPMC10218527
OpenAlexW4376645512

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.