Evidence map›Paper›PMID 36691481›Full record

ArticlePeerJ2023

Acteoside alleviates UUO-induced inflammation and fibrosis by regulating the HMGN1/TLR4/TREM1 signaling pathway.

Yan Mao, Jiali Yu, Jingjing Da, Fuxun Yu, Yan Zha

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.4field-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

14 citing papers in PubMed, 33 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

5 authors at 2 institutions in 1 country.

Yan MaoSchool of Medicine, Guizhou University, Guiyang, Guizhou, China.
Jiali YuSchool of Medicine, Guizhou University, Guiyang, Guizhou, China.
Jingjing DaSchool of Medicine, Guizhou University, Guiyang, Guizhou, China.
Fuxun YuSchool of Medicine, Guizhou University, Guiyang, Guizhou, China.
Yan ZhaSchool of Medicine, Guizhou University, Guiyang, Guizhou, China.
Guizhou University · CNGuizhou Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Acteoside (Act), a phenylethanoid compound that was first isolated from mullein, has been widely used for the investigation of anti-inflammatory and anti-fibrotic effect. However, the mechanism of Act against unilateral ureteral obstruction (UUO)-mediated renal injury is largely unknown. Therefore, this study aimed to explore the effects of Act on UUO rats and possible mechanisms. Methods: A total of 20 Sprague-Dawley (SD) rats were divided randomly into three groups ( Results: The results of renal function indexes and histopathological staining showed that Act could improve renal function by reducing serum creatinine, blood urea nitrogen and urine protein at the same time, Act could alleviate renal inflammation and fibrosis. In addition, the results of immunohistochemistry showed that Act could reduce the expression of inflammation and kidney injury-related proteins F4/80, Mcp-1, KIM-1 proteins, as well as the expression of fibrosis-related protein Conclusion: These data demonstrate that Act can ameliorate UUO-induced renal inflammation and fibrosis in rats probably through triggering HMGN1/TLR4/TREM-1 pathway.

Indexed as

HMGN1 ProteinKidney DiseasesUreteral ObstructionAnimalsFibrosisGlucosidesInflammationPolyphenolsRatsRats, Sprague-DawleySignal TransductionToll-Like Receptor 4Transcription FactorsTriggering Receptor Expressed on Myeloid Cells-1acteosideGlucosidesHMGN1 ProteinHMGN1 protein, ratPolyphenolsTlr4 protein, ratToll-Like Receptor 4Transcription FactorsTREM1 protein, ratTriggering Receptor Expressed on Myeloid Cells-1ActeosideHMGN1InflammationObstructive nephropathyRenal fibrosis

Identifiers

PMID36691481
PMCPMC9864189
OpenAlexW4317393609

What OpenQuestion holds

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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.