Evidence map›Paper›PMID 34057544›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2021

Protective effect of myricetin on LPS-induced mastitis in mice through ERK1/2 and p38 protein author.

Xingchi Kan, Juxiong Liu, Yingsheng Chen, Wenjin Guo, Dianwen Xu, Ji Cheng, Yu Cao, Zhanqing Yang, Shoupeng Fu

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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
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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

9 authors at 1 institution in 1 country.

Xingchi Kan *Department of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.ORCID http://orcid.org/0000-0002-3541-4997
Juxiong Liu *Department of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Yingsheng ChenDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Wenjin GuoDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Dianwen XuDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Ji ChengDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Yu CaoDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Zhanqing YangDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China.
Shoupeng FuDepartment of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, China. fushoupeng@jlu.edu.cn.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inflammatory reaction of mammary gland tissue in dairy cattle leads to the occurrence of mastitis disease and causes huge economic loss. Myricetin (Myr), a flavonoid natural product, is extracted from the root, stem, and leaves of Myrica rubra. It has a wide range of biological activities, such as anti-oxidant, anti-inflammatory, and anti-tumor. The purpose of this experiment is to further explore the effect of Myr on mastitis and further explore its potential mechanism in LPS-induced mice mastitis model and LPS-induced mice mammary epithelial cells (mMECs). The results showed that Myr could significantly inhibit the expression of TNF-α, IL-6, and IL-1β in the mammary gland of mice. Furthermore, the results of mechanism studies show that Myr can significantly inhibit P38 and ERK1/2 protein phosphorylation levels in mice mammary tissue, and this result has been further verified at the cellular level. These results confirm that Myr can significantly inhibit mammary inflammation, and its potential mechanism is to play a protective role by inhibiting the phosphorylation level of P38 and ERK1/2 protein.

Indexed as

AnimalsAnti-Inflammatory AgentsDisease Models, AnimalFemaleFlavonoidsInflammationLipopolysaccharidesMastitisMiceMice, Inbred BALB CMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myricap38 Mitogen-Activated Protein KinasesPhosphorylationAnti-Inflammatory AgentsFlavonoidsLipopolysaccharidesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3myricetinp38 Mitogen-Activated Protein KinasesERK1/2LPSMastitisMyricetinP38

Identifiers

PMID34057544
OpenAlexW3164336423

What OpenQuestion holds

Textmetadata
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.