Evidence map›Paper›PMID 31737165›Full record

ArticleOxidative medicine and cellular longevity2019

Niacin Protects against Butyrate-Induced Apoptosis in Rumen Epithelial Cells.

Dan Luo, Zhipeng Peng, Le Yang, Mingren Qu, Xiaowen Xiong, Lanjiao Xu, Xianghui Zhao, Ke Pan, Kehui Ouyang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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  10. Frontiers in veterinary science · 2022
    Article
  11. Genome-Protecting Compounds as Potential Geroprotectors.International journal of molecular sciences · 2020
    Review
  12. 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

9 authors at 2 institutions in 1 country.

Dan LuoJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.ORCID https://orcid.org/0000-0003-4058-4496
Zhipeng PengMenon Animal Nutrition Technology Co. Ltd., Shanghai 201800, China.
Le YangKaihua County Animal Husbandry and Veterinary Bureau, Quzhou 324000, China.
Mingren QuJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.
Xiaowen XiongJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.
Lanjiao XuJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.
Xianghui ZhaoJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.
Ke PanJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.
Kehui OuyangJiangxi Provincial Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Nanchang 330045, China.ORCID https://orcid.org/0000-0002-3837-9824
Jiangxi Agricultural University · CNShandong Province Animal Husbandry and Veterinary Bureau · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effects and underlying mechanisms of butyrate and butyrate+niacin on apoptosis in sheep rumen epithelial cells were investigated. Cells were exposed to butyrate (0-140 mM) for 6 h. A low concentration (20 mM) of butyrate increased cell viability and promoted growth whereas high concentrations (40-140 mM) inhibited proliferation. Cells were then cocultured with 120 mM butyrate and niacin (0-100 mM) for 6 h. Niacin addition attenuated butyrate-induced cellular damage and promoted proliferation at 20-80 mM; 40 mM presented the optimal effect. Higher concentrations (100 mM) of niacin resulted in low cell viability. Subsequent experiments confirmed that 120 mM butyrate increased intracellular reactive oxygen species (ROS) production and reduced the intracellular total antioxidant capacity (T-AOC) versus the untreated control. Compared with 120 mM butyrate, cotreatment with 40 mM niacin significantly reduced the intracellular ROS content and increased the intracellular T-AOC. Flow cytometry analysis revealed that 120 mM butyrate increased the proportion of apoptotic cells by 17.8% versus the untreated control, and 120 mM butyrate+40 mM niacin treatment reduced the proportion of apoptotic cells by 28.6% and 39.4% versus the untreated control and butyrate treatment, respectively. Treatment with 120 mM butyrate increased caspase-9 and p53 mRNA levels and decreased the expression of Bcl-2 and Bax, and the Bcl-2/Bax ratio versus the untreated control. Treatment with 120 mM butyrate+40 mM niacin downregulated the expression of caspase-3 and p53 and increased the expression of Bcl-2 and Bax versus butyrate treatment alone but had no effect on the Bcl-2/Bax ratio. Thus, high concentrations of butyrate may induce rumen epithelial cell apoptosis by increasing oxidative stress and inducing caspase-9 and p53 expression. Cotreatment with niacin regulates apoptosis-related gene expression by reducing intracellular ROS production and DNA damage and downregulating caspase-3 and p53 expressions to protect rumen epithelial cells against butyrate-induced apoptosis.

Indexed as

AnimalsAntioxidantsApoptosisbcl-2-Associated X ProteinButyratesCattleCells, CulturedCytoprotectionEpithelial CellsGene Expression RegulationNiacinOxidative StressRumenSheepTumor Suppressor Protein p53Antioxidantsbcl-2-Associated X ProteinButyratesNiacinTumor Suppressor Protein p53

Identifiers

PMID31737165
PMCPMC6815573
OpenAlexW2980057575

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.