Evidence map›Paper›PMID 28934296›Full record

ArticlePloS one2017

Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice.

Wei-Syun Hu, Peramaiyan Rajendran, Bor-Show Tzang, Yu-Lan Yeh, Chia-Yao Shen, Ray-Jade Chen, Tsung-Jung Ho, Viswanadha Vijaya Padma, Yi-Hsing Chen, Chih-Yang Huang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in immunology · 2023
    Review
  4. Review
  5. Frontiers in immunology · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. 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

10 authors at 8 institutions in 2 countries.

Wei-Syun HuSchool of Medicine, College of Medicine, China Medical University, Taichung, Taiwan, ROC.
Peramaiyan RajendranGraduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan, ROC.
Bor-Show TzangInstitute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan, ROC.
Yu-Lan YehDepartment of pathology, Changhua Christian Hospital, Changhua, Taiwan, ROC.
Chia-Yao ShenDepartment of Nursing, Mei Ho University, Pingtung, Taiwan, ROC.
Ray-Jade ChenDepartment of Surgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan, ROC.
Tsung-Jung HoGraduate Institute of Chinese Medical Science, China Medical University, Taichung, Taiwan, ROC.
Viswanadha Vijaya PadmaDepartment of Biotechnology, Bharathiar University, Coimbatore, India.
Yi-Hsing ChenResearch and Development Department, GenMont Biotech Incorporation, Tainan, Taiwan, ROC.
Chih-Yang HuangGraduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan, ROC.ORCID http://orcid.org/0000-0003-2347-0411
China Medical University · TWAsia University · TWBharathiar University · INChung Shan Medical University · TWGenMont Biotech (Taiwan) · TWKang-Ning Junior College of Medical Care and Management · TWMeiho University · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a disease that mostly affects women. Accelerated atherosclerosis is a high-risk factor associated with SLE patients. SLE associated with cardiovascular disease is one of the most important causes of death. In this study, we demonstrated that Lactobacillus paracasei GMNL-32 (GMNL-32), a probiotic species, exhibits anti-fibrosis and anti-apoptotic effects on the cardiac tissue of NZB/WF1 mice. Female NZB/W F1 mice, a well-known and commonly used lupus-prone mouse strain, were treated with or without GMNL-32 administration for 12 weeks. Oral administration of GMNL-32 to NZB/WF1 mice significantly increased the ventricular thickness when compared to that of NZB/WF1 mice. Administration of GMNL-32 significantly attenuated the cardiac cell apoptosis that was observed in exacerbate levels in the control NZB/WF1 mice. Further, the cellular morphology that was slightly distorted in the NZB/WF1 was effectively alleviated in the treatment group mice. In addition, GMNL-32 reduced the level of Fas death receptor-related pathway of apoptosis signaling and enhanced anti-apoptotic proteins. These results indicate that GMNL-32 exhibit an effective protective effect on cardiac cells of SLE mice. Thus, GMNL-32 may be a potential therapeutic strategy against SLE associated arthrosclerosis.

Indexed as

Lacticaseibacillus paracaseiAdministration, OralAnimalsApoptosisBlotting, WesternCollagenCyclooxygenase 2Disease Models, AnimalFemaleFibrosisFluorescent Antibody TechniqueHeart VentriclesIn Situ Nick-End LabelingLupus Erythematosus, SystemicMatrix Metalloproteinase 9Mice, Inbred NZBCollagenCyclooxygenase 2Matrix Metalloproteinase 9Mmp9 protein, mousePtgs2 protein, mouse

Identifiers

PMID28934296
PMCPMC5608316
OpenAlexW2759704888

What Socratic 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 Socratic graph.