Evidence map›Paper›PMID 40402978›Full record

ArticlePloS one2025

Comprehensive safety assessment and therapeutic potential of Pediococcus acidilactici NMCC-B in attenuating arthritis progression.

Tayyaba Zulfiqar, Muhammad Khalid Tipu, Muhammad Tariq Khan, Amr S Abouzied, Bassam S M Al Kazman, Saud O Alshammari, Qamar A Alshammari, Abdulkarim Alshammari, Muhammad Nasir Hayat Malik, Amir Ali and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

12 authors.

Tayyaba ZulfiqarDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Muhammad Khalid TipuDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Muhammad Tariq KhanDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Amr S AbouziedDepartment of Pharmaceutical Chemistry, College of Pharmacy, University of Hail, Hail, Saudi Arabia.ORCID https://orcid.org/0000-0002-9202-3909
Bassam S M Al KazmanDepartment of Pharmacognosy, College of Pharmacy, Najran University, Najran, Saudi Arabia.
Saud O AlshammariDepartment of Pharmacognosy and Alternative Medicine, College of Pharmacy, Northern Border University, Rafha, Saudi Arabia.
Qamar A AlshammariDepartment of Pharmacology and Toxicology, College of Pharmacy, Northern Border University, Rafha, Saudi Arabia.
Abdulkarim AlshammariDepartment of Pharmacy Practice, College of Pharmacy, Northern Border University, Rafha, Saudi Arabia.
Muhammad Nasir Hayat MalikFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.ORCID https://orcid.org/0000-0002-2657-9810
Amir AliFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Muhammad Usama MazharDepartment of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.ORCID https://orcid.org/0000-0002-0748-5421
Hafsa JabeenFaculty of Pharmacy, Capital University of Science and Technology, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysbiosis of gut microbiota and loss of gut-barrier integrity contribute to the development and severity of rheumatoid arthritis (RA). The available treatments pose a burden of major adverse effects and new treatment strategies are therefore the need of time. In this study, Pediococcus acidilactici NMCC-B (Probiotic) was evaluated for its safety and efficacy in complete Freund's adjuvant (CFA)-induced mice model of RA. Mice were treated with either Escherichia coli (1 × 109 CFU/ml) or P. acidilactici NMCC-B (1 × 109 CFU/ml, 2 × 109 CFU/ml) to assess acute, sub-acute, and chronic toxicities. In RA model, mice were either pre-treated with daily dose of P. acidilactici NMCC-B or treated concurrently (day 1-day 27) or post-treated (day 28-day 42). P. acidilactici NMCC-B inhibited gut permeability, lessened joint inflammation, and ameliorated RA progression. No signs of toxicity, pathogenicity or bacterial translocation were observed in animals treated with probiotic. P. acidilactici NMCC-B also restored total body weight, attenuated inflammation, improved antioxidants, alleviated soft tissue swelling, bone damage, and the expression of IL-1β, NF-κB and TNF-α in paw tissue. Based on current findings, it is perceivable that P. acidilactici NMCC-B could be a promising candidate for the management of RA.

Indexed as

Arthritis, ExperimentalArthritis, RheumatoidPediococcus acidilacticiProbioticsAnimalsDisease Models, AnimalDisease ProgressionFreund's AdjuvantGastrointestinal MicrobiomeMaleMiceFreund's Adjuvant

Identifiers

PMID40402978
PMCPMC12097640

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.