Evidence map›Paper›PMID 37512876›Full record

ArticleMicroorganisms2023

Protective and Therapeutic Effects of Lactic Acid Bacteria against Aflatoxin B1 Toxicity to Rat Organs.

Hayat Ashi, Meshal H K Almalki, Enas A Hamed, Wafaa S Ramadan, Tahani F H Alahmadi, Outour Tariq Alami, Sara H Arafa, Atheer K Alshareef, Fatimah S Alsulami, Areej F Alharbi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  3. 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

16 authors at 3 institutions in 2 countries.

Hayat AshiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Meshal H K AlmalkiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0009-0004-6517-1529
Enas A HamedDepartment of Medical Physiology, Faculty of Medicine, Assiut University, Assiut 71515, Egypt.
Wafaa S RamadanDepartment of Anatomy, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-8479-6426
Tahani F H AlahmadiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Outour Tariq AlamiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Sara H ArafaDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Atheer K AlshareefDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Fatimah S AlsulamiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Areej F AlharbiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Manahil S Al-HarbiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Ebtehal H AlqurashiDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Shirin AashiCollege of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Youssef A AlzahraniCollege of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0009-0008-3521-4793
Khaled ElbannaDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Hussein H AbulreeshDepartment of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0000-0002-3289-696X
Umm al-Qura University · SAKing Abdulaziz University · SAAssiut University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAflatoxin (AF), a metabolite of

methodsThirty adult male rats were divided into six groups (five each) to perform the experiments. The control (Co) group was fed a basal diet and water. Each of the following periods lasted 21 days: the milk (MK) group orally received milk (500 µL); LAB suspension (500 µL) containing 10

resultsThe results revealed a significant decrease in RBCs, lymphocytes, total proteins, eosinophil count, albumin, and uric acid, whereas the levels of WBCs, monocytes, neutrophils, creatinine, urea, aspartate aminotransferase, alkaline phosphatase, alanine aminotransferase, lactate dehydrogenase, and creatinine kinase significantly increased in the AF group in comparison to the control group. The histological examination of the AF group revealed necrosis and apoptosis of the kidney's glomeruli and renal tubules, nuclei vacuolization and apoptosis of hepatocytes, congestion of the liver's dilated portal vein, lymphoid depletion in the white pulp, localized hemorrhages, hemosiderin pigment deposition in the spleen, and vacuolization of seminiferous tubules with a complete loss of testis spermatogenic cells. Meanwhile, protective and therapeutic LAB administration in AF-treated rats improved the hematological, biochemical, and histological changes.

conclusionsThe study revealed LAB-based amelioration to AFB1-induced disruptions of the kidney, liver, spleen, and testis by inhibiting tissue damage. The therapeutic effects of LAB were comparatively more pronounced than the protective effects.

Indexed as

aflatoxinkidneylactic acid bacterialiverprotectiveratsspleenstructuretestestherapeutic

Identifiers

PMID37512876
PMCPMC10385160
OpenAlexW4382790732

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Registered trials

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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.