Evidence map›Paper›PMID 25152589›Full record

ArticleWorld journal of gastroenterology2014

Beneficial effect of butyrate, Lactobacillus casei and L-carnitine combination in preference to each in experimental colitis.

Mahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Amir Hossein Abdolghaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi

Open access · hybridAbstract readComparative Study
In one paragraph

Article in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Mahsa MoeinianMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Seyedeh Farnaz Ghasemi-NiriMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Shilan MozaffariMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Amir Hossein AbdolghaffariMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Maryam BaeeriMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Mona Navaea-NigjehMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Mohammad AbdollahiMahsa Moeinian, Seyedeh Farnaz Ghasemi-Niri, Shilan Mozaffari, Maryam Baeeri, Mona Navaea-Nigjeh, Mohammad Abdollahi, Department of Toxicology and Pharmacology, Toxicology and Poisoning Research Center, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Tehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the beneficial effect of the combination of butyrate, Lactobacillus casei, and L-carnitine in a rat colitis model.

methodsRats were divided into seven groups. Four groups received oral butyrate, L-carnitine, Lactobacillus casei and the combination of three agents for 10 consecutive days. The remaining groups included negative and positive controls and a sham group. Macroscopic, histopathological examinations, and biomarkers such as tumor necrosis factor-alpha (TNF-α) and interlukin-1β (IL-1β), myeloperoxidase (MPO), thiobarbituric acid reactive substances (TBARS), and ferric reduced ability of plasma (FRAP) were determined in the colon.

resultsThe combination therapy exhibited a significant beneficial effect in alleviation of colitis compared to controls. Overall changes in reduction of TNF-α (114.66 ± 18.26 vs 171.78 ± 9.48 pg/mg protein, P < 0.05), IL-1β (24.9 ± 1.07 vs 33.06 ± 2.16 pg/mg protein, P < 0.05), TBARS (0.2 ± 0.03 vs 0.49 ± 0.04 μg/mg protein, P < 0.01), MPO (15.32 ± 0.4 vs 27.24 ± 3.84 U/mg protein, P < 0.05), and elevation of FRAP (23.46 ± 1.2 vs 15.02 ± 2.37 μmol/L, P < 0.05) support the preference of the combination therapy in comparison to controls. Although the monotherapies were also effective in improvement of colitis markers, the combination therapy was much better in improvement of colon oxidative stress markers including FRAP, TBARS, and MPO.

conclusionThe present combination is a suitable mixture in control of experimental colitis and should be trialed in the clinical setting.

Indexed as

AnimalsAnti-Inflammatory AgentsAntioxidantsBiomarkersButyric AcidCarnitineColitisColonCombined Modality TherapyDisease Models, AnimalGastrointestinal AgentsInflammation MediatorsLacticaseibacillus caseiMaleOxidative StressProbioticsAnti-Inflammatory AgentsAntioxidantsBiomarkersButyric AcidCarnitineGastrointestinal AgentsInflammation MediatorsTrinitrobenzenesulfonic AcidButyrateColitisInflammatory bowel diseaseLactobacillus caseiL-carnitineOxidative stressProbiotic

Identifiers

PMID25152589
PMCPMC4138466
OpenAlexW2008857572

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.