Evidence map›Paper›PMID 38592518›Full record

ArticleEuropean journal of nutrition2024

The effect of novel paraprobiotic cocktail on dextran sodium sulfate induced acute colitis control focusing on autophagy signaling pathway.

Niloofar Rezaie, Fatemeh Ashrafian, Fatemeh Shidvash, Shadi Aghamohammad, Mahdi Rohani

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Article in European journal of nutrition, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Niloofar RezaieDepartment of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
Fatemeh AshrafianClinical Research Department, Pasteur Institute of Iran, Tehran, Iran.
Fatemeh ShidvashDepartment of Microbiology, Science and Research Campus, Islamic Azad University, Tehran, Iran.
Shadi AghamohammadDepartment of Bacteriology, Pasteur Institute of Iran, Tehran, Iran. shadi.aghamohammad@yahoo.com.
Mahdi RohaniDepartment of Bacteriology, Pasteur Institute of Iran, Tehran, Iran. kia.rohani@gmail.com.

Funding

Pasteur Institute of Iran B-9740
6 · The paper itself

Abstract

purposeParaprobiotics are a non-viable form of probiotics that are reported to provide significant health benefits. Nevertheless, little is known about the beneficial effects of paraprobiotics on inflammatory bowel disease. Although probiotics show potential as therapeutic agents for a range of diseases, including inflammatory bowel disease (IBD), there are certain risks associated with their use. These risks include toxin production, hemolytic potential, antibiotic resistance, and the need to analyze metabolic activities. Hence Using paraprobiotic with the lower aforementioned risk would therefore be the preferable option. Here, we conducted an in vivo study to evaluate the preventive effect of our native paraprobiotic cocktail against dextran sulfate sodium (DSS)-induced murine colitis by affecting the autophagy signaling pathway.

methodsFour-week-old male C57Bl/6 mice were randomly divided into three groups after a two-week acclimation period with normal standard laboratory food diet. Mice were administered PBS (PBS group as control), PBS along with DSS (DSS group, as a control), and a cocktail of paraprobiotics along with DSS (Para group). The severity of colitis, length and histopathology of the colon were evaluated. In addition, the expression of autophagy was assessed using real-time PCR.

resultsThe results showed that administration of the paraprobiotic cocktail to DSS-treated mice inhibited the severity of colitis symptoms, as evidenced by the inhibition of weight loss and DAI, as well as histopathological scores in the study colon, as well as shortening of colon length caused by DSS. In contrast to the DSS group, the cocktail was able to modulate inflammation through upregulation of autophagy-related genes (becline 1, atg5, atg7, atg12, and atg13).

conclusionAlthough there are some limitations in our investigation, such as the dosage and duration of treatments, our native paraprobiotic blend effectively prevented the advancement of colitis. This suggests that it plays a vital role in regulating inflammation and preventing colitis by promoting the autophagy mechanism in cases where the consumption of probiotics may have negative consequences.

Indexed as

AutophagyColitisDextran SulfateMice, Inbred C57BLProbioticsSignal TransductionAnimalsColonDisease Models, AnimalMaleMiceDextran SulfateAutophagyColitisIBDParaprobiotic

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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.