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Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats

Gastrointestinal (GI) adverse effects such as erosion and increased permeability are common during the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Our objective was to assess whether Bifidobacterium animalis ssp. lactis 420 protects against NSAID-induced GI side effects in a rat model. A t...

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Autores principales: Lyra, Anna, Saarinen, Markku, Putaala, Heli, Olli, Kaisa, Lahtinen, Sampo J., Ouwehand, Arthur C., Madetoja, Mari, Tiihonen, Kirsti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405648/
https://www.ncbi.nlm.nih.gov/pubmed/22848210
http://dx.doi.org/10.1155/2012/615051
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author Lyra, Anna
Saarinen, Markku
Putaala, Heli
Olli, Kaisa
Lahtinen, Sampo J.
Ouwehand, Arthur C.
Madetoja, Mari
Tiihonen, Kirsti
author_facet Lyra, Anna
Saarinen, Markku
Putaala, Heli
Olli, Kaisa
Lahtinen, Sampo J.
Ouwehand, Arthur C.
Madetoja, Mari
Tiihonen, Kirsti
author_sort Lyra, Anna
collection PubMed
description Gastrointestinal (GI) adverse effects such as erosion and increased permeability are common during the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Our objective was to assess whether Bifidobacterium animalis ssp. lactis 420 protects against NSAID-induced GI side effects in a rat model. A total of 120 male Wistar rats were allocated into groups designated as control, NSAID, and probiotic. The NSAID and probiotic groups were challenged with indomethacin (10 mg/kg(−1); single dose). The probiotic group was also supplemented daily with 10(10) CFU of B. lactis 420 for seven days prior to the indomethacin administration. The control group rats received no indomethacin or probiotic. The permeability of the rat intestine was analysed using carbohydrate probes and the visual damage of the rat stomach mucosa was graded according to severity. B. lactis 420 significantly reduced the indomethacin-induced increase in stomach permeability. However, the protective effect on the visual mucosal damage was not significant. The incidence of severe NSAID-induced lesions was, nevertheless, reduced from 50% to 33% with the probiotic treatment. To conclude, the B. lactis 420 supplementation protected the rats from an NSAID-induced increase in stomach permeability and may reduce the formation of more serious GI mucosal damage and/or enhance the recovery rate of the stomach mucosa.
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spelling pubmed-34056482012-07-30 Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats Lyra, Anna Saarinen, Markku Putaala, Heli Olli, Kaisa Lahtinen, Sampo J. Ouwehand, Arthur C. Madetoja, Mari Tiihonen, Kirsti Gastroenterol Res Pract Research Article Gastrointestinal (GI) adverse effects such as erosion and increased permeability are common during the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Our objective was to assess whether Bifidobacterium animalis ssp. lactis 420 protects against NSAID-induced GI side effects in a rat model. A total of 120 male Wistar rats were allocated into groups designated as control, NSAID, and probiotic. The NSAID and probiotic groups were challenged with indomethacin (10 mg/kg(−1); single dose). The probiotic group was also supplemented daily with 10(10) CFU of B. lactis 420 for seven days prior to the indomethacin administration. The control group rats received no indomethacin or probiotic. The permeability of the rat intestine was analysed using carbohydrate probes and the visual damage of the rat stomach mucosa was graded according to severity. B. lactis 420 significantly reduced the indomethacin-induced increase in stomach permeability. However, the protective effect on the visual mucosal damage was not significant. The incidence of severe NSAID-induced lesions was, nevertheless, reduced from 50% to 33% with the probiotic treatment. To conclude, the B. lactis 420 supplementation protected the rats from an NSAID-induced increase in stomach permeability and may reduce the formation of more serious GI mucosal damage and/or enhance the recovery rate of the stomach mucosa. Hindawi Publishing Corporation 2012 2012-07-17 /pmc/articles/PMC3405648/ /pubmed/22848210 http://dx.doi.org/10.1155/2012/615051 Text en Copyright © 2012 Anna Lyra et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lyra, Anna
Saarinen, Markku
Putaala, Heli
Olli, Kaisa
Lahtinen, Sampo J.
Ouwehand, Arthur C.
Madetoja, Mari
Tiihonen, Kirsti
Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title_full Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title_fullStr Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title_full_unstemmed Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title_short Bifidobacterium animalis ssp. lactis 420 Protects against Indomethacin-Induced Gastric Permeability in Rats
title_sort bifidobacterium animalis ssp. lactis 420 protects against indomethacin-induced gastric permeability in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405648/
https://www.ncbi.nlm.nih.gov/pubmed/22848210
http://dx.doi.org/10.1155/2012/615051
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