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Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis

Inflammatory bowel disorders can be associated with alterations in gut microbiota (dysbiosis) and behavioral disturbances. In experimental colitis, administration of fish oil (FO) or cannabinoids, such as cannabidiol (CBD), reduce inflammation. We investigated the effect of combined FO/CBD administr...

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Autores principales: Silvestri, Cristoforo, Pagano, Ester, Lacroix, Sébastien, Venneri, Tommaso, Cristiano, Claudia, Calignano, Antonio, Parisi, Olga A., Izzo, Angelo A., Di Marzo, Vincenzo, Borrelli, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580385/
https://www.ncbi.nlm.nih.gov/pubmed/33162890
http://dx.doi.org/10.3389/fphar.2020.585096
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author Silvestri, Cristoforo
Pagano, Ester
Lacroix, Sébastien
Venneri, Tommaso
Cristiano, Claudia
Calignano, Antonio
Parisi, Olga A.
Izzo, Angelo A.
Di Marzo, Vincenzo
Borrelli, Francesca
author_facet Silvestri, Cristoforo
Pagano, Ester
Lacroix, Sébastien
Venneri, Tommaso
Cristiano, Claudia
Calignano, Antonio
Parisi, Olga A.
Izzo, Angelo A.
Di Marzo, Vincenzo
Borrelli, Francesca
author_sort Silvestri, Cristoforo
collection PubMed
description Inflammatory bowel disorders can be associated with alterations in gut microbiota (dysbiosis) and behavioral disturbances. In experimental colitis, administration of fish oil (FO) or cannabinoids, such as cannabidiol (CBD), reduce inflammation. We investigated the effect of combined FO/CBD administration on inflammation and dysbiosis in the dextran sulphate sodium (DSS) model of mouse colitis, which also causes behavioral disturbances. Colitis was induced in CD1 mice by 4% w/v DSS in drinking water for five consecutive days followed by normal drinking water. FO (20–75 mg/mouse) was administered once a day starting two days after DSS, whereas CBD (0.3–30 mg/kg), alone or after FO administration, was administered once a day starting 3 days after DSS, until day 8 (d8) or day 14 (d14). Inflammation was assessed at d8 and d14 (resolution phase; RP) by measuring the Disease Activity Index (DAI) score, change in body weight, colon weight/length ratio, myeloperoxidase activity and colonic interleukin (IL)-1β (IL-1β), IL-10, and IL-6 concentrations. Intestinal permeability was measured with the fluorescein isothiocyanate-dextran. Behavioral tests (novel object recognition (NOR) and light/dark box test) were performed at d8. Fecal microbiota composition was determined by ribosomal 16S DNA sequencing of faecal pellets at d8 and d14. DSS-induced inflammation was stronger at d8 and accompanied by anxiety-like behavior and impaired recognition memory. FO (35, 50, 75 mg/mouse) alone reduced inflammation at d8, whereas CBD alone produced no effect at any of the doses tested; however, when CBD (3, 10 mg/kg) was co-administered with FO (75 mg/mouse) inflammation was attenuated. FO (20 mg/mouse) and CBD (1 mg/kg) were ineffective when given alone, but when co-administered reduced all inflammatory markers and the increased intestinal permeability at both d8 and d14, but not the behavioral impairments. FO, CBD, and their combination affected gut bacteria taxa that were not affected by DSS per se. Akkermansia muciniphila, a species suggested to afford anti-inflammatory action in colitis, was increased by DSS only at d14, but its levels were significantly elevated by all treatments at d8. FO and CBD co-administered at per se ineffective doses reduce colon inflammation, in a manner potentially strengthened by their independent elevation of Akkermansia muciniphila.
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spelling pubmed-75803852020-11-05 Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis Silvestri, Cristoforo Pagano, Ester Lacroix, Sébastien Venneri, Tommaso Cristiano, Claudia Calignano, Antonio Parisi, Olga A. Izzo, Angelo A. Di Marzo, Vincenzo Borrelli, Francesca Front Pharmacol Pharmacology Inflammatory bowel disorders can be associated with alterations in gut microbiota (dysbiosis) and behavioral disturbances. In experimental colitis, administration of fish oil (FO) or cannabinoids, such as cannabidiol (CBD), reduce inflammation. We investigated the effect of combined FO/CBD administration on inflammation and dysbiosis in the dextran sulphate sodium (DSS) model of mouse colitis, which also causes behavioral disturbances. Colitis was induced in CD1 mice by 4% w/v DSS in drinking water for five consecutive days followed by normal drinking water. FO (20–75 mg/mouse) was administered once a day starting two days after DSS, whereas CBD (0.3–30 mg/kg), alone or after FO administration, was administered once a day starting 3 days after DSS, until day 8 (d8) or day 14 (d14). Inflammation was assessed at d8 and d14 (resolution phase; RP) by measuring the Disease Activity Index (DAI) score, change in body weight, colon weight/length ratio, myeloperoxidase activity and colonic interleukin (IL)-1β (IL-1β), IL-10, and IL-6 concentrations. Intestinal permeability was measured with the fluorescein isothiocyanate-dextran. Behavioral tests (novel object recognition (NOR) and light/dark box test) were performed at d8. Fecal microbiota composition was determined by ribosomal 16S DNA sequencing of faecal pellets at d8 and d14. DSS-induced inflammation was stronger at d8 and accompanied by anxiety-like behavior and impaired recognition memory. FO (35, 50, 75 mg/mouse) alone reduced inflammation at d8, whereas CBD alone produced no effect at any of the doses tested; however, when CBD (3, 10 mg/kg) was co-administered with FO (75 mg/mouse) inflammation was attenuated. FO (20 mg/mouse) and CBD (1 mg/kg) were ineffective when given alone, but when co-administered reduced all inflammatory markers and the increased intestinal permeability at both d8 and d14, but not the behavioral impairments. FO, CBD, and their combination affected gut bacteria taxa that were not affected by DSS per se. Akkermansia muciniphila, a species suggested to afford anti-inflammatory action in colitis, was increased by DSS only at d14, but its levels were significantly elevated by all treatments at d8. FO and CBD co-administered at per se ineffective doses reduce colon inflammation, in a manner potentially strengthened by their independent elevation of Akkermansia muciniphila. Frontiers Media S.A. 2020-10-08 /pmc/articles/PMC7580385/ /pubmed/33162890 http://dx.doi.org/10.3389/fphar.2020.585096 Text en Copyright © 2020 Silvestri, Pagano, Lacroix, Venneri, Cristiano, Calignano, Parisi, Izzo, Di Marzo and Borrelli http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Silvestri, Cristoforo
Pagano, Ester
Lacroix, Sébastien
Venneri, Tommaso
Cristiano, Claudia
Calignano, Antonio
Parisi, Olga A.
Izzo, Angelo A.
Di Marzo, Vincenzo
Borrelli, Francesca
Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title_full Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title_fullStr Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title_full_unstemmed Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title_short Fish Oil, Cannabidiol and the Gut Microbiota: An Investigation in a Murine Model of Colitis
title_sort fish oil, cannabidiol and the gut microbiota: an investigation in a murine model of colitis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580385/
https://www.ncbi.nlm.nih.gov/pubmed/33162890
http://dx.doi.org/10.3389/fphar.2020.585096
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