Dietary Flaxseed and Flaxseed Oil Differentially Modulate Aspects of the Microbiota Gut–Brain Axis Following an Acute Lipopolysaccharide Challenge in Male C57Bl/6 Mice

Author:

Livingston Dawson B. H.1ORCID,Sweet Allison1ORCID,Rodrigue Alexane1,Kishore Lalit2,Loftus Julia3ORCID,Ghali Farida2,Mahmoodianfard Salma4ORCID,Celton Colleen5,Hosseinian Farah56,Power Krista A.12ORCID

Affiliation:

1. Faculty of Medicine, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1H 8L1, Canada

2. Faculty of Health Science, School of Nutrition Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada

3. Faculty of Science, Department of Biochemistry, University of Ottawa, Ottawa, ON K1N 6N5, Canada

4. Faculty of Health Science, School of Human Kinetics, University of Ottawa, Ottawa, ON K1N 6N5, Canada

5. Faculty of Science, Department of Chemistry, Carleton University, Ottawa, ON K1S 5B6, Canada

6. Faculty of Science, Institute of Biochemistry, Carleton University, Ottawa, ON K1S 5B6, Canada

Abstract

The microbiota gut–brain axis (mGBA) is an important contributor to mental health and neurological and mood disorders. Lipopolysaccharides (LPS) are endotoxins that are components of Gram-negative bacteria cell walls and have been widely shown to induce both systemic and neuro-inflammation. Flaxseed (Linum usitatissimum) is an oilseed rich in fibre, n3-poly-unsaturated fatty acid (alpha-linolenic acid (ALA)), and lignan, secoisolariciresinol diglucoside, which all can induce beneficial effects across varying aspects of the mGBA. The objective of this study was to determine the potential for dietary supplementation with flaxseed or flaxseed oil to attenuate LPS-induced inflammation through modulation of the mGBA. In this study, 72 5-week-old male C57Bl/6 mice were fed one of three isocaloric diets for 3 weeks: (1) AIN-93G basal diet (BD), (2) BD + 10% flaxseed (FS), or (3) BD + 4% FS oil (FO). Mice were then injected with LPS (1 mg/kg i.p) or saline (n = 12/group) and samples were collected 24 h post-injection. Dietary supplementation with FS, but not FO, partially attenuated LPS-induced systemic (serum TNF-α and IL-10) and neuro-inflammation (hippocampal and/or medial prefrontal cortex IL-10, TNF-α, IL-1β mRNA expression), but had no effect on sickness and nest-building behaviours. FS-fed mice had enhanced fecal microbial diversity with increased relative abundance of beneficial microbial groups (i.e., Lachnospiraceae, Bifidobacterium, Coriobacteriaceae), reduced Akkermansia muciniphila, and increased production of short-chain fatty acids (SCFAs), which may play a role in its anti-inflammatory response. Overall, this study highlights the potential for flaxseed to attenuate LPS-induced inflammation, in part through modulation of the intestinal microbiota, an effect which may not be solely driven by its ALA-rich oil component.

Funder

Natural Sciences and Engineering Research Council of Canada

uOttawa Nutrition and Mental Health Scholarship and Fellowship

NSERC Undergraduate Student Research Awards Program

uOttawa Undergraduate Research Opportunity Program (UROP) Award

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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