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Adipose tissue inflammation in human obesity and response to chronic marine omega-3 fatty acid supplementation: the BIOCLAIMS study at the University of Southampton

Published online by Cambridge University Press:  27 October 2021

H. Fisk ,
R. Ayres ,
C. Childs ,
O. Kuda ,
J. Kopecky ,
E. Antoun ,
K. Lillycrop  and
P. Calder
H. Fisk
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
R. Ayres
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
C. Childs
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
O. Kuda
Affiliation:
Department of Adipose Tissue Biology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic
J. Kopecky
Affiliation:
Institute for Clinical and Experimental Medicine, Prague, Czech Republic
E. Antoun
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
K. Lillycrop
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
P. Calder
Affiliation:
Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, UK
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Abstract

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Proceedings of the Nutrition Society , Volume 80 , Issue OCE5: Summer Conference, 6–8 July 2021, Nutrition in a changing world , 2021 , E160
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Copyright © The Authors 2021

This abstract was presented as the Cellular and Molecular Nutrition Theme highlight.

Obesity is an excess of adipose tissue (AT) and is linked with increased inflammation that enhances risk of type-2 diabetes and cardiovascular disease(Reference Dewhurst-Trigg, Hulston and Markey1,Reference Boden2,Reference Rogero M and Calder3) . The BIOCLAIMS Study assessed subcutaneous white AT (sWAT) inflammation in metabolically healthy obesity in which metabolic syndrome had not yet manifested, and responses to chronic supplementation with omega-3 fatty acid (FA) which are widely investigated for their anti-inflammatory actions(Reference Rogero M and Calder3).

sWAT biopsies were collected pre- and post-12-week supplementation with 1.1 g EPA + 0.8 g DHA/day or corn oil. sWAT FA composition, lipid mediator profile, whole transcriptome expression, protein expression, morphology, and immune cell infiltration were assessed by gas chromatography, coupled UPLC-mass spectrometry, RNA-Sequencing, immunoblotting, and immuno-histochemical staining respectively.

Metabolically healthy obesity was associated with dysregulated FA and lipid mediator profiles exhibiting higher concentrations of arachidonic acid (AA) and respective oxylipins, lower concentrations of DHA oxylipins, and alteration of the endocannabinoid system (ECS) (P <0.05). Metabolically healthy obesity was further associated with altered transcriptome expression suggestive of enhanced inflammation, immune response, tissue remodelling, and expansion. This was concordant with tissue morphology in which metabolically healthy obesity was associated with adipocyte hypertrophy and presence of macrophages arranged in crown like structures (P <0.05); however, total and pericellular fibrosis was not altered in metabolically healthy obese individuals but was positively correlated with HOMA 2-IR (P <0.05). Chronic supplementation with EPA+DHA increased concentrations of sWAT omega-3 FAs and derived oxylipins (P < 0.01), and decreased AA oxylipins, with particular effect on the ECS predominantly in normal weight individuals (P < 0.05). EPA+DHA modulated the sWAT transcriptome suggesting promotion of tissue remodelling and down regulation of chronic inflammatory response (P < 0.05).

These data suggest enhanced sWAT inflammation in the context of tissue expansion and remodelling is associated with metabolically healthy obesity. Furthermore, that sWAT of metabolically healthy obese individuals without type-2 diabetes maintains some degree of normal function in that it is still sensitive to dietary lipid manipulation. EPA+DHA are able to modulate synthesis of EPA, DHA and AA derived oxylipins and transcriptome expression but obesity may involve resistance to these effects particularly on the ECS.

References

Dewhurst-Trigg, R, Hulston, CJ & Markey, O (2020) Proc Nutr Soc 17, 1–15.Google Scholar
Boden, G (2011) Curr Opin Endocrinol Diabetes Obes 18 (2), 139–143.CrossRefGoogle Scholar
Rogero M, Macedo & Calder, PC (2018) Nutrient 10 (4), 432.10.3390/nu10040432CrossRefGoogle Scholar