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A high fat anti-inflammatory diet improves widespread allodynia despite worsening metabolic outcomes in adult mice exposed to neonatal maternal separation

View ORCID ProfileOlivia C. Eller, View ORCID ProfileRebecca M. Foright, View ORCID ProfileAaron D. Brake, Michelle K. Winter, Leonidas E. Bantis, View ORCID ProfileE. Matthew Morris, View ORCID ProfileJohn P. Thyfault, View ORCID ProfileJulie A. Christianson
doi: https://doi.org/10.1101/2020.09.29.317297
Olivia C. Eller
1Department of Anatomy and Cell Biology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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Rebecca M. Foright
1Department of Anatomy and Cell Biology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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Aaron D. Brake
1Department of Anatomy and Cell Biology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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Michelle K. Winter
2Kansas Intellectual and Developmental Disabilities Research Association, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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Leonidas E. Bantis
3Department of Biostatistics and Data Science, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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E. Matthew Morris
4Department of Molecular and Integrative Physiology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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John P. Thyfault
4Department of Molecular and Integrative Physiology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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Julie A. Christianson
1Department of Anatomy and Cell Biology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
5Department of Anesthesiology, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA
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  • For correspondence: jchristianson@kumc.edu
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Abstract

Inflammation plays a key role in the progression and maintenance of chronic pain, which impacts the lives of millions of Americans. Despite growing evidence that chronic pain can be improved by treating underlying inflammation, successful treatments are lacking and pharmaceutical interventions are limited due to drug side effects. Here we are testing whether an anti-inflammatory diet (AID) containing a combination of key anti-inflammatory compounds, at clinically relevant doses, improves pain-like behaviors in a preclinical model of chronic widespread hypersensitivity induced by neonatal maternal separation (NMS). Our results demonstrate a benefit of the AID on pain-like behaviors, despite the diet being high in fat, which led to increased caloric intake, adiposity, and weight gain. The AID specifically increased measures of metabolic syndrome and inflammation in female mice, compared to an isocaloric, macronutrient-matched diet lacking the anti-inflammatory compounds. Male mice, especially those exposed to NMS, were equally susceptible to both diets worsening metabolic measures. This work highlights important sexual dimorphic outcomes related to early life stress exposure and dietary interventions, as well as a potential disconnect between improvements in pain-like behaviors and metabolic measures.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted October 01, 2020.
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A high fat anti-inflammatory diet improves widespread allodynia despite worsening metabolic outcomes in adult mice exposed to neonatal maternal separation
Olivia C. Eller, Rebecca M. Foright, Aaron D. Brake, Michelle K. Winter, Leonidas E. Bantis, E. Matthew Morris, John P. Thyfault, Julie A. Christianson
bioRxiv 2020.09.29.317297; doi: https://doi.org/10.1101/2020.09.29.317297
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A high fat anti-inflammatory diet improves widespread allodynia despite worsening metabolic outcomes in adult mice exposed to neonatal maternal separation
Olivia C. Eller, Rebecca M. Foright, Aaron D. Brake, Michelle K. Winter, Leonidas E. Bantis, E. Matthew Morris, John P. Thyfault, Julie A. Christianson
bioRxiv 2020.09.29.317297; doi: https://doi.org/10.1101/2020.09.29.317297

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