A Multiomics Evaluation of the Countermeasure Influence of 4-Week Cranberry Beverage Supplementation on Exercise-Induced Changes in Innate Immunity.

Blake R Rushing, Susan J Sumner, Wimal Pathmasiri, Camila A Sakaguchi, Ashraf M Omar, James C Williams, Qibin Zhang, David C Nieman, Fayaj A Mulani, Susan McRitchie, Jongmin Woo, Jackie Lawson, Kevin C Lambirth

Journal: Nutrients 2024;16(19):

PMID: 39408218

Plain Language Summary

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Intensive exercise can affect the immune system and increase inflammation, which can have detrimental health affects in the body. Cranberries may contain beneficial naturally occurring chemicals known as polyphenols, which can have anti-inflammatory and immune regulatory effects. However, evidence in humans is currently still inconsistent. This randomised control trial of 25 non-elite cyclists aimed to investigate how a 4-week intake of unsweetened cranberry beverage affects the body's immune response after exercise. The researchers compared the effects of the cranberry drink, which contains polyphenols (natural compounds thought to have health benefits), to a placebo (a drink with no active ingredients).

The results showed that cranberry juice intake improved the level of proteins related to activation of the immune system. There were no changes in the assessed stress hormone or markers of muscle damage.

It was concluded that cranberry beverage supplementation may help moderate the immune changes that occur after intense exercise. This could be important for athletes or active individuals looking to support their immune health during training.This study could be used by healthcare professionals to understand the potential benefits of cranberry beverage supplementation on immune function following exercise.

Abstract

OBJECTIVES

This study examined the effect of a 4-week unsweetened cranberry beverage (CRAN) (317 mg polyphenols) versus placebo beverage (PLAC) ingestion (240 mL/day) on moderating exercise-induced changes in innate immunity.

METHODS

Participants included 25 male and female non-elite cyclists. A randomized, placebo-controlled, double-blind crossover design was used with two 4-week supplementation periods and a 2-week washout period. Supplementation periods were followed by an intensive 2.25 h cycling bout. Six blood samples were collected before and after supplementation (in an overnight fasted state) and at 0 h, 1.5 h, 3 h, and 24 h post-exercise. Stool and urine samples were collected pre- and post-supplementation. Outcome measures included serum creatine kinase, myoglobin, and cortisol, complete blood counts, plasma untargeted proteomics, plasma-targeted oxylipins, untargeted urine metabolomics, and stool microbiome composition via whole genome shotgun (WGS) sequencing.

RESULTS

Urine CRAN-linked metabolites increased significantly after supplementation, but no trial differences in alpha or beta microbiota diversity were found in the stool samples. The 2.25 h cycling bout caused significant increases in plasma arachidonic acid (ARA) and 53 oxylipins (FDR q-value < 0.05). The patterns of increase for ARA, four oxylipins generated from ARA-cytochrome P-450 (CYP) (5,6-, 8,9-, 11,12-, and 14,15-diHETrEs), two oxylipins from linoleic acid (LA) and CYP (9,10-DiHOME, 12,13-DiHOME), and two oxylipins generated from LA and lipoxygenase (LOX) (9-HODE, 13-HODE) were slightly but significantly higher for the CRAN versus PLAC trial (all interaction effects, < 0.05). The untargeted proteomics analysis showed that two protein clusters differed significantly between the CRAN and PLAC trials, with CRAN-related elevations in proteins related to innate immune activation and reduced levels of proteins related to the regulation of the complement cascade, platelet activation, and binding and uptake of ligands by scavenger receptors. No trial differences were found for cortisol and muscle damage biomarkers.

CONCLUSIONS

CRAN versus PLAC juice resulted in a significant increase in CRAN-related metabolites but no differences in the gut microbiome. CRAN supplementation was associated with a transient and modest but significant post-exercise elevation in selected oxylipins and proteins associated with the innate immune system.

Address: Human Performance Laboratory, Appalachian State University, North Carolina Research Campus (NCRC), Kannapolis, NC 28081, USA.; UNCG Center for Translational Biomedical Research, University of North Carolina at Greensboro, North Carolina Research Campus (NCRC), Kannapolis, NC 28081, USA.; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.; Nutrition Research Institute, University of North Carolina at Chapel Hill, North Carolina Research Campus (NCRC), Kannapolis, NC 28081, USA.; Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.; College of Computing and Informatics, University of North Carolina at Charlotte, North Carolina Research Campus (NCRC), Kannapolis, NC 28081, USA.

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