REVIEW article

Front. Neurosci., 22 February 2022

Sec. Gut-Brain Axis

Volume 16 - 2022 | https://doi.org/10.3389/fnins.2022.833202

Enhancing the Cognitive Effects of Flavonoids With Physical Activity: Is There a Case for the Gut Microbiome?

  • 1. Department of Psychology and Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States

  • 2. Human Performance Lab, Department of Biology, Appalachian State University, Kannapolis, NC, United States

  • 3. Department of Food, Bioprocessing and Nutrition Sciences, Plants for Human Health Institute, North Carolina State University, Kannapolis, NC, United States

Abstract

Age-related cognitive changes can be the first indication of the progression to dementias, such as Alzheimer’s disease. These changes may be driven by a complex interaction of factors including diet, activity levels, genetics, and environment. Here we review the evidence supporting relationships between flavonoids, physical activity, and brain function. Recent in vivo experiments and human clinical trials have shown that flavonoid-rich foods can inhibit neuroinflammation and enhance cognitive performance. Improved cognition has also been correlated with a physically active lifestyle, and with the functionality and diversity of the gut microbiome. The great majority (+ 90%) of dietary flavonoids are biotransformed into phytoactive phenolic metabolites at the gut microbiome level prior to absorption, and these prebiotic flavonoids modulate microbiota profiles and diversity. Health-relevant outcomes from flavonoid ingestion may only be realized in the presence of a robust microbiome. Moderate-to-vigorous physical activity (MVPA) accelerates the catabolism and uptake of these gut-derived anti-inflammatory and immunomodulatory metabolites into circulation. The gut microbiome exerts a profound influence on cognitive function; moderate exercise and flavonoid intake influence cognitive benefits; and exercise and flavonoid intake influence the microbiome. We conclude that there is a potential for combined impacts of flavonoid intake and physical exertion on cognitive function, as modulated by the gut microbiome, and that the combination of a flavonoid-rich diet and routine aerobic exercise may potentiate cognitive benefits and reduce cognitive decline in an aging population, via mechanisms mediated by the gut microbiome. Mechanistic animal studies and human clinical interventions are needed to further explore this hypothesis.

Introduction

The brain can be a neglected aspect of human health. Typically, brain health is not a consideration until people reach their 50s or 60s, when brain function can become less reliable. Moreover, lifestyle choices are hardly ever considered as detrimental to brain health in an otherwise healthy adult. Importantly, the number of Americans aged 65 and older is projected to nearly double from 52 million in 2018 to 95 million by 2060 (United States Census Bureau, 2021). As the life expectancy of the world’s population increases, dementia (age-related decline from previously attained cognitive levels) is a looming threat to the individual’s healthspan, and causes a heavy economic burden to families and to society. Researchers have put considerable effort into developing interventions for those who have been diagnosed with a dementia (e.g., Alzheimer’s disease, Parkinson’s disease, and Dementia with Lewy Bodies). We posit that validating proactive strategies to prevent cognitive dysfunction in the aging demographic should be a high priority.

In this review, we will explore the case for flavonoids as a prophylactic against declining brain health, investigate the modulating role(s) of the gut microbiome, and consider evidence for the potentiating influence of moderate–to-vigorous physical activity (MVPA) combined with flavonoid intake. Improved cognition is associated with a physically active lifestyle, a healthy diet, and a robust, diverse gut microbiome (the gut-brain axis) (Schlegel et al., 2019; Westfall and Pasinetti, 2019). We and others have demonstrated that flavonoid-rich food interventions (such as cocoa, berries, or tea) can attenuate biomarkers of inflammation including neuroinflammation, effectively mitigate cognitive dysfunction and decline, and sharpen cognitive function (Macready et al., 2009; Whyte et al., 2020). Dietary flavonoids act as prebiotics; as such, they can alter the profiles and the diversity of the gut microbiome, and exercise accelerates the circulation and transport of flavonoid metabolites after gut microbiome catabolism. Here we review the extant literature and weave the three – flavonoids, exercise, and the gut microbiome – together to form a more complete picture of how lifestyle affects cognition and how we can prevent the deterioration of cognitive abilities across the lifespan.

Flavonoids and Brain Health

Flavonoids, a ubiquitous group of plant secondary metabolites with a 15-carbon structure (two phenyl rings and a heterocyclic ring; C6-C3-C6) are an indispensable component of traditional medicines, current nutraceuticals, and functional foods. Dietary flavonoids are found in tea, berryfruit, citrus and other fruit and legumes, although it is estimated that consumption in the United States falls well below dietary guidance (U.S. Department of Health and Human Services and U.S. Department of Agriculture, 2015). Over a decade ago, the potential for flavonoids to attenuate neurodegeneration was recognized (Spencer, 2009), and growing epidemiological, in vivo, and clinical evidence suggests that supplementation with flavonoid-rich foods benefits cognitive function (Letenneur et al., 2007; ; Rajaram et al., 2019; Westfall and Pasinetti, 2019; Ruotolo et al., 2020; Whyte et al., 2020). In part, the underlying mechanisms may include flavonoids’ anti-inflammatory capacity and influences on endothelial function and peripheral blood flow (; Morais et al., 2016; Warner et al., 2017; Rajaram et al., 2019). We and others have established that dietary flavonoid metabolites pass the blood brain barrier and can be localized in brain tissues (,b; Strathearn et al., 2014; ; ; Westfall and Pasinetti, 2019). Importantly, the flavonoid metabolites have been shown to deposit in brain regions that underlie learning and memory, specifically the hippocampus (Sokolov et al., 2013; ). Flavonoids are able to exert neuroprotective activity (even at the relatively low concentrations that reach the brain) by virtue of their ability to modulate protein and lipid kinase signaling pathways, and by inhibiting neuroinflammation, rather than merely through antioxidant activity. Absorbed flavonoids and their metabolites from foods (cocoa, berry, and tea) appear to directly interact with cellular and molecular targets (e.g., ERK and PI3-kinase/Akt signaling pathways) to improve neuronal connectivity and increase expression of neuromodulatory proteins (Williams and Spencer, 2012). Mechanistically, dietary flavonoid consumption promotes peripheral and cerebral vascular flow as well as neuronal survival and differentiation. Mounting evidence supports an association between flavonoid-rich plant-based diets and improved domains of cognition in aging, notably in executive functions, which are higher-order cognitive abilities subserved by the prefrontal lobe (Rajaram et al., 2019). These detriments in executive function begin to develop in midlife.

Preclinical and clinical studies with flavonoid-rich foods indicate that higher levels of flavonoid intake are related to improved cognitive performance and tempered cognitive decline (Macready et al., 2009; ; Whyte et al., 2020). Cocoa flavanol intake, for example, has been linked to greater brain oxygenation, and higher performance during cognitive challenge (), with apparent dose-dependent improvements in working memory, attention and processing speed (Socci et al., 2017). A systematic review concluded that green tea intake has a positive influence on cognition through the combined influence of green tea extract constituents, including flavonoids, L-theanine, and caffeine (Mancini et al., 2017). In preclinical experiments, however, it was administration of the green tea catechins (primarily EGCG) that were credited with improved spatial cognition learning ability in rats (improved reference and working memory) (). Berries (a dietary resource with a highly diversified flavonoid profile), have been the intervention of choice for several trials on flavonoids and cognition (; McGuire et al., 2006; Lau et al., 2007; ; Williams et al., 2008; Small et al., 2014; Shukitt-Hale et al., 2015; Miller et al., 2018; ; Whyte et al., 2020). Human clinical interventions with flavonoid subgroups anthocyanins, flavanol and flavanone over the past several years indicate potential to limit or reverse age-related declines in cognition (; ; ). Blueberry-supplemented rats demonstrated elevated hippocampal levels of cAMP-response element-binding protein and extracellular signal-related kinase, and brain-derived neurotrophic factor (BDNF) compared to age-matched controls. Alteration of these signaling proteins led to better performance on a spatial working memory task (Williams et al., 2008; Vauzour et al., 2021). BDNF, known for differentiation and survival of neurons of the CNS, plays a crucial role in delay of cognitive aging by improving hippocampal plasticity, long-term memory, and neurogenesis (). Recently, clinical results showed that even a single acute dose of a flavonoid-rich blueberry beverage (equivalent to 200 g fresh berries; recognized as a reasonable, achievable dose) attenuated a decrease in plasma concentration of BDNF, whereas BDNF levels dropped in the placebo group (). Other gut-derived neuropeptides (GLP-1, GLP-2, glucagon, etc.) affect brain activity, and can be modulated by flavonoid consumption (; ; ; ), suggesting another mechanism through which flavonoids enhance brain function.

The protective effects of flavonoid consumption occur primarily in the hippocampus, a brain area critical for memory function. A 3-month intervention with blueberry extract in non-impaired older adults showed significant improvements in delayed recognition and repetition errors (Whyte et al., 2018). Krikorian et al. (2010) investigated blueberry supplementation in older adults with mild cognitive impairment (MCI), finding robust improvement in a verbal paired-associate learning test. In a trial on working memory (WM), a significant increase in signaling in the left inferior parietal gyrus and left pre-central gyrus (enhanced neural activation) was found in older adults consuming blueberries, although behaviorally, performance on the WM task improved only marginally (p = 0.08) (). More recently, a 24-week combined blueberry and/or fish oil intervention in older adults with cognitive deficits concluded that blueberry intervention improved cognitive efficiency for everyday life activities and resilience against extraneous disturbances during recognition memory tasks (McNamara et al., 2018).

In one of the longest duration blueberry interventions to date (), we randomized older adults (aged 65–80) who were experiencing age-related cognitive changes to 6 months of wild blueberry or placebo. Participants who were not experiencing cognitive changes were included as a reference group. Participants were tested for cognitive abilities using the Montreal Cognitive Assessment (MoCA) (Nasreddine et al., 2005). Age-related cognitive change was operationalized as 1–1.5 SD below the standardized mean. Participants with lower scores (>1.5 SD below the mean) were excluded from participation and referred to their physician. Cognitive abilities were gauged using the Cambridge Neuropsychological Test Automated Battery (CANTAB) and an electrophysiological technique known as event-related potentials (ERP). Those who consumed 35 g lyophilized blueberry powder/day (equivalent to ∼300 g or 2 cups fresh fruit) did not experience any further decline in abilities, whereas those on placebo did. In addition, those who consumed blueberries daily exhibited improvement in speed of processing (a basic cognitive ability that underlies all other cognitive abilities) (Figure 1, left). This improvement was evidenced in the behavioral tests (CANTAB) as well as the electrophysiological tests (ERP). In addition, recognition memory improved to the level of the reference group in the group consuming blueberries (Figure 1, right). That is, as measured in the ERP component N2, those consuming blueberries showed greater differentiation between processing (N2) in response to novel versus familiar stimuli relative to those consuming placebo. Thus, consumption of wild blueberries halted cognitive decline and improved speed of processing and recognition memory ().

FIGURE 1

In sum, consumption of foods containing flavonoids appears to act in the brain to improve function (Letenneur et al., 2007; ). Flavonoids may enhance brain blood flow and block beta-amyloid plaque buildup (a hallmark of Alzheimer’s disease) in the brain. As prevention is generally preferred and more readily achieved than remediation, we propose that consumption of flavonoid foods are central to the prevention of cognitive decline and quite possibly other brain functions such as executive function, attention, and memory (Socci et al., 2017; Westfall and Pasinetti, 2019).

Gut Microbiome and Cognition

The gut microbiome, an interactive community of microorganisms in the gastrointestinal tract, is highly influenced by diet (Westfall and Pasinetti, 2019; Zmora et al., 2019). Until very recently, only loosely attributed theories about the gastrointestinal microbial community’s impact on brain function and behavior were available, based on highly controlled animal studies. Recent trials, however, have shown that institutionalized study participants experiencing cognitive decline have altered gut bacterial composition compared to participants with typical cognitive ability (Scheperjans et al., 2015; ). These studies imply that the composition and diversity of gut microbiota may significantly modulate gut-brain communication, contributing to changes in cognition during aging (; Manderino et al., 2017). It has even been suggested that “westernization” of lifestyles, including western diets and the habitual use of antibiotic treatments which disrupt the gut microbiome, may contribute to neurological dysfunction (Novotny et al., 2019).

A comparative review of almost a score of recent human clinical trials suggested that deliberate intervention to change gut microbiota composition can produce a positive bacteria-cognition relationship, eliciting improvements in visuospatial memory, verbal learning, and attention (Tooley, 2020). In this narrative review, the importance of recognizing microbiota signatures associated with cognitive performance, and identifying potential gut microbiota interventions (including diet and lifestyle) were highlighted. In another clinical trial, an increased prevalence of Bacteroides in the gut microbiome was associated with mild cognitive impairment in geriatric patients, evidenced by impaired memory and lower global cognitive function scores (Saji et al., 2019). The gut microbiota-brain axis has previously been implicated in development of neurological diseases including Alzheimer’s disease, and is proposed as a target for cognitive decline therapeutics (). Deliberate modulation of gut microbiome profiles, either by fecal transplantation or probiotic interventions, is gaining research momentum in the quest to control the pathogenesis of Alzheimer’s disease (Wang and Dykes, 2021).

The microbiota-gut-brain communication is bidirectional; changes in the composition of the gut microbiota are associated with behavioral and cognitive alternations, and, perturbations in behavior also alter the composition of the gut microbiota (Mu et al., 2016; ). Gut microbial metabolites (including postbiotics such as bile acids, short chain fatty acids, and tryptophan metabolites, as well as phenolic metabolites from flavonoid catabolism) are major mediators of the microbiome-gut-brain axis (; ). We posit that cognition (memory and executive function) are linked to the composition, functionality, and diversity of the gut microbiota, in part because gut microbiota regulate the production and delivery of microbiome-catabolized phenolic metabolites into circulation following intake of flavonoid-rich foods (; Manderino et al., 2017; ).

Using clinically validated behavioral measures and electrophysiological measures of brain activity on a cohort of older adults between 67 and 83 years of age and a diversity metric for the gut microbiome, we recently found that gut microbial diversity, as modulated by diet/flavonoid intake, was a predictor of cognitive performance in free-living aging adults (). We saw a significant association between behavioral measures of paired-associate learning and spatial working memory, and the α-diversity of the gut microbiome of older adults; poorer performance (indicative of cognitive dysfunction) predicted lower gut microbiome diversity (). Poorer performance on spatial working memory tests and paired associates learning was related to lower Shannon α-scores (a diversity metric) (Peet, 1974) in the gut microbiome (Figure 2). Electrophysiology waveforms related to attention differentially predicted gut microbiome diversity, such that those with better attention allocation and better sustained attention abilities had more diverse gut microbiomes. Thus, higher gut microbiome diversity is related to better brain function as measured by cognitive tests. Importantly, in this same sample, we related free-living consumption of berries to the diversity score and found that those who reported eating more servings of berries across three 24-h diet recalls had a more diverse gut microbiome) (). Interacting ingested flavonoids can serve a pivotal role in changing or reshaping the gut microbiota, increasing populations of Lactobacilli spp. and Bifidobacteria spp. and inhibiting gut pathogens (Wang et al., 2021). Reduced abundance of pathogenic bacteria in the gut (Clostridium perfringens, C. difficile, and gram-negative Bacteroides spp.) without inhibition of commensal bacteria (clostridia and lactobacilli) has been linked to prebiotic polyphenol intake (Lee et al., 2006; Tuohy et al., 2012; ). Separate in vivo feeding trials with berry species (cranberry and grape) led to consistent decrease in proportion of Firmicutes to Bacteroidetes, and remarkable increase in growth of Akkermansia muciniphila in the microbial community (; Roopchand et al., 2015; Wang et al., 2021).

FIGURE 2

.

In sum, consumption of flavonoids is related to improved speed of processing and recognition memory; consumption of berry flavonoids is related to a more highly diverse gut microbiome; and higher α-diversity in the gut microbiome is related to better cognitive abilities (). The next section will further explore how flavonoid consumption alters the gut microbiome.

Flavonoids and the Gut Microbiome

Interactions between the microbiome and dietary flavonoids have dual impacts on human health. First, diet, including prebiotic flavonoid-rich foods, has a dramatic influence on the composition and consequently the functionality of the gut microbiome. The term prebiotic usually refers to indigestible dietary fibers that benefit the gut microbiota, and flavonoids are considered to have prebiotic-like effects as their consumption also feeds/benefits commensal bacteria in the gut. Ingesting prebiotics alters gut microbial community structure, favoring beneficial commensal bacteria, and reducing levels of opportunistic species (; Roopchand et al., 2015; Westfall et al., 2018). Prebiotic flavonoids’ metabolites also have a profound influence on inflammation in the gut, improving the epithelial barrier’s integrity and activating tight junctions (; Westfall and Pasinetti, 2019). Interestingly, the flavonoids do not even need to be absorbed to exert these benefits; as xenobiotic compounds, they induce cellular stress and an overcompensation reaction to maintain homeostasis, producing a hormetic response that improves cell and barrier function (). The same gut-derived flavonoid metabolites that suppress chronic intestinal inflammation are integral to inhibition of neuroinflammation (Spencer et al., 2012).

In tandem, the gut microbiome significantly impacts flavonoid bioavailability via extensive pre-systemic metabolism to release active metabolites with therapeutic efficacy, including for cognitive benefits. Only a small percentage of dietary flavonoids are absorbed from the small intestine, before they reach the colonic microbiota. Instead, most dietary flavonoids are biotransformed by commensal gut microbiota into diverse bioactive phenolic metabolites, and are delivered into circulation where they elicit health-protective effects (). The bioavailability of flavonoids is therefore largely dependent on their catabolism by the gut microbiome and subsequent secondary xenobiotic biotransformation in the liver before entering circulation in the form of phenolic metabolites (; Williamson et al., 2018; Westfall and Pasinetti, 2019). Thus, flavonoid bioavailability depends, in part, on the polyphenol-microbiota interactions, which ultimately regulate both bioavailability and bioactivity ().

Extensive evidence indicates that biotransformed metabolites from lower-intestinal bacterial catabolism of dietary flavonoids mediate anti-inflammatory activity in multiple tissues of the body (Moco et al., 2012; Morais et al., 2016; Tomas-Barberan et al., 2016; Schell et al., 2019; ; Martin and Ramos, 2021). Notably, diseases which cause chronic low-grade inflammation (metabolic syndrome, diabetes, and arthritis) are strongly linked to cognitive decline in aging (Santoro et al., 2014; Noble et al., 2017). Strategies to attenuate the chronic, low grade inflammatory status characteristic of aging adults (inflammaging) can evoke systemic benefits on both physical and cognitive health. The gut microbiota is also essential for producing the full battery of bioavailable plasma- and brain-bioactive metabolites that have neuroprotective capacity (Westfall and Pasinetti, 2019). Long-term supplementation with a probiotic could promote health by introducing colonic microbiota that make flavonoids more bioavailable (Pereira-Caro et al., 2015; Westfall and Pasinetti, 2019).

Evidence from our team and others shows that gut microbial-derived metabolites of dietary flavonoids are anti-inflammatory and immunomodulatory, can have greater bioactivity than their parent/precursor structures, and have additive or synergistic effects collectively (; ; ; Nieman et al., 2017, 2018; Warner et al., 2017). Indeed, daily consumption of anthocyanins in a diet-induced obese mouse model with either healthy or antibiotic-disrupted gut microbiota resulted in reduced body weight gain and improved glucose metabolism, but only in mice with intact gut microbiota (). The bidirectional breakdown of flavonoids into active and more bioaccessible metabolites and concurrent modulation of the gut microbial community by these metabolites, both contribute to positive health outcomes.

So far, we have described the positive associations between flavonoid ingestion and cognitive health; the connections between a robust microbiome and cognitive health; and the two-way interactions between the gut microbiome and ingested flavonoids, which mediate both the potency and bioavailability of flavonoid metabolites; and the composition and functionality of the microbiome. How might lifestyle factors, aside from diet, have a bearing on these cognition-relevant influences?

Physical Activity as a Mediator

A physically active lifestyle is intrinsically linked to brain health. Physically active people are less likely to demonstrate cognitive decline, all-cause dementia, vascular dementia, and Alzheimer’s disease; most data support MVPA for at least 150 min per week (Middleton et al., 2008; Voss et al., 2011; ; Napoli et al., 2014; Piercy and Troiano, 2018; Minghui, 2019; ). MVPA for elderly adults has benefits for cognitive performance, brain function, and brain structure (Voss et al., 2011). Most meta-analyses and systematic reviews support that regular MVPA improves various aspects of cognitive function including executive function (EF), language ability, visuospatial ability, and memory in older adults with cognitive impairment (; Zhou et al., 2020). When physical activity was directly monitored, participants engaging in recommended levels of MVPA had lower incidence of cognitive impairment and better maintenance of EF and memory (Zhu et al., 2016).

The Physical Activity Guidelines for Americans state that some benefits of physical activity on cognitive health occur immediately after a session of MVPA (acute effect); these include reduced anxiety, improved sleep, and improved cognitive function (Piercy and Troiano, 2018). With regular MVPA by older adults with or without impaired cognitive health (chronic effect), even greater cognitive benefits are experienced including improvements in EF, attention, memory, crystallized intelligence, and processing speed (Weng et al., 2015; Tsukamoto et al., 2017; Piercy and Troiano, 2018). The substantial cognitive benefits observed with at least 150 min per week MVPA are further amplified when MVPA is increased to 300 min per week. Potential mechanisms for MVPA’s positive impacts on cognition include changes in brain structures (Rovio et al., 2010; ), increases in cerebral blood flow and oxygentation (Rooks et al., 2010; Tsubaki et al., 2021), enhanced immune function, reductions in inflammation including neuroinflammation, and/or increase neurotrophic factors (Nieman et al., 2013; ; ; Rehfeld et al., 2018; Minghui, 2019). Habitual walking in late adulthood has been correlated with higher gray matter volume, coincident with reduced risk of cognitive dysfunction (). Flavonoid benefits coincident with physical exertion are in part due to antioxidant and anti-inflammatory effects, but also since these polyphenols activate the same adaptive cell signaling pathways as physical exertion, they are believed to complement adaptive benefits of exercise and support performance ().

Moderate-to-vigorous physical activity combined with flavonoid ingestion may improve post-exercise metabolic recovery (; Nieman et al., 2019, 2020), and augment cognitive function (Tsukamoto et al., 2018). Effects of MVPA and flavonoid ingestion may be mediated in part through elevations in circulating gut-derived phenolic metabolites, but this linkage has not yet been conclusively established (Nieman et al., 2013, 2018). MVPA does enhance the release of gut-derived phenolic metabolites following chronic flavonoid ingestion. In a randomized trial with long-distance runners featuring a 17-day intervention with a flavonoid-rich supplement (or placebo), serum metabolic signatures from colonic flavonoid metabolites (derived from green tea or berries) were significantly elevated for at least 14 h coincident with a 3-day intensified exercise period, and these changes persisted through post-exercise recovery (Nieman et al., 2013). Microbial metabolites were dramatically elevated once the workout commenced – the release of the metabolites into plasma was stimulated by physical exertion. Release of these microbial metabolites into circulation significantly countered the athletes’ typical post-exercise susceptibility to virus infection, by depressing ex vivo viral replication and attenuating virulence ().

In another study, the combination of 2 weeks of flavonoid supplementation and acute exercise (both 45 min brisk walking and 2.5 h running) enhanced the translocation of gut-derived phenolics into circulation (Figure 3; Nieman et al., 2018). The pre-study plasma concentration of gut-derived phenolic metabolites was 40% higher in the leaner and fitter runners than in the walkers. These data indicated that acute exercise bouts (both brisk walking and intensive running) combined with flavonoid supplementation, and an elevated fitness status associated with habitual running, were linked to elevations in plasma levels of gut-derived phenolics.

FIGURE 3

Several underlying mechanisms could explain these results including flavonoid- and exercise-induced changes in gut permeability and transporter function, increases in gut microbiota richness, and altered gastrointestinal motility and transport rate (Nieman et al., 2018). Chronic MVPA can modify the composition and functional capacity of the gut microbiota (). Cross-sectional human studies have revealed greater α-diversity and an enriched profile of short chain fatty acids (SCFAs) in athletes compared to sedentary controls (; Mailing et al., 2019; Nieman and Pence, 2020; Zhu et al., 2020). One examination of phenotypic features across 3,400 individuals found a linkage between microbiome diversity and MVPA frequency and duration that was independent of major dietary factors and BMI (Manor et al., 2020) and longitudinal MVPA studies support some selective changes on the gut microbiome, especially when vigorous exercise training is sustained for months (; ; ). The interaction between MVPA and the gut microbiota is bidirectional. As already noted, flavonoids are catabolized by and influence composition of the microbiota, and exercise stimulated the bioavailability of flavonoid metabolites (Nieman et al., 2018). The gut microbiota also has an influence on exercise performance by producing SCFAs that increase muscle blood flow and insulin sensitivity, and can be utilized as fuel ().

It is therefore reasonable to posit that the connection between physical activity (e.g., exercise), dietary flavonoids, and improved cognition (memory and executive function) is linked to their demonstrated influence on the microbiome (diversity and functionality) (Figure 4).

FIGURE 4

Conclusion

A complex interaction of factors (lifestyle, diet, genetics, and environment) all appear to exert influence on cognition in the aging brain. Emerging evidence suggests that there may be potentiating interactions between some of these, including flavonoid intake, microbiome, and physical activity levels (exercise). What are the mechanisms responsible for the benefits to cognition, and how can they be fully demonstrated? We hypothesize that it is the phytoactive metabolites from flavonoid ingestion, after catabolism at the gut microbiome level, that interact with cellular and molecular targets (signaling pathways) to improve neuron connectivity and promote vascular and peripheral flow in the brain. Exercise has demonstrated ability to provoke a surge of these phytoactive flavonoid metabolites into circulation. It follows that the positive cognitive benefits from dietary flavonoids and regular moderate exercise may be a consequence of the enhanced circulation of gut-derived flavonoid metabolites, mediated by the activities of the colonic microbiota.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Statements

Author contributions

CC: cognition. DN: physical movement. AN: microbiome. ML: flavonoids/metabolites. All authors contributed to and approved the manuscript.

Funding

Some of the work described in this review was partially funded through USDA-ARS Project Nos. 0204-41510-001-24S and USDA NIFA Hatch Project 02689.

Acknowledgments

First and foremost, we thank the generous people who participate in our research. Without them, our research would literally be impossible.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  • 1

    AhlesS.JorisP. J.PlatJ. (2021). Effects of berry anthocyanins on cognitive performance, vascular function and cardiometabolic risk markers: a systematic review of randomized placebo-controlled intervention studies in humans.Int. J. Mol. Sci.22:6482. 10.3390/ijms22126482

  • 2

    AhmedM.HensonD. A.SandersonM. C.NiemanD. C.GillittN. D.LilaM. A. (2014). The protective effects of a polyphenol-enriched protein powder on exercise-induced susceptibility to virus infection.Phytother. Res.2818291836. 10.1002/ptr.5208

  • 3

    AllenJ. M.MailingL. J.NiemiroG. M.MooreR.CookM. D.WhiteB. A.et al (2018). Exercise alters gut microbiota composition and function in lean and obese humans.Med. Sci. Sports Exerc.50747757. 10.1249/MSS.0000000000001495

  • 4

    AminH. P.CzankC.RaheemS.ZhangQ.BottingN. P.CassidyA.et al (2015). Anthocyanins and their physiologically relevant metabolites alter the expression of IL-6 and VCAM-1 in CD40L and oxidized LDL challenged vascular endothelial cells.Mol. Nutr. Food Res.5910951106. 10.1002/mnfr.201400803

  • 5

    AndersonJ. R.CarrollI.Azcarate-PerilM. A.RochetteA. D.HeinbergL. J.PeatC.et al (2017). A preliminary examination of gut microbiota, sleep, and cognitive flexibility in healthy older adults.Sleep Med.38104107.

  • 6

    AngelinoD. C.CarregosaD.Domenech-CocaC.SaviM.FigueiraI.BrindaniN.et al (2019). 5-(hydroxyphenyl)–valerolactone-sulfate, a key microbial metabolite of flavan-3-ols, is able to reach the brain: evidence from different in silico, in vitro and in vivo experimental models.Nutrients11:2678.

  • 7

    AnheF. F.RoyD.PilonG.DudonnéS.MatamorosS.VarinT. V.et al (2014). A polyphenol-rich cranberry extract protects from diet-induced obesity, insulin resistance and intestinal inflammation in association with increased Akkermansia spp. population in the gut microbiota of mice.Gut64872883.

  • 8

    AyazM.SadiqA.JunaidM.UllahF.OvaisM.UllahI.et al (2019). Flavonoids as prospective neuroprotectants and their therapeutic propensity in aging associated neurological disorders.Front. Aging Neurosci.11:155. 10.3389/fnagi.2019.00155

  • 9

    BadshahH.UllahI.KimS. E.KimT. H.LeeH. Y.KimM. O. (2013). Anthocyanins attenuate body weight gain via modulating neuropeptide Y and GABAB1 receptor in rats hypothalamus.Neuropeptides47347353. 10.1016/j.npep.2013.06.001

  • 10

    BajajJ. S.AhluwaliaV.SteinbergJ. L.HobgoodS.BolingP. A.GodschalkM.et al (2016). Elderly patients have an altered gut-brain axis regardless of the presence of cirrhosis.Sci. Rep.6:38481. 10.1038/srep38481

  • 11

    BanfiD.MoroE.BosiA.BistolettiM.CerantolaS.CremaF.et al (2021). Impact of microbial metabolites on microbiota-gut-brain axis in inflammatory bowel disease.Int. J. Mol. Sci.22:1623. 10.3390/ijms22041623

  • 12

    BartonW.PenneyN. C.CroninO.Garcia-PerezI.MolloyM. G.HolmesE.et al (2018). The microbiome of professional athletes differs from that of more sedentary subjects in composition and particularly at the functional metabolic level.Gut67625633. 10.1136/gutjnl-2016-313627

  • 13

    BirdR. J.HoggardN.Aceves-MartinsM. (2021). The effect of grape interventions on cognitive and mental performance in healthy participants and those with mild cognitive impairment: a systematic review of randomized controlled trials. Nutr. Rev.nuab025. 10.1093/nutrit/nuab025

  • 14

    BoespflugE. L.EliassenJ. C.DudleyJ. A.ShidlerM. D.KaltW.SummerS. S.et al (2018). Enhanced neural activation with blueberry supplementation in mild cognitive impairment.Nutr. Neurosci.21297305. 10.1080/1028415X.2017.1287833

  • 15

    BorsomE. M.LeeK.CopeE. K. (2020). Do the bugs in your gut eat your memories? relationship between gut microbiota and Alzheimer’s disease.Brain Sci.10:814. 10.3390/brainsci10110814

  • 16

    CalabreseV.CorneliusC.Dinkova-KostovaA. T.IavicoliI.Di PaolaR.KoverechA.et al (2012). Cellular stress responses, hormetic phytochemicals and vitagenes in aging and longevity.Biochim. Biophys. Acta1822753783. 10.1016/j.bbadis.2011.11.002

  • 17

    CanipeL. G.SiodaM.CheathamC. L. (2021). Diversity of the gut-microbiome related to cognitive behavioral outcomes in healthy older adults.Arch. Gerontol. Geriatr.96:104464. 10.1016/j.archger.2021.104464

  • 18

    CheathamC.MillsapG.ChaiS. C.CanipeG.SheppardK. W.LilaM. A. (2022). Consumption of wild blueberries for 6 months improves speed of processing in 65- to 80-year-olds experiencing mild cognitive decline. Am. J. Clin. Nutr.

  • 19

    ChenF. T.EtnierJ. L.ChanK. H.ChiuP. K.HungT. M.ChangY. K. (2020). Effects of exercise training interventions on executive function in older adults: a systematic review and meta-analysis.Sports Med.5014511467. 10.1007/s40279-020-01292-x

  • 20

    ChuC.MurdockM. H.JingD.WonT. H.ChungH.KresselA. M.et al (2019). The microbiota regulate neuronal function and fear extinction learning.Nature574543548. 10.1038/s41586-019-1644-y

  • 21

    CremoniniE.DaveriE.MastaloudisA.OteizaP. I. (2021). (-)-Epicatechin and anthocyanins modulate GLP-1 metabolism: evidence from C57BL/6J mice and GLUTag cells.J. Nutr.15114971506. 10.1093/jn/nxab029

  • 22

    CroninO.BartonW.SkuseP.PenneyN. C.Garcia-PerezI.MurphyE. F.et al (2018). A prospective metagenomic and metabolomic analysis of the impact of exercise and/or whey protein supplementation on the gut microbiome of sedentary adults.mSystems3:e00044-18. 10.1128/mSystems.00044-18

  • 23

    CryanJ. F.DinanT. G. (2012). Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour.Nat. Rev. Neurosci.13701712. 10.1038/nrn3346

  • 24

    CunhaC.BrambillaR.ThomasK. (2010). A simple role for BDNF in learning and memory?Front. Mol. Neurosci.3:1. 10.3389/neuro.02.001.2010

  • 25

    DeleddaA.AnnunziataG.TenoreG. C.PalmasV.ManzinA.VelluzziF. (2021). Diet-derived antioxidants and their role in inflammation, obesity and gut microbiota modulation.Antioxidants10:708. 10.3390/antiox10050708

  • 26

    DevenneyK. E.SandersM. L.LawlorB.Olde RikkertM. G. M.SchneiderS., and NeuroExercise Study Group (2017). The effects of an extensive exercise programme on the progression of mild cognitive impairment (MCI): study protocol for a randomised controlled trial.BMC Geriatr.17:75. 10.1186/s12877-017-0457-9

  • 27

    DinanT. G.StillingR. M.StantonC.CryanJ. F. (2015). Collective unconscious: how gut microbes shape human behavior.J. Psychiatr. Res.6319. 10.1016/j.jpsychires.2015.02.021

  • 28

    DocampoM.OlubuA.WangX.PasinettiG.DixonR. A. (2017). Glucuronidated flavonoids in neurological protection: structural analysis and approaches for chemical and biological synthesis.J. Agric. Food Chem.6576077623. 10.1021/acs.jafc.7b02633

  • 29

    DoddG. F.WilliamsC. M.ButlerL. T.SpencerJ. P. E. (2019). Acute effects of flavonoid-rich blueberry on cognitive and vascular function in healthy older adults.Nutr. Heal. Aging5119132.

  • 30

    Duda-ChodakA.TarkoT.SatoraP.SrokaP. (2015). Interaction of dietary compounds, especially polyphenols, with the intestinal microbiota: a review.Eur. J. Nutr.54325341. 10.1007/s00394-015-0852-y

  • 31

    DuffyK. B.SpanglerE. L.DevanB. D.GuoZ.BowkerJ. L.JanasA. M.et al (2008). A blueberry-enriched diet provides cellular protection against oxidative stress and reduces a kainate-induced learning impairment in rats.Neurobiol. Aging2916801689.

  • 32

    EricksonK. I.RajiC. A.LopezO. L.BeckerJ. T.RosanoC.NewmanA. B.et al (2010). Physical activity predicts gray matter volume in late adulthood: the cardiovascular health study.Neurology7514151422. 10.1212/WNL.0b013e3181f88359

  • 33

    EspinJ. C.Gonzalez-SarriasA.Tomas-BarberanF. (2017). The gut microbiota: a key factor in the therapeutic effects of (poly)phenols.Biochem. Pharmacol.1398293.

  • 34

    EspositoD.DamsudT.WilsonM.GraceM. H.StrauchR.LiX.et al (2015). Black currant anthocyanins attenuate weight gain and improve glucose metabolism in diet-induced obese mice with intact, but not disrupted, gut microbiome.J. Agric. Food Chem.6361726180. 10.1021/acs.jafc.5b00963

  • 35

    FlanaganE.MullerM.HornbergerM.VauzourD. (2018). Impact of flavonoids on cellular and molecular mechanisms underlying age-related cognitive decline and neurodegeneration.Curr. Nutr. Rep.74957. 10.1007/s13668-018-0226-1

  • 36

    GalliR. L.BielinskiD. F.SzprengielA.Shukitt-HaleB.JosephJ. A. (2006). Blueberry supplemented diet reverses age-related decline in hippocampal HSP70 neuroprotection.Neurobiol. Aging27344350.

  • 37

    GardenerS. L.Rainey-SmithS. R.WeinbornM.BondonnoC. P.MartinsR. N. (2021). Intake of products containing anthocyanins, flavanols, and flavanones, and cognitive function: a narrative review.Front. Aging Neurosci.13:640381. 10.3389/fnagi.2021.640381

  • 38

    GowA. J.MortensenE. L.AvlundK. (2012). Activity participation and cognitive aging from age 50 to 80 in the Glostrup 1914 cohort.J. Am. Geriatr. Soc.6018311838. 10.1111/j.1532-5415.2012.04168.x

  • 39

    GrattonG.WeaverS. R.BurleyC. V.LowK. A.MaclinE. L.JohnsP. W.et al (2020). Dietary flavanols improve cerebral cortical oxygenation and cognition in healthy adults.Sci. Rep.101940919409. 10.1038/s41598-020-76160-9

  • 40

    GuY.YuS.ParkJ. Y.HarvatineK.LambertJ. D. (2014). Dietary cocoa reduces metabolic endotoxemia and adipose tissue inflammation in high-fat fed mice.J. Nutr. Biochem.25439445. 10.1016/j.jnutbio.2013.12.004

  • 41

    HaqueA. M.HashimotoM.KatakuraM.TanabeY.HaraY.ShidoO. (2006). Long-term administration of green tea catechins improves spatial cognition learning ability in rats.J. Nutr.13610431047.

  • 42

    HeinS.WhyteA. R.WoodE.Rodriguez-MateosA.WilliamsC. M. (2019). Systematic review of the effects of blueberry on cognitive performance as we age.J. Gerontol. A Biol. Sci. Med. Sci.74984995. 10.1093/gerona/glz082

  • 43

    HughesR. L.HolscherH. D. (2021). Fueling gut microbes: a review of the interaction between diet, exercise, and the gut microbiota in athletes.Adv. Nutr.1221902215.

  • 44

    HurstR. D.LyallK. A.RobertsJ. M.PerthanerA.WellsR. W.CooneyJ. M.et al (2019). Consumption of an anthocyanin-rich extract made from New Zealand blackcurrants prior to exercise may assist recovery from oxidative stress and maintains circulating neutrophil function: a pilot study.Front. Nutr.6:73. 10.3389/fnut.2019.00073

  • 45

    JanleE. M.LilaM. A.GrannanM.WoodL.HigginsA.YousefG. G.et al (2010a). Method for evaluating the potential of C14 labeled plant polyphenols to cross the blood-brain barrier using accelerator mass spectrometry.Nucl. Instrum. Methods Phys. Res. B26813131316. 10.1016/j.nimb.2009.10.161

  • 46

    JanleE. M.LilaM. A.GrannanM.WoodL.HigginsA.YousefG. G.et al (2010b). Pharmacokinetics and tissue distribution of 14C-labeled grape polyphenols in the periphery and the central nervous system following oral administration.J. Med. Food13926933. 10.1089/jmf.2009.0157

  • 47

    JenningsA.KochM.JensenM. K.BangC.KassubekJ.MüllerH. P.et al (2019). The role of the gut microbiome in the association between habitual anthocyanin intake and visceral abdominal fat in population-level analysis.Am. J. Clin. Nutr.111340350.

  • 48

    KashiwabaraM.AsanoK.MizuyoshiT.KobayashiH. (2016). Suppression of neuropeptide production by quercetin in allergic rhinitis model rats.BMC Complement Altern. Med.16:132. 10.1186/s12906-016-1123-z

  • 49

    KernT.BlondM. B.HansenT. H.RosenkildeM.QuistJ. S.GramA. S.et al (2020). Structured exercise alters the gut microbiota in humans with overweight and obesity-A randomized controlled trial.Int. J. Obes44125135. 10.1038/s41366-019-0440-y

  • 50

    KrikorianR.ShidlerM. D.NashT. A.KaltW.Vinqvist-TymchukM. R.Shukitt-HaleB.et al (2010). Blueberry supplementation improves memory in older adults.J. Agric. Food Chem.5839964000. 10.1021/jf9029332

  • 51

    LauF. C.BielinskiD. F.JosephJ. A. (2007). Inhibitory effects of blueberry extract on the production of inflammatory mediators in lipopolysaccharide-activated BV2 miroglia.J. Neurosci. Res.8510101017. 10.1002/jnr.21205

  • 52

    LeeH. C.JennerA. M.LowC. S.LeeY. K. (2006). Effect of tea phenolics and their aromatic fecal bacterial metabolites on intestinal microbiota.Res. Microbiol.157876884. 10.1016/j.resmic.2006.07.004

  • 53

    LetenneurL.Proust-LimaC.Le GougeA.DartiguesJ.Barberger-GateauP. (2007). Flavonoid intake and cognitive decline over a 10-year period.Am. J. Epidemiol.16513641371. 10.1093/aje/kwm036

  • 54

    LilaM. A.Burton-FreemanB.GraceM.KaltW. (2016). Unraveling anthocyanin bioavailability for human health.Annu. Rev. Food Sci. Technol.7375393. 10.1146/annurev-food-041715-033346

  • 55

    MacreadyA. L.KennedyO. B.EllisJ. A.WilliamsC. M.SpencerJ. P.ButlerL. T. (2009). Flavonoids and cognitive function: a review of human randomized controlled trial studies and recommendations for future studies.Genes Nutr.4227242. 10.1007/s12263-009-0135-4

  • 56

    MailingL. J.AllenJ. M.BufordT. W.FieldsC. J.WoodsJ. A. (2019). Exercise and the gut microbiome: a review of the evidence, potential mechanisms, and implications for human health.Exerc. Sport Sci. Rev.477585. 10.1249/JES.0000000000000183

  • 57

    ManciniE.BeglingerC.DreweJ.ZanchiD.LangU. E.BorgwardtS. (2017). Green tea effects on cognition, mood and human brain function: a systematic review.Phytomedicine342637.

  • 58

    ManderinoL.CarrollI.Azcarate-PerilM. A.RochetteA.HeinbergL.PeatC.et al (2017). Preliminary evidence for an association between the composition of the gut microbiome and cognitive function in neurologically healthy older adults.J. Int. Neuropsychol. Soc.23700705. 10.1017/S1355617717000492

  • 59

    ManorO.DaiC. L.KornilovS. A.SmithB.PriceN. D.LovejoyJ.et al (2020). Health and disease markers correlate with gut microbiome composition across thousands of people.Nat. Commun.11:5206. 10.1038/s41467-020-18871-1

  • 60

    MartinM. A.RamosS. (2021). Impact of dietary flavanols on microbiota, immunity and inflammation in metabolic diseases.Nutrients13:850. 10.3390/nu13030850

  • 61

    McGuireS. O.SortwellC. E.Shukitt-HaleB.JosephJ. A.HejnaM. J.CollierT. J. (2006). Dietary supplementation with blueberry extract improves survival of transplanted dopamine neurons.Nutr. Neurosci.9251258. 10.1080/10284150601086134

  • 62

    McNamaraR. K.KaltW.ShidlerM. D.McDonaldJ.SummerS. S.SteinA. L.et al (2018). Cognitive response to fish oil, blueberry, and combined supplementation in older adults with subjective cognitive impairment.Neurobiol. Aging64147156.

  • 63

    MiddletonL. E.MitnitskiA.FallahN.KirklandS. A.RockwoodK. (2008). Changes in cognition and mortality in relation to exercise in late life: a population based study.PLoS One3:e3124. 10.1371/journal.pone.0003124

  • 64

    MillerM. G.HamiltonD. A.JosephJ. A.Shukitt-HaleB. (2018). Dietary blueberry improves cognition among older adults in a randomized, double-blind, placebo-controlled trial.Eur. J. Nutr.5711691180. 10.1007/s00394-017-1400-8

  • 65

    MinghuiR. (2019). Risk Reduction of Cognitive Decline and Dementia.Geneva: World Health Organization. WHO guidelines.

  • 66

    MocoS.MartinF. P.RezziS. (2012). Metabolomics view on gut microbiome modulation by polyphenol-rich foods.J. Proteome Res.1147814790. 10.1021/pr300581s

  • 67

    MoraisC.de RossoV.EstadellaD.PisaniL. (2016). Anthocyanins as inflammatory modulators and the role of the gut microbiota.J. Nutri. Biochem.3317.

  • 68

    MuC.YangY.ZhuW. (2016). Gut microbiota: the brain peacekeeper.Front. Microbiol.7:345. 10.3389/fmicb.2016.00345

  • 69

    NapoliN.ShahK.WatersD. L.SinacoreD. R.QuallsC.VillarealD. T. (2014). Effect of weight loss, exercise, or both on cognition and quality of life in obese older adults.Am. J. Clin. Nutr.100189198. 10.3945/ajcn.113.082883

  • 70

    NasreddineZ. S.PhillipsN. A.BedirianV.CharbonneauS.WhiteheadV.CollinI.et al (2005). The Montreal cognitive assessment, MoCA: a brief screening tool for mild cognitive impairment.J. Am. Geriatr. Soc.53695699.

  • 71

    NiemanD.GillittN.ChenG.ZhangQ.ShaW.KayC. D.et al (2020). Blueberry and/or banana consumption mitigate cytochrome P450 oxylipin generation during recovery from 75-km cycling: a randomized trial.Front. Nutr.7:121. 10.3389/fnut.2020.00121

  • 72

    NiemanD.PenceB. (2020). Exercise immunology: future directions.J. Sport Health Sci.9432445.

  • 73

    NiemanD. C.GillittN. D.KnabA. M.ShanelyR. A.PappanK. L.JinF.et al (2013). Influence of a polyphenol-enriched protein powder on exercise-induced inflammation and oxidative stress in athletes: a randomized trial using a metabolomics approach.PLoS One8:e72215. 10.1371/journal.pone.0072215

  • 74

    NiemanD. C.KayC. D.RathoreA. S.GraceM. H.StrauchR. C.StephanE. H.et al (2018). Increased plasma levels of gut-derived phenolics linked to walking and running following two weeks of flavonoid supplementation.Nutrients10:1718. 10.3390/nu10111718

  • 75

    NiemanD. C.LilaM. A.GillittN. D. (2019). Immunometabolism: a multi-omics approach to interpreting the influence of exercise and diet on the immune system.Annu. Rev. Food Sci. Technol.10341363. 10.1146/annurev-food-032818-121316

  • 76

    NiemanD. C.RamamoorthyS.KayC. D.GoodmanC. L.CappsC. R.ShueZ. L.et al (2017). Influence of ingesting a flavonoid-rich supplement on the metabolome and concentration of urine phenolics in overweight/obese women.J. Proteome Res.1629242935.

  • 77

    NobleE. E.HsuT. M.KanoskiS. E. (2017). Gut to brain dysbiosis: mechanisms linking Western diet consumption, the microbiome, and cognitive impairment.Front. Behav. Neurosci.11:9. 10.3389/fnbeh.2017.00009

  • 78

    NovotnyM.KlimovaB.ValisM. (2019). Microbiome and cognitive impairment: can any diets influence learning processes in a positive way?Front. Aging Neurosci.11:170. 10.3389/fnagi.2019.00170

  • 79

    PeetR. (1974). The measurement of species diversity.Annu. Rev. Ecol. Syst.5285307.

  • 80

    Pereira-CaroG.OliverC. M.WeerakkodyR.SinghT.ConlonM.BorgesG.et al (2015). Chronic administration of a microencapsulated probiotic enhances the bioavailability of orange juice flavanones in humans.Free Radic. Biol. Med.84206214.

  • 81

    PiercyK. L.TroianoR. P. (2018). Physical activity guidelines for Americans From the US department of health and human services.Circ. Cardiovasc. Qual. Outcomes11:e005263.

  • 82

    RajaramS.JonesJ.LeeG. J. (2019). Plant-based dietary patterns, plant foods, and age-related cognitive decline.Adv. Nutr.10(Suppl._4), S422S436. 10.1093/advances/nmz081

  • 83

    RehfeldK.LudersA.HokelmannA.LessmannV.KaufmannJ.BrigadskiT.et al (2018). Dance training is superior to repetitive physical exercise in inducing brain plasticity in the elderly.PLoS One13:e0196636. 10.1371/journal.pone.0196636

  • 84

    RooksC. R.ThomN. J.McCullyK. K.DishmanR. K. (2010). Effects of incremental exercise on cerebral oxygenation measured by near-infrared spectroscopy: a systematic review.Prog. Neurobiol.92134150. 10.1016/j.pneurobio.2010.06.002

  • 85

    RoopchandD. E.CarmodyR. N.KuhnP.MoskalK.Rojas-SilvaP.TurnbaughP. J.et al (2015). Dietary polyphenols promote growth of the gut bacterium Akkermansia muciniphila and attenuate high-fat diet-induced metabolic syndrome.Diabetes6428472858. 10.2337/db14-1916

  • 86

    RovioS.SpulberG.NieminenL. J.NiskanenE.WinbladB.TuomilehtoJ.et al (2010). The effect of midlife physical activity on structural brain changes in the elderly.Neurobiol. Aging3119271936. 10.1016/j.neurobiolaging.2008.10.007

  • 87

    RuotoloR.MinatoI.La VitolaP.ArtioliL.CurtiC.FranceschiV.et al (2020). Flavonoid-derived human phenyl-gamma-valerolactone metabolites selectively detoxify amyloid-beta oligomers and prevent memory impairment in a mouse model of Alzheimer’s disease.Mol. Nutr. Food Res.2020:e1900890. 10.1002/mnfr.201900890

  • 88

    SajiN.MurotaniK.HisadaT.TsudukiT.SugimotoT.KimuraA.et al (2019). The relationship between the gut microbiome and mild cognitive impairment in patients without dementia: a cross-sectional study conducted in japan.Sci. Rep.9:19227. 10.1038/s41598-019-55851-y

  • 89

    SantoroA.BrigidiP.GonosE. S.BohrV. A.FranceschiC. (2014). Mediterranean diet and inflammaging in the elderly: the European project NU-AGE. preface.Mech. Ageing Dev.1312. 10.1016/j.mad.2014.01.006

  • 90

    SchellJ.BettsN. M.LyonsT. J.BasuA. (2019). Raspberries improve postprandial glucose and acute and chronic inflammation in adults with type 2 diabetes.Ann. Nutr. Metab.74165174. 10.1159/000497226

  • 91

    ScheperjansF.AhoV.PereiraP. A.KoskinenK.PaulinL.PekkonenE.et al (2015). Gut microbiota are related to Parkinson’s disease and clinical phenotype.Mov. Disord.30350358. 10.1002/mds.26069

  • 92

    SchlegelP.NovotnyM.KlimovaB.ValisM. (2019). “Muscle-gut-brain axis”: can physical activity help patients with Alzheimer’s disease due to microbiome modulation?J. Alzheimers Dis.71861878. 10.3233/JAD-190460

  • 93

    Shukitt-HaleB.BielinskiD. F.LauF. C.WillisL. M.CareyA. N.JosephJ. A. (2015). The beneficial effects of berries on cognition, motor behaviour and neuronal function in ageing.Br. J. Nutr.11415421549. 10.1017/S0007114515003451

  • 94

    SmallB. J.RawsonK. S.MartinC.EiselS. L.SanbergC. D.McEvoyC. L.et al (2014). Nutraceutical intervention improves older adults’ cognitive functioning.Rejuvenation Res.172732. 10.1089/rej.2013.1477

  • 95

    SocciV.TempestaD.DesideriG.De GennaroL.FerraraM. (2017). Enhancing human cognition with cocoa flavonoids.Front. Nutr.4:19. 10.3389/fnut.2017.00019

  • 96

    SokolovA. N.PavlovaM. A.KlosterhalfenS.EnckP. (2013). Chocolate and the brain: Neurobiological impact of cocoa flavanols on cognition and behavior.Neurosci. Biobehav. Rev.37(10 Pt 2), 24452453. 10.1016/j.neubiorev.2013.06.013

  • 97

    SpencerJ. P.VafeiadouK.WilliamsR. J.VauzourD. (2012). Neuroinflammation: modulation by flavonoids and mechanisms of action.Mol. Aspects Med.338397. 10.1016/j.mam.2011.10.016

  • 98

    SpencerJ. P. E. (2009). Flavonoids and brain health: multiple effects underpinned by common mechanisms.Genes Nutr.4243250.

  • 99

    StrathearnK. E.YousefG. G.GraceM. H.RoyS. L.TambeM. A.FerruzziM. G.et al (2014). Neuroprotective effects of anthocyanin- and proanthocyanidin-rich extracts in cellular models of Parkinsons disease.Brain Res.15556077. 10.1016/j.brainres.2014.01.047

  • 100

    Tomas-BarberanF. A.SelmaM. V.EspinJ. C. (2016). Interactions of gut microbiota with dietary polyphenols and consequences to human health.Curr. Opin. Clin. Nutr. Metab Care19471476. 10.1097/MCO.0000000000000314

  • 101

    TooleyK. L. (2020). Effects of the human gut microbiota on cognitive performance, brain structure and function: a narrative review.Nutrients12:3009. 10.3390/nu12103009

  • 102

    TsubakiA.MorishitaS.HottaK.TokunagaY.QinW.KojimaS.et al (2021). Changes in the laterality of oxygenation in the prefrontal cortex and premotor area during a 20-min moderate-intensity cycling exercise.Adv. Exp. Med. Biol.1269113117. 10.1007/978-3-030-48238-1_18

  • 103

    TsukamotoH.SugaT.IshibashiA.TakenakaS.TanakaD.HiranoY.et al (2018). Flavanol-rich cocoa consumption enhances exercise-induced executive function improvements in humans.Nutrition469096.

  • 104

    TsukamotoH.TakenakaS.SugaT.TanakaD.TakeuchiT.HamaokaT.et al (2017). Effect of exercise intensity and duration on post-exercise executive function.Med. Sci. Sports Exerc.49774784. 10.1249/MSS.0000000000001155

  • 105

    TuohyK. M.ConternoL.GasperottiM.ViolaR. (2012). Up-regulating the human intestinal microbiome using whole plant foods, polyphenols, and/or fiber.J. Agric. Food Chem.6087768782. 10.1021/jf2053959

  • 106

    U.S. Department of Health and Human Services and U.S. Department of Agriculture (2015). 2015–2020 Dietary guidelines for Americans, 8th Edn. London: Pearson.

  • 107

    United States Census Bureau (2021). Population Projections.Suitland, MA: US Census Bureau.

  • 108

    VauzourD.RendeiroC.D’AmatoA.Waffo-TéguoP.RichardT.MérillonJ. M.et al (2021). Anthocyanins promote learning through modulation of synaptic plasticity related proteins in an animal model of ageing.Antioxidants10:1235. 10.3390/antiox10081235

  • 109

    VossM. W.NagamatsuL. S.Liu-AmbroseT.KramerA. F. (2011). Exercise, brain, and cognition across the life span.J. Appl. Physiol.11115051513. 10.1152/japplphysiol.00210.2011

  • 110

    WangL.GaoM.KangG.HuangH. (2021). The potential role of phytonutrients flavonoids influencing gut microbiota in the prophylaxis and treatment of inflammatory bowel disease.Front. Nutr.8:798038. 10.3389/fnut.2021.798038

  • 111

    WangY.DykesG. A. (2021). Direct modulation of the gut microbiota as a therapeutic approach for Alzheimer’s disease.CNS Neurol. Disord. Drug Targets211425. 10.2174/1871527320666210806165751

  • 112

    WarnerE. F.SmithM. J.ZhangQ.RaheemK. S.O’HaganD.O’ConnellM. A.et al (2017). Signatures of anthocyanin metabolites identified in humans inhibit biomarkers of vascular inflammation in human endothelial cells.Mol. Nutr. Food Res.61:1700053. 10.1002/mnfr.201700053

  • 113

    WengT.PierceG.DarlingW.VossM. (2015). Differential effects of acute exercise on distinct aspects of executive function.Med. Sci. Sports Exerc.4714601469. 10.1249/MSS.0000000000000542

  • 114

    WestfallS.LomisN.PrakashS. (2018). A novel polyphenolic prebiotic and probiotic formulation have synergistic effects on the gut microbiota influencing Drosophila melanogaster physiology.Artif. Cells Nanomed. Biotechnol.46441455. 10.1080/21691401.2018.1458731

  • 115

    WestfallS.PasinettiG. M. (2019). The gut microbiota links dietary polyphenols with management of psychiatric mood disorders.Front. Neurosci.13:1196. 10.3389/fnins.2019.01196

  • 116

    WhyteA. R.ChengN.FromentinE.WilliamsC. (2018). A randomized, double-blinded, placebo-controlled study to compare the safety and efficacy of low dose enhanced wild blueberry powder and wild blueberry extract (ThinkBlue™) in maintenance of episodic and working memory in older adults.Nutrients10:660.

  • 117

    WhyteA. R.RahmanS.BellL.EdirisingheI.KrikorianR.WilliamsC. M.et al (2020). Improved metabolic function and cognitive performance in middle-aged adults following a single dose of wild blueberry.Eur. J. Nutr.6015211536. 10.1007/s00394-020-02336-8

  • 118

    WilliamsC. M.El MohsenM. A.VauzourD.RendeiroC.ButlerL. T.EllisJ. A.et al (2008). Blueberry-induced changes in spatial working memory correlate with changes in hippocampal CREB phosphorylation and brain-derived neurotrophic factor (BDNF) levels.Free Radic. Biol. Med.45295305. 10.1016/j.freeradbiomed.2008.04.008

  • 119

    WilliamsR. J.SpencerJ. P. (2012). Flavonoids, cognition, and dementia: actions, mechanisms, and potential therapeutic utility for Alzheimer disease.Free Radic. Biol. Med.523545. 10.1016/j.freeradbiomed.2011.09.010

  • 120

    WilliamsonG.KayC.CrozierA. (2018). The bioavailability, transport, and bioactivity of dietary flavonoids: a review from a historical perspective.Compr. Rev. Food Sci. Food Saf.1710541112.

  • 121

    ZhouX. L.WangL. N.WangJ.ZhouL.ShenX. H. (2020). Effects of exercise interventions for specific cognitive domains in old adults with mild cognitive impairment: a meta-analysis and subgroup analysis of randomized controlled trials.Medicine99:e20105. 10.1097/MD.0000000000020105

  • 122

    ZhuQ.JiangS.DuG. (2020). Effects of exercise frequency on the gut microbiota in elderly individuals.Microbiologyopen9:e1053. 10.1002/mbo3.1053

  • 123

    ZhuW.WadleyV.HowardV.HuttoB.BlairS.HookerS. (2016). Objectively measured physical activity and cognitive function in older adults.Med. Scie. Sports Exer.494753. 10.1249/MSS.0000000000001079

  • 124

    ZmoraN.SuezJ.ElinavE. (2019). You are what you eat: diet, health and the gut microbiota.Nat. Rev. Gastroenterol. Hepatol.163556. 10.1038/s41575-018-0061-2

Summary

Keywords

age-related, cognition, neuroprotective, phenolic metabolites, prebiotic flavonoids, exercise, microbiome

Citation

Cheatham CL, Nieman DC, Neilson AP and Lila MA (2022) Enhancing the Cognitive Effects of Flavonoids With Physical Activity: Is There a Case for the Gut Microbiome?. Front. Neurosci. 16:833202. doi: 10.3389/fnins.2022.833202

Received

10 December 2021

Accepted

20 January 2022

Published

22 February 2022

Volume

16 - 2022

Edited by

David Vauzour, University of East Anglia, United Kingdom

Reviewed by

Silvia Turroni, University of Bologna, Italy; Naiman A. Khan, University of Illinois at Urbana-Champaign, United States

Updates

Copyright

*Correspondence: Mary Ann Lila,

This article was submitted to Gut-Brain Axis, a section of the journal Frontiers in Neuroscience

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics