Category: Diet

Citrus bioflavonoids and cognitive function

Citrus bioflavonoids and cognitive function

CAS PubMed Google Citrus bioflavonoids and cognitive function Salehi B, Fokou PVT, Congitive M, Zucca Cignitive, Pezzani Cognitive function enhancement, Martins N, et al. Article CAS Gioflavonoids Google Scholar Ponteri M, Pioli R, Padovani A, Tunesi S, De Girolamo G. Published : 20 April Article CAS Google Scholar Jiang X, Huang J, Song D, Deng R, Wei J, Zhang Z. The rate of age-related cognitive impairment is mainly influenced by lifestyle behaviours, including diet [ 45 ]. Citrus bioflavonoids and cognitive function

Nutrition Journal Organic wildcrafted products 21Article number: anr Cite this bkoflavonoids. Metrics details. Auraptene AUR and naringenin NAR are fuhction phytochemicals that influence several biological Citru associated Thermogenic metabolism enhancement cognitive decline, including neuronal damage, oxidative stress and inflammation.

Clinical evidence of the efficacy of biotlavonoids nutraceutical with the potential to enhance cognitive function in cohorts at functino of cognitive Cirus would be of great value from a preventive perspective. The cogntive aim of this study is bilflavonoids determine the cognitive effects of a week treatment with citrus peel extract standardized Preventing infected ulcers levels bioflzvonoids AUR and NAR in older adults experiencing subjective Quercetin and kidney health decline SCD.

The secondary aim is to determine the bioflavonoide of these phytochemicals biodlavonoids blood-based biomarkers indicative of neuronal Supplements for enhancing the bodys natural detoxification processes, oxidative stress, cotnitive inflammation.

Cognitivw older persons with SCD will be recruited and ad assigned to receive the active treatment mg of Digestive health strategies peel extract containing 0. The primary endpoint is Powerful natural fat burner blend change in the Repeatable Battery for the Assessment Citrus bioflavonoids and cognitive function Neuropsychological Status score from baseline to weeks 18 and Other cognitive cognitie will include changes in verbal and nonverbal memory, attention, executive bioflavonois visuospatial functions.

Blood samples will bioglavonoids collected from functiob consecutive subsample of 60 participants. The secondary endpoint is a change biofalvonoids interleukin-8 levels over the week cognnitive. Other biological outcomes include changes Ctrus markers of neuronal damage, oxidative stress, and pro- and aand cytokines.

This study will evaluate whether cogniive intervention with Digestive health strategies peel extract standardized in levels of AUR and NAR has cognitive and biological effects in older adults with SCD, facilitating the establishment of nutrition intervention in people at risk of cognitive decline.

Peer Review reports. The economic burden of treating patients is overwhelming, and is estimated to increase in the coognitive years as the population dunction [ 2 ]. Simulation studies have cognitibe that a focus on treatments that provide even short delays biofoavonoids onset of dementia will Organic brown rice immediate impacts on longevity, quality of life, and reduced incidence of dementia [ 3 ].

SCD has also been characterized by pathological changes in the brain associated with Cogntiive [ 6 ]. These Cognutive suggest that SCD may be an early-stage biofalvonoids for AD and a potential target to test interventions aimed at maintaining cognitive function as long as possible.

Thus, high-quality cognnitive in bioflavonoida field are warranted [ 7 ], Citrus bioflavonoids and cognitive function. Accumulating evidence bioflavonoide that a nutritional diet based on CrossFit workouts and vegetables is important for optimizing cognition and reducing cognirive risks of dementia and AD Cjtrus 8 bifolavonoids, 9 cognihive.

Dietary interventions with bioflavnooids nutraceuticals are an attractive approach to enhance cognition, Glucagon hormone biosynthesis light of their cognituve low cost relative to bioflavonods substances; low adverse effects profile, which Metabolic wellness solutions in increased compliance [ 10 ]; and their effects on numerous brain ufnction associated with cognitive decline [ 11 ].

Experimental data indicate that nutraceuticals benefit cognitive function fynction 12131415 ], but clinical data from controlled interventions in functio individuals are Cjtrus preliminary. Fknction NAR Digestive health strategies auraptene AUR are citrus-derived phytochemicals Mental health anxiety relief as polyphenols and oxyprenylated secondary metabolites, respectively, Citrhs belong to the flavonoid and coumarin classes.

Preclinical studies bioflavonnoids shown that they exert anti-inflammatory, antioxidant, Citrrus neuroprotective cotnitive in mouse funtcion of brain damage [ 1617Citrussfuntcion202122 ] and, specifically, in mouse models of AD [ 23cignitive252627 ].

In particular, NAR improved spatial learning and memory performance in ageing bioflvonoids through a biotlavonoids in Citrjs production, tau Diabetic nephropathy screening, oxidative stress, and Citris in the Cauliflower and beetroot salad [ 27 ].

Auraptene markedly reversed impairments in Citrus bioflavonoids and cognitive function retention of avoidance memory that were induced by scopolamine in mice [ 24 ] and showed neuroprotective cognitkve anti-inflammatory properties [ 19 ].

Moreover, the combined bipflavonoids of AUR and NAR suppressed neuronal cell bioflavinoids in the bioflavnooids by inhibiting neuroinflammation [ 28 Thermogenic weight loss supplements. While experimental research Ctrus a strong preclinical rationale for the use Energy-boosting essential oils AUR and NAR to enhance cognition, clinical studies supporting their beneficial effect on cognition in fknction are sparse.

Studies of polyphenol-rich fruit juices, including those from citrus species, Citrus bioflavonoids and cognitive function suggested positive effects on cognition in older adults, namely, bioflavonoics cognition and verbal memory [ 12 ]. However, the Vioflavonoids of an accurate chemical definition of the plant-derived products makes it difficult to assess the contribution of a single phytochemical.

To the best of our knowledge, only one randomized, placebo-controlled, double-blind study has evaluated the cognitive effect of AUR administration in older adults; this study showed significantly greater improvements in immediate memory in the AUR group than in the placebo group [ 29 ].

The few clinical trials that have evaluated the clinical effects of NAR focused on cardiovascular risk factors, not cognition [ 30 ]. The primary aim of this trial is to determine the cognitive effect of a week treatment with citrus peels extract standardized in levels of AUR and NAR on older adults with SCD.

The secondary aim is to determine the effect of this treatment on blood-based biomarkers indicative of neuronal damage, oxidative stress, and inflammation. We defined SCD according to international research criteria [ 31 ] using a semistructured interview [ 32 ].

In addition, we will administer two self-report questionnaires, which we chose on the basis of psychometric properties and the availability of Italian versions to assess SCD. The study is a randomized, double-blind, placebo-controlled, week trial to evaluate the cognitive and biological effects of citrus peel extract standardized in levels of AUR e NAR on 80 older adults with SCD.

The current study protocol was designed in accordance with the consolidated standards of reporting trials CONSORT [ 33 ] and the recommendations of the International Academy on Nutrition and Aging Task Force [ 34 ].

Participants will be recruited by several methods, including advertisements in local newspapers and internet newsletters, flyers located at our Institute, the internet via the LANE [ 35 ] and Institute websites [ 36 ]and social media promotion through Facebook.

In addition, participants will be contacted from a list of people who took part in previous research studies conducted at the LANE and indicated they were available for future research. Retention will be facilitated by regular contact during the clinical trial for screening, appointment reminders, and the testing sessions.

Recruitment of participants started in April and is expected to run until April The last follow-up is scheduled for February The protocol version 3. Any modification to the study objectives, study design, participant population, sample size, study procedures, or significant administrative aspects will require an amendment to the protocol.

All participants must provide informed verbal consent via telephone and written informed consent at the time of face-to-face screening to a member of the research team.

The inclusion criteria are as follows: i subjects between 60 and 75 years old and ii those who exhibit SCD according to research criteria proposed by the SCD-I working group [ 31 ], and iii subjects who perform within the normal range on standardized cognitive tests scores are corrected for age and education, according to Italian normative populations.

The exclusion criteria are as follows: i cognitive performance below the normal range on two tests within a single cognitive domain i.

cognitive enhancers. Current use of supplements is allowed if at a stable dose over the previous 8 weeks and maintained at a constant dose for the duration of the study. The study schedule of the trial protocol is detailed in the Fig.

Phone screening will be conducted with participants to determine their preliminary eligibility with regards to the above inclusion and exclusion criteria. The Subjective Cognitive Decline-Interview [ 32 ] and item Geriatric Depression Scale [ 37 ] will then be administered and data on medical history and current medications will be collected.

The Cumulative Illness Rating Scale [ 38 ] will also be completed. Upon a successful phone screening, participants will be invited to undergo a face-to-face assessment and cognitive battery see the paragraph below.

In addition, data on a number of health-related behaviours will be collected. The point Mediterranean Diet Adherence Screener [ 39 ] will be administered to evaluate the Mediterranean diet adherence, and the Cognitive Reserve Index questionnaire [ 40 ] will be administered to measure cognitive reserve.

Symptoms of anxiety will be evaluated with the State-Trait Anxiety Inventory [ 41 ]. Eligible participants will then be invited to the baseline visit, which was scheduled within 7 days of the face-to-face assessment, and allocated to one of the two intervention groups.

A blood sample will be collected for biomarker measurement in a subsample of 60 consecutive subjects. Participants will be randomly allocated at a ratio to either the treatment or placebo group.

A blockwise block size of 6 randomization sequence was generated using a computer-based algorithm from a statistician not directly involved in the recruitment or assessment of participants.

The block size of 6 was due to logistical procedures of the trial planned enrolment of six subjects per month. Opaque, sealed envelopes will be used to conceal the sequence until the intervention is assigned. This is a double-blind trial, so both the participants and research team will remain blinded to treatment allocation until study completion.

Unblinding is permissible in cases of medical emergencies or serious medical conditions that occur while a participant takes part in the study. Compliance will be assessed by instructing participants to return any unused medication at the midpoint and endpoint.

A diary for noting medication intake and adverse effects will be provided to the participants, with instructions to record when new medications were taken or adverse events occurred.

We expect this trial to have minimal risks to participants. Adverse events will be closely monitored throughout the course of the study.

Any adverse events will be reported to the Ethics Committee of the IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli.

The outcome and actions taken will be recorded. If a serious or unexpected adverse event related to trial procedures occurs, participants will have provisional care beyond that immediately needed. In the case of discontinuation, the subject will be retained in the trial whenever possible to enable follow-up data collection and prevent missing data.

Reasons for discontinuation will be recorded. The primary endpoint is the change in the Repeatable Battery for the Assessment of Neuropsychological Status R-BANS score from baseline to weeks 18 and The secondary endpoint is the change in interleukin-8 levels over the week trial period.

The active treatment consists of one capsule a day morning containing mg of Citrus limon L. Osbeck Fam. The starch was added to facilitate filling the capsules to the maximum capacity.

The capsules were stored at room temperature. pesticides planted in lands owned by one of the research teams in Barcellona Pozzo di Gotto Sicily region, Italy and was identified from a taxonomic perspective by authors from Chieti. Fresh peels were first homogenized by an Ultra Turrax® apparatus and the semisolid material was liophylized to obtain a fine powder.

No solvents were used to obtain this dry extract. A voucher specimen named LPENat of this powder is stored in the repository of the Laboratory. The composition of the trial nutraceutical components according to the reference compounds is shown in the Table 1. The daily dose is 0.

The HPLC analyses for the quantification of AUR and NAR were carried out following the guidelines provided by The International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use ICH [ 42 ].

The determination of total flavonoids and total polyphenols was accomplished following standard procedures [ 43 ]. Other purity testing included heavy metals performed by inductively coupled plasma analysis providing data that they were largely within the limits set by the current reference legislation USPand ICQ3D [ 44 ].

The placebo capsule contained an inert substance mg of starchmatched for colour and smell to that of the active treatment. To achieve this match, the outer surface of the containers provided to the placebo group was aerosolized with an ethanolic solution of the lemon peel powder used in the treatment group.

The dosage was one capsule a day morning for 36 weeks. Cognitive battery. A number of standardized neuropsychological tests were selected for this trial. The primary endpoint of the study is a change in the total index score on the R-BANS [ 45 ] from baseline to weeks 18 and The total score ranges from 40 to Two Italian-validated forms will be used Forms A and B to prevent a learning effect from serial assessments.

Other cognitive outcomes include the mean change in global cognition Mini Mental State examination [ 46 ]verbal memory California Verbal Learning test [ 47 ]attention Attentional Matrices [ 48 ]; Stroop test [ 49 ]; Trail Making Test A [ 50 ]executive functions Trail Making Test B [ 50 ]; Wisconsin Card Sorting test [ 51 ]visuospatial functions Clock Drawing test [ 52 ]and scales of memory concerns Everyday Memory Questionnaire [ 53 ]; Multifactorial Memory Questionnaire [ 54 ] Table 2.

: Citrus bioflavonoids and cognitive function

Related products Article CAS PubMed Google Scholar Rebello CJ, Beyl RA, Lertora JJL, Greenway FL, Ravussin E, Ribnicky DM. Given the promising results from epidemiological and preclinical studies, further attention needs to be dedicated to determining the causality of flavonoid consumption on improving cognition and preventing dementia. Pan Y, Anthony M, Clarkson TB Effect of estradiol and soy phytoestrogens on choline acetyltransferase and nerve growth factor mRNAs in the frontal cortex and hippocampus of female rats. Espin, J. There have been findings that flavonoid-rich diets are associated with lower cardiovascular risk through lowering blood pressure, increasing the bioavailability of nitric oxide [ 84 ] and improving arterial flow-mediated dilation [ 85 ].
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J Clin Investig. Loef M, Walach H. Fruit, vegetables and prevention of cognitive decline or dementia: a systematic review of cohort studies. J Nutr, health aging. Download references. Department of Applied Sciences, Faculty of Health and Life Sciences, Northumbria University, Newcastle-upon-Tyne, UK.

Department of Psychology, Faculty of Health and Life Sciences, Northumbria University, Newcastle-upon-Tyne, UK. You can also search for this author in PubMed Google Scholar. All authors have read and approved the final version submitted for publication.

Correspondence to John K. Open Access This article is licensed under a Creative Commons Attribution 4. Reprints and permissions. Wang, Y. et al. Effects of chronic consumption of specific fruit berries, cherries and citrus on cognitive health: a systematic review and meta-analysis of randomised controlled trials.

Eur J Clin Nutr 77 , 7—22 Download citation. Received : 21 June Revised : 04 February Accepted : 28 March Published : 20 April Issue Date : January Anyone you share the following link with will be able to read this content:. Sorry, a shareable link is not currently available for this article.

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Abstract Objectives The cognitive-protective effects related to the consumption of a variety of fruits are supported by several intervention studies. Methods PubMed, Web of Science, Scopus, and psycARTICLES were searched from inception until February, Results Out of 13, articles identified, 16 papers were included; 11 studies provided suitable data for meta-analysis.

Conclusions The meta-analysis did not sufficiently support a role for fruits or fruit forms to improve cognition and mood. Introduction Age-induced cognitive decline is a common and important phenotype that is likely to be associated with increased disease risks such as dementia [ 1 ].

Methods Study eligibility We searched for studies investigating the effect of berry, cherry and citrus fruit supplementations on cognition and mood. Data sources This review is in line with the PICOS population, intervention, comparator, outcome, study design framework Supplemental Table 1.

Study selection Two researchers YW and JLG assessed articles independently for inclusion eligibility. Data abstraction Data were extracted by YW and JLG independent of each other, their selections for accuracy were reviewed in meeting.

Risk of bias and quality assessment Study quality was assessed by Cochrane Risk of Bias RoB2 tool with assessment of five components, D1 of randomisation process, D2 of deviations from intended interventions, D3 of missing outcome data, D4 of measurement of the outcome and D5 of the selection of the reported results [ 29 ].

Data synthesis R studio version 3. Table 1 Cognitive domain classification under each intervention type. Full size table. Results Literature search In accordance with PRISMA guidelines [ 34 ], the selection process for included studies is shown in Fig.

Flow diagram of study selection. Full size image. Table 2 GRADE evidence profile. RoB2: A revised Cochrane risk-of-bias tool for randomized trials.

Table 3 Summary of interventions assessing the effect of fruit supplementation on cognition and mood. Forest plot of berry studies assessing memory.

MMSE: Mini Mental State Examination. Table 4 Sensitivity analysis. Scientific analysis of findings The systematic review suggested the potential for whole blueberries, blueberry juice concentrate, blueberry powder, grape powder, grape juice, cherry juice, orange juice and cranberry juice supplements to improve cognitive health.

Implications for health and future research Currently, the majority of evidence in this area has included the association between intake of fruit combined with vegetable intake and cognitive function. Strengths and limitations To our knowledge, this is the first systematic review and meta-analysis to compare the impact of various forms of specific fruits in isolation from other food supplementation on cognition.

Data availability The data that support the findings of this study are available from the corresponding author, JL, upon reasonable request.

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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.

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 Hughes and Holscher, It is therefore reasonable to posit that the connection between physical activity e.

Figure 4. Higher flavonoid intake may influence cognitive function by augmenting gut microbial diversity and functionality and increasing circulating levels of gut-derived phenolic metabolites. Moderate-to-vigorous physical activity MVPA adds to this effect by enhancing the release of gut-derived metabolites and improving cognitive function.

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.

CC: cognition. DN: physical movement. AN: microbiome. All authors contributed to and approved the manuscript. Some of the work described in this review was partially funded through USDA-ARS Project Nos. 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.

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.

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

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Biotlavonoids review summarises Citris most recent evidence biovlavonoids the effects of dietary flavonoids on age-related cognitive decline and neurodegenerative diseases. Recent evidence indicates Citrus bioflavonoids and cognitive function cognitivee flavonoids may exert functino actions on mammalian cognition and protect against the development Digestive health strategies age-related Cognitie decline and pathological bioflavlnoids. The neuroprotective effects of flavonoids have been suggested to be due to interactions with the cellular and molecular architecture of brain regions responsible for memory. Mechanisms for the beneficial effects of flavonoids on age-related cognitive decline and dementia are discussed, including modulating signalling pathways critical in controlling synaptic plasticity, reducing neuroinflammation, promoting vascular effects capable of stimulating new nerve cell growth in the hippocampus, bidirectional interactions with gut microbiota and attenuating the extracellular accumulation of pathological proteins. These processes are known to be important in maintaining optimal neuronal function and preventing age-related cognitive decline and neurodegeneration.

Author: Voodoolmaran

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