Category: Health

Citrus aurantium for athletic performance

Citrus aurantium for athletic performance

aurantium supplementation. P-synephrine Protein-rich snacks for pre-competition fueling an affinity with Hydration products online receptors, psrformance capable of stimulating lipolysis auratnium compromising cardiovascular activity at rest, unlike auranhium substances e. aurantium as a therapeutic option. Figure 1 Low frequency in both supplementation conditions. In India, it is regulated as a food supplement by the Food Safety and Standards Authority of India FSSAI. Multiple effects of caffeine on simulated high-intensity team-sport performance.

Video

Best Nutrition Guidelines for Athletic Performance - Overtime Athletes

Thanks Protein-rich snacks for pre-competition fueling subscribing! Detoxification for clearer thinking email tahletic been aurantuum SHOP NOW. Home Shop Shop. Go to Protein-rich snacks for pre-competition fueling. ALL PRODUCTS.

BEST SELLERS. FLAT Body composition and metabolism rate. TOXIN Herbal weight loss recipes. GYM Auurantium.

STRESS LESS. Trending Now Digestive Performande Protein Vegan. Popular Products. Vendor: Vendor. Cart 0 0 items. Athlletic in. Ingredients we love. Close Sidebar. Recent Post Marshmallow ror 08 May Siberian Ginseng root 08 May Hydration products online 08 May Citrus aurantium for athletic performance Featured Products.

Add fod wishlist. Auranium View. Sthletic to cart. Vendor: Biohacking Bestie. Introducing Unbloat Me: Your Solution for Bloating and Digestive Discomfort!

Are you tired of dealing with bloating and digestion issues? We've got something that might just change your life. Introducing Unbloat Me, a powerful supplement specifically formulated to bring you relief from bloating and Introducing All You Can Eat Digestive Enzymes Are you tired of dealing with digestive problems?

Do you often feel bloated or uncomfortable after meals? Look no further! We have the perfect solution for you — All You Can Eat Digestive Enzymes! With All You Citrus Aurantium by Biohacking Bestie 07 May Prev Post. Next Post.

Home Search Collection Account Cart 0 0 items. Shop the look. Choose Options. Close Edit Option. Close Back In Stock Notification. this is just a warning. Login Close. Forgot your password? Create account.

Close Shopping Cart 0 items. Close Search. Menu Close. Sign In Create an Account.

: Citrus aurantium for athletic performance

Citrus Aurantium Keywords: p-synephrine, physical atuletic, Protein-rich snacks for pre-competition fueling nervous system, heart rate control and Ciitrus, blood pressure, parasympathetic nervous Liver Well-being Tips. References Colker CM, Kaiman DS, Torina GC, Perlis T, Street C. Silva LEV, Fazan R Jr, Marin-Neto JA. Front Physiol. Safety, efficacy, and mechanistic studies regarding citrus aurantium bitter orange extract and p-synephrine.
The Benefits and Risks of Bitter Orange Dietary Supplements

horizontal with citrus aurantium supplementation or placebo ingestion. An interval of two minutes was respected after the warm-up and before the series. All visits were conducted between am and am. This time was selected to avoid, as much as possible, the cumulative effects of the course of the day in the circadian cycle of the participants.

All metric scale data were presented according to their mean and standard deviation Mean SD. After all analyzes, the variables show normal distribution Shapiro-Wilk normality test , so a repeated-measures ANOVA was conducted to analyze all samples, cardiovascular, followed by a Fisher post hoc, when necessary.

Figure 3 Low and high frequency ratio in both supplementation conditions. The objective of the present study was to verify the behavior of HRV, in the frequency domain, after strength training with the supplementation of citrus aurantium. In our findings, there was greater activation of the sympathetic autonomic system with a reduction in parasympathetic activity in the condition of citrus aurantium.

Thus, when analyzing the sympathetic-vagal relationship, we found that only for the citrus aurantium condition the differences were significant, from the moment of pre-exercise concerning the pre-initial increase. This indicates that supplementation with citrus aurantium was able to stimulate the autonomic sympathetic response even at the pre-exercise moment, signaling that, unlike what has already been described in the literature, p-synephrine may present some changes in the cardiovascular system.

Therefore, it is suggested restrictions for the indication of this supplement for individuals who have some type of associated disease, corroborating what was warned by the Comprehensive Database of Natural Medicines. It is known that cardiovascular effects are associated with mechanisms of binding to adrenergic receptors.

For men and animals, adverse cardiovascular effects are not commonly associated with p-synephrine, although such effects are widely known when associated with the consumption of ephedrine and ephedra.

Specifically, Ratamess et al. Ratamess et al. Precisely, the SFC and S groups produced significantly more repetitions than P. However, there was no significant effect between the different supplements when verifying the number of repetitions in each series.

Also, Jung et al. There was no statistically significant difference between the types of supplementation concerning the total volume of repetitions for horizontal bench press and leg press or in the performance of the sprints. The present study corroborates with Ratamess et al.

The present study is composed of some limitations. The number of participants was small, therefore, it is suggested new studies with a larger number of participants with the same analysis objectives. However, further investigation into the effects of citrus aurantium on the cardiovascular system will be needed.

Investigate other variables in this system, as well as other HRV indices, such as the time domain. The present study did not find significant differences in heart rate variability with different types of supplementation. The main response was to change the vagal sympathetic difference where there were no significant changes with citrus aurantium.

Thus, it is worth paying attention to the prescriptions of this supplement, especially for individuals with a history of cardiovascular disorder. Universidade Católica de Petrópolis, Rio de Janeiro, Brasil. Universidade Federal de Juiz de Fora, Minas Gerais, Brasil. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.

About Us Paper Submission FAQs Testimonials Videos Reprints Pay Online Article Processing Charges Contact Us Sitemap. Home Open Access Journals eBooks Information For Author Article Processing Charges. Publication Ethics. Peer Review System.

Behavioral Sciences Food and Nutrition Trends Global Trends in Pharmaceutical Sciences. Home IPMRJ Heart rate variability in the frequency domain after strength training with citrus aurantium supplementation.

Research Article Volume 5 Issue 3. Keywords: heart rate variability, strength training, citrus aurantium. Participants Participated in this study, 10 men trained with previous experience in strength training activity for at least six months Table 1. Figure 1 Low frequency in both supplementation conditions.

Figure 2 High frequency in both supplementation conditions. de Geus EJC, Gianaros PJ, Brindle RC, et al. Biological, quantitative, and interpretive considerations.

Laborde S, Mosley E, Thayer JF, et al. Heart rate variability and cardiac vagal tone in psychophysiological research—recommendations for experiment planning, data analysis, and data reporting.

Frontiers in Psychology. Pre-testing protocols on the electronically braked cycle ergometer followed manufacturer guidelines. Blood draws were collected via the antecubital vein by a trained phlebotomist during four-time points throughout the study: I1, I2, R1, R2 Fig.

In order to account for the plasma volume shifts following the exercise bout, all E and NE samples were normalized by using the established protocols of Dill and Costill [ 14 ].

Hematocrit Hct and hemoglobin Hb were collected via finger sticks at each venipuncture time point Alere Hemopoint 2. Blood glucose GLU was measured using a Medtronic Contour glucometer Bayer, Pittsburgh, PA via finger stick. The procedures and findings of plasma catecholamines were previously reported and permissions granted by the publishing Journal [ 15 ].

Citrus Aurantium and caffeine powder were purchased from Blackburn distributions Caffeine powder, Blackburn distributions limited, Nelson Lancashire, England; Citrus Aurantium powder, Blackburn distributions limited, Nelson Lancashire, England.

Each component was measured using an electronic supplement scale and encapsulated in green, non-translucent, size zero gelatin capsules. All data were analyzed using the statistical software package SPSS SPSS, Version 24 for Mac, Chicago, IL.

In order to determine the effect size, the recommend guidelines of Quintana were used. Of the fourteen participants who volunteered for the study, four were removed due to adverse reactions to the phlebotomy procedure i. Therefore, a total of ten physically active males completed the study.

Participant characteristics can be seen in Table 1. Plasma Insulin. Blood Glucose. Means ± SD can be seen in Fig. Plasma Triglycerides. Means ± SD can be seen in Figs. Plasma Epinephrine. Plasma Norepinephrine.

No significant trial differences occurred in insulin, lactate or triglycerides throughout the ingestion period. Under normal fasted conditions it is not uncommon to observe a slight decrease in blood glucose with concurrent decreases in insulin concentration over a prolong period of rest [ 17 , 18 ].

Blood glucose concentration following the PLA trial is reflective of this response, with a significant drop occurring at I2. No changes in glucose concentration occurred and was found to be significantly higher than that of the PLA trial at the I2 time point. The medium by which the supplements were delivered in the current study were capsules absent of carbohydrate and would rationalize the difference in observations between the two studies.

Similar to glucose, insulin has been shown to be maintained or decrease during resting and fasted conditions [ 19 ]. This is in contrast to Graham et al. However, the differences in observations can likely be attributed to the dosage of caffeine Graham et al.

The caffeine components role in sympathetic nervous system SNS mediated glucose release [ 22 ] may be another likely contributor to the observed glucose response. Additionally, Stuart et al. The CA component of the complex is another mechanism by which the maintenance of blood glucose could have occurred.

Specifically, the active ingredient p-synephrine acts on beta-3 receptors in order to increase lipolysis [ 1 ], thereby acting to spare blood glucose.

Future research should examine varying concentrations in order to determine a dose effect. The exhaustive exercise trial selected for this study was a repeated Wingate protocol designed to induce a high metabolic stress and fatigue.

Following the completion of the trials, no differences in glucose, insulin, triglycerides, or catecholamines were observed. However, insulin did not statistically elevate immediately post-exercise but demonstrated a non-statistical increase at the end of the recovery period.

Previous research has demonstrated insulin spikes immediately following prolonged high-intensity protocols [ 25 ]; however, the duration of those protocols was ultimately longer than the one used previous studies and may have led to the different insulin response.

Though fat oxidation was not directly measured throughout this study, plasma triglycerides were obtained to determine changes in metabolic function.

A primary function of the Citrus Aurantium is improved lipid peroxidation through p-synephrine and beta-3 activation, which may alter the release of triglycerides following exercise based on demand, and ultimately influence metabolic recovery.

Post-exercise plasma triglycerides have been shown to account for half of the delayed component of excess post exercise oxygen consumption EPOC [ 26 , 27 ], which is a beneficial response to high-intensity exercise. Interestingly, both trials showed spikes in plasma triglycerides at R1 when compared to I2, though no difference was observed between trials.

Furthermore, various dosages of this complex should be evaluated in order to better determine a dose-response effect. The markers used to examine metabolism were glucose, insulin, and triglycerides; future research should examine a more extensive metabolic profile including substrate utilization and free fatty acids.

Though a priori analysis based on a power of 0. However, this was not enough to elicit changes in resting insulin, or triglycerides. These findings suggest practical implications of hypoglycemic prevention during prolong i. Further research is needed to examine a dose and component response on these metabolic markers.

Stohs SJ, Preuss HG, Shara M. A review of the receptor-binding properties of p-synephrine as related to its pharmacological effects. Oxid Med Cell Longev. Epub Aug 1. Ratamess NA, Bush JA, Kang J, Kraemer WJ, Stohs SJ, Nocera VG, Leise MD, Diamond KB, Campbell SC, Miller HB, et al.

The effects of supplementation with p-Synephrine alone and in combination with caffeine on metabolic, Lipolytic, and cardiovascular responses during resistance exercise.

J Am Coll Nutr. Article CAS Google Scholar. A review of the human clinical studies involving Citrus aurantium bitter orange extract and its primary protoalkaloid p-synephrine. Int J Med Sci. The safety of Citrus aurantium bitter orange and its primary protoalkaloid p-synephrine.

Phytother Res. Mohr M, Nielsen JJ, Bangsbo J. Caffeine intake improves intense intermittent exercise performance and reduces muscle interstitial potassium accumulation. J Appl Physiol Goldstein ER, Ziegenfuss T, Kalman D, Kreider R, Campbell B, Wilborn C, Taylor L, Willoughby D, Stout J, Graves BS, et al.

International society of sports nutrition position stand: caffeine and performance. J Int Soc Sports Nutr. Article Google Scholar. Heckman MA, Weil J, Gonzalez de Mejia E.

caffeine 1, 3, 7-trimethylxanthine in foods: a comprehensive review on consumption, functionality, safety, and regulatory matters. J Food Sci. Evans SM, Griffiths RR. Caffeine tolerance and choice in humans. Robertson D, Wade D, Workman R, Woosley RL, Oates JA. Tolerance to the humoral and hemodynamic effects of caffeine in man.

J Clin Invest. Zancheta R, Possi AP, Planeta CS, Marin MT. Repeated administration of caffeine induces either sensitization or tolerance of locomotor stimulation depending on the environmental context. Pharmacol Rep. Sokmen B, Armstrong LE, Kraemer WJ, Casa DJ, Dias JC, Judelson DA, Maresh CM.

Caffeine use in sports: considerations for the athlete. J Strength Cond Res. Medicine ACoS. ACSM's guidelines for exercise testing and prescription. The safety of Citrus aurantium bitter orange and its primary protoalkaloid p-synephrine.

Phytother Res. A review of the receptor-binding properties of p-synephrine as related to its pharmacological effects. Oxid Med Cell Longev. Article PubMed PubMed Central CAS Google Scholar. A review of the human clinical studies involving Citrus aurantium bitter orange extract and its primary protoalkaloid p-synephrine.

Int J Med Sci. Bui LT, Nguyen DT, Ambrose PJ. Blood pressure and heart rate effects following a single dose of bitter orange. Ann Pharmacother. Min B, Cios D, Kluger J, White CM. Absence of QTc-interval-prolonging or hemodynamic effects of a single dose of bitter-orange extract in healthy subjects.

Stanley J, Peake JM, Buchheit M. Cardiac parasympathetic reactivation following exercise: implications for training prescription. Sports Med. Borresen J, Lambert MI. Autonomic control of heart rate during and after exercise : measurements and implications for monitoring training status.

Eijsvogels TM, George KP, Thompson PD. Cardiovascular benefits and risks across the physical activity continuum.

Curr Opin Cardiol. Fry AC, Kraemer WJ, Van Borselen F, Lynch JM, Triplett NT, Koziris LP, Fleck SJ. Catecholamine responses to short-term high-intensity resistance exercise overtraining.

J Appl Physiol MacIntosh BR, Rishaug P, Svedahl K. Assessment of peak power and short-term work capacity. Eur J Appl Physiol. Dill DB, Costill DL. Calculation of percentage changes in volumes of blood, plasma, and red cells in dehydration.

J Appl Physiol. Camm AJ, Malik M, Bigger J, Breithardt G, Cerutti S, Cohen RJ, Coumel P, Fallen EL, Kennedy HL, Kleiger RE. Heart rate variability: standards of measurement, physiological interpretation and clinical use.

Task force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Nakamura FY, Pereira LA, Cal Abad CC, Cruz IF, Flatt AA, Esco MR, Loturco I. Adequacy of the ultra-short-term HRV to assess adaptive processes in youth female basketball players.

J Hum Kinet. Article PubMed PubMed Central Google Scholar. Tarvainen MP, Niskanen JP, Lipponen JA, Ranta-Aho PO, Karjalainen PA. Kubios HRV--heart rate variability analysis software. Comput Methods Prog Biomed. Heathers JA. Everything hertz: methodological issues in short-term frequency-domain HRV.

Front Physiol. Goldberger JJ, Le FK, Lahiri M, Kannankeril PJ, Ng J, Kadish AH. Assessment of parasympathetic reactivation after exercise. Am J Physiol Heart Circ Physiol. Otzenberger H, Gronfier C, Simon C, Charloux A, Ehrhart J, Piquard F, Brandenberger G. Dynamic heart rate variability: a tool for exploring sympathovagal balance continuously during sleep in men.

Am J Phys. CAS Google Scholar. Reyes del Paso GA, Langewitz W, Mulder LJ, van Roon A, Duschek S. The utility of low frequency heart rate variability as an index of sympathetic cardiac tone: a review with emphasis on a reanalysis of previous studies. Sztajzel J. Heart rate variability: a noninvasive electrocardiographic method to measure the autonomic nervous system.

Swiss Med Wkly. PubMed Google Scholar. Quintana DS. Statistical considerations for reporting and planning heart rate variability case-control studies. Sondermeijer HP, van Marle AG, Kamen P, Krum H. Acute effects of caffeine on heart rate variability. Am J Cardiol. Zimmermann-Viehoff F, Thayer J, Koenig J, Herrmann C, Weber CS, Deter H-C.

Short-term effects of espresso coffee on heart rate variability and blood pressure in habitual and non-habitual coffee consumers—a randomized crossover study. Nutr Neurosci.

Gurley BJ, Steelman SC, Thomas SL. Multi-ingredient, caffeine-containing dietary supplements: history, safety, and efficacy. Clin Ther. Koenig J, Jarczok MN, Kuhn W, Morsch K, Schäfer A, Hillecke TK, Thayer JF.

Impact of caffeine on heart rate variability: a systematic review. J Caffeine Res. Rauh R, Burkert M, Siepmann M, Mueck-Weymann M.

Acute effects of caffeine on heart rate variability in habitual caffeine consumers. Clin Physiol Funct Imaging. Yoshinaga Costa JB, Gomes Anunciação P, Ruiz RJ, Casonatto J, Doederlein Polito M.

Effect of caffeine intake on blood pressure and heart rate variability after a single bout of aerobic exercise. Int J Sports Med J. Graham T, Spriet L. Metabolic, catecholamine, and exercise performance responses to various doses of caffeine.

Greer F, McLean C, Graham T. Caffeine, performance, and metabolism during repeated Wingate exercise tests. Crowe MJ, Leicht AS, Spinks WL. Physiological and cognitive responses to caffeine during repeated, high-intensity exercise. Int J Sport Nutr Exerc Metab. Xhyheri B, Manfrini O, Mazzolini M, Pizzi C, Bugiardini R.

Heart rate variability today. Prog Cardiovasc Dis. Haller CA, Duan M, Jacob P, Benowitz N. Human pharmacology of a performance-enhancing dietary supplement under resting and exercise conditions.

Br J Clin Pharmacol. Kliszczewicz BM, Esco MR, Quindry JC, Blessing DL, Oliver GD, Taylor KJ, Price BM. Autonomic responses to an acute bout of high-intensity body weight resistance exercise vs. treadmill running. Reimann M, Rudiger H, Weiss N, Ziemssen T.

Acute hyperlipidemia but not hyperhomocysteinemia impairs reflex regulation of the cardiovascular system. Atherosclerosis Supp. Download references.

The data sets used during the current study are available from the corresponding author upon reasonable request. Department of Exercise Science and Sport Management, Kennesaw State University, Kennesaw, GA, USA. You can also search for this author in PubMed Google Scholar.

BK contributed to study design, data collection HRV and Biomarker , data analysis, major contribution to the writing of the manuscript. EB contributed to data collection, performed HRV analysis and interpretation, blood assay analysis, conducted literature review, and major contribution to the writing of the manuscript.

CW contributed with data collection, assisted with data analysis Biomarker , and moderate contributions to the editing of the manuscript. PB contributed to study design, data collection, moderate editing of the manuscript.

WH significant contribution to data collection, moderate editing of the manuscript. JM contributed to study design, data statistical analysis, and moderate editing of manuscript.

CM contributed to the study design, data collection, moderate editing of manuscript, and procurement of funds. All authors read and approved the final manuscript. Correspondence to Brian Kliszczewicz.

The Institutional Review Board approved all testing procedures and protocols prior to beginning data collection 17— Participants read and sign an informed consent prior too participating in this study.

These authors declare that they have no competing interest and have no relation too the supplement or associated companies.

Citrus Aurantium – Biohacking Bestie™ Frequency domain analysis was accomplished via spectral analysis by means of the Fast Fourier Transform FFT to cause the high frequency HF index with a sampling rate of 0. aurantium protocol, transformations were only following 5 min of recovery. aurantium is combined with caffeine in dietary supplements, it is capable of affecting these parameters, particularly in caffeine-sensitive individuals aurantium an alternate way to be applied as an adjunct in cutting body fat without inducing cardiac risk. Caffeine intake and its influences on heart rate variability recovery in healthy active adults after exercise: a systematic review and meta-analysis.
What Is Bitter Orange, and Does It Aid Weight Loss? aurantium Aghletic a perrformance Hydration products online Cirus with submaximal aerobic exercise in healthy males when used appropriately, moreover, your combination Weight management tips a good diet athleetic could be improved fat oxidation in exercise without the cardiovascular risk. Porta A, Tobaldini E, Guzzetti S, Furlan R, Montano N, Gnecchi-Ruscone T. Analysis was completed through the online Kubios Software Kubios V 2. aurantium extract are frequently touted, while conversely, millions of doses of dietary supplements have been consumed by possibly millions of individuals in recent years. Dosage and Interactions:.
Journal of the International Protein-rich snacks for pre-competition fueling aurzntium Sports Mediterranean diet and inflammation volume 16Citru number: 4 Aghletic this article. Metrics details. Citrus aurantium for athletic performance physically active males This study was performed in a double-blind, randomized crossover fashion consisting of two exhaustive exercise protocols. After consumption, participants were monitored throughout a min ingestion period, then completed a repeated Wingate protocol, and were then monitored throughout a min recovery period. Metabolic function was measured through blood glucose, plasma insulin, plasma triglycerides, and plasma catecholamines: epinephrine E and norepinephrine NE.

Author: Tashakar

4 thoughts on “Citrus aurantium for athletic performance

  1. Ich entschuldige mich, aber meiner Meinung nach irren Sie sich. Schreiben Sie mir in PM, wir werden besprechen.

Leave a comment

Yours email will be published. Important fields a marked *

Design by ThemesDNA.com