Category: Home

Citrus aurantium for muscle recovery

Citrus aurantium for muscle recovery

Bitter auantium may also interact with certain medications. All analyzes were Pre-game meal tips using SPSS version Curr Ther Res. Kubios HRV--heart rate variability analysis software. A review of the receptor-binding properties of p -synephrine as related to its pharmacological effects.

Video

Upper Body Stretch - Muscle Recovery and Stress Relief

Citrus aurantium for muscle recovery -

Get science-backed tips to achieve your goals sent directly to your email every week:. My Cart. All Products New Best Sellers Stacks 2-Packs Gift Card View All. by category Pre Workout Strength Energy Focus Health Performance Recovery Sleep Weightloss. by category Strength Energy Focus Health Performance Recovery Sleep Weight Loss All Articles Recent Popular.

featured article. Home » News » Bitter Orange Extract Increases Energy and Speeds Weight Loss. science nutrition blog. Therefore, the actual amount of p -synephrine consumed in the majority of the studies was not verified.

Finally, nine studies involving the administration of bitter orange extract alone or in combination with other constituents have demonstrated an increase in metabolic rate without an increase in heart rate or blood pressure [ 18 - 20 , 26 , 30 - 32 , 35 , 36 ]. These results suggest that bitter orange extract and p -synephrine may be beneficial in weight management.

The results involving both published and unpublished clinical studies indicate that p -synephrine alone or in combination with caffeine does not appear to produce significant adverse cardiovascular effects or pose a risk to human health at doses commonly ingested orally.

No adverse effects have been directly attributable to bitter orange extract or p- synephrine. The results indicate that bitter orange extract and p -synephrine increase metabolism and energy expenditure. The data accumulated to date do not support hypothesized concerns regarding potential adverse effects of p -synephrine particularly with respect to the cardiovascular system due to a paucity of binding to α-, β-1 and β-2 adrenergic receptors while exhibiting modest binding to β-3 adrenergic receptors.

All authors have served as consultants for Nutratech, Inc. Nutratech Inc. provided some of the unpublished research reports.

Chen JK, Chen TT. Zhi Shi Fructus Aurantii Immaturus. Chinese Medical Herbology and Pharmacology. City of Industry, CA USA: Art of Medicine Press. Stohs SJ, Shara M. A review of the safety and efficacy of Citrus aurantium in weight management.

In: ed. Bagchi D, Preuss HG. Obesity: Epidemiology, Pathophysiology, and Prevention. Boca Raton, FL, USA: CRC Press. Pellati F, Benvenuti S. Chromatographic and electrophoretic methods for the analysis of phenethylamine alkaloids in Citrus aurantium.

J Chromatog A. Sander LC, Putzbach K, Nelson BC. et al. Certification of standard reference materials containing bitter orange. Analyt Bioanalyt Chem.

Evans RL, Pho AN, Roman MC, Betz JM. Penzak SR, Jann MW, Cold JA. Seville sour orange juice: synephrine content and cardiovascular effects in normotensive adults. J Clin Pharmacol.

Bent S, Padula A, Neuhaus J. Safety and efficacy of Citrus aurantium for weight loss. Amer J Cardiol. Nasir JM, Durning SJ.

Exercise-induced syncope associated with QT prolongation and ephedra-free Xenadrine. Mayo Clinic Proceed. Stephensen TA, Sarlay JrR. Ventricular fibrillation associated with use of a synephrine containing dietary supplement.

Military Med. 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 Long. Stohs SJ, Preuss HG. Stereochemical and pharmacological differences between naturally occurring p -synephrine and synthetic p -synephrine.

J Funct Foods. McGuffin M. Media spins numbers on bitter orange AERs based on erroneous information from FDA. The Safety of bitter orange Citrus aurantium and its primary protoalkaloid p -synephrine.

The safety of Citrus aurantium bitter orange and its primary protoalkaloid p -synephrine. Phytother Res. Colker CM, Kalman DS, Torina GC, Perlis T, Street C. Effects of Citrus aurantium extract, caffeine, and St. John's wort on body fat loss, lipid levels, and mood states in overweight healthy adults.

Curr Therap Res. Dulloo AG, Duret C, Rohrer D. Efficacy of a green tea extract rich in catechin polyphenols and caffeine in increasing h energy expenditure and fat oxidation in humans.

Amer J ClinNutr. Kendall-Reed P. Study on the effectiveness of Ultra Slim Down ® for the reduction of body weight. Unpublished report.

Kalman DS, Oxford S, Schwartz HI, Krieger DR. A double blind clinical evaluation of the metabolic effects of Xenadrine EFX TM compared to two ephedra-containing products in normal healthy volunteers. Presented at the annual meeting of the American College of Nutrition, Abstract No.

J Amer Coll Nutr. Kalman DS, Rubin S, Martinez T, Schwartz HI. Presented at a meeting of NIH-National Institute of Diabetes and Digestive and Kidney Diseases. Kalman DS, Rubin S, Schwartz HI. An acute clinical trial to evaluate the safety and efficacy of a popular commercial weight loss supplement when used with exercise.

Presented at Federation of American Societies of Experimental Biology. Kalman DS, Colker CM, Shi Q, Swain MA. Effects of a weight-loss aid in healthy overweight adults: double-blind, placebo-controlled clinical study. Curr Ther Res. Kalman DS, Incledon T, Gaunaurd I. An acute clinical trial evaluating the cardiovascular effects of an herbal ephedra-caffeine weight loss product in healthy overweight adults.

Int J Obes. Kalman DS. Comment on: An acute clinical trial evaluating the cardiovascular effects of an herbal ephedra-caffeine weight loss product in healthy overweight adults. Int J Obes Relat metab Disord. Gurley BJ, Gardner SF, Hubbard MA.

In vivo assessment of botanical supplementation on human cytochrome P phenotypes: Citrus aurantium , Echinacea purpurea , milk thistle, and saw palmetto. Clin Pharmacol Therap. Zenk JL, Kuskowski MA. Zenk JL, Leikam SA, Kassen LJ, Kuskowski MA.

Effect of Lean System 7 on metabolic rate and body composition. 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.

Haller CA, Benowitz N, Peyton J III. Hemodynamic effects of ephedra-free weight loss supplements in humans. Amer J Med. Bui LT, Nguyen DT, Ambrose PJ. Blood pressure and heart rate affects following a single dose of bitter orange.

Ann Pharmacodyn. Sale C, Harris RC, Delves S, Corbett J. Metabolic and physiological effects of ingesting extracts of bitter orange, green tea and guarana at rest and during treadmill walking in overweight males. Int J Obesity. Gougeon R, Harrigan K, Tremblay JF.

Increase in the thermic effect of food in women by adrenergic amines extracted from Citrus aurantium. Obesity Res. Hoffman JR, Kang J, Ratamess A. Thermogenic effect from nutritionally enriched coffee consumption.

J Int Soc Sports Nutr. Citrus aurantium extract has no effect on blood pressure or heart rate in healthy adults. Unpublished report Talbott SM, Christopulos AM, Richards E. Haller CA, Duan M, Peyton J III, Benowitz N. Human pharmacology of a performance-enhancing dietary supplement under resting and exercise conditions.

Brit J Clin Pharmacol. Seifert JG, Nelson A, Devonish J. Effect of acute administration of an herbal preparation on blood pressure and heart rate in humans.

International J Med Sci. Stohs SJ, Preuss HG, Keith SC. Effects of p -synephrine alone and in combination with selected bioflavonoids on resting metabolism, blood pressure, heart rate and self-reported mood changes.

Int J Med Sci. Shara M, Stohs SJ. Safety evaluation of bitter orange extract p -synephrine in healthy volunteers. Presented at the annual meeting of the American College of Nutrition.

Abstract No. Bloomer RJ, Canale RE, Blankenship MM. Effects of the dietary supplement Meltdown on catecholamine secretion, markers of lipolysis, and metabolic rate in men and women: a randomized, placebo controlled, cross-over study.

Lipids Health Disease. Bloomer R, Fisher-Wellman KH, Hammond KG. Dietary supplement increases plasma norepinephrine, lipolysis, and metabolic rate in resistance trained men. Hoffman JR, Kang J, Ratamess NA. Thermogenic effect of an acute ingestion of a weight loss supplement.

Stohs SJ. Assessment of the adverse event reports associated with Citrus aurantium bitter orange from April to October Dragull K, Breksa AP, Cain B.

Synephrine content of juice from Satsuma mandarins Citrus unshiu Marcovitch. J Agric Food Chem. Uckoo RM, Jayaprakasha GK, Nelson DS, Pati BS. Rapid simultaneous determinations of amines and organic acids in citrus using high-performance liquid chromatography.

Karch SB. Peer review and the process of publishing of adverse drug event reports. J Forensic Legal Med. Hengtmann JH, Aulepp H. Pharmacokinetics and metabolism of synephrinc. Arzneimittel Forschung.

Hansen DK, George NI, White GE. Physiological effects following administration of Citrus aurantium for 28 days in rats. Toxicol Appl Pharmacol. Reagan-Shaw S, Nihal M, Ahmed N. Dose translation from animal to human studies revisited. FASEB J. Rozec B, Gauther C. β3-Adrenoreceptors in the cardiovascular system: Putative roles in human pathologies.

Pharmacol Therap. 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. Google Scholar. 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. Kliszczewicz B, Bechke E, Williamson C, Bailey P, Hoffstetter W, McLester J, McLester C. The influence of citrus aurantium and caffeine complex versus placebo on the cardiac autonomic response: a double blind crossover design.

Quintana DS. Statistical considerations for reporting and planning heart rate variability case-control studies. Garg S, Jovanovic L. Relationship of fasting and hourly blood glucose levels to HbA1c values: safety, accuracy, and improvements in glucose profiles obtained using a 7-day continuous glucose sensor.

Diabetes Care. Legro RS, Finegood D, Dunaif A. A fasting glucose to insulin ratio is a useful measure of insulin sensitivity in women with polycystic ovary syndrome. J Clin Endocrinol Metab. CAS PubMed Google Scholar. Dekker MJ, Gusba JE, Robinson LE, Graham TE.

Glucose homeostasis remains altered by acute caffeine ingestion following 2 weeks of daily caffeine consumption in previously non-caffeine-consuming males. Br J Nutr. Graham TE, Sathasivam P, Rowland M, Marko N, Greer F, Battram D. Caffeine ingestion elevates plasma insulin response in humans during an oral glucose tolerance test.

Can J Physiol Pharmacol. Shi X, Xue W, Liang S, Zhao J, Zhang X. Acute caffeine ingestion reduces insulin sensitivity in healthy subjects: a systematic review and meta-analysis. Nutr J. Petersen MC, Vatner DF, Shulman GI. Regulation of hepatic glucose metabolism in health and disease. Nat Rev Endocrinol.

Graham TE, Spriet LL. Performance and metabolic responses to a high caffeine dose during prolonged exercise. Stuart GR, Hopkins WG, Cook C, Cairns SP. Multiple effects of caffeine on simulated high-intensity team-sport performance. Med Sci Sports Exerc. Kliszczewicz B, Buresh R, Bechke E, Williamson C.

Metabolic biomarkers following a short and long bout of high-intensity functional training in recreationally trained men.

Journal Citrus aurantium for muscle recovery Whole grain snacking options International Society of Sports Aurantim volume 15Article number: 34 Cite this reovery. Fat intake and food allergies details. Redovery physically active males Gor After consumption, participants were monitored mudcle a min ingestion period, then completed a repeated Wingate protocol, and were then monitored throughout a min recovery period. Cardiac autonomic function Heart Rate HR and Heart Rate Variability HRV and plasma epinephrine E and norepinephrine NE were taken at four different time points; Ingestion period: baseline I1post-ingestion period I2 ; Recovery period: immediately post-exercise R1post-recovery period R2. Heart rate variability was assessed in 5-min increments. The cultivation of commercially available supplements has substantially increased throughout recent years, making the use of pharmacologic ergogenic aids more prevalent and readily available to the general population and athletic community. Citrus aurantium for muscle recovery The scientific name Citrus Aurantium refers to a citrus recoverh Citrus aurantium for muscle recovery Orange that is native to southern Aurwntium but has Citrus aurantium for muscle recovery to many parts of the world. Due to the Fat intake and food allergies musclee and aurantim taste of the revovery orange fruit; it is not commonly eaten instead the active ingredient Optimal nutrition for team sports performance is extracted from the peel and is used in fat burners and thermogenics. The main function of Citrus Aurantium is increasing metabolic rate and it is an effective fat burning ingredient. Studies have shown that when Citrus Aurantium has been taken before a workout the body will burn more fat than carbohydrates. Citrus Aurantium is a legal substance and is often confused with the now-banned substance Ephedrine because of how similar the effects are. Ephedrine strongly stimulates the alpha-1 and alpha-2 adrenoreceptors leading to increased heart rate and blood pressure, however, Citrus Aurantium is less potent and only weakly stimulates these receptors.

Author: Netilar

0 thoughts on “Citrus aurantium for muscle recovery

Leave a comment

Yours email will be published. Important fields a marked *

Design by ThemesDNA.com