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* SPEED TRAINING REPORT *
8 Specially Prepared Techniques for More Explosive POWER and SPEED!
>> Get it FREE Now! <<
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Contributed by: Flawless Fitness Media
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90 Tablets |
Supplement Facts
Serving Size 2 Tablets
Servings Per Container 45
2 Tablets = 2728.3mg |
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| Proprietary FX1 Power
Vita™ Matrix, Including, 130.7mg: |
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|
Vitamin B1 (Thiamine)..................%DV: 1333
Vitamin B5 (Calcium Pantothenate).%DV:1000
Vitamin B6(Pyridoxine HCL)............%DV: 500
Vitamin B9 (Folic Acid)...................%DV: 100
Vitamin B12 (Cobalamin)..............%DV: 5000
* %DV = % of Daily Value based on RDA
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| Proprietary FX2 Thunder™ Matrix, Including: 1227.5mg: |
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Beta-Alanine..........................................*mg
Methylxanthines
(Caffeine Anhydrous USP).................................................225mg
NADH (Nicotinamide Adenine
Dinucleotide)..........................................*mg
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| Proprietary FX3 Lightning™ Matrix, Including, 905.1mg: |
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Acetyl L-Carnitine...................................*mg
N-Acetyl-Tyrosine..................................*mg
DL-Phenylalanine...................................*mg
Vinpocetine...........................................*mg
Huperzine A..........................................*mg
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| FX4 ROS Defence™ Matrix, Including, 425mg: |
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| N-Acetyl Cysteine...................................*mg
R-ALA....................................................*mg |
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| FX5 Speed
Stream™ Delivery Matrix, Including, 40mg: |
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| Bioperine™.............................................*mg
Capsicum annuum L. (fruit) 40 000 H.U......*mg |
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| Other
Ingredients: |
| Stearic Acid, Microcrystalline Cellulose, Dicalcium Phosphate,
Magnesium Stearate, Croscarmellose Sodium, and Silicon Dioxide |
Directions and Warnings |
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Retailed in the USA by:
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The Science Behind MUSCLESPEED™
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MUSCLESPEED™ - Supplement Facts |
Discover MUSCLESPEED's™ nutritional profile and all of its benefits. Learn about each ingredient, examine the research and understand why this supplement is the right choice for extreme sport athletes. After constant refinement and product innovation, we proudly offer the most effective supplement for power and speed. Now, it's time to give away some of our secrets - Enjoy!
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FX1 Power Vita Blend™
A matrix that blends a precise ratio of B vitamins designed to: |
Boost energy levels, assist in the production of neurotransmitters, stimulate the brain, improve the transmission of certain nerve cells, fight against depression and anxiety, manufacture amino acids, enhance the proper utilization of fats, carbohydrates and protein. |
B1 (thiamine): Thiamine works with the other B vitamins to change protein, carbohydrate, and fat to energy. Every cell of the body requires vitamin B1 to form the fuel the body runs on - ATP.
[+,-] Read About it
Thiamine may be used to support nerve health, and minimize numbness and tingling, helping to protect against this condition.
Thiamine is essential for the transmission of certain types of nerve signal between the brain and the spinal cord.
It is especially involved in carbohydrate metabolism in the brain.
Tests on volunteers at higher doses have claimed an increase in mental acuity[1]
References
1- Thiamine's Mood-Mending Qualities, Richard N. Podel, Nutrition Science News, January 1999.
B5 (pantothenic acid): Pantothenic Acid is essential for the propagation of nerve signals and the contraction of large muscle groups. Your ability to generate power will be determined not only by the strength of your muscles, but by your bodys ability to signal them to contract.
[+,-] Read About it
Pantothenic acid is essential for life and is involved in a wide range of bodily functions, including making fats, neurotransmitters, hormones, haemoglobin, and other important molecules that are involved in growth, reproduction and normal functioning of the body.
Vitamin B5 is a precursor of coenzymes that are part of important chemical reactions in the body necessary for the production of energy from food.
Pantothenic acid is used in the synthesis of coenzyme A (CoA). The transfer of carbon atoms by coenzyme A is important in cellular respiration, as well as the biosynthesis of many important compounds such as fatty acids, cholesterol, and acetylcholine.
From the TCA cycle, acetyl-CoA can also initiate the fatty acid synthesis pathway[1]
Pantothenic acid also helps the body absorb and utilize vitamin B6, vitamin B12 and vitamin C.
Panthothenic acid is also used as a supplement for people who suffer from depression or anxiety.
References
1- Combs, G.F. The Vitamins: Fundamental Aspects in Nutrition and Health. 2008.San Diego: Elsevier Inc.
B6 (pyridoxine): Vitamin B6 is involved with more than 101 chemical reactions that occur in our bodies
[+,-] Read About it
It helps us by aiding in the manufacturing of amino acids.
Vitamin B6 helps us to make what's called neurotransmitters.[1] Neurotransmitters are chemicals that connect one nerve cell to the next and enable these two nerve cells to communicate with one another. Some of these neurotransmitters are serotonin, norepinephrine, dopamine and what's called GABA.
It assists in metabolizing our foods and converting these foods into energy we need to get us through our day.
Vitamin B6 helps our bodies to produce what's called Lymphocytes. These are white blood cells that are called out to attack foreign invaders in our bodies called antigens.
References
1- Combs, G.F. The Vitamins: Fundamental Aspects in Nutrition and Health. 2008. San Diego: Elsevier
B9 (folic acid): Vitamin B9 (also called folate or folacin), is needed for energy production and a strong immune system.
[+,-] Read About it
Folate is necessary for the production and maintenance of new cells[1]. It helps to form the DNA and RNA in our genes, which are needed to regulate cell formation, red blood cells, skin cells, and the cells that line your small intestine.
folic acid is actually better absorbed into the system in its supplemental form, especially when combined with vitamin B12 and vitamin C. Vitamin C prevents folic acid from being broken down too quickly in your body.
Folic acid may also help prevent heart disease and stroke by reducing homocysteine in the blood. Homocysteine is an amino acid found in meats that can damage arterial walls and contribute to development of atherosclerosis, a condition that often leads to early heart attack.
Folic acid is also thought to be helpful to improving ulcerative colitis symptoms, and may help prevent cancer of the cervix and the colon.
References
1- Kamen B (1997). "Folate and antifolate pharmacology". Seminars in oncology 24 (5 Suppl 18): S1830S1839
B12 (cobalamin): Vitamin B-12 (Cobalamin) aids in the production of red blood cells, normal functioning of the nervous system, and helps to metabolize protein and fat.
[+,-] Read About it
The coenzymes of Vitamin B-12 assist in the metabolism of fatty acids and amino acids that contribute to the formation and maintenance of the nerves, blood, and other cells.
It is also needed to make myelin, a protective fatty layer that coats nerve cells and keeps electrical impulses moving through the body.
This vitamin is essential for cell replication and plays a critical role in the production of DNA and RNA.
Without enough vitamin B12 the nervous system can "short out" and cause interruptions in mental function--symptoms of B12 deficiency can be so severe that they actually mimic senility.
Some Possible Benefits
Prevent anemia by forming and regenerating red blood cells
Help maintain a healthy nervous system and reduce depression and irritability
Alleviate nerve pain, numbness, and tingling
Enhance proper utilization of fats, carbohydrates, and protein
Increase energy
Reduce heart disease risks
Sharpen mental agility, concentration, memory, and balance due to its "brain booster" effects
Keeps the immune system healthy
May slow the progression of HIV infection to AIDS
Improve ability to fight off disease
References
1- Victor Herbert (1988). "Vitamin B-12: plant sources, requirements, and assay". American Journal of Clinical Nutrition 48: 8528.
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FX2 Thunder™
Features a high-caliber formulation that is designed to help you max-out muscle fiber contractions, quicken reaction time, fight fatigue and boost your metabolism.
Beta Alanine: Beta-Alanine raises Carnosine concentrations mainly in type II muscle fibers. These are the "fast-twitch" fibers that are so important for explosive sports, such as sprinting and weight training. This is largely accomplished by its ability to slow down the increase in H+ (hydrogen ions) which cause a lowering of our muscles pH (more acidic) and causing performance to degrade. Essentially, Carnosine acts as an intracellular buffer allowing muscles to continue to contract forcibly for a longer period of time.
[+,-] Read About it
A research study published by Stout et al on Nov 7th 2008 suggests that by improving intracellular pH control, BA improves muscle endurance.[1]
In another published study the 11th of February 2009, Smith et al concluded: The use of HIIT to induce significant aerobic improvements is effective and efficient. Chronic BA supplementation may further enhance HIIT, improving endurance performance and lean body mass.[2]
a 10-week study on the effects of Beta-Alanine was conducted on football players. The results of this study showed that the group of players who supplemented with Beta-Alanine plus creatine gained more muscle and lost more fat than the creatine or placebo group alone. [3]
In a 4 week study subjects who consumed Beta-Alanine significantly improved their exercise performance and power output over the placebo group. Researchers found that Beta-Alanine also increased Carnosines ability to buffer lactic acid. [4]
The use of beta-alanine results in higher training volumes and lower subjective feelings of fatigue. BA use indicated that as the duration of supplementation continued, the efficacy of beta-alanine supplementation in highly trained athletes became apparent. [5]
References
1- Stout et al; The effect of beta-alanine supplementation on neuromuscular fatigue in elderly (5592 Years): a double-blind randomized study. Published: 7 November 2008, Department of Health and Exercise Science, University of Oklahoma, Norman, OK, USA
2- Smith et al; Effects of ί-alanine supplementation and high-intensity interval training on endurance performance and body composition in men; a double-blind trial. Published: 11 February 2009. Metabolic and Body Composition Laboratory, Department of Health and Exercise Science, University of Oklahoma, Norman, OK 73019, USA
3- International Journal of Sports Nutrition and Exercise Metabolism. 2006 Aug;16(4):430-46. Effect of creatine and Beta-Alanine supplementation on performance and endocrine responses in strength/power athletes.
4- Amino Acids. 2007 Feb; 32(2):225-33. Influence of Beta-Alanine supplementation on skeletal muscle carnosine concentrations and high intensity cycling capacity.
5- Nutr Res. 2008 Jan;28(1):31-5.Short-duration beta-alanine supplementation increases training volume and reduces subjective feelings of fatigue in college football players.Hoffman JR, Ratamess NA, Faigenbaum AD, Ross R, Kang J, Stout JR, Wise JA.Department of Health and Exercise Science, The College of New Jersey, PO Box 7718, Ewing, NJ 08628, USA. hoffmanj@tcnj.edu
Methylxanthines: Caffeine Anhydrous USP, is a fast-acting substance that delivers the right molecular structure to your energy systems for maximum energy and power output. It increases mental alertness and neurologically provides the surge you need to maximize your training.
Studies have proven this powerful substance reaches deep into muscle cells to provide lasting power and delaying the onset of muscle fatigue.
[+,-] Read About it
The precise amount of caffeine necessary to produce effects varies from person to person depending on body size and degree of tolerance to caffeine. It takes less than an hour for caffeine to begin affecting the body and a mild dose wears off in three to four hours.[1]
Caffeine is an ergogenic: increasing the capacity for mental or physical labor. A study conducted in 1979 showed a 7% increase in distance cycled over a period of two hours in subjects who consumed caffeine compared to control tests.[2] Other studies attained much more dramatic results; one particular study of trained runners showed a 44% increase in "race-pace" endurance, as well as a 51% increase in cycling endurance[3]. The extensive boost shown in the runners is not an isolated case; additional studies have reported similar effects. Another study resulted in subjects cycling 29% longer during high intensity circuits.[4]
Caffeine also exerts some direct physical effects on muscle that may also help explain its ergogenic effects. As long ago as 1910, scientists discovered that caffeine administration increased the contractile ability of isolated muscle[5] and also that this effect was (up to a point) dose dependent[6]. This almost certainly occurs because caffeine stimulates the release of calcium ions (Ca2+) from a region of the cell known as the sarcoplasmic reticulum. Ca2+ ions are involved in the process of initiating a sequence of chemical and electrical events that eventually lead to muscular contraction, and we now know that impaired calcium release can contribute to muscular fatigue[7]. Although the isolated muscle tissue studies on caffeine stimulated Ca2+ release used much higher levels of caffeine than would be found after even large amounts of caffeine ingestion, we now know that other naturally occurring molecules in the body such as cyclic ADP-ribose can dramatically increase the sensitivity of the Ca2+ release system to caffeine5.
Typically, caffeine can significantly delay the onset of fatigue during endurance exercise at 70-85% VO2max lasting more than 30 minutes and enables higher work rates to be maintained during exercise with a reduced perception of effort. Studies have involved cyclists, runners and other endurance athletes in a range of test protocols (time-trials, incremental intensity tests, tests to exhaustion etc.) and over a wide range of distances/durations.
In recent years its become clear that caffeine-mediated CNS stimulation plays a much greater role enhancing performance than was first thought. Consequently there have been more good quality studies into the effects of caffeine in shorter events and the results look promising. For example, a look at the most recent research shows the following:
- Caffeine administered to runners 1 hour before an 8km run produced an average improvement of 23.8 seconds over the distance compared to an inert placebo[8];
- Compared to placebo, trained rugby players who underwent simulated rugby play (seven circuits in each of two 40-minute halves separated by a 10-minute break) performed significantly better in sprinting, driving and passing drills when they took caffeine compared to placebo[9];
- Intermittent cycle sprinting (2 sets of eighteen 4-second sprints with 2 minutes of active rest in between sprints) resulted in an 8.5% increase in the total amount of sprinting work performed and a 7% increase in mean sprint power when caffeine was consumed[10];
- Caffeine produced an improvement of 1.2% in the times for 2000m ergo rowing and a corresponding increase in power of 2.7% compared to placebo[11];
The perception of leg muscle discomfort associated with cycling was significantly reduced in female cyclists when caffeine was administered when compared to placebo[12].
References
1-Bolton, Ph.D., Sanford; Gary Null, M.S. (1981). "Caffeine: Psychological Effects, Use and Abuse". Orthomolecular Psychiatry 10 (3): 202211. doi:10.1152/physrev.00004.2004 br (inactive 2008-06-25). Retrieved on 2006-08-12.
2- Ivy, JL; Costill DL, Fink WJ, Lower RW (1979 Spring). "Influence of caffeine and carbohydrate feedings on endurance performance". Med Sci Sports 11 (1): 611. PMID 481158.
3- Graham, TE; Spriet, LL (1991 December). "Performance and metabolic responses to a high caffeine dose during prolonged exercise". J Appl Physiol 71 (6): 22928. PMID 1778925.
4- Trice, I; Haymes, EM (March 1995). "Effects of caffeine ingestion on exercise-induced changes during high-intensity, intermittent exercise". Int J Sport Nutr 5 (1): 3744. doi:10.1152/physrev.00004.2004. PMID 7749424.
5- Proc. R. Soc. Lond. B Biol. Sci 1910; 82:568574
6-. J. Physiol 1968; 194:5174
7- Exp Physiol 1995; 80:497-527
8- J Sports Sci. 2006; 24(4):433-9
9- Med Sci Sports Exerc. 2005;37(11):1998-2005
10- Med Sci Sports Exerc. 2006;38(3):578-85
11- Med Sci Sports Exerc. 2000;32(11):1958-63
12- Med Sci Sports Exerc. 2006;38(3):598-604
NADH: Nicotinamide Adenine Dinucleotide is a very safe, effective substance, not toxic even in high concentrations and has no side effects. NADH can
increase cellular energy production and can also extend cell life. Even seasoned athletes found that NADH helped
them to surprisingly improve their athletic performance and oxygen capacity. These same athletes improved their reaction time by 10-20%!
[+,-] Read About it
The results of a European research study were reported in April, 1996, in the International Journal of Sports Medicine. This study measured the reaction times and ergometric performance of competition level cyclists and long distance runners. The athletes took 5 mg. of NADH daily for 4 weeks. After 4 weeks, 16 of the 17 athletes had decreased their reaction times by an astounding 10 to 20%. These are impressive improvements for young, well-conditioned competitive athletes. The athletes themselves were also quite impressed that their reaction times had shortened. In addition, their spiro-ergometric parameters, maximum oxygen uptake (VO2 max/kg) and maximum heart frequency were also improved. There were no negative side effects. The athletes commented that they
also experienced greater mental acuity and alertness.
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FX3 Lightning™
Achieve mental clarity, alertness, focus, and a sense of well-being to perform at your highest level.
Acetyl L-Carnitine: ALC facilitates both the release and synthesis of Acetylcholine. It has the ability to increase the synthesis of Acetylcholine occurs as a result of it donating its Acetyl group towards the production of Acetylcholine. ALC increases the Brain's levels of Choline Acetylase (which in turn facilities the production of Acetylcholine). Furthermore, it enhances the release of Dopamine from Dopaminergic Neurons and improves the binding of Dopamine to Dopamine Receptors.
[+,-] Read About it
ALC facilitates both the release and synthesis of acetylcholine. It has the ability to increase the synthesis of acetylcholine which occurs as a result of it donating its Acetyl group towards the production of acetylcholine. ALC increases the Brain's levels of choline acetylase (which in turn facilities the production of acetylcholine). Furthermore, it enhances the release of dopamine from dopaminergic Neurons and improves the binding of dopamine to dopamine receptors.
Additional benefits of ALC :
ALC improves (eye to hand) Coordination [supplemental ALC @ 1.5 grams per day for 30 days improved eye to hand coordination in healthy, sedentary subjects by a factor of 300-400%].
ALC given prior to exercise increased the maximum running speed of animals.
ALC increases plasma Testosterone levels (via its influence on Acetylcholine neurotransmission in the Striatal Cortex of the Brain) and prevents the depletion of Testosterone caused by exposure to excessive Stress [research - rats].
ALC improves the Energy metabolism of Neurons (by enhancing the transport of Medium-Chain Saturated Fatty Acids and Short-Chain Saturated Fatty Acids across the Cell Membranes of Neurons into the Mitochondria).
ALC transports Lipids into the Mitochondria of Cells.
ALC improves the quality of Sleep and reduces the quantity of Sleep required.
ALC reverses the age-related decline that occurs in Cholinergic Receptors (i.e. the Receptors that receive Acetylcholine).
Acetyl-L-Carnitine (ALC) improves Learning ability [women aged 22 - 27 were supplemented with ALC for 30 days. Complex video game tests before and after supplementation concluded that supplemental ALC caused large increases in speed of Learning, speed of reaction and reduction in errors].
ALC improves both Short-Term Memory and Long-Term Memory.
ALC improves Mood [ALC improves Mood in 53% of healthy subjects].
ALC stimulates and maintains the growth of new Neurons within the Brain (both independently of Nerve Growth Factor (NGF) and as a result of preserving NGF) and helps to prevent the death of existing Neurons [ALC inhibits Neuron death in the Striatal Cortex, Prefrontal Cortex and the Occipital Cortex of the Brain].
References
1- De Falco, F. A., et al. Effect of the chronic treatment with L-acetylcarnitine in Downs syndrome. Clin Ther. 144:123-127, 1994.
2- Bowman, B. Acetyl-carnitine and Alzheimers disease. Nutr Rev. 50:142-144, 1992.
3- Bruno, G., et al. Acetyl-L-carnitine in Alzheimer disease: a short-term study on CSF neurotransmitters and neuropeptides. Alzheimer Dis Assoc Disord (USA). 9(3):128-131, 1995.
4- Calvani, M., et al. Action of acetyl L-carnitine in neurodegeneration and Alzheimers disease. Annals of the New York Academy of Sciences (USA). 663:483-486, 1993.
5- Carta, A., et al. Acetyl L-carnitine: a drug able to slow the progress of Alzheimers Disease? Annals of the New York Academy of Sciences (USA. 640:228-232, 1991.
6- Guarnaschelli, C., et al. Pathological brain ageing: evaluation of the efficacy of a pharmacological aid. Drugs under Experimental and Clinical Research. 14(11):715-718, 1988.
7- Passeri, M., et al. Acetyl L-carnitine in the treatment of mildly demented elderly patients. International Journal of Clinical Pharmacology Research. 10(1-2):75-79, 1990.
8- Pettegrew, J. W., et al. Clinical and neurochemical effects of acetyl-L-carnitine in Alzheimers disease. Neurobiol Aging. 16:1-4, 1995.
9- Rai, G., et al. Double-blind, placebo controlled study of acetyl-L-carnitine in patients with Alzheimers dementia. Current Medical Research and Opinion. 11(10):638-647, 1989.
10- Sano, M., et al. Double-blind parallel design pilot study of acetyl levocarnitine in patients with Alzheimers disease. Arch Neurol. 49:1137-1141, 1992.
11- inforiani, E., et al. Neuropsychological changes in demented patients treated with acetyl-L-carnitine. International Journal of Clinical Pharmacology Research. 10(1-2):69-74, 1990.
12- Spagnoli, A. U., et al. Long-term acetyl-l-carnitine treatment in Alzheimers disease. Neurology. 41(11):1726-1732, 1991.
N-Acetyl-Tyrosine: It is a precursor of the neurotransmitter dopamine, as well as a precursor to the adrenal hormones norepinephrine and epinephrine.[1] L-tyrosine may help athletes avoid overtraining, due to its ability to offset fatigue.[2] Because L-tyrosine is a precursor of Dopamine, supplementing with L-tyrosine may heighten mental alertness, increase feelings of well being, and offset physical and mental fatigue.[3],[4]
[+,-] Read About it
Athletes, people trying to lose weight, and the elderly. Hard training athletes may benefit from supplementing with L-tyrosine as it helps to offset fatigue and stress associated with intense training.
People attempting to lose weight may benefit from supplemental L-tyrosine. The thyroid is responsible for the manufacture of T-cells. L-tyrosine influences the manufacture of thyroxin [T-cells], which influences basal metabolic rate. Because of this, L-tyrosine may prove effective for weight loss.
References
1- Wurtman, RJ, and Lewis MC. Exercise, plasma composition and neurotransmission. In: Advances in Nutrition and Top Sport, edited by Brouns F.. Basel: Karger, 1991, vol. 32, p. 94-109.
2- Romanowski, W, and Grabiec S. The role of serotonin in the mechanism of central fatigue. Acta Physiol Pol 25: 127-134, 1974.
3- Lieberman, HR, Corkin S, Spring BJ, Wurtman RJ, and Growden JH. The effects of dietary neurotransmitter precursors on human behavior. Am J Clin Nutr 42: 366-370, 1985.
4- Banderet, LE, and Lieberman HR. Treatment with tyrosine, a neurotransmitter precursor, reduces environmental stress in humans. Brain Res Bull 22: 759-762, 1989.
DL-Phenylalanine: DLPA, otherwise known as DL-phenylalanine, is a special form of the essential amino acid phenylalanine. It is believed to reduce chronic pain, fight depression, muscle cramps, soreness, and migraines through the release of endorphins. Endorphins are neurotransmitters that are found in the brain. They are your body's natural painkillers. Not only does it relieve pain, it also has been connected to "euphoric" feelings, such as the "feel good" feeling that comes with prolonged, strenuous exercise, often known as "runner's high".
[+,-] Read About it
DLPA, otherwise known as DL-phenylalanine, is a special form of the essential amino acid phenylalanine. It is believed to reduce chronic pain, fight depression, muscle cramps, soreness, and migraines through the release of endorphins. Endorphins are neurotransmitters that are found in the brain. They are your body's natural painkillers. Not only does it relieve pain, it also has been connected to "euphoric" feelings, such as the "feel good" feeling that comes with prolonged, strenuous exercise, often know as "runner's high".
Research has shown that DLPA offers good, if not excellent, relief from pain in patients. [1]
A 1979 study at the University of Chicago conducted by Dr. Ehrenpreis [2] In treating various arthritic conditions with DLPA daily, highly significant results were obtained; better than 75 percent of the chronic pain patients experienced good to complete relief within a period of one week to one month.
May support fat loss by helping curb sugar and carbohydrate cravings.
References
[1] # Pert, C. "Oplole Antagonist Counters Obesity," Science News, Feb. 14, 1981.
[2] Op. Clt., Ehrenpreis, et al., 1979, pp. 379-382.
Vinpocetine: Vinpocetine supports healthy blood circulation[1,2] and oxygen flow to the brain[3,4]. It's a powerful antioxidant and it also enhances the delivery of glucose to the brain. Glucose is the brains primary fuel source, and without it the brain will shut-down. Athletes who supplement with Vinpocetine report significant improvement in visual acuity, memory and focus. Athletes also report that Vincamine is extremely thermogenic. It causes rapid losses in body fat, and it accomplishes this by stimulating the release of the hormone norepinephine.
[+,-] Read About it
Vinpocetine improves oxygen utilization which means that the brain should be more effective at producing ATP (the energy A currency@ of the body). In fact, research has shown that vinpocetine effectively elevated cerebral concentrations of ATP, as well as ATP concentrations in red blood cells.
In addition to its circulation and oxygen enhancing properties, another mechanism of Vinpocetine s action is that it seems to work as part of the cholinergic pathway. This is the pathway that involves the production of the memory neurotransmitter, acetylcholine. Specifically, Vinpocetine increase the firing rate of certain nerve cells.
References
1- Miyazaki M. The effect of a cerebral vasodilator, vinpocetine, on cerebral vascular resistance evaluated by the Doppler ultrasonic technique in patients with cerebrovascular diseases. Angiology 1995;46:53-8.
2- Solti F, Iskum M, Czako E. Effect of ethyl apovincaminate on the cerebral circulation. Studies in patients with obliterative cerebral arterial disease. Arzneimittelforschung 1976;26:1945-7.
3. Bonoczk P, Panczel G, Nagy Z. Vinpocetine increases cerebral blood flow and oxygenation in stroke patients: a near infrared spectroscopy and transcranial Doppler study. Eur J Ultrasound. 2002 Jun;15(1-2):85-91.
4. Depresseux JC. The effect of vincamine on the regional cerebral blood flow in man. Eur Neurol. 1978;17(2):100-7.
Huperzine A: Huperzine A inhibits the enzyme acetylcholinesterase(AChE). This enzyme breaks down acetylcholine, a substance that plays an important role in mental function and muscle contraction. When AChE is released into the neuromuscular junction by the muscle cell, it inactivates acetylcholine within 1/500 of a second. If the enzyme that breaks it down is inhibited, acetylcholine levels in the brain tend to rise.
[+,-] Read About it
Acetylcholine is less known by lay people for its role in stimulates skeletal muscle contraction. Specifically, acetylcholine binds to receptor sites on the muscle fiber membrane which, with the help of a sodium ion, causes the muscle fiber to contract. Without acetylcholine muscular contraction (and athletic activity) would not be possible.
The chemical action of huperzine A is very precise and specific. It "fits" into a niche on the enzyme where acetylcholine is supposed to attach.[1],[2] Because huperzine A is in the way, the enzyme can't grab and destroy acetylcholine. This mechanism has been demonstrated by considerable scientific work, including sophisticated computer modeling of the shape of the molecule.[3] Huperzine may also help protect nerve cells from damage.[5-7]
Since Huperzine is a selective AChE inhibitor, it may have benefits for athletes who wish to improve cognitive function and concentration. It may also have the side benefit of promoting muscular contraction for effective athletic performance.
References
1- Raves ML, Harel M, Pang YP, et al. Structure of acetylcholinesterase complexed with the nootropic alkaloid, (-)-huperzine A. Nat Struct Biol. 1997;4:5763.
2- Ashani Y, Peggins JO III, Doctor BP. Mechanism of inhibition of cholinesterases by huperzine A. Biochem Biophys Res Commun. 1992;184:719726.
3- Pang YP, Kozikowski AP. Prediction of the binding sites of huperzine A in acetylcholinesterase by docking studies. J Comput Aided Mol Des. 1994;8:669681.
4- Ved HS, Koenig ML, Dave JR, et al. Huperzine A, a potential therapeutic agent for dementia, reduces neuronal cell death caused by glutamate. Neuroreport. 1997;8:963968.
5- Zhou J, Zhang HY, Tang XC. Huperzine A attenuates cognitive deficits and hippocampal neuronal damage after transient global ischemia in gerbils. Neurosci Lett. 2001;313:137-140.
6- Zhou J, Fu Y, Tang XC. Huperzine A protects rat pheochromocytoma cells against oxygen-glucose deprivation. Neuroreport. 2001;12:2073-2077.
7- Wang LM, Han YF, Tang XC. Huperzine A improves cognitive deficits caused by chronic cerebral hypoperfusion in rats. Eur J Pharmacol. 2000;398:65-72.
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| FX4 ROS Defence™
Protects against cellular damage, muscular fatigue, and scavenges for free radicals!
N-Acetylcysteine: N-acetylcysteine (NAC) enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise in endurance-trained individuals. NAC is one of the most important antioxidants for athletes. NAC is known for its positive effects on muscle trauma caused by lifting weights or intense cardio training. This highly bio-available form L-cysteine assists in combating exercise-induced damage to muscle tissue, helps detoxify the liver, builds connective tissue, fights viral infections, helps fight aging, and aids in joint health.
[+,-] Read About it
NAC is the stable form of L-Cysteine. This allows your body to make use of the supplement and release glutathione in the body, which fights the cellular damage of oxidative stress.
N-acetylcysteine enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise in endurance-trained individuals
NAC is used by elite athletes who have suffered tears and partial tears of connective tissue to help them recover from injuries. In less serious cases, it can help reduce joint inflammation and the pain.
Supplementation with NAC has been shown to illicit a protective effect on muscle and other related tissues after intense exercise.
It aids in recovery and consistent use may help maintain and even add muscle.
NAC has shown the ability to inhibit viral replication may assist in fighting viral infections from HIV to the flu.
NAC helps neutralize the byproducts of ingested fats and alcohol metabolism and protect the body from the damaging effects of chemotherapy, cigarette smoke, heavy metals, and various other substances.
N-acetylcysteine on respiratory muscle fatigue during heavy exercise.
N-acetylcysteine attenuates the decline in muscle Na+,K+-pump activity and delays fatigue during prolonged exercise in humans.
N-acetylcysteine enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise in endurance-trained individuals
References
1- Sen CK, Rankinen T, Vδisδnen S, Rauramaa R., Oxidative stress after human exercise: effect of N-acetylcysteine supplementation. J Appl Physiol. 1994 Jun;76(6):2570-7.
2- Horowitz, J.D., et al., "Combined Use of Nitroglycerin and N-acetylcysteine in the Management of Unstable Angina Pectoris," Circulation 77.4 (1988) : 787-94.
3- Kinscherf, R., et al., "Low Plasma Glutamine in Combination with High Glutamate Levels Indicate Risk for Loss of Body Cell Mass in Healthy Individuals: the Effect of N-Acetyle-Cysteine," J Mol Med 74.7 (1996) : 393-400.
4- Marchetti, G., et al., "Use of N-Acetylcysteine in the Management of Coronary Artery Diseases," Cardiologia 44.7 (1999) : 633-7.
5- Mold'eus, P., et al., "Lung Protection by a Thiol-Containing Antioxidant: N-Acetylcysteine," Respiration 50 suppl 1 (1986) : 31-42.
6- N-acetylcysteine enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise in endurance-trained individuals. I. Medved,1 M. J. Brown,2 A. R. Bjorksten,3 K. T. Murphy,1 A. C. Petersen,1 S. Sostaric,1 X. Gong,1 and M. J. McKenna1, First published June 11, 2004; doi:10.1152/japplphysiol.00371.2004
7- Effects of N-acetylcysteine on respiratory muscle fatigue during heavy exercise.Kelly MK, Wicker RJ, Barstow TJ, Harms CA. Department of Kinesiology, Kansas State University, 1A Natatorium, Manhattan, KS 66506, United States. Respir Physiol Neurobiol. 2009 Jan 1;165(1):67-72. Epub 2008 Oct 17.
8- N-acetylcysteine attenuates the decline in muscle Na+,K+-pump activity and delays fatigue during prolonged exercise in humans. McKenna MJ, Medved I, Goodman CA, Brown MJ, Bjorksten AR, Murphy KT, Petersen AC, Sostaric S, Gong X. School of Human Movement, Recreation and Performance, Victoria University, PO Box 14428, Melbourne, Victoria, Australia, 8001. michael.mckenna@vu.edu.au. J Physiol. 2006 Oct 1;576(Pt 1):279-88. Epub 2006 Jul 13.
9- N-acetylcysteine enhances muscle cysteine and glutathione availability and attenuates fatigue during prolonged exercise in endurance-trained individuals. Medved I, Brown MJ, Bjorksten AR, Murphy KT, Petersen AC, Sostaric S, Gong X, McKenna MJ. Muscle, Ions and Exercise Group, School of Human Movement, Recreation and Performance (FO22 Victoria University of Technology, PO Box 14428, MCMC, Melbourne, Victoria 8001, Australia. J Appl Physiol. 2004 Oct;97(4):1477-85. Epub 2004 Jun 11.
R-Alpha-Lipoic Acid: R-ALA is a potent antioxidant, which in contrast to other antioxidants; is both fat and water soluble, enabling it to exert an effect in almost any part of the body. Most ALA supplements feature a 50-50 blend of R and S isomers, but the R isomer is the only form that occurs naturally in the human body thus making it the most useful form. ALA is important for sports performance because it promotes increased glucose uptake and utilization. By improving the regulation of blood sugar glycation is reduced and our protein structures maintained. Alpha lipoic acid increases blood flow to the nerves and improves the transmission of nerve impulses.
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ALA stimulates blood flow by enhancing the activity of the Endothelial Nitric Oxide Synthase (eNOS) enzyme, supports energy production, and also functions as a cognitive enhancer.
This powerful antioxidant will help with heart strength, liver toxicity, boost the immune system preserve brain cells, and help in energy production.
Alpha Lipoic Acid improves nerve blood flow, reduces oxidative stress, and improves nerve conduction.
It significantly lowers blood sugar levels while increasing glycogen storage in muscles and liver.
Besides its antioxidant function alpha lipoic acid is the first coenzyme necessary in the conversion of glucose to ATP, and helps cells take up sugar and use it for fuel much more efficiently.
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Delivery boosters were introduced to MULTIPLY the power of the supplement, FAST. Additionally, expect a rise in thermogenesis, protect against inflammation, reduce pain, and much more…
Bioperine™: An ingredient that acts to increase the bioavailability of various compounds making your supplements more effective. This is like using high octane fuel while saving you money.
Capsicum annuum L. (fruit): The cayenne pepper is a member of the Capsicum family of vegetables, which are more commonly known as chili peppers. It is known botanically as Capsicum annuum. Cayenne helps the body to create hydrochloric acid, which is necessary for good digestion and assimilation, especially of proteins. It acts as a catalyst and increases the effectiveness of other herbs when used with it.
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Chili and even sweet peppers have been found to contain substances that significantly increase thermogenesis (heat production) and oxygen consumption for more than 20 minutes after they are eaten. They can help you lose weight.
All chili peppers, including cayenne, contain capsaicin, which in addition to giving cayenne its characteristic heat, is a potent inhibitor of substance P, a neuropeptide associated with inflammatory processes.
Capsaicin is being studied as an effective treatment for sensory nerve fiber disorders, including pain associated with arthritis, psoriasis, and diabetic neuropathy.
Cayenne and other red chili peppers have been shown to reduce blood cholesterol, triglyceride levels, and platelet aggregation, while increasing the body's ability to dissolve fibrin, a substance integral to the formation of blood clots.
Capsaicin is know to reduce pain
Its peppery heat stimulates secretions that help clear mucus from your stuffed up nose or congested lungs. Capsaicin is similar to a compound found in many cold remedies for breaking up congestion, except that capsaicin works much faster.
Cayenne may have an undeserved reputation for contributing to stomach ulcers. Not only does it not cause ulcers, hot peppers, in general, may help prevent them by killing bacteria you may have ingested, while powerfully stimulating the cells lining the stomach to secrete protective buffering juices that prevent ulcer formation.
References
1- Ensminger AH, Esminger M. K. J. e. al. Food for Health: A Nutrition Encyclopedia. Clovis, California: Pegus Press; 1986 1986. PMID:15210.
2- Gonzalez R, Dunkel R, Koletzko B, et al. Effect of capsaicin-containing red pepper sauce suspension on upper gastrointestinal motility in healthy volunteers. Dig Dis Sci 1998 Jun;43(6):1165-71 1998. PMID:18140.
3- Hautkappe M, Roizen MF, Toledano A, et al. Review of the effectiveness of capsaicin for painful cutaneous disorders and neural dysfunction. Clin J Pain 1998 Jun;14:97-106 1998.
4- Kempaiah RK, Srinivasan K. Integrity of erythrocytes of hypercholesterolemic rats during spices treatment. Mol Cell Biochem 2002 Jul;236(1-2):155-61 2002.
5- Sambaiah K, Satyanarayana MN. Hypocholesterolemic effect of red pepper & capsaicin. Indian J Exp Biol 1980 Aug;18(8):898-9 1980. PMID:18150.
6- Wood, Rebecca. The Whole Foods Encyclopedia. New York, NY: Prentice-Hall Press; 1988 1988. PMID:15220.
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