ATP Energy
Adenosine triphosphate, also referred to as ATP, is nature’s energy store. Every living organism needs ATP energy in order to carry out the processes that maintain life within that organism, including us humans for whom a continuous energy source is essential for our biochemistry, movement of fluids and the involuntary muscular movements exemplified by our heartbeat, respiration and digestion.
ATP energy is also required on occasion, such as for the contraction of muscle cells during exercise and athletic performance, and each of these activities, conscious or not, requires adenosine triphosphate to enable muscular contraction. As will be discussed, ATP is the source of all of that energy and so the more that can be produced during athletic performance, then the better you will perform.
ATP, and thus energy from ATP, can be produced in a number of ways within your body, such as how it uses its emergency energy store of creatine phosphate to add a phosphate group to adenosine diphosphate to generate the triphosphate. However, that is only useful for a few seconds, and the two major ATP energy creating routes involve cellular respiration of glucose to pyruvate followed either by the aerobic or anaerobic breakdown of that to adenosine triphosphate.
Here is each of these explained in slightly more detail:
Aerobic Respiration
Aerobic respiration proceeds from cellular respiration by using oxygen and an ignition source to burn the fuel: glycolysis initially converts glucose to pyruvate as the fuel, and then aerobic exercise provides oxygen, with cellular charge as the ignition source. Very similar to a regular fire: fuel, oxygen and ignition source. GSH Ignite promotes this ignition of oxygen and pyruvate to generate ATP energy under aerobic conditions.
The aerobic exercise you use to promote this includes jogging, floor exercises, step-ups and circuit training: anything that makes you breathe hard. You take in oxygen and use it to ignite the oxidation reaction of pyruvate to ATP, CO2 and water, using up ADP (adenosine diphosphate) in the process. The greater the cellular charge, then the more efficient is the cellular respiration, in the same way that the newer a lighter flint, the faster and for longer it will ignite the gas.
Aerobic respiration is the source of ATP energy for your everyday living and for non-explosive athletic events. It is the phosphate bonds in the unstable ATP molecule that generate energy when they are broken back down to ADP. If you remove one of the three phosphate groups, then the molecule is much more stable, and in doing that you also liberate 7.3 Kcal/mol of energy1.
GSH Ignite provides the ignition source that makes best use of the cellular electrical charge that enables your cellular respiration system to operate at maximum efficiency. Protein Extreme Energy also helps by maximizing that cellular charge on each cell in your body.
Anaerobic Respiration
Anaerobic respiration is respiration without oxygen, and enables adenosine triphosphate to be generated without oxygen being present. It is not as efficient a means of generating adenosine triphosphate as aerobic respiration, but it can enable rapid short-term ATP energy production for immediate explosive power.
In the absence of oxygen, the pyruvate mentioned above undergoes a form of fermentation that creates lactic acid and adenosine triphosphate. This is sufficient to offer you maximum athletic performance for a period of 2 -3 minutes, after which the lactic acid builds up and you can no longer function without anaerobic respiration. Sprinters use anaerobic conditions, and Usain Bolt can break a work 100m record with just one deep breath. That provides all the ATP needed before lactic acid kicks in.
The more you train, the more you are able to expend energy under low oxygen conditions, and that is why those that train more can run farther at higher speeds than those that train less: their cellular respiration is more efficient at producing ATP energy from the available oxygen before anaerobic respiration has to make up the balance. Likewise, their muscles can work longer under anaerobic conditions before lactic acid seizes up their muscles, and more oxygen is needed.
GSH Ignite supports cellular respiration, and also destroys the free radicals that are by-products of respiration. Free radical damage results from small oxygenated molecules that can destroy the membranes of the cells that generate adenosine triphosphate, and GSH Ignite offers the free radical killer glutathione and the enzyme superoxide dismutase that help maintain efficient cellular respiration through preventing these free radicals from destroying the cells that provide your ATP energy source.
Normal ATP Requirement
Around 160Kg of adenosine triphosphate can be created and used in the human body each day2; although at any one time you will have no more than around 250 grams available for use. In other words, your body can turn over its own weight of this amazing ATP molecule every day and athletes turn over even more ATP.
In summary, cellular respiration is responsible for the production of ATP in the mitochondria of your body cells, and the more effective your cellular respiration in oxidizing glucose ultimately to adenosine triphosphate, then the more ATP energy will be available to you to enable maximum athletic performance. It is therefore essential that your biochemistry is tuned to producing as much ATP as possible, and that is dependent on many factors, of which cellular respiration is the most important.
By maximizing your cellular charge and reducing the damaging effects of the free radicals that are a natural by-product of the process, you will maximize the production of adenosine triphosphate.
Protein Extreme Energy increases the cellular electrical charge that enables effective oxidation of glucose, and also enables more effective hydrolysis of adenosine triphosphate to energy plus ADP, whereas GSH Ignite negates the effects of free radicals and enables maximum efficiency in the conversion of ATP to energy.
1. Campbell, Neil. Biology, Third Edition. Benjamin Cummings, 1993: 97-101.
2. Törnroth-Horsefield S, Neutze R (December 2008). Opening and closing the metabolite gate. Proc. Natl. Acad. Sci. U.S.A.
105 (50): 19565–6.
Other reading:
Karp, Gerald (2008). Cell and Molecular Biology (5th edition). Hoboken, NJ: John Wiley & Sons.pp. 194.
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