Creatine Research and Information on the Benefits of Creatine
A substantial body of creatine research studies have discovered that creatine may have a wide
variety of benefits. In fact, creatine is being studied as a supplement that may help with diseases affecting the
neuromuscular system, such as muscular dystrophy.
Although creatine offers an array of benefits, most people think of it simply as a supplement that body builders
and other athletes use to gain strength and muscle mass. Nothing could be further from the truth.
Recent creatine research suggests creatine may have therapeutic applications in aging populations for
wasting syndromes, muscle atrophy, fatigue, gyrate atrophy, Parkinson's disease, Huntington's disease and other
brain pathologies.
Several creatine studies have shown creatine can reduce cholesterol by up to 15% and it has been used to
correct certain inborn errors of metabolism, such as in people born without the enzyme(s) responsible for making
creatine.
Some research has found that creatine may increase growth hormone production.
Creatine Studies : What is Creatine?
Creatine is formed in the human body from the amino acids methionine, glycine and arginine. The average person's
body contains approximately 120 grams of creatine stored as creatine phosphate. Certain foods such as beef, herring
and salmon, are fairly high in creatine. However, a person would have to eat pounds of these foods daily to equal
what can be obtained in one teaspoon of creatine.
Creatine is directly related to adenosine triphosphate (ATP). ATP is formed in the powerhouses of the cell, the
mitochondria. ATP is often referred to as the "universal energy molecule" used by every cell in our bodies. An
increase in oxidative stress coupled with a cell's inability to produce essential energy molecules such as ATP, is
a hallmark of the aging cell and is found in many disease states.
Key factors in maintaining health are the ability to: (a) prevent mitochondrial damage to DNA caused by reactive
oxygen species (ROS) and (b) prevent the decline in ATP synthesis, which reduces whole body ATP levels. It would
appear that maintaining antioxidant status (in particular intra-cellular glutathione) and ATP levels are essential
in fighting the aging process.
It is interesting to note that many of the most promising anti-aging nutrients such as CoQ10, NAD,
acetyl-l-carnitine and lipoic acid are all taken to maintain the ability of the mitochondria to produce high energy
compounds such as ATP and reduce oxidative stress. The ability of a cell to do work is directly related to its ATP
status and the health of the mitochondria.
Heart tissue, neurons in the brain and other highly active tissues are very sensitive to this system. Even small
changes in ATP can have profound effects on the tissues' ability to function properly. Of all the nutritional
supplements available to us currently, creatine research indicates that creatine appears to be the most effective
for maintaining or raising ATP levels.
Creatine Information : How Does Creatine Work?
In a nutshell, creatine works to help generate energy. When ATP loses a phosphate molecule and becomes adenosine
diphosphate (ADP), it must be converted back to ATP to produce energy. Creatine is stored in the human body as
creatine phosphate also called phosphocreatine. When ATP is depleted, it can be recharged by creatine phosphate.
That is, creatine phosphate donates a phosphate molecule to the ADP, making it ATP again.
An increased pool of creatine phosphate means faster and greater recharging of ATP, which means more work can be
performed. This is why creatine has been so successful for athletes. For short-duration explosive sports, such as
sprinting, weight lifting and other anaerobic endeavors, ATP is the energy system used.
To date, creatine research has shown that ingesting creatine can increase the total body pool of creatine
phosphate which leads to greater generation of energy for anaerobic forms of exercise, such as weight training and
sprinting. Other effects of creatine may be increases in protein synthesis and increased cell hydration.
Creatine research has shown spotty results in affecting performance in endurance sports such as swimming, rowing
and long distance running, with some creatine studies showing no positive effects on performance in endurance
athletes. Whether or not the failure of creatine to improve performance in endurance athletes was due to the nature
of the sport or the design of the studies is still being debated.
Creatine can be found in the form of creatine monohydrate, creatine citrate, creatine phosphate,
creatine-magnesium chelate and even liquid versions. However, the vast majority of creatine research to date
showing creatine to have positive effects on pathologies, muscle mass and performance, used the monohydrate form.
Creatine monohydrate is over 90% absorbable. What follows is a review of some of the more interesting and promising
creatine research and creatine studies.
Creatine Facts and Neuromuscular Diseases
One of the most promising areas of creatine research is its effect on neuromuscular diseases such as Muscular
Dystrophy. One creatine study looked at the safety and efficacy of creatine monohydrate in various types of
muscular dystrophies using a double blind, crossover trial.
Thirty-six patients (12 patients with facioscapulohumeral dystrophy, 10 patients with Becker dystrophy, eight
patients with Duchenne dystrophy and six patients with sarcoglycan-deficient limb girdle muscular dystrophy) were
randomized to receive creatine or placebo for eight weeks.
The creatine research found there was a "mild but significant improvement" in muscle strength in all groups. The
creatine research also found a general improvement in the patients' daily-life activities as demonstrated by
improved scores in the Medical Research Council scales and the Neuromuscular Symptom scale. creatine was well
tolerated throughout the study period, according to the study.(1)
Another group of creatine researchers fed creatine monohydrate to people with neuromuscular disease at 10 grams
per day for five days, then reduced the dose to 5 grams per day for five days. The first creatine study used 81
people and was followed by a single-blinded creatine study of 21 people. In both creatine studies, body weight,
handgrip, dorsiflexion and knee extensor strength were measured before and after treatment.
The creatine research found, "creatine administration increased all measured indices in both studies."
Short-term creatine monohydrate increased high-intensity strength significantly in patients with neuromuscular
disease.(2)
There have also been many clinical observations by physicians that creatine improves the strength, functionality
and symptomology of people with various diseases of the neuromuscular system.
Creatine and Neurological Protection - Brain Injury
If there is one place creatine really shines, it's in protecting the brain from various forms of neurological
injury and stress. A growing number of creatine studies have found that creatine can protect the brain from
neurotoxic agents, certain forms of injury and other insults. Several in vitro creatine research found that neurons
exposed to either glutamate or beta-amyloid (both highly toxic to neurons and involved in various neurological
diseases) were protected when exposed to creatine.(3) The creatine research
hypothesized that, "... cells supplemented with the precursor creatine make more phosphocreatine (PCr) and create
larger energy reserves with consequent neuroprotection against stressors."
More recent creatine research, in vitro and in vivo in animals, have found creatine to be highly neuroprotective
against other neurotoxic agents such as N-methyl-D-aspartate (NMDA) and malonate.(4)
Another creatine study found that feeding rats creatine helped protect them against tetrahydropyridine (MPTP),
which produces parkinsonism in animals through impaired energy production.
The results were impressive enough for this creatine research to conclude, "These results further implicate
metabolic dysfunction in MPTP neurotoxicity and suggest a novel therapeutic approach, which may have applicability
in Parkinson's disease."(5) Other creatine research has found creatine protected
neurons from ischemic (low oxygen) damage as is often seen after strokes or injuries.(6)
Yet more creatine research has found that creatine may play a therapeutic and or protective role in Huntington's
disease (7,8) as well as ALS (amyotrophic lateral sclerosis).(9) This
creatine research found that, "...oral administration of creatine produced a dose-dependent improvement in motor
performance and extended survival in G93A transgenic mice, and it protected mice from loss of both motor neurons
and substantia nigra neurons at 120 days of age. Creatine administration protected G93A transgenic mice from
increases in biochemical indices of oxidative damage. Therefore, creatine administration may be a new therapeutic
strategy for ALS."
Amazingly, this is only the tip of the iceberg showing creatine may have therapeutic uses for a wide range of
neurological disease as well as injuries to the brain. One creatine researcher who has looked at the effects of
creatine commented, "This food supplement may provide clues to the mechanisms responsible for neuronal loss after
traumatic brain injury and may find use as a neuroprotective agent against acute and delayed neurodegenerative
processes."
Creatine Research and Heart Disease
Because it is known that heart cells are dependent on adequate levels of ATP to function properly, and that
cardiac creatine levels are depressed in chronic heart failure, creatine research has looked at supplemental
creatine to improve heart function and overall symptomology in certain forms of heart disease.
It is well known that people suffering from chronic heart failure have limited endurance, strength and tire
easily, which greatly limits their ability to function in everyday life. Using a double blind, placebo-controlled
design, 17 patients aged 43 to 70 years with an ejection fraction >40 were supplemented with 20 grams of
creatine daily for 10 days. Before and after creatine supplementation, the creatine research looked at:
- Ejection fraction of the heart (blood present in the ventricle at the end of diastole and expelled during
the contraction of the heart)
- 1-legged knee extensor (which tests strength)
- Exercise performance on the cycle ergometer (which tests endurance)
Biopsies were also taken from muscle to determine if there was an increase in energy-producing compounds (i.e.,
creatine and creatine phosphate). Interestingly, but not surprisingly, the ejection fraction at rest and during the
exercise phase did not increase. However, the biopsies revealed a considerable increase in tissue levels of
creatine and creatine phosphate in the patients getting the supplemental creatine. More importantly, patients
getting the creatine had increases in strength and peak torque (21%, P > 0.05) and endurance (10%, P > 0.05).
Both peak torque and 1-legged performance increased linearly with increased skeletal muscle phosphocreatine (P >
0.05).
After just one week of creatine supplementation, the creatine research concluded: "Supplementation to patients
with chronic heart failure did not increase ejection fraction but increased skeletal muscle, energy-rich
phosphagens, and performance as regards both strength and endurance. This new therapeutic approach merits further
attention."(10)
Another creatine study looked at the effects of creatine supplementation on endurance and muscle metabolism in
people with congestive heart failure.(11) In particular the creatine research looked
at levels of ammonia and lactate, two important indicators of muscle performance under stress. Lactate and ammonia
levels rise as intensity increases during exercise and higher levels are associated with fatigue. High-level
athletes have lower levels of lactate and ammonia during a given exercise than non-athletes, as the athletes'
metabolism is better at dealing with these metabolites of exertion, allowing them to perform better.
This creatine research found that patients with congestive heart failure given 20 grams of creatine per day had
greater strength and endurance (measured as handgrip exercise at 25%, 50% and 75% of maximum voluntary contraction
or until exhaustion) and had lower levels of lactate and ammonia than the placebo group. This shows that creatine
supplementation in chronic heart failure augments skeletal muscle endurance and attenuates the abnormal skeletal
muscle metabolic response to exercise.
It is important to note that the whole-body lack of essential high energy compounds (e.g. ATP, creatine,
creatine phosphate, etc.) in people with chronic congestive heart failure is not a matter of simple malnutrition,
but appears to be a metabolic derangement in skeletal muscle and other tissues.(12)
Supplementing with high energy precursors such as creatine monohydrate appears to be a highly effective, low cost
approach to helping these patients live more functional lives, and perhaps extend their life spans.
Conclusion on Creatine Research
Creatine is quickly becoming one of the most well researched and promising supplements for a wide range of
diseases. It may have additional uses for pathologies where a lack of high energy compounds and general muscle
weakness exist, such as fibromyalgia. People with fibromyalgia have lower levels of creatine phosphate and ATP
levels compared to controls.(13) Some creatine studies also suggest it helps with the
strength and endurance of healthy but aging people as well.
Though additional creatine research is needed, there is a substantial body of creatine research showing creatine
is an effective and safe supplement for a wide range of pathologies and may be the next big find in anti-aging
nutrients. Although the doses used in some creatine studies were quite high, recent studies suggest lower doses are
just as effective for increasing the overall creatine phosphate pool in the body. Two to three grams per day
appears adequate for healthy people to increase their tissue levels of creatine phosphate. People with the
aforementioned pathologies may benefit from higher intakes, in the 5-to-10 grams per day range.
Article on Creatine Research - References:
- Walter MC, et al. Creatine monohydrate in muscular dystrophies: A double blind, placebo-controlled
clinical study. Neurology 2000 May 9; 54(9): 1848-50.
- Tarnopolsky M, et al. Creatine monohydrate increases strength in patients with neuromuscular
disease. Neurology 1999 Mar 10; 52(4): 854-7.
- Protective effect of the energy precursor creatine against toxicity of glutamate and beta-amyloid in
rat hippocampal neurons. J Neurochem 1968-1978; 74(5).
- Malcon C, et al. Neuroprotective effects of creatine administration against NMDA and malonate
toxicity. Brain Res 2000; 860(1-2): 195-8.
- Matthews RT, et al. Creatine and cyclocreatine attenuate MPTP neurotoxicity. Exp Neurol 1999;
157(1): 142-9.
- Balestrino M, et al. Role of creatine and phosphocreatine in neuronal protection from anoxic and
ischemic damage. Amino Acids Abstract 2002; 23(1-3): 221-229.
- Matthews RT, et al. Neuroprotective effects of creatine and cyclocreatine in animal models of
Huntington's disease. J Neurosci 1998; 18(1): 156-163.
- Ferrante RJ, et al. Neuroprotective effects of creatine in a transgenic mouse model of Huntington's
disease. J Neurosci 2000; 20(12): 4389-97.
- Klivenyi P, et al. Neuroprotective effects of creatine in a transgenic animal model of amyotrophic
lateral sclerosis. Nat Med 1999; 5(3): 347-50.
- Gordon A, et al. Creatine supplementation in chronic heart failure increases skeletal muscle
creatine phosphate and muscle performance. Cardiovasc Res 1995 Sep; 30(3): 413-8.
- Andrews R, et al. The effect of dietary creatine supplementation on skeletal muscle metabolism in
congestive heart failure. Eur Heart J 1998 Apr; 19(4): 617-22.
- Broqvist M, et al. Nutritional assessment and muscle energy metabolism in severe chronic congestive
heart failure-effects of long-term dietary supplementation. Eur Heart J 1994 Dec; 15(12): 1641-50.
- Park JH, et al. Use of P-31 magnetic resonance spectroscopy to detect metabolic abnormalities in
muscles of patients with fibromyalgia. Arthritis Rheum 1998 Mar; 41(3): 406-13.
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