Creatine: More Than a
Sports Nutrition Supplement
By Will Brink. (Author of Muscle Building Nutrition
http://musclebuildingnutrition.com - a
complete guide bodybuilding supplements and eating to gain lean muscle, and Diet
Supplements Revealed http://aboutsupplements.com - a review of diet supplements and
guide to eating for maximum fat loss.) See FREE offer at the bottom of the
page.
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Creatine: More Than a
Sports Nutrition Supplement
Although creatine offers an array of benefits, most people think of it simply as a
supplement that bodybuilders and other athletes use to gain strength and muscle
mass. Nothing could be further from the truth.
A substantial body of research has found that creatine may have a wide variety
of uses. In fact, creatine is being studied as a supplement that may help with
diseases affecting the neuromuscular system, such as muscular dystrophy (MD). Recent studies suggest 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 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 studies have found that
creatine may increase growth hormone production.
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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 powdered 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 appears to be the most effective for maintaining or raising ATP levels.
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 (CP) also
called phosphocreatine. When ATP is depleted, it can be recharged by CP. That is, CP
donates a phosphate molecule to the ADP, making it ATP again. An increased pool of CP
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, research has shown that ingesting creatine can increase the total body pool of CP
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 has had spotty results in affecting performance in endurance sports such as
swimming, rowing and long distance running, with some 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 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
research studies with creatine.
Creatine and neuromuscular diseases
One of the most promising areas of research with creatine is its effect on neuromuscular
diseases such as MD. One 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 researchers found there was a "mild but significant
improvement" in muscle strength in all groups. The study 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 researchers.1
Another group of 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 study used 81 people and was followed by a single-blinded study of 21
people. In both studies, body weight, handgrip, dorsiflexion and knee extensor strength
were measured before and after treatment. The researchers 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 studies have found that creatine can
protect the brain from neurotoxic agents, certain forms of injury and other insults. Several
in vitro studies 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 researchers hypothesized that "… cells supplemented with the
precursor creatine make more phosphocreatine (PCr) and create larger energy reserves with
consequent neuroprotection against stressors."
More recent studies, 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 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 these researchers 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 studies
have found creatine protected neurons from ischemic (low oxygen) damage as is often seen
after strokes or injuries.6
Yet more studies have found creatine may play a therapeutic and or protective role in
Huntington's disease7, 8 as well as ALS (amyotrophic lateral sclerosis).9 This study 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
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 and heart function
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, researchers
have 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 researchers looked at:
1) Ejection fraction of the heart (blood present in the ventricle at the end of diastole and
expelled during the contraction of the heart)
2) 1-legged knee extensor (which tests strength)
3) 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 researchers 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 study looked at the effects of creatine supplementation on endurance and muscle
metabolism in people with congestive heart failure.11 In particular the researchers 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 study
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
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 studies also suggest it helps with the strength and endurance of healthy
but aging people as well. Though additional research is needed, there is a substantial body
of 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 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.
About the Author - William D. Brink
Will Brink is a columnist, contributing consultant, and writer for various health/fitness,
medical, and bodybuilding publications. His articles relating to nutrition, supplements,
weight loss, exercise and medicine can be found in such publications as Lets Live, Muscle
Media 2000, MuscleMag International, The Life Extension Magazine, Muscle n Fitness,
Inside Karate, Exercise For Men Only, Body International, Power, Oxygen, Penthouse,
Women’s World and The Townsend Letter For Doctors. He is the author of Priming The
Anabolic Environment and Weight Loss Nutrients Revealed. He is the Consulting Sports
Nutrition Editor and a monthly columnist for Physical magazine and an Editor at
Large for Power magazine. Will graduated from Harvard University with a concentration in the natural
sciences, and is a consultant to major supplement, dairy, and pharmaceutical companies.
He has been co author of several studies relating to sports nutrition and health found in
peer reviewed academic journals, as well as having commentary published in JAMA. He runs
the highly popular web site BrinkZone.com which is strategically positioned to fulfill the
needs and interests of people with diverse backgrounds and knowledge. The BrinkZone site
has a following with many sports nutrition enthusiasts, athletes, fitness professionals,
scientists, medical doctors, nutritionists, and interested lay people. William has been
invited to lecture on the benefits of weight training and nutrition at conventions and
symposiums around the U.S. and Canada, and has appeared on numerous radio and television programs.
William has worked with athletes ranging from professional bodybuilders, golfers, fitness
contestants, to police and military personnel.
See Will's ebooks online here:
Muscle Building Nutrition http://musclebuildingnutrition.com
A complete guide bodybuilding supplements and eating to gain lean muscle
Diet Supplements Revealed http://aboutsupplements.com
A review of diet supplements and guide to eating for maximum fat loss
He can be contacted at: PO Box 812430
Wellesley MA. 02482.
BrinkZone.com
Email: wbrink@earthlink.net
Article References:
1. Walter MC, et al. Creatine monohydrate in muscular dystrophies: A double blind,
placebo-controlled clinical study. Neurology 2000 May 9; 54(9): 1848-50.
2. Tarnopolsky M, et al. Creatine monohydrate increases strength in patients with
neuromuscular disease. Neurology 1999 Mar 10; 52(4): 854-7.
3. Protective effect of the energy precursor creatine against toxicity of glutamate and
beta-amyloid in rat hippocampal neurons. J Neurochem 1968-1978; 74(5).
4. Malcon C, et al. Neuroprotective effects of creatine administration against NMDA and
malonate toxicity. Brain Res 2000; 860(1-2): 195-8.
5. Matthews RT, et al. Creatine and cyclocreatine attenuate MPTP neurotoxicity. Exp Neurol
1999; 157(1): 142-9.
6. 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.
7. Matthews RT, et al. Neuroprotective effects of creatine and cyclocreatine in animal
models of Huntington's disease. J Neurosci 1998; 18(1): 156-163.
8. Ferrante RJ, et al. Neuroprotective effects of creatine in a transgenic mouse model of
Huntington's disease. J Neurosci 2000; 20(12): 4389-97.
9. Klivenyi P, et al. Neuroprotective effects of creatine in a transgenic animal model of
amyotrophic lateral sclerosis. Nat Med 1999; 5(3): 347-50.
10. 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.
11. 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.
12. 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.
13. 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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