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Drugs |
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IGF-1
has anti-aging effects
IGF-1 is a highly
anabolic hormone secreted
by the liver and stimulated
by growth hormone
(GH) and testosterone.
It affects every cell
in the body, particularly
muscle, cartilage,
bane and nerves by
promoting cell growth
and regulating DNA
synthesis (gene activity).
Spanish researchers
showed that IGF-1
therapy administered
to aging rats prevented
insulin resistance,
reduced cholesterol
and triglycerides
and decreased body
fat. IGF-1 also reduced
metabolic damage in
the brain and liver
and improved mitochondrial
function through out
the body. The mitochondria
are the powerhouses
of the cells and supply
energy for almost
all metabolic functions.
IGF-1 is synthesized
by yeast and bacteria
in the laboratory
and is manufactured
in the United States
by Tercica. Studies
by John Linderman
from the University
of Toledo showed that
administration of
GH and IGF-1 was more
effective for increasing
muscle mass and strength
than either hormone
by itself. IGF-1 is
an effective anabolic
drug, but it is not
readily available.
(Endocrinology, 149: 2433-2442, 2008)
Ibuprofen
does not block gains
in strength and muscle
size.
Active people
are hooked on nonsteroidal
anti-inflammation
drugs (NSAIDs) like
ibuprofen to help
them cope with sore
muscles and joints.
NSAIDs may decrease
pain, but might also
interfere with the
healing process. They
worked by blocking
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stress
chemicals called prostaglandins,
which are critical for generating
muscle stem cells called satellite
cells. During hypertrophy and
muscle tissue repair, the muscle
cells create satellite cells.
Muscle growth factors can cause
the satellite cells to combine
with muscle cells that were
stressed or damaged during training
and assist in cell repair and
adaptation. Canadian researchers,
led by Joel Krents, found that
low doses of ibuprofen (400
milligrams per day) did not
interfere with muscle hypertrophy
or muscle soreness. This was
a short-term study involving
only 18 subjects. Several studies
have demonstrated that NSAIDs
interfere with protein synthesis,
so it is a good idea to use
these drugs sparingly. (Applied
Physiology Nutrition Metabolism,
33:470-475, 2008)
Government evaluates
new version of oxycontin
Oxycontin, sometimes
called “hillbilly heroin,” has
replaced marijuana and cocaine
as the recreational drug of
choice in many young people.
They sometimes take oxycontin
by first crushing the pill and
then either snorting it or diluting
it in water and injecting it.
The drug was hailed as a breakthrough
for treating chronic pain when
it was introduced in the 1990s.
However, drug abusers found
that they could get a heroin-like
high by administering the drug
all at once. The maker of Oxycontin
Purdue Pharma LP wants to coat
the pill in plastic to make
it more tamper resistant. The
FDA wants the company to perform
studies to determine if the
plastic coat reduces abuse.
Preliminary studies show that
the new drug dissolves slowly
and provides long-term relief
of pain. Other companies are
also working on abuse resistant
forms of the drug. (Associated
Press, May 1, 2008)
Heavy drinking damages
the heart and blood vessels
Moderate alcohol consumption
reduces the risk of heart disease
and premature death. Heavy drinking,
however, has the opposite effect.
It promotes domestic violence
and accidents and is destructive
to the heart, kidneys, liver
and metabolism. An Irish study
showed that men who drank more
than 21 drinks per week and
women who drank more than 14
drinks per week were more likely
to develop high blood pressure,
stiff arteries and enlarged
hearts. Enlarged hearts increase
the risk of heart failure, heart
attack and stroke by five to
six times. Once a heart is enlarged
and weakened, it is very difficult
to restore it to normal. We
can infer from scientific studies
that moderate alcohol consumption
(one or two drinks per day)
is healthy and promotes longevity
for most people. However, excessive
consumption causes damage to
the heart and blood vessels.
(Paper presented at the American
Society of Hypertension annual
meeting, May 2008)
Aspirin lowers blood
sugar
Many people take an
aspirin every day to prevent
heart attack and stroke. Aspirin
decreases blood clot formation,
which causes most heart attacks.
Also aspirin decreases inflammation,
which triggers blood vessel
disease. Aspirin might also
have an effect on metabolic
health by enhancing insulin
metabolism. Spanish researchers,
in a study on rats and human
tissue, found that an aspirin-like
drug (trifluomethyl salicylate)
decreased blood sugar and increased
insulin secretion, but had no
effects on insulin sensitivity.
Problems with blood sugar metabolism
cause high blood pressure, abdominal
fat deposition, abnormal blood
fats, blood clotting abnormalities
and type 2 diabetes all of which
increase the risk of heart attack
and stroke. This study supported
taking an aspirin every day
to prevent heart attacks. (Journal
Clinical Endocrinology Metabolism,
in press; published online May
6. 2008)
Ritalin increases heat
stroke risk during exercise
Ritalin (methylphenidate)
is a stimulant used to treat
attention deficit hyperactivity
disorder, drowsiness and chronic
fatigue syndrome. It is a commonly
prescribed drug, particularly
to young people. Belgian researchers
showed that the drug could have
deadly side effects during exercise
in the heat. Cyclists took either
Ritalin (20mg) or a placebo
(fake Ritalin) before exercising
for 1 hour in a room temperature
of either 64 or 80 degrees.
Ritalin increased exercise capacity
in the hot, but not the cool
environment. Care temperature
rose when the subjects took
the drug, but there was no change
in the perception of effort
or thermal stress. Ritalin allowed
athletes to drive up their body
temperatures during exercise
in the heat and took away the
perception they were getting
overheated, which would increase
their risk of heat stroke. People
taking Ritalin should be careful
not to push too hard during
exercise in the heat. (Medicine
Science Sports Exercise, 40:
879-885, 2008) |
Nandrolone
could cause liver
problems
Most bodybuilders
are well aware that
oral anabolic steroids
are toxic to the liver.
So, many use inject
able drugs such as
nandrolone because
they feel are more
liver-friendly. Brazilian
researchers, in a
study on rats, found
that low, normal and
high doses of nandrolone
administered for five
weeks increased key
liver enzymes (aspartate
aminotransferase,
AST; alanine aminotransferase,
ALT; and alkaline
phosphates, ALP ).
Changes were highest
in the high-dose group,
but liver function
tests remained within
the normal range in
all groups. The authors
concluded that administering
higher than clinical
doses could damage
the liver. There are
no long-term studies
showing the effects
of nandrolone or any
other anabolic steroid
on liver function.
(Medicine Science
Sports Exercise, 40:
842-847, 2008)
Why athletes
take drugs
In a 1990s
poll, 75 percent of
elite athletes said
they would take a
pill that would guarantee
an Olympic gold medal,
but kill them five
years later. They
changed their tune
when they were older.
Many former East German
athletes said that
they would gladly
give back their gold
medals if they could
get their health back.
Australian psychologists
analyzed why athletes
take drugs in the
first place. Athletes
constantly set goals
and make decisions
on how to achieve
these goals. Most
athletes who take
drugs see them as
training aids.
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They realize that a pill is
no substitute for hard work,
determination and commitment
to goals. In deciding whether
to use drugs, athletes must
choose between the expected
positive outcomes and negative
consequences. The negative consequences
might deal with personal or
moral issues or the more practical
possibility that they will test
positive on a drug test. The
researchers concluded that the
motivation for drug use in athletes
is complicated and that getting
them to stop requires careful
analysis of factors that make
them vulnerable to drug use
in the fist place. (Substance
Abuse Treatment, Prevention,
and policy, 3:7 published online
March 10, 2008)
EPO might increase muscle
and capillary growth
Erythropoietin (EPO0
is a hormone produced by the
kidneys that stimulates red
blood cell production in the
bone marrow. Scientists developed
a synthetic version of EPO using
recombinant DNA technology (genetically
alters bacteria to produce EPO).
It is very popular with cyclists
and distance runners who take
it to increase maximal oxygen
consumption and endurance. The
drug increases the ability to
deliver oxygen to the muscles
and boost exercise capacity
by 10 percent or more. EPO is
a banned substance in most sports
and has been at the center of
recent doping scandals in the
tour de France and the Olympics.
It does more than increase red
boost cell production. Danish
researchers found EPO receptors
in muscle and in cells lining
blood vessels. EPO is involved
in muscle hypertrophy and promoting
capillary density in response
to training, but its role is
not very well understood. (Journal
Applied Physiology, 104:1154-1160,
2008)
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Steroid
users have bad images
During the recent congressional
hearings on drug use in baseball,
the news media portrayed athletes
who used anabolic steroids at
about the same level as heroine
addicts, burglars and check
forgers. It is little wonder
that the perception of the average
person is similarly misinformed.
French psychologists found that
people viewed steroid users
as less committed and motivated,
poor sportsmen and more likely
to deliberately injure an opponent.
The study showed that in the
general population, steroid
use is socially undesirable
and steroid users are viewed
in a bad light. The average
non-medical used of steroids
is in his early 30s and takes
the drugs for self-improvement.
Most steroid users seek to increase
strength, muscle mass and physical
attractiveness and decrease
body fat. They follow structured
diets and exercise programs
and do not play sports. Most
are well educated and employed
and take the drugs as part of
a health-centered lifestyle.
It isn’t likely that the image
of anabolic steroids will improve
anytime soon. If you use steroids,
keep quiet about it. (Scandinavian
Journal Medicine Science Sports,
in press; published online February
4, 2008)
Levothyroxine therapy
maintains levels of T3
Many bodybuilders take
levothyroxine, a synthetic form
of the thyroid, hormone thyroxin
(T4), to help cut fat and normalize
thyroid function when taking
growth hormone and anabolic
steroids. The thyroid gland
releases thyroxine (T4) and
triiodothyronine (T3). Both
hormones stimulate metabolism.
T3 is more powerful than T4.
Also, most T4 is converted to
T3 in tissues outside thy thyroid
gland. Metabolism decreases
by 50 percent when your body
can’t secrete these hormones.
Likewise, metabolic rate increases
60-100 percent if your body
secretes too much. Georgetown
Medical School researchers found
that levothyroxine increased
levels of T4 and T3 in patients
without thyroid glands. This
study showed that taking levothyroxine
by itself was sufficient for
maximizing thyroid therapy and
that it was not necessary to
also take T3 medications such
as cytomel. (Journal American
Association, 299:769-777, 2008)
Inhaled insulin could
cause lung cancer
People with type 1
diabetes and many people with
type 2 diabetes need insulin
injections to regulate blood
sugar. The injections are relatively
painless, but they are inconvenient
and embarrassing. Pfizer Inc.,
Nektar Thepapeutics and Sanofi-Aventis
SA developed in inhaled insulin
product called exubera that
effectively lowers blood sugar
in type 1 diabetes who were
taking low doses of injected
insulin. The food and drug administration
approved the drug in 1996, but
the companies stopped clinical
trials after reporting an increased
incidence of lung cancer in
patients using the drug. All
patients who developed lung
cancer smoked cigarettes and
there were so few cases that
it was difficult to say whether
the drug triggered the cancer.
Physicians have been reluctant
to prescribe the drug, so it
has not been the financial success
that the companies had hoped.
(Reuters, April 9, 2008) |
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