GH - The Hormone
Growth hormone (GH) is a 191-amino acid protein or peptide that's naturally
released from the pituitary gland. GH, much like Testosterone, is released in a
pulsatile or episodic manner. The GH pulse occurs every 2-3 hours so each and
every day we get about 8-12 big doses of all-natural growth hormone (Hartman et
al 1991). The sum of these GH peaks amounts to about 0.5 mg of GH produced per
day. The following is an example of what normal 24 hr GH production might look
like, with the highest peaks occurring during the first few hours of sleep:
According to the research review published in a new textbook entitled "Growth
Hormone in Adults," the release of GH from the pituitary is governed by a
balancing act between 2 hormones; GHRH (growth hormone releasing hormone) and
somatostatin. GHRH is responsible for stimulating both the synthesis and the
release of GH from the pituitary. Essentially, GHRH initiates the strength of
the GH pulse.
GHRH's arch rival, somatostatin, counters these effects, however, by
inhibiting GH release. Therefore, somatostatin prevents the GH pulse. In the
end, GH release occurs when GHRH is at its peak in stimulating the pituitary,
while somatostatin is at its low in inhibiting the pituitary. The result of this
high GHRH and low somatostatin period is a big spike in blood levels of GH (Juul,
The following is a chart adapted from Basic and Clinical Endocrinology, 5th
Edition depicting other factors influencing the GH secretion spike:
Elevated Blood Free
High Amino Acids
in the Blood
Low Blood Sugar
Any hypoglycemic agent
Once the GH pulse occurs, blood GH is free to affect target tissues. Some of
the well-documented actions of GH are increases in longitudinal bone growth
(longer bones), increased bone mineralization (thicker, stronger bones),
anabolism (protein building), lipolysis (fat loss), and anti-diuretic actions (Bengtsson,
1999). GH treatment is common in congenital syndromes of GH deficiency and in
cases of hypothalamic or pituitary damage.
In addition, it's been recognized that around the age of 30, there's a
progressive decline in GH secretion from the pituitary, so much so that by the
age of 60, GH production can drop as much as 60%! This means that an aging
pituitary that once produced 0.5 mg of GH per day would now produce only 0.2 mg
per day, and this is definitely physiologically relevant. In fact, these
production levels are often equivalent to those of GH deficient young adults.
This age-related GH decline has been termed somatopause by some researchers and
treatment requires GH replacement therapy.
GH deficiencies in different populations can occur as a result of impaired
GHRH activity or increased somatostatin activity, impaired GH production and
release within the pituitary, and/or impaired GH interactions with GH receptors
on target tissues (Bengtsson, 1999). Basically GH either isn't produced or the
GH is knockin' but it can't come in. Regardless of the mechanism behind GH
deficiencies, these conditions can lead to a whole host of physiological
In children, GH deficiency leads to a reduced growth rate. This can occur due
to the lack of GH specific effects on bone and connective tissue growth. In
addition, skeletal muscle growth can be retarded due to other metabolic
abnormalities associated with GH deficiency (decreased protein anabolism).
In adults, there are a number of abnormalities associated with GH deficiency.
First, GH deficient adults tend to suffer from a host of psychological symptoms.
These symptoms include reduced energy levels, reduced vitality, increased
anxiety, reduced emotional reaction, depression, hampered learning capacity, and
social isolation (Bjorck, 1989).
Secondly, GH-deficient adults suffer from negative changes in body
composition such as increased fat mass, especially in the abdominal area (called
android fat distribution), decreased lean body mass and muscle volume, and
reduced bone mineral content (Binnerts 1992, Bengtsson 1993, Rosen 993). As a
result of these negative changes in body composition, decreased muscular
strength, poor exercise capacity, and poor power output are a result (Cuneo
Finally, GH deficiency can lead to other symptoms such as dehydration,
reduced heart size, reduced cardiac performance (measured by cardiac
contractility and output), hypertension, and hypothyroidism (due to low T4 to T3
conversion) (Henneman 1960, Shahi 1992, Jogensen 1989).
The bottom line is that if you can't get GH to do its job in the body, your
psychological state, body composition, muscular performance, and cardiac
performance will suffer. So you'd better get some GH.
Hey Doc, How's My GH?
So how do you know if you need GH treatment? That's a good question that
scientists are still trying to answer. And you can bet that if they're having a
hard time with this question, most physicians are quite a bit behind them. Since
the symptoms of GH deficiency in adulthood (increased adiposity, decreased
muscle mass, reduced strength and exercise capacity, and psychological
disturbances) are non-specific, a deficency based on clinical symptoms is
difficult to diagnose. Therefore, biochemical markers must be used.
Random sampling of plasma GH isn't a sufficient measure due to the
unpredictable pulsatile nature of GH secretion shown in the graph above. If you
pull a sample at the peak of a GH burst, it looks like you're fine, but if you
pull one at the "trough"; it looks like you need some GH. Normal fasted levels
of GH are less than 5 ng/ml, but again, the utility of random sampling is
limited. By taking a 24-hour integrated measure, you could get a good
approximation of total GH secretion, but who wants to sit in the doctor's office
for 24 hours and have 24 blood samples taken; one every hour? Not me!
Therefore, the best clinical test for GH secretory deficiency is an ITT or
insulin tolerance test. With this test, a single dose of insulin is administered
to promote hypoglycemia. If you check your chart above, you'll notice that
hypoglycemia is a good GH secretory stimulant. So, as insulin goes up and blood
glucose goes down, GH secretion should go up. Since this test only measures GH
secretion and not GH action at the receptor level, other tests are required to
determine GH deficiency.
Serum measures of IGF-1 and IGFBP-3 are two markers of GH activity but their
utility has been questioned (more on these later). Since daily IGF-1 levels tend
to be stable, in the clinical setting, low IGF-1 levels can indicate the need
for further assessment of GH secretion and function. Normal IGF-1 levels are
90-318 micrograms/l while IGFBP-3 levels are 2.0-4.9 milligrams/l.
Effects of GH Replacement
Since GH deficiency leads to the aforementioned frightening list of
psychological and physiological abnormalities, the treatment of GH deficiency
has received much attention within the medical community.
In clinical trials, most of which were referenced above in the "deficiency"
section, GH replacement has been shown to remedy most of the physiological
abnormalities. The major benefits of GH therapy include positive protein balance
(synthesis exceeds breakdown), increased lean body mass, decreased fat mass,
increased insulin sensitivity, normalized body water, increased bone remodeling,
and increased T4 to T3 conversion.
What about side effects? In GH deficient patients, replacement therapy is
usually associated with minimal side effects. The most common side effects
typically occur with the onset of therapy but often tend to normalize within a
few months' time. These negative side effects include include fluid retention,
carpal tunnel syndrome, myalgia (muscle pain), and arthralgia (joint pain). In
addition, fasted and post-prandial (post-meal) blood glucose levels tend to be
higher in GH replacement as a result of the mild insulin insensitivity that can
occur with doses in excess of the exact requirement. Finally, it's been
suggested, but not verified, that GH replacement may lead to a risk of
malignancy and some cancers.
Although there are a few risks with GH replacement, the risk to benefit ratio
of GH therapy in grossly deficient humans remains positive. Since GH can be
relatively safe in replacement situations, as well as the fact that GH treatment
can greatly impact body composition, researchers and clinicians have begun to
explore the use of GH in treating the negative physiological conditions caused
by HIV or age-related muscle wasting, obesity, severe physiological stressors
(surgery or burn injuries), nutrient restriction, glucocorticoid therapy, and
impaired immunity. Unfortunately, the data are mixed in regard to GH therapy in
these populations with some studies showing positive results in muscle mass and
fat loss and others showing nothing but side effects.
One reason for this may be the fact that in some studies, GH treatment has
been given alone while in others, GH treatment was given with several other
hormones that may have acted synergistically with the GH to promote the positive
changes. One thing is clear though; there is no clarity! At the doses given in
research studies, there is no clear consensus on whether GH therapy is warranted
in any population other than those with GH deficiency. More research is needed
to make this determination.
How GH Works - The GH/IGF-1 AXIS
Due to the rise in recombinant GH availability, the research has been
abundant and a clearer picture is emerging of GH action. But make no mistake,
the picture isn't all that clear. It may be more like one of those
computer-generated 3D pictures that you have to look at in just the right way
for just the right amount of time to make any sense of it at all. And no one has
yet to look long enough at this particular picture.
With all of this GH floating around, the black market supply of GH has also
been on the rise. So after we talk GH action, let's talk bodybuilding. If GH can
potentially get bodybuilders big and ripped, then to some, it's a drug worth
exploring. So for you die-hard muscle heads, here's a little GH primer with
special focus on the pursuit of lean mass.
Circulating GH is thought to act through two distinct but interrelated
mechanisms. The first is direct. GH can act directly on many cells in the body
via the GH receptor. Once released into the blood from the pituitary, GH either
circulates as free GH or circulates bound to GHBP for transport (GH Binding
Protein). Free GH is available to interact with cellular receptors to create a
Once free GH has interacted with the cellular receptors, it's thought that
more GHBPs are formed. With this increased GHBP, some researchers believe that
more GH is rendered temporarily unavailable. But at the same time, it stays in
the system for a longer amount of time. So although GHBP-bound GH has a much
longer half-life, it cannot interact with cellular receptors while bound.
Unfortunately, there's no clear consensus as to whether it's more important
to cellular GH action to prolong the half-life of GH (to allow for higher levels
to circulate for longer), or to decrease GHBP to allow for higher levels of free
GH. And this debate holds true for not only GH, but for other hormones like
Testosterone as well. Although the researchers tend to contradict each other and
sometimes even themselves on this point, the bottom line is that the
effectiveness of GH (and other hormones) is tied up in this balance between
bound and unbound GH and the presence of binding proteins.
Binding proteins aside, once free GH does reach the cells, its direct actions
include the promotion of lipolytic and hyperglycemic effects. GH can decrease
glucose utilization in favor of fat release and oxidation (lipolysis).
Unfortunately, because of this shift from carb to fat use, GH also increases
insulin resistance. Hyperglycemia is a result of this insulin insensitivity. So
although GH itself can make you lean due to lipolysis, this might come at the
expense of insulin resistance and might ultimately lead to a diabetic state. As
a result, you'll be a lean diabetic rather than a chubby normal guy. I guess
it's a trade-off.
The second mechanism by which GH exerts its effects is indirectly through
IGF-1. In the liver, circulating GH is converted into IGF-1 and 2 which can
travel through the blood to promote their effects. IGF is also bound to one of 6
plasma proteins (IGFBP's 1-6). About 1-5% of IGF-1 is free while 95-99% is
bound. Again, this balance is important for hormone action. This systemic IGF is
also free to interact with cellular receptors.
In addition to the systemic effects of liver IGF-1, IGF can act locally. Let
me explain. GH binding to cells can lead to what is called peripheral conversion
of IGF-1. At this specific location (skeletal muscle for example), IGF-1 acts in
an autocrine or paracrine fashion to promote its effects. This means that unlike
GH, which has endocrine function (it is produced in the pituitary and travels
elsewhere to do its work), IGF-1 can both be produced in, and promote changes
in, the same tissue or those immediately adjacent to it.
Perhaps the most relevant effect of IGF-1 to this discussion is the ability of
IGF-1 to increase protein synthesis by increasing cellular mRNA formation (mRNA
makes protein) as well as increasing uptake of amino acids. This effect on
protein synthesis can lead to increased lean mass. The research indicates that
this effect is dependent on GH presence as well. So IGF-1 alone does not promote
such effects. Nor does GH. It appears the combination of the two most
consistently lead to increased protein synthesis.
In addition, IGF-1 can also counteract the hyperglycemic effects of GH via
insulin-like actions on glucose uptake. Since IGF-1 is typically elevated to a
small extent with GH elevations, IGF action is not sufficient to neutralize the
hyperglycemic effects of GH, but perhaps it minimizes extreme insulin
The bottom line is that GH and IGF-1 seem to be necessary bedmates. Although
each may act most strongly in different tissue types, they are thought to work
together to promote anabolism and stimulate lipolysis (Ney 1999, Yarasheski
1994). But all this synergy comes at a price. Both hormones negatively feed back
on the pituitary to slow GH production. And this impacts normal GH secretion as
well as GH treatment.
When plasma GH levels and IGF-1 levels are elevated with GH treatment, this
elevation is non-physiologic. What this means is that after a GH injection, GH
levels are elevated for some time and then come crashing down to normal, often
being suppressed for hours thereafter. So the pattern seen in the graph above is
not the one seen when using exogenous GH. This is probably due to the fact that
both GH and IGF-1 are negative regulators of GH release so an increase in either
(from a GH injection) reduces the secretion of GH.
So when examining the GH/IGF-1 axis, a few things should be considered. With
strong feedback mechanisms in place, it's difficult to maintain consistently
high levels of GH without constant exogenous dosing. And that's a hassle. In
addition, just like with insulin, there may be something known as GH
insensitivity (Grinspoon 1998). It appears that with chronically high levels of
GH, liver and peripheral conversions of GH to IGF-1 are decreased. So even with
the constant use of exogenous GH, the body may simply try to regulate itself and
the actions of GH by preventing the availability of what is thought to be GH's
It seems like a no-win situation. And perhaps this is best. The body has
feedback mechanisms for a reason... protection. If GH action isn't kept in
check, the medical condition known as acromegaly can result. Acromegaly is
characterized by abnormal skeletal growth characterized by enlarged jaw and
hands. Individuals suffering from this have abnormally high levels of GH, IGF-1,
and IGFBPs. It's apparent, then, that the feedback mechanisms of these
individuals aren't working all that well.
Often times, GH users smugly tell me that acromegaly is BS because they've
been using GH for X amount of time and they didn't get it. Well guys, guess
what? Normal individuals probably won't get it because of the feedback
mechanisms described above. You know what else? You're probably not getting
muscle building results either.
The Perfect Physique?
GH, Muscle Function, and Body Composition Research
Since most of the benefits of GH were originally thought to impact muscle
mass, scores of rodent studies were conducted to examine the effect of GH on
muscle mass and contractile ability. The findings did indicate a small increase
in muscle mass but no increase in contractile strength. One study looked at rat
quads (no they didn't squat) and they did get bigger (quads), but not stronger (Bigland,
1953). In addition, in other rat studies, although there were small increases in
body mass, there were absolutely no increases in strength. How could this be?
More muscle equals more strength, right? Well, researchers concluded that the
increase in quad mass was not contractile protein. The mass could have been
fluid or connective tissue.
Since animals did benefit from increased muscle mass, the next step was to
take these findings to humans. In cases of GH deficiency, small increases were
found in muscle volume (~6-8%) and lean body mass (~11%). Exercise capacity was
elevated in such patients (~12%), but strength was either not changed or mildly
increased by about 8% (Jorgensen 1989, Salomon 1989). As stated earlier, most of
the observed benefits of GH have been seen in GH deficient animals and humans.
Also, as mentioned earlier, there's certainly not much to get excited about
in other populations. When GH is administered alone, very few studies have shown
any increase in size or strength. In two recent HIV studies, patients given huge
doses of up to 27 IU per day (9 milligrams) had no gains in muscle mass. But
remember, according to what I said earlier, IGF-1 was the protein anabolic
agent. And GH has its biggest effect on lipolysis. And the combination of the
two may lead to the greatest results.
So in examining the research, it's been speculated that the levels of IGF-1
adminstered weren't great enough (in conjunction with GH) to make an impact, or
that the individuals became GH resistant. Also, since IGF-1 would lower GH
secretion, it doesn't make much sense to give it alone. Remember, GH and IGF-1
often work together to change body composition. Newer studies have shown that
when adding IGF-1 to the mix, it appears that there's a definite increase in
protein synthesis and muscle mass as well as some increase in strength.
So perhaps GH alone is useless at increasing muscle mass while a combination
of GH and IGF-1 may be effective if protein anabolism and increased contractile
protein is the goal (Kupfer 1993, Snyder 1988). But even the increases seen in
these studies were moderate and a cost/benefit analysis is warranted since this
combination might also lead to severe side effects.
So what about GH and fat mass? Most studies have shown modest decreases in
body fat and skinfold measures with GH treatment (Jorgensen 1989, Salomon F,
Tagliaferri 1998). Decreases in fat mass of about 16% and decreases in thigh
adipose mass of about 7% have been reported. But remember, a 16% fat decrease
doesn't mean they went from 20% to 4% body fat. It more likely means that a 200
lb person with 20% bodyfat or 40 lbs of fat would have their fat mass decreased
to about 35.5 lbs. This would put them at about 193.5 lbs and 18% fat.
In another study, obese women on GH lost 2 more lbs than placebo group in a
one-month period. So although it does appear that GH can decrease fat mass in
clinical populations, when looking at the actual fat loss numbers, it appears
that the good old ECA stack or MD6 would be more effective than GH.
GH and The Athlete
I've never been sure why the use of GH has become popular in athletes and
bodybuilders. Perhaps it's the name... Growth Hormone. Sounds like it'll make me
big. Or perhaps it's the legend of Pump de Leon. Either way, the research on GH
use in bodybuilders and men on resistance training programs has shown it to be
all but useless. And this is probably due to the feedback mechanisms like the
negative feedback on the pituitary and the GH resistance discussed earlier.
In two landmark GH studies conducted at the Washington University School of
Medicine, a world-renowned GH researcher named Kevin Yarasheski studied the
effects of GH in combination with weight training (Yarasheski 1992, 1993).
In the first study, 18 untrained men were given either GH and exercise or
placebo and exercise for 12 weeks. GH subjects were given 40 micrograms/kg of
recombinant GH and all subjects were evaluated before and after treatment for
fat mass, fat free mass, total body water, whole body protein synthesis, insulin
sensitivity, muscle size and muscle strength. Due to the development of carpal
tunnel syndrome, 2 subjects were forced to withdraw from the study.
When comparing the GH+exercise group with the placebo+exercise group, the
data showed that there was no fat loss, no change in insulin sensitivity, no
increase in muscle size, and no increase in strength! Whole body protein
synthesis was increased in the GH group relative to the placebo, but muscle
protein synthesis wasn't. In addition, lean body mass was increased, but again,
this wasn't muscle mass, but probably a combination of water retention, organ
mass, and connective tissue instead. The researchers, who seemed quite objective
in their conclusions, decided that non-muscle proteins were being formed instead
of muscle contractile protein.
In the follow-up study, Dr. Yarasheski pursued the effects of GH on
experienced weight-lifters. Since the GH didn't positively impact strength or
body comp in the untrained guys, Dr. Yarasheski wondered if well-trained
athletes might be different. So another study was conducted to examine protein
synthetic rates in GH-treated athletes. After 2 weeks of GH treatment
(40micrograms/kg), the data were clear that short term GH had no effect on whole
body protein synthesis or breakdown. The reason they chose 2 weeks was that in a
number of previous studies on clinical populations, any increases in protein
synthesis had only lasted for about a month and then ceased due to some type of
down-regulation (Perhaps GH insensitivity?). In this population, however, GH
didn't even promote protein synthesis within this time frame.
With all this negative data, it should be mentioned that one study showed
something positive happening, but again, it wasn't all that exciting (Crist
1988). This particular study showed a small 4% gain in lean body mass and a
modest 12% loss in body fat with GH doses of 8IU per day (2.6 milligrams).
Muscle mass wasn't measured, so there was no way to determine the make-up of the
increased LMB (lean body mass).
So it's pretty apparent that in weight trained men, GH alone doesn't increase
muscle mass. Resulting lean mass gains from GH treatment are probably a combo of
water, connective tissue, or organ mass. I say probably because organ mass and
connective tissue mass are hard to measure. The indirect evidence is pretty
Since non-muscle protein gains and the development of carpal tunnel syndrome
(due to growth in the connective tissue sheath in the wrist) were apparent in
these studies, connective tissue gain is a reasonable speculation. In addition,
acromegaly patients have increased organ mass as a result of the high
responsiveness to GH, so it would stand to reason that this could have occurred
in these studies, too.
The next logical question is this: Since a lot of guys are still using GH,
what are the implications of increased organ mass and connective tissue? Well,
to be honest, we don't know.
Acromegaly patients do not have high rates of organ malfunction or
pathophysiology, so although growing large organs isn't ideal, the current
literature doesn't indicate that the problem is immediately life-threatening.
But, acromegaly patients do die prematurely, so if they were to live longer,
perhaps these organ changes could have long-term impact.
As far as the issue of increases in connective tissue, the increases
themselves may not be too terrible, as long as they don't become
pathophysiological. Of course, developing carpel tunnel syndrom is no picnic. On
the other hand, if the strength of connective tissue increases with connective
tissue growth, athletes could become more injury-resistant. Connective tissue
growth will not lead to strength increases in well-trained guys if contractile
protein mass doesn't go up, but these connective tissue increases may allow
individuals to train with heavier weights with less risk of injury. This,
however, merely results from me taking off the "science hat" and speculating a
Let's Get Ready to Rumble
GH vs Testosterone and Beta-Agonists
With all this data flying, I think it's important to put things into
perspective. Currently, far and away, the most popular bodybuilding drug for
building muscle mass is Testosterone, while the most popular fat-loss drugs are
the beta agonists clenbuterol and ephedrine. So if GH is to have any relevance
to bodybuilders and athletes, it has to show itself to be superior to these
drugs in terms of effectiveness, safety, or price. Since we all know that the
price of GH is astronomical (it can run $1000 ++ for a month's supply), the
price situation is a losing one on the GH front. What about the other two
As stated in the above sections, fat loss with GH is moderate and GH can
probably be outperformed with a simple ECA stack. In addition, it appears that
even Testosterone, while not known for its fat-burning abilities, does a nice
job of its own. In two studies, Testosterone was shown to decrease fat mass by
5% and 6% (Anawalt 1999, Blackman 1999). In one of the same studies, GH was also
administered and decreased fat mass by 12%. So although doubly effective when
compared to test, I think that GH would be bested by ECA in a fat-loss contest.
As far as muscle mass, do we even need to waste our time on this discussion?
Testosterone is clearly the winner of the muscle building battle, hands down. No
And what about safety profiles? Well, it's not all that safe for healthy
individuals to mess with endocrine profiles in the first place. But since both
Testosterone and GH clearly have their risks, it appears to me that when
comparing the doses needed for a positive effect, Testosterone is much less
likely to cause any serious harm. So, in the end, when looking at the total cost
to benefit profile, it is clear that GH loses the battle with both Testosterone
and even with the over-the-counter ECA stack. Sorry GH.
Here's a little chart that's adapted from the June 3, 1999 New England Journal
of Medicine comparing the costs of different drug therapies if you were to
obtain them legitimately with a prescription. I've also added the cost of MD-6
for a little comparison:
Testosterone Analogs (IM)
So Long GH
New Options in GH Manipulation
Over the last few years, GH has been a relative disappointment in terms of
treating catabolic/wasting disorders. And it has obviously been a disappointment
for athletes and bodybuilders. So the pharmacologists got to work and built a
better mouse trap. It has been proposed that GH has been disappointing because
of the feedback mechanisms described earlier as well as the non-physiologic
nature of GH treatment. What this means is that since GH is normally pulsatile,
the body may be best adapted to this situation. Perhaps it likes to see frequent
short bursts of GH rather than huge single increases followed by hours of
Since GH treatment results in these non-physiologic GH responses,
pharmacologists have speculated that an oral GH secretagogue that could increase
the burst frequency and burst amplitude (height) might offer the distinct
advantages of less negative feedback, less GH resistance, a better risk profile,
and a better mode of delivery (oral).
Lo and behold, such secretagogues, called Growth Hormone Releasing Peptides
have been found. Growth hormone releasing peptide 6 (GHRP 6), Hexarelin, and
MK-0677 are available and fit the bill. Whereas a GH injection might cause a
large spike in GH and the suppress GH for hours thereafter, these drugs,
increase GH frequency and amplitude in a more physiological manner as shown
As shown, the GH secretagogues offer a pulsatile GH release that is more
physiologic than the GH burst that a GH injection gives. Of additional interest
is the fact that the inclusion of GHRH injection with GHRP (not shown) can lead
to this same profile with huge, rapid peaks in GH release.
With an understanding of natural GH release it is clear that these new types of
GH therapy may offer future treatment options for GH deficiency. In the absence
of good safety or body compostion data, it is uncertain as to how they will be
used or what populations will benefit the most from their use. If these drugs do
become more popular treatment options, I would expect that bodybuilders will be
testing them out as well and will provide feedback on their efficacy.
If you'll permit me to speculate about potential body comp implications,
since GH has shown to be a more effective fat loss agent than anabolic agent,
these secretagogues may offer a new and better fat loss approach. Since even
just a physiological burst of GH increases lipolysis (Gravholt 1999), especially
in the abdominal area, the very large bursts seen with GH injections may not be
necessary. They may not lead to increased lipolysis above normal or mildly
supraphysiological pulses. And since GH secretagogues mildly increase frequency
and amplitude of GH secretion, this increased GH activity may be even more
effective at promoting fat loss than GH alone. So if some supplement company
comes out with a real-deal, honest-to-goodness, GH secretagogue that really
works, it may be a great supplement to promote lipolysis. But for now, the only
effective secretagogues I know of are the ones discussed in this article.
Within the last few years, the bodybuilding community has taken drug use to a
new high. Being extremists by nature, bodybuilders are always looking for the
next drug or combination of drugs to take their muscle mass to the next level.
To this end, the new generation of bodybuilders have sworn by a combination of
Testosterone, GH, IGF-1, Insulin, and Thyroid drugs. A discussion of these
combinations is beyond the scope of this article and beyond the scientific
literature at the current time. There is quite a bit of indirect evidence
suggesting that, in theory, there may be a synergistic response to a
polypharmacy of this type, but there have been very few trials looking directly
at such combinations (Mani Maran 2000, Painson 2000, Demling 1999, Grinspoon
1998 and 1999, Juul 1998, Keenan 1996).
The body of anecdotal evidence is greater and I've talked to tons of guys who
have used GH, T, Insulin, Thyroid, etc. Many feel that the addition of GH to a
drug stack results in some pretty good gains while some say that they don't
think the GH helps them at all. But who really knows how much each drug
contributes? Since each person is different, uses different doses, and may or
may not have real drugs, comparisons are difficult. At a price tag of $1000+ per
month for the GH alone, I just don't think that the gains would be worth it
My personal feeling is that when drug use gets to this extreme level where it
is "necessary" to take 5 or 6 dramatically powerful, incompletely understood,
and potentially dangerous hormones to compete, I think it has gone way too far.
Although it's pretty interesting to think that we could control our body
compositions by taking the endocrine system off auto pilot and controlling it
manually for a while, we may get more than we bargained for.
Auto pilot may never work again and you'll be trying to figure out how you're
gonna pay the hormone replacement bills for the rest of your lives. I just don't
want to be 65 years old and still giving myself a dozen injections per day
because I turned my pituitary into a shriveled, dangling waste of endocrine
tissue hanging from my atrophied brain mass.