Thread: Thoughts on this.......
01-20-2005, 06:51 PM #1New Member
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- Jan 2005
Thoughts on this.......
I found this and thought it was a great read any thoughts on this cycle??
Maximum Human Growth Hormone for Dummies
Maximum Human Growth Hormone for Dummies
by L. Rea
Growth hormone (GH) has been surrounded by a cloud of mystique for many years carried by whispered hushes of freak status and a shot at the Mr. O for those who venture its use. Warnings of facial disfigurement and hopes of sexual appendage elongation alike have accompanied the strange tales of this hormone’s power. Wow, get a life!
The truth is that GH works very well indeed…if it is properly employed. If An athlete has trained and eaten correctly (many do not of course) the net gain in lean tissue mass can be as much as a 14% increase in total lean mass in a matter of weeks with a similar corresponding loss in adipose (fat) tissue. But the effects are far positive effects of a GH protocol can be far reaching in that the protocol allows continued progress where none has been realized for quite some time. Many lose much of the potential possible progress during the actual GH protocol and almost all give up the long-term gains that they could have realized by simply understanding a few facts of reality concerning GH use. Employment of these facts usually results in realizing the 14% net gain possible and keeping them post-protocol while adding a few more freaky pounds. Been there done that.
There are several hormones, hormone-like substances, and a few supplements that act anabolically enough to result in an increase in lean muscle mass without any degree of androgenic activity. Many of these substances are highly anti-catabolic as well. If an athlete’s goal is to make continuous progress either an anabolic or anti-catabolic environment must be maintained without creating uncontrolled negative reactions to the intended anabolic or anti-catabolic action. In the case of Absolute Anabolics this means that the anabolic signaling method must be phased or cycled in the appropriate time frames as well as utilization of the correct products to aid an athlete in working with instead of against their bodies. We will first discuss the hormone and then discuss OTC products that either positively affect them or those that mimic their activity.
Growth Hormone (GH) GH is probably the best known of the hormones we refer to as Absolute Anabolics. GH is often heralded to be a fountain of youth for the aging and a mandatory addition to the drug protocols of the elite competitive athlete. It is also naturally produced within the body.
The average healthy adult produces between 0.5-1.5 iu (international units) of GH daily. This is not to say that the body cannot produce a great deal more GH, only that this is all the body wants to produce for our declining post-adolescent years. (Which really sucks) After all, we are past our hormonal prime as males at age 18-25 (yet we are not in our muscular prime for well over a decade after).
A growing child produces 4-7 GH pulses of about 2iu each for 4-5 days but not necessarily on consecutive days. This amounts to as much as 70iu of GH entering the circulatory system in a rather brief period. (Gee, and I wonder why I have to buy clothes for my kid about every other week?)
As we have discussed in earlier books and articles, the two types of muscle proteins capable of growth are structural and contractile proteins. Contractile proteins are called actin and myosin. Their job is to induce body movement through contractions that result in the shortening of the muscle fibers. This is quite similar to a ratcheting effect in action. The structural proteins hold the entire muscle and connective tissue complex together. Both proteins add to total muscle mass, strength potential and density. GH has a profound positive effect upon structural protein anabolism while providing a degree of increased protein synthesis within contractile proteins. Additionally, GH use results in a very powerful anticatabolic effect. By increasing total structural protein content we realize a very obvious increase in lean muscle mass and strength potential while benefiting actual structural integrity. This is important when considering long-term potential and results. Structural integrity can be a dramatic limiting factor or growth stimulus. The lack of supporting tissues obviously also limits potential training weight-loads for the affected muscle groups. Therefore a greater degree of structural protein synthesis results in an increase in contractile protein synthesis due to adaptation to a greater weight-load. (Gee, ya think so? Duh)
Consider this aspect of structural integrity: Would you try to do bar squats on loose sand? Of course not! And the reason is due to a lack of structural integrity. So why would anyone seeking to build the perfect beast disregard the necessity of a complete musculature?
Yes, there are a few other benefits to increased GH levels to consider… *Increased lean mass tissue *Improved memory *Increased strength *Improved stamina *Increased Libido *Stronger bones *Lower blood pressure *Lower bodyfat percentage *Increased rate of recovery and regeneration of tissues *Regeneration of skin proteins and improved skin elasticity *Anticatabolic/lean tissue sparing during calorie restricted periods *Increased use of fat stores as an energy source.
Some older athlete’s have reported an increase in hair growth on the pate and a decrease in gray hair.
Many of the effects of GH can be attributed to the known 8 growth factors resulting from its elevation in the circulatory system. Of these the most noted growth factor in the sports community is IGF-1, and less so FGF. Many who have used GH with poor results simply did not realize the chain of events that GH use induces and therefore missed the long-term gains that they had at their finger-tips. Of course some simply totally screwed up the protocol.
Okay, Science Geek Time!
I realize that reading through the science behind a given subject can be as boring as watching mold grow on a kitchen sink (actually had to do this in a biology class years ago…had two very hot lab partners though) but the ability to create protocols of specific intent with a known out come requires some degree of knowledge relating to the Action/Reaction Factors that effect it…and therefore us.
There are immature cells that sit out-side of, but joined to, muscle fibers called satellite-cells or stem-cells. These are metabolically active cells that do not have the capacity to (yet) join in with all of the other muscle cells and fibers to produce contractile force. They also lack fiber-type and much of a growth capacity (duh!). So picture this as a sort of muscle cell nursery. The proliferation/multiplication of these satellite-cells is induced by FGF (Fibroblast Growth Factor) when it merges/binds with existing cell receptors. The result is an up-regulation in satellite-cell count and production (more cells).
The mature satellite-cells sit around the muscle cell nursery stealing food from the immature satellite-cells and pretty much do nothing. (Like most adolescents. Gee I miss those days). Some type of (there are several) an Action Factor occurs that results in the production/release of IGF-1 (Insulin -Like Growth Factor-1). When IGF-1 binds to its satellite-cell receptor the inclusion process of that cell into its adjoined muscle fiber results. The eventual out come is more muscle cells and fibers. These two events are called hyperplasia.
Now that the mature satellite-cells have become muscle cells, it is time to get a job. In the presence of high circulatory androgen/testosterone levels , massive muscle cell androgen receptor/testosterone binding occurs. The result is that, at the expense of type-I muscle fibers, an increase in type-II muscle fiber count occurs. The second Reaction Factor that happens is increased muscle cell contractile protein synthesis (anabolism/growth). This is called hypertrophy because each affected cell is getting larger. If anyone missed the point, this means that we can change low growth potential type-I fibers into high growth potential type-II muscle fibers.
Insulin binding with its cell receptor initiates a series of events that results in increased cellular up-take of glucose (from carbohydrates), fatty-acids (from fats), amino acids (from proteins), and micro-nutrients. This means that insulin has the ability to increase cellular growth nutrient up-take to a point of triggering anabolism/growth/hypertrophy. Unfortunately supraphysiological insulin levels result in the up-take of only about half of the necessary amino acids for cell growth. (Which sucks, but the process is yet unfinished)
When GH binds to its healthy muscle cell receptor, several good things happen: The cell increases IGF-1 production. The cell switches to favoring fat as a main energy source. An increase in structural protein synthesis occurs (anabolism) The up-take of the other half of the necessary amino acids for cell growth significantly increases.
Thyroid Hormones regulate the body’s metabolic rate. That is: The rate at which cells absorb and utilize calories. The rate of protein synthesis occurs. The rate at which fat is oxidized (burned).
*The liver readily forms circulatory IGF-1 in the presence of GH and Insulin. Metabolically active cells secrete IGF-1 as a result of meeting up with GH, estrogens, or as a result of a chemical cascade originating from cellular and tissue elongation (stretching).
The human body is an amazingly adaptive organism that is basically lazy. In short it fights change by doing as little as possible. The body prefers to slowly degrade into mediocrity through preservation of homeostasis. Homeostasis simply means a state of no change. Yup: Weenie status. Anytime the hormone ratio/profile that supports this slide in the oblivion is altered the body either attempts to shut down the offending organ or gland, or inhibits the effect at the cellular level. Obviously GH and its growth factor substrates are no different in this aspect.
Control Of The GH/IGF-1 Axis There are two recognized peptide hormones known to regulate the body’s GH levels. When the hypothalamus secretes GHRH (growth hormone releasing hormone) it contacts its receptors of the pituitary gland resulting in a pulsitile release of GH. If there were no inhibiting hormone, or negative feed-back loop, the levels of circulatory GH and resulting IGF-1 would reach a very profound measure indeed (Oh darn). Somatostatin is the hormone that tells the pituitary to decrease or stop GH secretion. But of course it does not stop there. Somatostatin triggers GH/IGF-1 receptor down-regulation and a decrease in sensitivity as well as acting to decrease the secretion of TSH (thyroid stimulating hormone). The result is a decrease in metabolic rate and a reduction in net anabolism. Sucks, huh? Ya, so does the correlating decrease in calorie expenditure from fat stores and an increase in muscle catabolism (fat dude status). So, all we have to do is decrease or stop the somatostatin release and shredded freak status will soon be ours…right?
There is a second inhibitive pathway to regulate GH levels is called a negative feed-back loop. When circulatory GH or Somatostatin makes its way back to the hypothalamus and/or the pituitary gland the over abundance of either will shut down its own respective receptors as well.
Bottom-Line When an athlete administers supraphysiological dosages of GH for a prolonged period of time without correctly anticipating and responding to Action/Reaction Factors the pituitary and hypothalamus respond to the increasing negative feed-back loop by shutting down first GHRH release and second shutting off the GH supply. So GH release is suppressed on two levels. Next the release of Somatostatin gradually increases to beyond normal levels to further inhibit what the body assumes to be pituitary release of GH. Of course the GH/IGF-1 receptors are beaten up pretty bad by the chronic elevation of Somatostatin and the dosages of GH administered are required to increase to match. During the protocol this means higher dosages with fewer returns and post protocol it means suppressed endogenous GH secretion and a great deal of lean tissue loss. Not bad enough? How about the fat accumulation and loss of long term results? Like 2 steps forward and 1.5 back, huh?
The body does not respond by totally shutting down the GH/IGF-1 axis simply because an individual administers a couple of iu of GH. In fact the body fails to “significantly” suppress GH release on a long-term basis until after more than 2 weeks of continuous multiple daily injections are administered. So what is a wanna-be freak suppose to do? There is always the option of winning the Mr. O and investing your winnings and endorsement money into BioTech stocks such as Genentech for non-stop administration protocols, or work with, instead of against, the body’s Action/Reaction Factors.
For Every Action There Is A Profitable Reaction The human physiology commonly begins a significant multi-level fight for homeostasis against exogenous GH use at just over the 14 day continuous administration period. This is due to an increase in Somatostatin and a down-regulation of GHRH release. The result is a decrease in GH/IGF-1 receptor sensitivity and a shut-down in GH secretion by the pituitary respectively.
Estrogens promote cellular and hepatic IGF-1 secretion and pituitary release of GH. Though it seems that most high androgens can inhibit this process to some extent, those that foster its formation tend to promote it…as do certain blood meds employed to control the elevation in blood pressure realized from estrogen induced water retention.
A few chemicals called GH secretagogues have shown the unique ability to restore the GH/IGF-1 Axis to normal function. In fact some of these drugs have been clinically documented to elicit GH release levels as much as 40 times normal with consecutive dosages realizing nearly the same degree of elevation…multiple times daily. The down fall of GH secretagogues drugs like MK-677, Hexarelin and GHRP-2 is that the body begins to react to them as well after a bout 2 weeks with a decrease in GH secretion of about 40%.
(Come on now, you had to have seen this coming) Maximum GH/IGF-1 For Dummies…and Me Example Protocol (With AAS)
Day 1. Testosterone Propionate 150-200mg/GHRP-2 4xd 2. Testosterone Propionate 100-150mg/GHRP-2 4xd 3. Testosterone Propionate 100-150mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 4. Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 5. GH 4iu 2xd/Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd 6. GH 4iu 2xd/Trenbolone Acetate 75-100mg 7. GH 4iu 2xd/Testosterone Propionate 150-200mg 8. Testosterone Propionate 100-150mg/GHRP-2 4xd 9. Testosterone Propionate 100-150mg/GHRP-2 4xd 10. Testosterone Propionate 100-150mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 11. Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 12. GH 4iu 2xd/Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd 13. GH 4iu 2xd/Trenbolone Acetate 75-100mg 14. GH 4iu 2xd/Testosterone Propionate 150-200mg 15. Testosterone Propionate 100-150mg/GHRP-2 4xd 16. Testosterone Propionate 100-150mg/GHRP-2 4xd 17. Testosterone Propionate 100-150mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 18. Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 19. GH 4iu 2xd/Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd 20. GH 4iu 2xd/ Trenbolone Acetate 75-100mg 21. GH 4iu 2xd/Testosterone Propionate 150-200mg 22. Testosterone Propionate 100-150mg/GHRP-2 4xd 23. Testosterone Propionate 100-150mg/GHRP-2 4xd 24. Testosterone Propionate 100-150mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 25. Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd/GHRP-2 4xd 26. GH 4iu 2xd/Trenbolone Acetate 75-100mg/Clonidine 0.5mg 2xd 27. GH 4iu 2xd/Trenbolone Acetate 75-100mg 28. GH 4iu 2xd/Testosterone Propionate 150-200mg *Nolvadex 20mg 2xd *GHRP-2 is continued for 7 days post-cycle and the protocol is repeated *10g L-Arginine AM/PM on exogenous GH days *Optional: Add methandrostenolone 30mg on Testosterone days and oxandrolone on trenbolone days.
Testosterone aromatizes to estrogens thus promoting GH/IGF-1 release and formation. With the synergistic effect of increase pituitary release of GH resulting from clonidine and GHRP-2 administration, GH/IGF-1 levels are Significant. This structure allows an over-lapping effect during exogenous GH administration periods evolving into an additive effect (endogenous + exogenous = A lot of GH).
So why the intermittent use of GH? As I explained prior the human body has an amazing ability to adapt. Consider the amount of growth that occurs from the intermittent GH pulses natural to children and the results that transpire. Nature can be highly effective, huh?
By utilizing the fast-acting and brief half-life qualities of testosterone propionate and non-aromatizing trenbolone acetate the protocol allows for near immediate response and a high androgenic environment to maximize the value of GH use.
There are other options for the replacement of GHRP-2 that I will list, but considering the fact that there is an over the counter product that contains it available. (Intragrowth).
Pyridostigmine: A cholinergic agonist that decreases hypothalamic somatostatin has been effective at a dose of 120mg/d
MK-677: A GH secretagogue has been effective at 50mg/d
Hexarelin: A GH secretagogue has been effective at a dosage of 2mcg/kg of bodyweight 3xd.
01-20-2005, 06:53 PM #2Anabolic Member
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- Mar 2004
Interesting article. L. Rea really does know his stuff in case you're wondering about the author.
01-20-2005, 06:56 PM #3New Member
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- Jan 2005
I really need thoughts on the cycle, I think it looks good due to the fact it is low in gear and HGH but also uses GHRP-2 which we all know release natural GH and it keeps all gear switched up. Any thoughts or has anyone tried L.Rea cycles before? Thanks bros
01-20-2005, 07:12 PM #4VET Retired
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- Dec 2001
I'll take some heat for this but sometimes I think he over complicates things when discussing anabolics (intentionally or unintentionally). So when I total noob looks at his work the person would be like "whoa this dude knows his stuff!!" his work that I’ve read is good but I usually find myself disagreeing with some of the cycle advise he gives. JMO.
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