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  Bulking Steroids:

  Anabol 5mg British Dispensary
Anabol 50mg - British Dragon
Anabol 50mg, C&K, China
Anabol 5mg - C&K
Anadrol 50 / oxymetholone
Anapolon 50 mg
Andriol / Testosterone Undecanoate
Androlic 50mg British Dragon
Androlic 50mg British Dispensary
Androlic 50mg, C&K, China
Averbol 25
BONALONE (Oxymetholone)
Clomid 50mg, Global Napi
Cypioject 10 ml vial (200 mg/ml) Testosterone cypionate
Cypionax (Testosterone cypionate)
Danabol, 10mg, 500tabs, DS
Deca Durabolin (Norma)
Deca Durabolin (Organon)
Deca-durabolin 100mg
Deca-durabolin 50mg
Decabol 250 British Dragon
Decaject 200
Durabol British Dragon
Durabol 200
Durabolin 25
Halotestex British Dragon
Halotestin 5mg
Mastabol 100 British Dragon
Mastabol Depot 200 BD
Metanabol 5mg Poland, Jelfa
Methanabol 10mg 100tabs British Dragon
Methanabol 10mg 500tabs BD
Methanabol 50mg 100tabs BD
Methandriol Dipropionate 75
Methandrostenoloni - 5mg
Nandrolone decanoate
Nandrolone Phenylpropionate
Naposim 5mg
Oxanabol 10mg 50tabs
Oxanabol, 5mg, C&K
Oxydrol 50Mg, 100tabs BritishDragon
Primoteston Depot 1ml amp
SustaJect 250 (Ec labs - Eurochem)
Sustanon 250 Pakistan
Sustanon 250mg/1ml Nile
Testabol Cypionate
Testabol Depot, British Dragon
Testabol Enanthate British Dragon
Testabol Propionate 100, 10ml
Testex Elmu Prolongatum 250mg/2ml
TestoJect / 4x testosterone blend
Testosteron Depo 1ml/amp
Testosterone cypionate 200mg
Testosterone Enanthate 250
Testosterone Enanthate 250 Norma
Testosterone Propionate 50mg/ml, Farmak
Testosterone suspension / Aquaviron
Testoviron Depot / Schering
TESTOVIS / testosterone-propionate
Trenabol 75 / British Dragon
Tri-Trenabol 150 BD
Turanabol 10mg

  Cutting Steroids:

  Anadiol Depot, Ilium
Boldabol / British Dragon
Bonavar / Oxandrolone
Cetabon (anabolic formula)
Equipoise 50mL / 50mL - 50mg/1ml
Fluoxymesterone 10mg
Stanabolic 50mg/ml Ilium
Lasix (furosemide)
Orabolin / etylestrenol, 2 mg/tab
PARATABS - Parabolan (trenbolone acetate), 60 tabs (25 mg/tab)
Primobol 100 British Dragon
Primobol tabs, British Dragon
Primobolan Depot
Primoject 10ml
Stanabol 10mg
Stanabol 50injectable (Stanozolol)
Stanabol 50mg British Dragon
Stanabol 50mg C&K
Stanabol 5mg, C&K
Stanoject / Stanozolol
STANOL (stanozolol) 5 mg 200tab
Stanol 50mg/1ml
Stanol 50mg/1ml
STANOZOLOL 1ml x 50mg/ml, LA
Stanozolol 10mg 100Tabs / LA, Italy
Testolic 2ml testosteron propianate
TESTOPIN-100 2 ml vial
Trenabol depot 100mg/1ml
Trenbolone Acetate tabs, BD
Virormone 2ml (Testosterone Propionate) 100mg/1ml
Voltaren 75

  Man's Health:

  Caverject 10mcg, Syringes
Caverject 20mcg
Caverject 20mcg
Propecia 1mg (Finasteride) 28 tabs

  Human Hormones:

Choriomon 15000IU
Igtropin IGF1 LR3 100mcg
Jintropin 10IU(100IU/box)
Jintropin 10IU(200IU/kit)
Jintropin 4IU(40IU/box)
Jintropin 4IU(80IU/box)
Pregnyl 5000 IU Organon
Pregnyl 3 X 5000 IU (HCG)

  Anti Estrogens:

  Anastrozole, - British Dragon
Arimidex / Anastrozole
Aromasin 20 mg / British Dragon
Aromasin 25 mg / Pfizer
Aromasin 25 mg
Clenbuterol / Hubei Huangshi
Clomid 50mg C&K
Clomid 50mg, Aventis
Clomid 50mg, Brunno Farmaceutici
Clomifen 25 mg
Clomiphene 50mg
Clomiphene citrate 50mg
Mesterolone BD (Proviron)
Nolvadex 10mg
Nolvadex, 20mg, AstraZeneca
Nolvadex, 40mg, AstraZeneca
Nolvadex, 50mg, C&K China
Omifin 50 mg 30 tabs
Proviron 25mg (Mesterolone)
Provironum 25mg Schering
Tamoxifen 20mg British Dragon
Teslac (Testolactone) 50mg / 100 tabs

  Anti Depressants:

Dumirox (Fluvoxamine) 50mg
Rivotril (CLONAZEPAM) 0.5 mg
Rivotril (CLONAZEPAM) 2 mg
Rivotril (CLONAZEPAM) 2 mg
Rohypnol (Flunitrazepam) 1mg
Valium (DIAZEPAM) 10mg
Valium (DIAZEPAM) 5mg

  Head Ache:

  Maxalt (Rizatripan) 10 mg
Relpax 40mg
Zomigon (Zolmitriptane) 2.5mg


  Famvir (Famciclovir) 125 mg
Viranet (Valacyclovir) 500mg
Zovirax (Acyclovir) 15 gr

  Muscle Relaxers:

  Baclofen 25mg
Muscoril Caps 20 x 4 mg
Norgesic (Orphenadrine)

  Pain Releaf:

  Advil (Ibuprofen) 200mg
Celebrex 200mg
Mesulid (Nimesulide) 100mg
Movatec (Meloxicam) 15mg
Naprosyn 500mg
Oruvail (Ketoprofen) 200mg
Vioxx 25mg

  Quit Smoking:

  Zyban (bupropion) 150 mg

  Skin Care:

  Harifin 5 (Finasteride) 5mg

  Weight Loss:

  Cynomel 0,025mg (25mcg) (Cytomel / T3) / Liothyronine Sodium
Cytomel / T4 50 mg
Phentermine (blue/clear) 30mg. 100 Caps
Reducil 28tabs 15mg
TRIACANA 0.35 mcg



  Genital Warts:

  Aldara cream 5% (Imiquimod)
Wartek (Podophyllotoxin) cream

Insulin The Anabolic Substance

Ask any of the elite who has become truly massive beasts which anabolic substance has had the most profound effect upon their physique and the answer from the largest mammals will unanimously be insulin.

Though GH has brought to the forefront of competitive stages the well retained lean muscle mass tissue displayed beneath an onion skin exterior of today, it is the symbiotic relationship insulin has with all other physical enhancement chemistry that has made beasts what they are in the new millenium.

Insulin is predominantly a storage hormone in that it initiates a cascade of cellular events that result in up-regulation of cellular nutrient content. It obviously goes without saying then that supraphysiological plasma levels of insulin result in supraphysiological cellular levels of nutrients. This in itself allows for a highly anabolic effect known as an osmotic response. A cellular osmotic response is nothing more than an increase in water and growth potentiating nutrients intracellularly that has a effect similar to increasing the amount of air in a balloon. More air in the balloon means a larger balloon. More water and proportionate growth nutrients means a larger cell. Interesting enough is the fact that this also triggers another survival mechanism that tells the stretched cell wall to increase in thickness to accommodate the osmotic response. This is due to an up-regulation in localized IGF-1 and MGF production and the synergistic response initialize. Oh ya. That is anabolism in the form of hypertrophy. Unfortunately, insulin is quite anabolic to fat cells too.

Since insulin is the body's main "storage" hormone it should come as no surprise to the reader that many diabetics and would-be beasts alike have become horribly fat as a result of improper insulin use and misguided dietary habits. Many bodybuilders have employed the 10-15 grams of carbohydrates per IU of insulin administered protocol with a great deal of success in spite of the inherent dangers of non-medical insulin use. However many, who have either become insulin resistant/insensitive or are genetically predisposed to inordinate adipose (fat) tissue accumulation, have endured a greater anabolism of adipose tissue than muscle. Some have foolishly put on more covering clothing and simply accepted this as a necessary side effect endured for the greater eventual goal. Others have added the additional potential negative side effects of heart arrhythmia/tachycardia, diabetes, and other not so fun stuff as well.

As I have pointed out many times before, adipose tissue is a major site for aromatase enzyme activity which in itself compounds the Big Fat Bastard problem. Many AAS (anabolic/androgenic steroids) are susceptible to the effects of aromatase enzyme conversion to estrogens as is endogenously produced (made inside the body) androgens such as testosterone. Obviously the greater the volume and activity of this enzyme that exists in the body, the greater the chance and degree of aromatization that occurs. Estrogen is directly anabolic to a minor degree to muscle tissue. Both fortunately and unfortunately it is highly anabolic to adipose tissue. Since estrogen is the hormone that induces female pattern fat deposits it is fortunate because a nice rack is a thing of beauty. Unfortunately I have as of yet not noted a single male bodybuilder who looked good or happy with boobs or any other fatty female attributes. So a greater degree of adipose tissue accumulation from insulin administration results in a compounded adipose tissue storage effect from aromatase enzyme susceptible AAS employment.
In some instances the result of this vicious cycle is bodybuilders who fail to ingest adequate calories during AAS protocols as a means of decreasing adipose tissue accumulation. Unless you are from another planet you realize this also limits muscular growth potential as well.

Before we discuss all of the interesting facts concerning the means of becoming a big fat bastard, it is necessary to have a fundamental understanding of the macronutrient product glucose.


Glucose is the body's preferred energy substrate. Though the brain's nutrient make-up is nearly 1/3 omega-3 fatty acids it is glucose that is without fail mandatory for continued sentience. So carb up a little and read closely as we learn a few things about the body we have been entrusted to play nice with.

When we ingest food stuffs in the form of the three macronutrients protein, carbohydrates, and fats the GI track introduces a series of chemical Action/Reaction Factors that result in the break-down of these nutrients to metabolic substrates.

  • Proteins=amino acids
  • Carbohydrates=glucose
  • Fats=fatty acids

It appears simple on the surface but in fact glucose can be converted to triglycerides and adipose tissue or lean tissue glycogen stores and toilet tinkle. Like wise fatty acids can be stored as fat or utilized as an energy substrate by the body's tissues but it cannot be converted to glucose. This is interesting when one considers the fact that carbohydrates can become glucose or fat, but fat cannot become glucose (though the cellular mitochondria can use fatty acids as an energy substrate as a keto response). Protein is ultimately destined to become amino acids employed for cellular repair and growth or intimate moments with the bathroom. But certain amino acids called gluconeogenic amino acids can be converted to glucose too. This can be disastrous for a bodybuilder who hopes to be a beast one day since lean muscle mass is predominantly made up of protein in the form of amino acids and a complete spectrum is necessary. We will get to this later. For now simply accept that glucose is necessary for life and bodybuilding progress alike.

The average circulatory value for glucose allows for about only 4 grams of glucose. It is actually uncommon for blood glucose levels to rise beyond an additional 1.5-2.0 grams or to drop below the 4 gram mark. A healthy individual who ingests a meal containing 50-150g of mixed carbohydrates will realize the normal increase in circulatory glucose for only about an hour. Interesting thing here is that endogenous (made by the body) insulin secretion will remain elevated for an additional 2 hours after glucose clearing. When the same individual ingests 300g of carbs (Fat Bastard) at one time the resulting insulin secretion levels will be 300% above normal for an additional 7 hours after blood glucose clearing. This is clearly a highly anabolic environment, but after tissue glycogen stores reach maximum levels a grotesque amount of the excess glucose finds its way to adipose tissue. And don't worry. If all of the existing fat cells are full, the body is way to happy to make new ones to secrete lots of aromatase enzyme. And herein awaits the key to greater lean mass tissue and a decrease in adipose tissue.


Gluconeogenesis is the biosynthesis of new glucose. This means that glucose is synthesized from other substrates than carbohydrates or glycogen stores. Obviously since the only source of fuel for the brain, testes, kidneys, and erythrocytes is glucose the body in its amazing adaptive manner can manufacture glucose from other materials. Those who are up on keto diets are aware of the fact that the body can derive energy from ketone bodies (which are converted into acetyl-CoA). But that is an entire different topic for now. In short the body utilizes the carbon structures within substrates to create energy in the eventual form of ATP (adenosine triphosphate). ATP is cellular energy that, as readers are aware, is the body's only energy currency. In the case of gluconeogenesis the carbon structures can come from other sources.

Triglycerides are structures consisting of three fatty acids adjoined by a glycerol molecule. By cleaving the fatty acids away from the glycerol molecule the body can utilize the freed glycerol molecule to make glucose through a series of conversions and subsequent carbon utilization.

With the exception of lysine and leucine all 20 (or 22 if you are of that school of thought) amino acids can be turned into TCA cycle intermediates which in turn allows for the carbon skeletons of the amino acids to be converted to pyruvate. The newly formed pyruvate can then be utilized by the gluconeogenic pathway to create glucose by way of another series of metabolic pathways. Let me explain that a little better. When glycogen stores in the liver and muscle are depleted the working/recovering muscles, brain and organs need another energy source. Catabolism of muscle tissue proteins to amino acids becomes the main source of carbon skeletons for the maintenance of mandatory blood glucose. As you will recall the body can clear 50 150 grams of carbohydrates in only a few hours.

So how much muscle do you think the gluconeogenic adaptive process can munch in the same period of inadequate nutrient supply from diet? By the way, the amino acid Alanine is the favorite gluconeogenic snack with Arginine and Glutamine coming in as close seconds.


In the presence of circulatory insulin elevation gluconeogenesis in the liver and muscle tissue decreases. During periods of circulating supraphysiological levels of amino acid muscle catabolism decreases. In the presence of both protein synthesis occurs.

So it would seem that the two choices a wanna-be beast faces is 300 grams of carbohydrates to induce a sufficient prolonged insulin spike and a Big Fat Bastard pose down or non-stop keto diets and declarations of "Hey, I may look like a weenie but I am really cut" for life.

  • The obvious solution is an elevation in both circulatory insulin and a corrected amino acid pool rendered highly efficient by design and not by chance.

Insulin administration is nothing new to the larger beasts of the bodybuilding world. Unfortunately neither is Big Fat Bastard status in the brief off-season. So it should come as no surprise to those who have entered the realm of the chemically enhance athlete to learn that insulin can make even the best genetically predisposed individual fat. It has been my experience that this is simply not necessary.

Insulin forces excessive amounts of amino acids into muscle cells when an adequate supply exists at the time of insulin exposure. Insulin also triggers increased muscle cell glycogen synthesis by way of positively effecting the rate limiting enzyme glycogen synthase. We also know the positive effects correct application of supraphysiological insulin levels has had upon the most catabolic pathway there is that affects muscle mass from reading my two prior books. Add to this the fact that insulin is synergistic to and with all other chemicals of muscular enhancement and realize the potential.

In relationship to goals it would seem evident that a protocol employing the attributes of insulin would necessitate the symbiotic relationship the hormone has with macronutrients as it applies to lean muscle mass tissue.

  1. Muscle is more than 80% protein by dry weight.

  2. ATP is the energy currency of muscular contractions, repair, and growth.

  3. Glucose is the prime source substrate for ATP synthesis and mandatory for proper brain and organ function (yes, that one also).

  4. Excess blood glucose will result in excess adipose tissue accumulation.

The Protocol

When this protocol was created its intent was rapid accumulation of lean mass tissue without an increase in adipose tissue deposits. Since the foundation of the diet was structured for efficient gluconeogenic dependant upon a correct ratio and amount of amino acids, a great deal of protein was consumed daily. The most effective protein intake minimum was the equivalent of 3 grams of protein per pound of bodyweight daily divided into at least 6 meals. Using a 200 pound individual as an example it was possible to reduce this slightly by simply eating 4 whole food meals daily providing 50 grams of whole protein each and sipping on whey protein drinks in water throughout the day providing the remaining 400 grams of protein. I preferred whey protein simply because it is one of the only two drinkable products I am aware of that allows for actual hyperaminoacid response in the circulatory system. Casein, egg, and (some people still use it) soy proteins fail to clear the GI track at a rate significant enough to induce the necessary supraphysiological amino acid concentrations for the protocol. The fact that whey protein is easily oxidized by the liver should be the first clue to the reason why results are superior. By the way, the other is Human Profile by Hazardous Materials (it is nearly 100% absorbed)

So here is the kicker. Though fat intake could be quite high, total daily carbohydrate intake could not exceed 0.5 grams per 25 pounds of bodyweight daily. The reason is simple: The goal was to force the body to employ the gluconeogenic pathway as a means of energy production. Any degree of actual glycogen regeneration resulted in the body returning to the glycosis pathway which allows for adipose tissue accumulation. The reason this worked so well was simplistic in nature. The making of ATP through amino acid gluconeogenesis is very inefficient thus allowing for a huge calorie expenditure similar to what occurs during DNP utilization. During calorie expenditure the body does not store fat but it does undergo protein anabolism. When enough protein was ingested the result was always a net increase in lean body mass of 5-8 pounds by the end of a two week protocol. Not bad for an experienced beasts, huh?

Additional Supplements

Since exogenous insulin was utilized during this protocol and, as mentioned prior, the gluconeogenic energy pathway loves certain amino acids it is easy to realize that the normal ratio of amino acids derived from whey protein and whole foods was not likely adequate. A mixture of 4 parts Alanine, 2 parts Glutamine, 2 parts Arginine and 1 part Taurine was created and capsulated. The dosage ingested was 1 gram of the supplemental mix per I.U. of insulin administered daily divided into 2 post administration dosages.

The preparation for this protocol required a liver glycogen depletion period of 24 hours prior to initial insulin administration. This was done to initiate the gluconeogenic pathway prior to protocol onset thus preventing any loss of lean tissue growth potential.

Though only a total idiot would ever assume that non-medical exogenous insulin use was safe, the utilization of a fast acting insulin was the better choice for this protocol. The first reason of course being that short acting chemistry also means shorter periods of potential exposure to negative side effects like a coma. Second is the fact that it was necessary due to the relevance in liver capacity for glucose manufacture by way of gluconeogenesis. Running out of adequate glucose reserves would introduce a series of potential negative side effects that would have required the ingestion of dextrose to inhibit.


Name of InsulinStart ActivityHighest ActivityEnds ActivityLow BS
Very short-acting (Humalog) 10 minutes1.5 hours3 hours2-4 hours
Short-acting (Regular/-R)20 minutes3-4 hours8 hours3-7 hours
Intermediate acting (Nor L)1.5-2 hours4-15 hours22-24 hours6-13 hours
Long-acting (Ultra Lente)4 hours10-24 hours36 hours12-28 hours
Combination: 70% N/30% R0-1 hour3-13 hours12-20 hours3-12 hours
Combination: 50% N/50% R0-1 hour3-12 hours12-20 hours3-12 hours

  • Humalog was administered about 15 minutes before an appropriate meal

  • Regular Type-R was administered 30 minutes before an appropriate


  • Low BS=Low blood sugar (Glucose).

As the reader can see when viewing the examples of insulin above, the employment of Humalog allowed for a total of 4 daily administrations of 10-15iu each and Humulin-R (Short-acting) only allowed for 3 daily administrations. This is not to say some have not increased the dosage or chose different insulin analogs, but it is to say that under these circumstances it was not necessary or more effective.

When looking at the following example consider these facts:

  1. Testosterone suspension has an active-life of about 24 hours tough plasma androgen levels remain elevated for about an additional 24 hours.

  2. Sex hormones such as testosterone and estrogens are inactive when bound by SHBG (sex hormone binding globulin) and free or active when not.

  3. Insulin is a powerful SHBG inhibitor.

  4. Insulin increases muscle glucose transporters and androgen receptors

Protocol Example

DayProtocol DayProtocol
1.Testosterone Sus. 150mg15.Testosterone Sus. 150mg
2.Humalog 10iu 4xd16.Humalog 10iu 4xd
3.Testosterone Sus. 150mg17.Testosterone Sus. 150mg
4.Humalog 10iu 4xd18.Humalog 10iu 4xd
5.Testosterone Sus. 150mg19.Testosterone Sus. 150mg
6.Humalog 10iu 4xd20.Humalog 10iu 4xd
7.Testosterone Sus. 150mg21.Testosterone Sus. 150mg
8.Humalog 10iu 4xd22.Humalog 10iu 4xd
9.Testosterone Sus. 150mg23.Testosterone Sus. 150mg
10.Humalog 10iu 4xd24.Humalog 10iu 4xd
11.Testosterone Sus. 150mg25.Testosterone Sus. 150mg
12.Humalog 10iu 4xd26.Humalog 10iu 4xd
13.Testosterone Sus. 150mg27.Testosterone Sus. 150mg
14.Humalog 10iu 4xd28.Humalog 10iu 4xd

Testosterone Sus.=testosterone suspension

150mg of testosterone suspension created a great deal of estrogen since it originates as a non-esterfied AAS. Estrogen up-regulated the muscle cells glucose transporters called GLUT-4 and increased androgen receptor sensitivity. This also meant that the administered testosterone was free or unbound from its inactivating protein SHBG. A great deal of the hormone entering the circulatory system was quickly bound, though not before a serious degree of anabolism occurred. But there is a portion left bound and in reserve.

Insulin inhibited SHBG resulting in a synergistic pro-anabolic response. By freeing the remaining prior days administered testosterone from SHBG an increase in androgenic activity was realized. Since SHBG is also estrogens binding protein the excretion of estrogens was dramatically accelerated. This resulted in rapid estrogen clearing and a notable increase in GH secretion which was amplified by the lack of the inhibitory effect normally caused by excess glucose. As most readers are aware, GH and insulin must both be present in the liver to produce IGF-1. The end result was adequate glucose regeneration at the expense of adipose tissue with a profound degree of lean tissue protein synthesis and growth. No more Big Fat Bastard!

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