| Content | GHRP-6 peptide which is structurally very similar to its predecessor, GHRP-2 The main difference is that the GHRP-6 increases appetite in some people. Both peptides can be used together to achieve better synergistic effects. Studies have shown that the highest concentrations of growth hormone in the blood is achieved just combinations of GHRP-6 and GHRP-2. GHRP-6 stimulates the pituitary gland to produce GH. GHRP can be effectively used in the treatment of growth hormone deficiency. GHRP-6 is highly effective in increasing blood levels of the hormone HGH and IGF-1.
GHRP-6 stimulates and strengthens the immune system, has a strong anabolic – for massive muscle gains and strength, helps burn body fat, has a very strong anti-aging effect, smooths wrinkles, improves the condition of hair and skin, gives a very good sleep and excellent regeneration, increases bone strength, has anti-inflammatory effects, brings a sense of the large influx of energy and vitality, and causing general overall rejuvenation of the body and all of its body tissues.
GHRP-6 helps very effectively to gain muscle mass, increase strength, recovery and burn fat. GHRP-6 improves energy metabolism.
Combining GHRP 6 with CJC 1295
The combined use of CJC 1295 peptide without DAC can greatly enhance its results in conjunction with GHRP 6.
Combining GHRP 6 with T3
The efficiency of GHRP 6 can greatly amplify with little high levels of T3 in the body. | Tesamorelin (Tesamorelin) is made with growth hormone-releasing factor (GRF).
Tesamorelin is used to reduce excess fat around the stomach that is caused by taking certain HIV medications. This condition is also called lipodystrophy (LYE-poe-DIS-troe-fee).
Tesamorelin is not a weight-loss medication and should not be used to treat obesity.
Tesamorelin (Tesamorelin for injection) is indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy.
Limitations of Use:
Since the long-term cardiovascular safety and potential long-term cardiovascular benefit of Tesamorelin treatment have not been studied and are not known, careful consideration should be given whether to continue Tesamorelin treatment in patients who do not show a clear efficacy response as judged by the degree of reduction in visceral adipose tissue measured by waist circumference or CT scan.
Tesamorelin is not indicated for weight loss management (weight neutral effect).
There are no data to support improved compliance with anti-retroviral therapies in HIV-positive patients taking Tesamorelin.
General Dosing Information
The recommended dose of Tesamorelin is 2 mg injected subcutaneously once a day.
The recommended injection site is the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel.
Reconstitution Procedure
Tesamorelin must be reconstituted with the diluent provided with the product.
Reconstitute the 2 mg vial of Tesamorelin with 2.1 mL of diluent. Mix by rolling the vial gently in your hands for 30 seconds. Do not shake.
Detailed instructions for reconstituting Tesamorelin are provided in the INSTRUCTIONS FOR USE leaflet enclosed in the boxes containing Tesamorelin and diluent.
Administer Tesamorelin immediately following reconstitution and throw away any unused Tesamorelin solution. If not used immediately, the reconstituted Tesamorelin solution should be discarded. Do not freeze or refrigerate the reconstituted Tesamorelin solution.
Administration
Reconstituted Tesamorelin solution should always be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Tesamorelin must be injected only if the solution is clear, colorless and without particulate matter.
Tesamorelin should be injected subcutaneously into the skin on the abdomen. Injection sites should be rotated to different areas of the abdomen. Do not inject into scar tissue, bruises or the navel. | Trenbolone Enanthate – injectable steroid that is used mainly in bodybuilding and weightlifting to achieve maximum growth of compacted muscle mass and a significant increase in power capacity.
Trenbolone Enanthate ester is characterized by a long period of exposure into the body (about six weeks).
Trenbolone Enanthate Effects
significant increase in muscle mass (average 10 kg per 8 weeks);
increasing the degree of endurance and power performance;
200% increase in the level of insulin-like growth factor stimulation and hyperplasia of the muscle;
fat burning effect (including the influence due to the release of growth hormone);
lowering cortisol levels (a hormone which facilitates the destruction of proteins, increased fat accumulation and glucose).
How to Use Trenbolone Enanthate: Dosage, Cycle, PCT
To create a cycle for Trenbolone Enanthate, which also would be effective and safe for the body, stick to a few rules:
Do not exceed the dosage of the drug and duration of the cycle (the optimal dose of Trenbolone Enanthate per week – 300 mg, cycle length – 6-8 weeks).
Always start with a minimum rate of injection to fix the body’s response to anabolic effects.
Take Gonadotropins, if the steroid cycle is designed for 5 weeks and more.
Do not neglect the power of sports complex and a special diet for weight gain.
Always consult a doctor before starting the cycle.
Trenbolone Enanthate Combination Cycles
Trenbolone Enanthate, to gain muscle mass, is often taken solo, because of its efficiency. In professional cycles at a dosage of 250 mg per week, can be stacked with Testosterone Enanthate, but this combination is only valid for the experienced athletes, and after a medical advice.
For drying period one can buy Winstrol, or Anavar without anti-estrogens, using half of the dosage.
As PCT on Trenbolone cycle is used Toremifene or Clomid.
Trenbolone Enanthate Reviews
After analyzing published on Trenbolone Enanthate reviews, it is easy to draw a conclusion about the quality of weight and severity of the effect: more than 90% of athletes and bodybuilders were satisfied with the results of the cycle. The absence of the phenomenon of rollback and flavoring also played a significant role in relation of athletes with this steroid.
Warnings: Keep out of reach of children. For adults only. | CJC-1295 is a synthetic GHRH (growth hormone releasing hormone) analogue made up of 30 amino acids. It has been found to be highly effective with regards to the increase of growth hormone secretion and IGF-1 without negatively affecting the pulsatility of GH secretion.
CJC-1295 is often combined with Ipamorelin due to its enhanced specificity as a GHRH. This peptide generates similar increases in growth hormone secretion, but without the appetite stimulation and increase in cortisol, acetylcholine, prolactin, and aldosterone seen with other peptides in its class. This peptide has been found to be very well-tolerated and perfect when combined with Ipamorelin.
Gland Stimulated: Pituitary
Benefits of CJC-1295:
Increased growth hormone secretion and IGF-1 Levels with no increase in prolactin
Increased Body Weight and Length through increased protein synthesis
Increased Muscle Growth
Increased Bone Density
Improved Immune Function
Improved Cognition and Memory
Increased Collagen Production
Increased Fat Loss
Increased Cellular Repair and Regeneration
CJC-1295 also promotes slow wave deep sleep, which is responsible for the highest level of muscle growth and memory retention and rejuvenation
Two types of CJC 1295:
GHRH (growth hormone releasing hormone) is produced in the hypothalamus. Its pulsatile release from the hypothalamus triggers a pulsatile release of GH from the pituitary gland. GHRH has a very short half-life of only a few minutes (half-life = the time required to remove half of the substance from the blood. The shorter the half-life, the more rapidly the substance is removed from the body, and the less its effect on the body).
The first 29 amino acids of GHRH is the active segment. They are available as a manufactured peptide called Sermorelin. Sermorelin was further modified to increase its half-life to 30 minutes. This is called CJC 1295. CJC-1295 was further modified by adding DAC (Drug Affinity Complex) to it. DAC binds to a blood protein called albumin, which increases it's half-life to 8 days. It is called CJC 1295 + DAC. CJC 1295 can also be compounded in a non-DAC form which mimics a more normal physiologic GH spike each night.
The longer half-life from the DAC binding to albumin means injections are only required once or twice per week. However, the long half-life and relatively constant blood level provide a constant stimulus for GH release from the pituitary through the GHRH receptor, which is not physiological. This can decrease the GH pulse amplitude which will result in decreased GH tissue stimulation.
Safety:
It is recommended when using a long-acting CJC molecule to have 'hormone holidays' of three months each three to six months, to allow the pituitary to 'recover'. During the holidays, Sermorelin is used instead of CJC 1295 + DAC.
The 'hormone holidays' may also minimize the risk of GH resistance developing. This resistance, or insensitivity, may occur via antibodies forming that bind to and inactivate GH, or by a decreased number of GH receptors on tissues (down-regulation). These are theoretical concerns as no long-term studies have been undertaken to clarify the issues.
Side effects of CJC-1295 may include injection site reactions (irritation, erythema, induration, pain, itching), headache, diarrhea, vasodilation (flushing, warmth, transient hypotension), nausea, abdominal pain. | | Insulin-like growth factor-1 (IGF-1) helps encourage normal bone and tissue growth and development and also has the ability to decrease blood glucose levels.
IGF-1 advances to fat cells and therefore burns fat. Subsequently, it increases lean body mass and decreases fat. These effects are desired mostly by athletes and bodybuilders. Increased IGF-1 levels are also comparable to weight gain. This weight gain is a result of lean body mass growth, not fat production.
IGF-1 is favored in the bodybuilding industry and for people who workout regularly. It helps enhance recovery time after workout and improves energy during the workout.
IGF-1 injections are common for adults and children if they have a growth hormone deficiency. IGF-1 contains many necessary amino acids that can help children who are not developing at a standard rate and supplement adults that are deficient.
Research has also shown that the anabolic effects of IGF-1 may reflect inhibited protein breakdown and stimulated protein synthesis in skeletal muscle and that this response may be caused by a direct effect of IGF-1 on muscle tissue, therefore assisting burns on the skin and other tissue abnormalities.
Mechanism of Action
IGF-1 is a hormone found naturally in human blood. Its primary function is to manage the effects of growth hormone in the body. Normal IGF-1 and growth hormone functions include tissue and bone growth. IGF-1 is formed in different tissues as a result of growth hormone in the blood.
IGF-1 promotes systemic body growth, and has growth-stimulating effects on mostly every cell in the body, mainly bone, cartilage, skeletal muscle, liver, kidney, nerve, skin and lung cells. As well as the insulin-like effects, IGF-1 can also manage cellular DNA synthesis.
Administration
Mode of Administration: Subcutaneous injection to a fleshy part of the body, typically to the stomach or abdominal area. IGF-1 can also be administered intramuscularly.
Before administering IGF-1, always be sure to use a clean and sterile syringe.
Hold the IGF-1 vial upright and insert the syringe in the center of the cap.
Draw the plunger until you have the correct amount (see ‘Dosage’ below) in the syringe and carefully remove it.
Before administering the syringe, use alcohol to cleanse the area of skin.
Pinch the skin around the area to be injected, leave about 2 cm on each side.
Hold the syringe at a 90 degree angle to your skin and swiftly insert the syringe.
Depress the plunger fully, until the syringe is empty, and carefully draw out.
Dosage
Dosage Amount: For lean muscle growth and fat loss
40 mcg - 50 mcg daily (men)
10 mcg - 20 mcg daily (women)
IGF-1 should not be injected more than twice daily
A typical dosage cycle of IGF-1 will continue for 2 to 12 weeks
Children and adults who are prescribed IGF-1 for development deficiency should consult with a care provider about correct dosing.
Side Effects
The side effects of IGF-1 can be similar to those of other growth hormones. These include growth of excess body tissue, also known as acromegaly, and damage to the joints, liver, and heart. IGF-1 could possibly cause joint pain, muscle pain, headaches and nausea. IGF-1 can also decrease levels of blood glucose, resulting in hypoglycemia. Researchers also associate IGF-1 with an increased risk of developing some cancers, such as lung, breast, colorectal and prostate.
Benefits
Facilitation of protein synthesis in the body
Regulation of stored fat and channeling it to be used for energy production, resulting in fat loss
Promotion of positive effects on metabolism and increasing lean body mass and muscle growth
Protection against autoimmune disease, heart disease and plaque buildup
Aid development in young children and adults deficient in essential amino acids
Improvement in blood sugar regulation
Promotion of optimal health, wellness and fitness in users |
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