basskiller's collection of Bodybuilding Peptide Articles

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  1. #46
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    appreciate the help!

    Yea I am not really good at math and been searching for someone to dummy proof some measurements as you did with the posting you have on IGF and really thankful for it. Just one thing if you could help me with PEG MGF ? I am gonna try to do 80 mcg if that sounds right, the peptide vile consist of Net Qty: 2.0 mg and I am planing to use the same style of syringe you have posted, 1 ml insulin syringe, the same thing. I have read that you're only suppose to reconstitute it with bacteriostatic water only, can I use acetate acid instead? Just wanna know two things if the markings are the same from IGF to PEG MGF? Only using of course 1 ml of either bacteriostatic water or acetate acid, and which leads me to my next question, do I use bacteriostatic water or acetate acid? I know I have read most people say water, but would it make any difference if I use acetate acid? Thank you for any input you will give me, and will follow more of your postings.

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    you can use AA to reconstitute it, but why do it.. You will still need the bacteriostatic water to cut the AA. You really don't want to inject straight AA/peg/mgf mix.

    you have a 2mg vial, add 2 mls of water or AA.. I would use the water for ease and one less step you have to do before injection.

    now once added, you now have 2000mcgs of peg/mgf
    you would use this picture to show you just how much you need






    2mgs is = to 2000mcgs

    Now as for dosage.. normally you would hit both muscles.. Right bi left bi, and you would use 80mcgs in each

    Now if you do use AA to reconstitute, once you draw up the desired amount, You now need to draw up some Bac water to dilute the AA that is now in the syringe.
    The amount doesn't really matter as long as you use some.. Your still getting that 80mcgs no matter how much bac water you now drawing into the syringe
    Last edited by basskiller; 05-09-2014 at 04:20 PM.

  3. #48
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    BPC 157 the healing peptide

    BPC 157 the healing peptide


    Bpc 157: specifications
    Molecular Formula : C62H98N16O22 Molecular Weight : 1419.5355 purity>99%
    Sequence: L-Valine, glycyl-L-alpha-glutamyl-L-prolyl-L-prolyl-L-prolylglycyl-L-lysyl-L-prolyl-L-alanyl-L-alpha-aspartyl-L-alpha-aspartyl-L-alanylglycyl-L-leucyl-; glycyl-L-alpha-glutamyl-L-prolyl-L-prolyl-L-prolylglycyllysyl-L-prolyl-L-alanyl-L-alpha-aspartyl-L-alpha-aspartyl-L-alanylglycyl-L-leucyl-L-valine


    BPC 157 Stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W. 1419) may be the new drug stable in human gastric juice, effective both in the upper and lower GI tract, and free of side effects. BPC 157, in addition to an antiulcer effect efficient in therapy of inflammatory bowel disease (IBD) (PL 14736) so far only tested in clinical phase II, has a very safe profile, and exhibited a particular wound healing effect. It also has shown to interact with the NO-system, providing endothelium protection and angiogenic effect, even in severely impaired conditions (i.e., it stimulated expression of early growth response 1 gene responsible for cytokine and growth factor generation and early extracellular matrix (collagen) formation (but also its repressor nerve growth factor 1-A binding protein-2)), important to counteract severe complications of advanced and poorly controlled IBD. Hopefully, the lessons from animal studies, particularly advanced intestinal anastomosis healing, reversed short bowel syndrome and fistula healing indicate BPC 157's high significance in further IBD therapy. Also, this supportive evidence (i.e., no toxic effect, limit test negative, LD1 not achieved, no side effect in trials) may counteract the problems commonly exercised in the use of peptidergic agents, particularly those used on a long-term basis.

    what is BPC 157 used for in humans/bodybuilders?
    well BPC 157 is known for super quick and professional Joint/tendon/ligament healing in all phases of clinical trials.. studies are shown here: BPC 157 has been shown in studies to heal torn quadriceps muscles, detached achilles tendon, muscles that have been damaged/crushed. Demonstrating dramatic fast recovery from muscle tears. Tendon to bone healing - increased ligament healing, BPC 157 has a variety of protective effects in the organs.

    Clinical trials demonstrate healing and prevention of stomach ulcers and it is being studied as a burn treatment. Trials show it may help repair some liver damage after prolonged chronic alcohol exposure. No adverse reactions have been seen in clinical trials.

    BPC 157 peptide has been shown to heal a variety of wounds in all areas researched, including internal organs, muscles, ligaments, tendons, skin, internal lacerations from surgery, etc.

    it can have a use in the medical industry help heal and get rid of stomach ulcers caused by people abusing NSAID drugs


    how long can i wait to see some effective results/benefits from this product?
    well personally for me ive been using for 1 week and the results are astounding! my right hip is now moveable im almost at a point where i can go in the gym and smash legs harder then before, my right bicep IM injections with it has had immaculate results thus far the pain is greatly diminished and im able to pick up things mildy heavy whereas 4 injections previously i was in bad pain/weakness and now... its feeling strong/harder then previous.

    usually results will take 4-6 weeks, because yes of course your injecting the drug but the human body has a set healing rate, but with BPC 157 the healing will be imo 100% faster then regular and the also the healing will be more complete whereas before you would only get around 80% of what you had before.



    How long can i run BPC 157 for?
    BPC 157 can be run for 4 weeks, followed by a 2 week rest. after this if you are still not feeling 100% itll be safe to run another course of BPC 157.


    How do you reconstitute BPC 157?
    simply pop the cap off, gently alchol swab the stopper, then let it dry, same goes with the BAC water vial. then dose out the correct amount of BAC water. then slowly put the needle in... then slowly but surely inject the BAC water along side the vial making sure you do not indirectly inject on the peptide powder, however once you have done the first dose and the powder i essentially mixed you can inject on the bac water, that is fine. Note* this is done with 2mls of bac water, that would be 2 whole 1ml/1cc insulin syringes.

    How do i Dose BPC 157 for optimal results?
    you can use anywhere from 200mcg being a medium dose up to 500mcg ... depending on severity of issue ( if severe) dose 2x a day at 350 mcg totaling 700 mcg.

    Is BPC 157 IM or sub q injection?BPC 157 is both, you can do IM or subq as close as you can to the injection site, preferably around 1-4 inches away to yield the most benefit to the injured area.


    what are the side effects of BPC 157?
    there are absolutely none that i know of well No one knows, however the first time i used it i got a head ache and felt generally sick, however this was only for a day. I'm now 100% this is most likely a coincidence, most probably a body reaction to the first time. to be honest there are no side effects, its in clinical trial phase 2 ATM and they have reported 0 effects, only positives.

    what syringe/needle size is good for this peptide?
    all needles would be good for this peptide depending on where you want to inject, however a 1ml/1cc 29 and half inch insulin syringe is optimal for most sites on the body.

    what is the cost of BPC 157?
    bpc 157 is relatively inexpensive and the results are worth the money as it could permanently strengthen your weak joints/connective tissues/muscles unlike a placebo supplement where it yields good results and once you come off, your joints are crying out for mercy. the general price is around $25-50 USD.

    How long will 1 bottle last?
    generally if run at the baseline 200mcg dose, 1 5mg vial will last 25 consecutive days. $25 usd for 1 bottle, is well worth it!

    where do i store this?
    just like another peptide keep it away from UV/sunlight. it can stay in room temp for up to 10 weeks, however for best storage/results store in a fridge and use until vial is run out then discard of it. For other BPC 157, they can stay in the fridge too as they;ll last up to 6 months, whereas if you had more you can store in the freezer( up to 2 years).

    thats everything you need to know about BPC 157 guys! hope you enjoy the read and this will help noobs/future injured athletes or current injured gym addicts try it.


    Huge thanks to HarryBrah for putting this all together
    by harrybrah
    Last edited by basskiller; 09-09-2014 at 11:47 PM.

  4. #49
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    Stable gastric pentadecapeptide BPC 157 is an anti-ulcer peptidergic agent, safe in inflammatory bowel disease clinical trials (GEPPPGKPADDAGLV, M.W. 1419, PL 14736) and wound healing, stable in human gastric juice and has no reported toxicity. We focused on BPC 157 as a therapy in peridontitis, esophagus, stomach, duodenum, intestine, liver and pancreas lesions. Particularly, it has a prominent effect on alcohol-lesions (i.e., acute, chronic) and NSAIDs-lesions (interestingly, BPC 157 both prevents and reverses adjuvant arthritis). In rat esophagitis and failed function of both lower esophageal sphincter (LES) and pyloric sphincters (PS), BPC 157 increased pressure in both sphincters till normal and reduced esophagitis. However, in healthy rats, it may decrease (PS) or increase (LES) the pressure in sphincters. It has strong angiogenic potential, it acts protectively on endothelium, prevents and reverses thrombus formation after abdominal aorta anastomosis, affects many central disturbances (i.e., dopamine and 5-HT system), the NO-system (either L-arginine and L-NAME effects), endothelin, acts as a free radical scavenger (counteracting CCl4-, paracetamol-, diclofenac-injuries) and exhibits neuroprotective properties. BPC 157 successfully heals the intestinal anastomosis, gastrocutaneous, duodenocutaneous and colocutaneous fistulas in rats, as well as interacting with the NO-system. Interestingly, the fistula closure was achieved even when the BPC 157 therapy was postponed for one month. In short-bowel syndrome escalating throughout 4 weeks, the constant weight gain above preoperative values started immediately with peroral and parental BPC 157 therapy and the villus height, crypth depth and muscle thickness (inner (circular) muscular layer) additionally increased. Thus, BPC 157 may improve gastrointestinal tract therapy.

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    Basskiller you always have some of the best info out there. Everyone always appreciates what you do for all the community's. It's been awhile bro hope you are doing good.

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    Quote Originally Posted by TEKLABS View Post
    Basskiller you always have some of the best info out there. Everyone always appreciates what you do for all the community's. It's been awhile bro hope you are doing good.
    I am.. and thank you.. Absolutely loved that test Enanthate from that contest.. quality gear!!!

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    Melanotan 2 information

    Melanotan 2 information




    Melanotan II is a cosmetic sunless tanning product that stimulates melanin production. Melanin is the main determinant of skin color in humans, a brown pigment which causes skin to become darker in appearance, instead of red when exposed to UV rays. Melanotan II users develop a gradual, natural looking tan with minimal exposure to the sun. It is particularly useful for fair-skinned individuals who find that they cannot tan naturally in the sun.

    Melanotan 2 peptide is not a treatment or cure for any disease, nor should it be used with the aim of preventing skin cancer. While melanin is known to have excellent photo protective properties, no clinical studies have ever indicated the efficiency of Melanotan II specifically in reducing UV damage.


    It is estimated that more than 90% of Melanotan users are familiar with the injectable Melanotan II. Melanotan I is usually only preferred by a small amount of long-term users who feel that Melanotan II makes them too dark, nauseated, and/or those who find the aphrodisiac side effect of Melanotan II to be a nuisance. These problems can be avoided by taking Melanotan II in lower dosages, administering before bed and using sunscreen and clothing to control tanning.

    Since Melanotan I has a large body of clinical evidence supporting its safety and efficacy, new users in particular often feel that it would be the better and safer option for usage. Unfortunately this is not the case when it comes to skin darkening and most new users who choose Melanotan I find themselves very disappointed at lack of tanning results since Melanotan I is not intended to be used for this purpose. To achieve similar cosmetic tanning results as seen with Melanotan II, a dose of 10x more per injection is required. Melanotan I is more expensive for tanning.
    Melanotan II Storage

    In powder (lyophilized) form vials should be stored at refrigerator temperature (2-8 degrees Celsius) where they will remain stable for up to 12 months. Reconstituted (mixed) vials should also be stored in the refrigerator, but use within 8 weeks or they may begin to degrade. They will still be safe to use after this time, but they may not be as effective as new vials.
    When to take Melanotan II

    The frequency of Melanotan II injections will depend largely on your skin type to begin with, therefore you should identify with which Fitzpatrick skin type you are

    Type 1: Pale skin, many freckles, blue/green eyes, red hair, never tans, always burns
    Type 2: Fair skin, few freckles, blue/hazel eyes, blonde/sandy hair, tans poorly, usually burns
    Type 3: Darker white skin, brown hair/eyes, usually tans, rarely burns
    Type 4: Light brown skin, darker brown hair/eyes, tans easily, burns minimally
    Sunless Tanning

    Loading: Take your Melanotan II dose 1 time per day and continue with daily injections until you are happy with the color of your tan.
    Maintenance: To maintain your desired tan, inject your Melanotan II dose just 2-3 times per week Cessation: You can continue the maintenance dosing indefinitely; however, if you choose to stop your Melanotan II injections, your tan will fade back to its pre-Melanotan II shade in 1-2 months.

    Assuming the right amount of UV exposure (sun or sun bed) is combined with your Melanotan II usage, then the amount of time it takes to achieve your desired tan (i.e. the loading phase) will usually take 4-8 weeks for skin types 1 and 2 and as little as 2-3 weeks for skin types 3 and 4.

    Melanotan II and UV Exposure
    The tanning activity of Melanotan II without the need for UV exposure has been proven by clinical trial; however, the majority of users report that results are achieved much quicker, and that the tan is a more natural color, when Melanotan II is combined with a small amount of UV exposure.

    Tanning should start after the third injection and occur 2-3 times per week if you wish to see tanning results quickly; otherwise one tanning session per week is sufficient to gradually build your tan

    Melanotan Advice

    If you are not seeing results then you need to increase the frequency of your outdoor or indoor UV exposure (especially if you are skin types 1 or 2). Never increase your recommended Melanotan II dose.

    Tanning sessions should be short, 5-10 minutes in a sun bed or 30-40 minutes in the sun on a warm day is sufficient each time. DO NOT overexpose yourself to UV rays.

    When starting out always use 30+ sunscreen on sensitive areas such as the face and neck. Because these areas are frequently exposed to UV rays they are more responsive to the melanin producing effects of Melanotan II and therefore will become darker quicker than the rest of the body. Covering these areas initially will allow other parts of the body to tan first, ensuring you achieve a well balanced tan.

    Melanotan II and UV exposure complement each other, so if you spend a lot of time tanning you will need less frequent injections of Melanotan II to obtain and maintain your tan. If you don't spend much time in the sun or sun beds then you will need frequent dosages of Melanotan II to develop and keep your tan ..

    Fair skinned folks who never tan, always burn in the sun, can achieve a natural tan when using Melanotan 2. For people with sun allergies these discoveries are life changing. The best defense against skin cancer is a natural tan developed over time. MT-2 was designed to reduce skin cancer rates and be effective as a sunless tanner.

    Athletes and fitness enthusiasts use Melanotan for sunless tanning, Libido increase and and appetite suppression. MT-2 was dubbed the Barbie drug and has been highlighted in wired magazine. Synthetic melanocortin use helps attain a tan with the least amount of exposure to harmful ultraviolet radiation.
    Fitzpatrick skin type: Skin type I and II, the lower of the skin types on the Fitzpatrick scale are the best candidates for Melanotan 2 who see the most dramatic results.

    Treatment: Melanotan stimulates melanin effectively, in particular those with low skin types.


    Shipping and Handling: Melanotan Peptides are durable and stable. Highlighted in study, the reconstituted MT-2 was shown to be stable at 37 degrees Celsius (98 degrees Fahrenheit) for at least 28 days. Shipping MT-2, even in summer months, is not a problem. Do not pay for cold shipping as it is not a premium. When receiving MT-2 it is recommended to store in the refrigerator.

    Mixing: Add BW to the vial when you are ready to begin MT-2 research.

    Remove plastic flip top from vial to expose rubber stopper. needle will pierce the stopper making way inside the vial to turn the white ****** into a clear liquid.

    Calculator: Add 100 units (1ml) of water to the vial. 1ml/100 units will minimize the volume that you have to inject and will simplify the arithmetic in your MT-2 experiment. Dosing measurements are often mentioned in both milligram (mg) and microgram (mcg). Example: .5mg = 500mcg

    Peptide Calculator

    Peptide Measurement

    1ml syringe (U100), 1ml BW to reconstitute
    Calculations for a desired 0.5mg dose:
    Step 1= 1ml
    Step 2= 10mg MT-II
    Step 3= 1ml bac water
    Step 4= 500mcg dose
    2-3 ticks on your insulin pin (approximately 1/20th of a U100 syringe)

    Some prefer to add more diluent which works fine, take note of the volume increase.

    Needles: 29-31 gauge X 1/2", 1 CC (100 unit). That is a typical insulin needle used to mix as well as inject. Use needles one time only. Once your technique perfected, injections are almost painless.

    Starting dose: Your first injection should be a very small dose, for example .25mg (250mcg). See how you react. Goal should be to feel nothing. Dose after dinner, before bed. Any dosing chart stating that you should take a high dose (according to your weight) is outdated and potentially dangerous.

    Loading dose: Load with 0.5-1mg once a day. People who have used doses in this range generally report getting excellent results. Don’t worry if you miss occasional days. It will not make much difference, focus on the cumulative effects.

    Maintenance dose: Maintenance is taking doses less frequently than daily to avoid becoming darker than you want. Yes, that will happen. With enough UVR, you will get much darker than you have even been before. A maintenance dose can help prolong super-physiological photo-protection MT-2 delivers.

    UV Radiation: Melanotan is a poor sunless tanner. UV (from sun or a tanning bed) light is necessary to develop a tan. Without it, almost nothing happens. In other words, NO UV = NO TAN. Well, user will pigment depending on skin type.... If you have loaded for a full month and then start UV exposure, you (and your friends) will be astounded by how fast you tan and how dark you get. Moreover, it is advisable to keep areas of your skin that ordinarily get exposure covered up with a towel and/or zinc oxide (nose/lips/face) and let less exposed areas develop pigmentation first. Areas of skin that are typically sun-exposed in your day to day life will respond more readily to the effects of the Melanotan Peptides.

    Fat Loss: The melanocortin (MC) system is a signaling pathway for leptin and insulin. The MC system is important for control of food intake and body weight. MT-2 treatment results in adipocyte lipolysis. MT-2 increases fatty acid oxidation(FAO) in which the MC5R plays a significant role. MT-2 improves insulin sensitivity through stimulating FAO in skeletal muscle tissue. Reduced food intake from the anorectic response of MT-2 is primarily responsible for weight loss.

    Watch yourself: Your tan can sneak up on you. A tan generally sets in 3 days after UV rays. Dose and expose yourself gradually to UVR when tanning. Love your skin.

    Avoid burning: You are protected from burning mostly by your tan, not the MT-2 peptide. Therefore, don’t overdo the rays at first. Start with only as much UV that you could tolerate without burring before you began Melanotan. It should not take many weeks before you can tolerate hours of strong sun without burning. Truly incredible for those who have never experienced freedom to enjoy the sun.

    Continue your regular dosing protocol until you have reached your desired tan and do not want to become darker. Cut injection frequency to once every 2, 3, 4, or even 7 days. Experiment to find the frequency that gives the tan you want.

    Storage: Store freeze dried and reconstituted (mixed) Peptides in the refrigerator.

    Do you have to inject MT-II?
    Yes. The best, most efficient method of administering Melanotan Peptides are subcutaneous (subq) injections. Nasal sprays are inconsistent and inefficient. No detectable levels were observed following oral dosing - pills do not work.

    when you start supplementing (Melanotan II) to tan keep in mind that tanning is literally a side effect. The tanning response is, in reality, a physiological repair mechanism to instant UV damage of the skin cells (. Melanocyte stimulating hormone is not going to color your skin, it is going to make your own skin create its own tan and that in turn creates protection. If you are looking to be some bronzed beach God with perfectly uniform and specific color then you are better off to going to mystic tan. Redheads, for example, naturally produce a variant form of melanin that is yellowish-red . Do not expect a brown tan on a ginger body right away.

    Know your skin type: Knowing your skin type is just one detail which will help create a public user log. There are 10s of thousands of Melanotan users worldwide who share the experience. Raise awareness and help others who want to hear success stories, complications and failures.
    Am I a good candidate for MT-II?
    Melanotan is best suited for the folks with skin types I & II. Prior sun damage, scars, tattoos, freckles, moles, hair color, etc are deciding factors prospective MT-2 users consider.

    How should I dose MT-II?
    Melanotan II dosage it is recommended to start out small and build up. A typical starting dose is around .25mg and max dose reaching 1mg. Desensitization happens quick, the first administration is an opportunity to dose low to avoid Melanotan 2 side effects. Same goes for Bremelanotide (PT-141) dosage unfortunately.

    Melanotan Instructions: There is no magic pill or formula. Instructions do not exist for research Peptides. Few dermatologists are familiar with Melanotan. The skin is a large, unpredictable organ. Feel comfortable and confident with MT-II before use. Check out as many before and after photos and user logs as you can. A skin type I individual may have to commit months of dedication before dialing in their desired results, be patient and ask questions.

    How much MT-II should I buy and how long will it last?
    Skin type I: 30-50mg
    Skin type II: 20-30mg
    Skin type III: 10mg
    Should last entire summer or season

    How soon will I begin to see results from Melanotan II?
    You should notice a change in your skin tone after three weeks. If you have freckles, expect them to get darker before your actual skin color changes.

    How long will the tan last?
    A tan developed using Melanotan 2 lasts much longer than an ordinary tan. A well-tanned person returning from a beach holiday will lose most of the tan in a month if they stop getting sun. But if they had been using Melanotan 2 and continued on maintenance after returning, they would still have most of their tan 3 months later.
    author ???
    Last edited by basskiller; 07-12-2014 at 09:53 AM.

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    Bodybuilders use Ipamorelin Peptide For Building solid Muscle

    Bodybuilders use Ipamorelin Peptide For Building solid Muscle

    Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. Like the GHRP-6 peptide (growth hormone releasing hexapeptide), it is a synthetic peptide that has powerful Growth Hormone releasing properties. And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat. Both Ipamorelin and GHRP-6 as well as numerous other peptides and research chemicals can be found at TruePeptide.com



    Whereas GHRP-6 is a hexapeptide, Ipamorelin is a penta-peptide. (Aib-His-D-2-Nal-D- Phe-Lys-NH2) And, the strength it displays may very well make regular old Growth Hormone (GH) obsolete. But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other GHRP peptides?
    Athletes are taking Ipamorelin in a 200mcg -300mcg dosage, two or three times daily, using a tiny insulin needle to inject. They usually start with the lower dose since side effects can include headaches or what feels like a head-rush. Ipamorelin can be taken at anytime but taking it about 30-45 minutes before a workout would seem ideal because of the pulse in Growth Hormone (GH) it creates allowing for maximum growth.


    Studies on the effects of Ipamorelin on bone growth, body weight, and GH release showed some interesting conclusions.
    In one experiment, various doses were administered over the course of 15 days to test the group’s reactions.
    There was a distinct and dose-dependent effect on body weight gain however, the treatment group did not show a change in total IGF-I levels. Nor did the treatment group produce serum markers of bone development. For example, the number of cells in the wide portion of the tibia (the shinbone) did not change significantly. This is a good thing because it suggests muscle growth with less potential for deformity of bone or cartilage.


    The reaction of the pituitary to an aggressive i.v. dose of Ipamorelin showed that plasma GH levels were notably reduced whereas they were unchanged after a comparable dose of GHRH. This is actually a good thing as it suggests that Ipamorelin may not decrease your body’s natural GH production – further demonstrating that Ipamorelin is a selective GH releaser.

    GHRP-2 Unlike GHRP-6, Ipamorelin does not induce hunger making it advantageous to those on a restricted calorie diet. And obviously, Ipamorelin’s side-effects are enhanced when combined with anabolic steroids since they too influence Growth Hormone/Insulin Growth Factor release and production.

    In another study in rats, Ipamorelin released GH from rat pituitary cells as effectively as GHRP-2.
    Another document states that in healthy swine, Ipamorelin released GH with a consistency that is very comparable to GHRP-6. Also noteworthy was that none of the GH releasers tested affected FSH, LH, PRL or TSH blood serum plasma levels.

    Ipamorelin in theory may increase Acetylchloine or Cortisol when used in higher dosages. However, and increase in Acetylchloine or Cortisol is even more likely with GHRP-2 and GHRP-6. In fact, in the case of Ipamorelin, there was little to no rise in Acetylcholine and Cortisol blood plasma levels even at injections more than 200 times higher than the effective dosage for comparable GH release.


    This clearly proves that Ipamorelin is the first successful GHRP receptor agonist or chemical that binds to a receptor of a cell and triggers a response by that cell with a specific selectivity for the promotion of GH release by itself.

    Another advantage to Ipamorelin is that it doesn’t cause sudden spikes in prolactin or cortisol as does GHRP-2 and GHRP-6. Ipamorelin is slower in its delivery unlike GHRP’s which spike GH levels at a more rapid rate. The slower release is more natural and has a more sustained effect.
    All in all it looks as if Ipamorelin is the new wave in GH releasing peptides. It appear to be more potent, longer lasting and potentially safer to use in the long run. More studies are being conducted all the time but as it stands, Ipamorelin looks like a serious contender in the arsenal of anabolic advancement.

    Both Ipamorelin and GHRP-2 as well as numerous other peptides and research chemicals can be found at " Check my signature"
    Last edited by basskiller; 09-09-2014 at 11:39 PM.

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    Growth Hormone Administration vs. CJC-1295/GHRP-6

    Growth Hormone Administration vs. CJC-1295/GHRP-6

    Units of Measurement
    Growth Hormone (GH) like other biologically active substances is measured in International Units (abbreviated as IU) which are based on the measured biological activity for that substance the establishment of which is determined by international agreement. International Units are specific to each substance and so one IU of one substance has no equivalence to one IU of another substance.

    While it is fairly straightforward to compare the amount of GH among various dosing administrations (a two (2) iu dose is twice the amount of a four (4) iu dose) and it is easy to ask the manufacture the weight of each iu (Nutropin reveals that 1 iu of their GH is equal to 333 mcg) it is not so simple to compare Growth Hormone to other "Growth Hormone Releasing" compounds such as CJC-1295 and GHRP-6.


    Practically all studies that use Growth Hormone (GH) or Growth Hormone Releasing Hormone (GHRH) or its analog CJC-1295 or Growth Hormone Releasing Peptides all take blood samples to measure the amount of GH present in blood plasma at various points in time. The unit of measurement is a standardized unit which can be used to make comparisons across different compounds.
    The studies either report results as "nanograms (ng) per milliliter (ml)" or "micrograms (ug) per liter (L)". For the reason that ng = 1/1000 ug and ml = 1/1000 L, ng/ml will always equal ug/L. So no matter how the studies report results comparison is straightforward. In making the cross-comparisons contained herein for simplicity I have chosen to report results as ng/ml.
    Therefore this examination will look to several studies involving administration of the compounds of interest and compare the blood plasma levels of IGF-1 and both peaks and total amount of GH blood plasma levels as a result of administration of each tested compound. The result of this cross-study examination will reveal the efficaciousness of various doses of GH, CJC-1295 and GHRH + GHRP-6 in increasing GH & IGF-1 in blood plasma.


    Studies used for comparison

    Growth Hormone Administration
    In "Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men", Toshiaki Tanaka, et al., Endocrine Journal 1999, 46 (4), 605-612, fifteen healthy normal Japanese adult males aged from 20 to 27 years were administered various doses of recombinant GH (Norditropin). The GH was administered in a single dose at 9:00 a.m. after overnight fasting. Blood samples were collected at 0, 1, 2, 3, 4, 5, 6, 9, 12 and 24 hours after the single injection.
    The doses administered were: .075iu/kg; .15iu/kg and .30iu/kg
    When the average weight of each test subject is accounted for the doses administered approximated: 5iu; 10iu and 20iu


    CJC-1295 Administration
    In "Prolonged Stimulation of Growth Hormone (GH) and Insulin-Like Growth Factor I Secretion by CJC-1295, a Long-Acting Analog of GH-Releasing Hormone, in Healthy Adults", Sam L. Teichman, et al. Journal of Clinical Endocrinology & Metabolism 91(3):799-805, sixty-six healthy normal men and women aged 21-61 were administered various doses of CJC-1295 (long-lasting GHRH analog). The CJC-1295 was administered in a single dose and again in some groups 7 days later and other groups 14 days later. For the reason that we are only examining a week's worth of data only the initial dose is of interest. Blood samples were collected before dosing and then at 15, 30, and 60 minutes and 2, 3, 4, 6, 8, 10, 12, and 24 hours afterdosing; and then every 8 hours on days 2–3, then daily on days 4, 5, 6, 7.
    The doses administered were: 30mcg/kg; 60mcg/kg; 125mcg/kg; 250mcg/kg

    GHRH + GHRP-6 Administration
    While we are limited in our choice of GH administration studies (because no other study administered such high doses in normal men) and CJC-1295 studies (there are only two, the results of which are available to the public) we have many available studies measuring the effects of co administration of GHRH and GHRPs.
    So we will briefly look at the results from two studies to give us an idea of how much GH release is contributed by the enhanced pulse brought on by this synergistic combination.
    They are, "Inhibition of growth hormone release after the combined administration of GHRH and GHRP-6 in patients with Cushing's syndrome", Alfonso Leal-Cerro, et al., Clinical Endocrinology 1994, 41 (5) , 649–654 and "Growth hormone (GH)-releasing peptide stimulates GH release in normal men and acts synergistically with GH-releasing hormone", Bowers, C.Y., et al. J. Clin. Endocrinol. Metab. 70, 975–982.

    What's Normal?
    Before we look at the studies lets take a brief look at how much growth hormone (GH) is secreted naturally. There is a large variability among age groups, gender, fitness level and among individuals within a single age group. So the best we can do is generalize. The charts below are derived from GH blood plasma data collected over a 24 hour period for a normal man, a normal man after a fast, a normal woman and a normal woman after a fast. All ages were mid-20s.
    Note that the night-time GH pulse peak for a man was about 20 ng/ml (aprox. 85% of 24hr GH release normally occurs at night).
    Total GH release was as follows:
    Men (Fed):
    Area Under the Curve (AUC): 94 ng/ml per 24 hours
    Men (Fasted):
    AUC: 274 ng/ml per 24 hours
    Women (Fed):
    AUC: 168 ng/ml
    Women (Fasted)
    AUC: 264 ng/ml per 24 hours


    Comparing GH administration to CJC-1295 administration
    It is difficult to compare based on the following GH release graphs so let's examine the numbers.



    Total GH Release:
    When GH was administered at 5iu, 10iu & 20iu the total GH levels (area under the curve (AUC)) were respectively:
    AUC: 311.5; 836.9; 1778.5 ng/ml per 24 hours

    When CJC-1295 was administered at 30mcg/kg; 60mcg/kg; 125mcg/kg and 250mcg/kg the total GH levels (area under the curve (AUC)) were respectively:
    AUC: 758; 969; 977; 1370 ng/ml per hour

    NOTE: This is per hour while the GH study is per 24 hours

    So based on the total GH concentration in blood plasma the lowest dose of CJC-1295 on a per hour basis results in more than twice the 24 hour GH secretion level of a 5iu dose of GH.

    Peak Concentration:
    However the GH release pattern results in a much higher mean maximum concentration for the GH administration than the CJC-1295 administration.
    The GH study resulted in dose respected peaks of 55.4; 93.8; 180 ng/ml

    The CJC-1295 study resulted in dose respected peaks of 6.6; 9.6; 9.9; 13.3 ng/ml

    The graph indicates that for the GH study the bulk of the peak lasts about 12 hours followed by low levels of GH. As an aside clearly GH administration would be better if it were administered in at least two doses per day.

    But even IF 5iu of GH were administered in the morning followed by 5iu twelve hours later the total amount of GH released would be less than a low dose of CJC-1295 (311.5 + 311.5 < 758 ng/ml). Furthermore the CJC-1295 was dosed just once in seven days while the GH would need to be dosed every one of those 7 days.

    IGF-1 Levels:

    CJC-1295 elevates IGF-1 within the first day or two where it stays elevated for seven days.
    GH elevates IGF-1 levels immediately where it stays elevated throughout the rest of the day.
    Both the GH & CJC-1295 studies demonstrated a dose dependent increase in elevated IGF-1 levels. The highest GH dose of 20iu resulted in a similar IGF-1 level as the highest CJC-1295 dose. The lowest GH dose of 5iu resulted in an IGF-1 level not much different then the lowest CJC-1295 dose.
    Again the CJC-1295 elevated IGF-1 for seven days from a single administration while GH would likely need to be dosed everyday (perhaps every other day) to match CJC-1295's chronic elevation of IGF-1.



    Can CJC-1295 plus GHRP-6 match GH adminstration's peaks?
    Adding GHRPs to CJC-1295 three times a day can amplify peaks and greatly add to the total GH secretion level.
    The Alfonso Leal-Cerro study demonstrated the following GH release:
    GHRH by itself dosed at 100mcg resulted in:
    (AUC) 120 minutes = 1420 * 330 ng/ml
    GHRP-6 by itself dosed at 100mcg resulted in:
    (AUC) 120 minutes = 2278 * 290 ng/ml
    GHRH + GHRP-6 dosed together at 100mcg each resulted in:
    (AUC) 120 minutes = 7332 * 592 ng/ml
    By adding GHRP-6 to CJC-1295 (long-lasting GHRH) it may be possible to add almost 6000 ng/ml of GH release at each GHRP-6 dosing. [Figure arrived at by taking synergy amount 7332 and subtracting GHRH's contribution of 1420]
    But what about those peaks?



    Clearly adding GHRP-6 has the effect of matching GH's peaking power as measured by amplitude. The difference is that GH results in big hills lasting up to 12 hours. This really amounts to an elevation rather than a pulse. GH does not mimic the physiological pulsatile release of GH that naturally occurs while GHRP-6 particularly in the presence of GHRH does result in such a natural pulse. These pulses last for about 2 hours. If dosed three times a day the result would be three 2-hour pulses each of which exceed GH's 5iu and 10iu elevations and approach GH's 20iu elevation.
    However 6 hours total of peak for the CJC-1295/GHRP-6 combination would be half of the 12 hours total of peak for the GH.
    I do not know if it matters. I do not know if these two different peaking characteristics would result in different effects concerning growth.


    In CONCLUSION, CJC-1295 appears to result in higher concentrations of GH in blood plasma than does GH administration. When CJC-1295 is combined with GHRP-6 the total GH release is exacerbated.
    GH administration results in higher GH maximum concentration or peaks then CJC-1295 alone. However when CJC-1295 is combined with GHRP-6 the peaking amplitude exceeds the 5iu & 10iu GH doses and approaches the 20iu dose. GH administration's peaks however last for 12 hours while CJC-1296/GHRP-6 results in a natural 2 hour peak at each dosing (i.e. 6 hours total).
    Both CJC-1295 and GH appear equally effective at elevating and sustaining IGF-1 levels.
    Last edited by basskiller; 07-12-2014 at 09:55 AM.

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    Hgh fragment 177-191, Clenbuterol & T3 fat burning synergy

    Hgh fragment 177-191, Clenbuterol & T3 fat burning synergy

    Growth hormone has many systematic effects, from improved strength, anti-aging effects on skin, tendon strengthening, increased IGF levels, better sleep, to name just a few.. but when Synthetic GH is taken.. most of these effects are minimized, as synthetic GH doesn't imitate the cascade of GH that subjects pituitary creates, and the effects it has…

    So what if you could harness say one aspect of GH specifically lets say.. The profound effect it has on fat loss, and produce a peptide that imitates GH in that regard. Introducing HGH Fragment



    Hgh fragment 177-191 is a stabilized analogue of the growth hormone-releasing factor (GRF) that induces Growth Hormone in a specific and physiological manner. To date, studies suggest that HGH Fragment 177-191 has several beneficial features: it reduces abdominal fat in particular visceral fat, without compromising glycemic control (blood glucose), it increases muscle mass and improves the lipid profile, so it looks to have a lot of key benefits.. but does it?



    Studies that can be found easily show that at a dosage of 500mcg, HGH Fragment 177-191 was shown to increase lipolytic activity in adipose tissue ,this HGH Fragment potently burns body fat, especially stubborn adipose body fat, and at the same time as it doesn't spike glucose levels, or cause any problems with insulin sensitivity, and improving your lipid profile, this really should be part of any dedicated athletes fat loss regime.

    Unlike GH, HGH fragment doesn't induce cell proliferation, it does not induce hyperglycemia or reduce insulin secretion. HGH fragment 177-191 does not compete for the hgh receptor, but of important note.. is the HGH Fragment’s ability to increase IGF-1 levels which translate into the HGH Fragment’s ability to give collateral anti-aging and anabolic effects along with its ability to induce fat loss in the most stubborn body fat (adipose tissue) while increasing energy expenditure and glucose and fat oxidation.

    The good news is, the subjects body is burning fat for fuel and energy!! And add to that a whole host of health benefits and everything looks great, However it does seem to cause the thyroid to become sluggish, not as potent as GH, but perhaps through its ability to increase cortisol it still slows the thyroid..
    So i suggest that HGH fragment should be stacked.


    CLENBUTEROL and T3

    Everyone these days has probably heard of both supplements, and the scare mongering that goes along with them, so lets make a few things clear..
    I have never seen a report with any evidence showing T3 shuts down subjects own pituitary, except when it has been abused, extremely large doses for long periods, 200mcg for 6 weeks or more without any proper tapering off the drug.

    In the case of Clenbuterol, if it respected, it can give outstanding results in the fat loss department, help aid in preventing muscle loss and it stacks well with T3 and HGH fragment.

    Cytomel is the most common brand name for a synthetic thyroid hormone- more specifically, it’s a synthetic version of T3 (triiodothyronine ). T3 is not produced directly by your thyroid gland, is actually converted from the T4 thyroid hormone, it has potent fat burning effects, and T3will enhance your body’s ability to synthesize protein, even at very low doses which can actually help add muscle. T3 when used in conjunction with HGH fragment will reduce nitrogen retention, this is a fact, so if your looking to get big and ripped, you need to add in something else, and this is where personally clen is often I feel overlooked.

    So you have the potent fat burning of HGH fragment, increased IGF levels, but without nitrogen retention, you will look flat, under perform, and find building any muscle close to impossible.. T3 will increase your ATP, ramp up your metabolism, burn fat.. and decrease your nitrogen levels that should be elevated by HGH fragment.
    Clenbuterol a powerful fat burner working on stimulating Beta 2 receptors which helps you to release and then burn stored fat. But interestingly not only is it extremely potent in this regard, but it increases Nitrogen retention.. I'm sure subjects who has taken it has noticed the pumps, and the increased fullness on Clen.

    If dosed accordingly, This cycle can transform your subjects physique and give them the sharp hardened features you desire, but only if your diet and training is on par with these exceptional supplements.
    By chris
    Last edited by basskiller; 09-09-2014 at 11:40 PM.

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    Peptide Guide Information

    Peptide Guide Information



    Peptides come in the form of lyophilized (freeze dried) powder. The amount of powder/product is stated in International Units (IU’s) or in Milligrams (MG).


    Melanotan peptides (Melanotan 1 & Melanotan 2), PT-141 Bremelanotide, GH Fragment, Ipamorelin, CJC-1295 & GHRPs (GRHP-2 & GHRP-6), HGH, HCG, et cetera use Bacteriostatic Water (BW). Bacteriostatic Water for injection, USP is a sterile, nonpyrogenic preparation of water for injection containing 0.9% of benzyl alcohol added as a bacteriostatic preservative. It is supplied in a multiple-dose container from which repeated withdrawals may be made to dilute or dissolve drugs for injection. The pH is 5.7 (4.5 to 7.0)

    For IGF use an acetic acid solution (.6%) which is 7 parts distilled water and 1 part vinegar to reconstitute. You must filter the distilled water and white wine vinegar through a sterile 20 micron syringe filter before use. Sodium Chloride (NaCl) is used to buffer the injection.

    1.) Take an alcohol swab to the stopper of both your peptide vial and the vial of the diluent.
    2.) Draw your preferred diluent (BW) with a 1cc syringe. Choose an amount that will make measuring the final product simple.
    1ml(cc) per 10 mg vial of Melanotan would mean each 10 tick marks on a U100 slin syringe would equal 1mg of Melanotan
    1ml(cc) per 10 IU vial of HGH would mean each 10 tick marks on a U100 slin syringe would equal 1 IU of HGH
    3.) Take the syringe with the diluent and push it into the vial of lyophilized powder letting the diluent dissolve the peptide. Many (not all) peptides are sealed with vacuum pressure, be careful
    4.) After diluent has been added to the vial, gentling swirl the vial until the lyophilized powder has dissolved and you are left with a clear liquid. The peptide is now reconstructed, ready for measurement and usage.
    5.) Store your now reconstituted research peptides in the refrigerator.





    Peptide Measurement
    After successfully reconstituting your peptide, measure the desired amount out for injection. Use a U100 insulin syringe to draw out and inject your product.

    Since you know the amount of IU’s/MG’s in your vial, we divide this out as follows:
    You will need to know the following to be successful: 1ml = 1cc = 100 IU’s

    We take our dose from the label of the dry lyophilized powder and we divide that into the amount of diluent used.

    Example- We used 1cc(ml) of water. We have a 10 IU vial of HGH.
    From our formula above we know that 1cc = 100 IU’s, so we have 100 IU’s of water.
    We now divide the 100 IU’s (the amount of our water) by 10 IU’s (the amount of our HGH)
    100 IU / 10 IU = 10

    This 10 will perfectly correspond with the markings on a U100 insulin syringe. In our example every 10 mark on our syringe will equal 1 IU of HGH. Want to draw out 2 IU’s of GH? ….draw out to the 20 mark on the syringe (1/5th of the syringe).

    Say you have a 1mg vial and you add 1ML you get
    1000mcg/1mL: 10 mcg per IU
    1000mcg/2mL: 5 mcg per IU







    Say you have a 10mg vial and you add 1ML you get
    10mg/1mL: 1 mg per 10 IU
    10mg/2mL: .5 mg per 10 IU

    Say you have a 20mg vial and you add 1ML you get
    20mg/1mL: 2 mg per 10 IU
    20mg/2mL: 1 mg per 10 IU

    Say you have a 10iu vial and you add 1ML you get
    10iu/1mL: 1 iu per 10 IU (on the syringe – 1/10th the product)
    10iu/2mL: 1 iu per 20 IU (on the syringe – still 1/10th the product)
    Say you have a 5000iu vial and you add 1ML you get
    5000iu/1mL: 500iu per 10 IU
    5000iu/2mL: 250iu per 10 IU
    Last edited by basskiller; 09-09-2014 at 11:42 PM.

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    Lgd-4033

    Lgd-4033


    One of the members of the Selective Androgen Receptor Modulator category, also known as SARM, is LGD-4033. It is an oral product that is non-steroidal, but it can offer many of the same benefits as some of the anabolic steroids. The use of LGD-4033 medically includes treatment of muscle wasting. This can be due to issues with cancer or muscle loss due to the natural aging process.

    The same benefits astestosterone are also offered with LGD-4033. The difference though is that the user doesn’t have to worry about potential side effects. With testosterone, there can be the risk of the body not responding well or even damage to the liver. Even though this product is taken orally, it isn’t toxic to the liver.

    This is one of the most common SARMS used due to how powerful it is. Yet it is also gentle on the body when compared to steroids. For the individual that wants the results but not all of the hassles, this could be exactly what they were looking for.


    How does it Work?
    This SARM works by binding the androgen receptors selectively. The results of anabolic activity in the muscles and bones occur rather than adversely affecting the glands or the prostate which can occur with the use of steroids. LGD-4033 was recently involved in a study involving volunteers called Phase I Multiple Ascending Dose. This was a random, double blind testing phase that involved a placebo. The goal was to establish that the use of LGD-4033 was safe and easy to tolerate with a dose not to exceed 22 mg per day.

    When to use LGD-4033
    For many bodybuilders and athletes, the use of LGD-4033 occurs for a bulking phase in order to offer lean body mass and to reduce overall body fat. The use of it can also increase overall strength which allows the individual to take on more challenging workout sessions. When used for bulking, an efficient diet that is high in protein is also necessary. Higher calorie intake may be necessary too if the person will be bulking up by 10 pounds or more. The recommended dose is 5 to 10 mg per day, for a period of 8 weeks.

    For a cutting cycle, it may be best to use LGD-4033 along with other SARMS including GW-501516 and S-4. This is called a SARMS triple stack. The goal is to add more size while cutting fat. The dose recommended for this type of cycle is 3 to 5 mg, for a period of 8 weeks.




    Risk Factors
    The results of various studies indicate that there is very little risk in regards to possible side effects associated with the use of LGD-4033. This is encouraging for those that would like to gain muscle and cut fat without using steroids that do have some harsh side effects associated with them.

    The fact that that SARMS don’t harm the liver is also another reason to consider taking them instead of steroids. They are also inexpensive so the average person can use them without worrying about their budget.
    Last edited by basskiller; 09-09-2014 at 11:42 PM.

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    About CJC-1295

    About CJC-1295



    CJC-1295 was developed for clinical trials in the year 2000. The drug was originally synthesized to remove visceral fat deposits in AIDS patients. CJC 1295 was ultimately successful on all research subjects, as increasing the level of growth hormone in the body proved to increase fat loss.
    Various experiments have been conducted to test the effectiveness of CJC-1295 in vivo and the Journal of Clinical Endocrinology & Metabolism has reported dose-dependent increases in mean plasma GH concentrations by 2-10 fold for more than 6 days and increased IGF-1 concentrations 1.5-3 fold for 9-11 days after a single injection
    .

    Not only that but they proved the mean half life to be 5.8-8.1 days and after multiple doses showed mean IGF-1 levels remained above baseline for up to 28 days following! No serious adverse reactions were reported in any group.

    Another very positive benefit of CJC-1295/CJC-1293 is its ability to promote slow wave sleep. Slow wave sleep is also known as deep sleep and is the portion of sleep responsible for the highest level of muscle growth and memory retention. SWS are decreased significantly in older adults and also with people who tend to exercise later in the evening.

    This peptide has a benefit to side effect ratio that exceeds all others currently being legally sold and would make a great addition to ones training regimen or post cycle therapy.

    CJC-1295 has the ability to make the body produce its own GH as compared to using synthetic HGH. GHRP-6 in conjunction with CJC-1295 is synergistic, amplifying the GH pulse considerably. Studies have shown that CJC-1295 also promotes slow-wave sleep, the kind of sleep responsible for muscle growth and increased memory retention.

    There are three popular and clinically proven GHRH analogs on the market today, CJC-1293, CJC-1295, CJC-1295 DAC, and Sermorelin. CJC-1293 is a longer lasting peptide- it is sometimes also referred to as tetrasubstituted GRF(1-29) or Modified Sermorelin.

    The half life of Research peptide CJC1295 is more desirable and establishes a significant enough of a GH pulse to increase IGF-1 levels and GH levels. However, it's pulsatile release is more of a sustained-consistent release that does not necessarily mimic that of the pituitary gland.

    The CJC-1295 & the total 24 hour dosing of GHRP-6 together comprise a single comparison with exogenic GH administration.
    Last edited by basskiller; 09-09-2014 at 11:43 PM.

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    Healing Peptides

    Healing Peptides

    ACT1 PEPTIDE: this peptide is cleaved from thymosin, it was created from a section of the thymosin (TB-500) amino acid chain.
    ACT1 is a synthetic peptide derived from the carboxyl-terminal sequence of the cellular gap junction protein connexin43. This novel peptide has recently been shown to modulate cutaneous wound healing, reduce scarring, and promote regenerative repair of the skin following injury. In this study, the authors investigated the ability of the ACT1 peptide to modulate the wound-healing response to biomedical device implantation.
    ACT1 PEPTIDE
    - promotes skin wound healing
    - closure at the wound site
    - reduced scarring at the site of injury
    - reduced inflammation at injury site
    - research is being conducted in healing of the heart(tons of successful studies on heart post injury), spinal cord, cornea.



    BPC 157:
    - BPC 157 has been shown in rat studies to heal torn quadriceps muscles, detached achilles tendon, muscles that have been damaged/crushed
    - dramatic fast recovery from muscle tears
    - tendon to bone healing
    - increased ligament healing
    - has a variety of protective effects in the organs
    - human trials demonstrate healing and prevention of stomach ulcers
    - no adverse reactions have been seen in human trials.
    Both ACT1 PEPTIDE and BPC 157 have been shown to heal a variety of wounds in all areas researched, including internal organs, muscles, ligaments, tendons, skin, internal lacerations from surgery, etc. Anyone at MHQ research these peptides?



    Thymosin beta4 wound healing: visions of the future.

    Abstract
    Persistent corneal epithelial defects and inflammation within the central cornea can directly distort visual acuity and may lead to permanent visual loss. Therefore, treatments with agents that enhance corneal reepithelialization and regulate the inflammatory response without the deleterious side effects of currently used agents such as corticosteroids would result in improved clinical outcome and would represent a major advance in the field. Despite much progress in the areas of corneal wound healing research, clinically available pharmacological therapies that can promote repair and limit the visual complications from persistent corneal wounds are severely limited and remains a major deficiency in the field. Prior studies from our laboratory have demonstrated the potent wound healing and anti-inflammatory effects of thymosin beta 4 (TB-500); TB500 in numerous models of corneal injury. We are studying the mechanisms by which Thymosin beta 4 suppresses inflammation and promotes repair. Herein, we discuss some of our new basic scientific directions that may lead to the use of tb-500 as a novel corneal wound healing and anti-inflammatory therapy.
    Last edited by basskiller; 09-09-2014 at 11:44 PM.

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    CJC-1295 Shows Promise HGH Release

    CJC-1295 Shows Promise HGH Release




    If you have used CJC-1295 please post your results below. What dose did you use?
    CJC-1295 is a peptide analogue of GHRH. Because of the way CJC-1295 is engineered its half life has been extended from ~7 minutes to greater than 7 days!
    Due to the extremely long half life of CJC-1295 it is plausible to use this peptide once per week with outstanding results. It would be wiser to use ˝ dosages twice per week to keep serum levels high and to get maximal.

    Various experiments have been conducted to test the effectiveness of CJC-1295 in vivo and the Journal of Clinical Endocrinology & Metabolism has reported dose-dependent increases in mean plasma GH concentrations by 2-10 fold for more than 6 days and increased IGF-1 concentrations 1.5-3 fold for 9-11 days after a single injection.

    Not only that but they proved the mean half life to be 5.8-8.1 days and after multiple doses showed mean IGF-1 levels remained above baseline for up to 28 days following! No serious adverse reactions were reported in any group.

    Another very positive benefit of CJC-1295 is its ability to promote slow wave sleep. Slow wave sleep is also known as deep sleep and is the portion of sleep responsible for the highest level of muscle growth and memory retention. SWS are decreased significantly in older adults and also with people who tend to exercise later in the evening. This peptide has a benefit to side effect ratio that exceeds all others currently being legally sold and would make a great addition to ones training regimen or post cycle therapy.

    Quotes:
    CJC 1295 is expensive whereas the GRF 1 – 29 & GHRP 6 are not, so I use GRF 1- 29 & GHRP 6 at doses of 100 mcg’s each morning. Before bedtime I inject 150 mcg’s of CJC 1295 & 100 mcg’s of GHRP 6. This seems to provide a good sleep & I wake in the morning feeling quite fresh & ready for another day at the uni.

    The most popular dosage used by body builders seems to be 100 mcg injections of both CJC 1295 & GHRP 6 * 3 times each day. It really depends on a person’s goals, because some people use what I consider to be massive doses once or twice each week. The general opinion, however, seems to be that regular small doses are healthier & more effective. I’ve found that better sleep, & better digestion are the obvious results of using these products.


    GHRP-6 is great for appetite stimulation and works very well taken with CJC-1295 and testosterone,Especially for those who have difficulty in gaining weight.
    My vote goes to real hgh,lots of chinese brands have popped up these days.And like Sly Stallone said,hgh and testosterone should really be over the counter.


    your best way to go is to take 100mcg of GRF1-29 and 100mcgs GHRP6 in the morning upon waking up, post workout and pre-bed. The 2 peptides has a synergistic effect without the other it would be not 100% effective.

    A GRF1-29 only wont do such…
    A GHRP6 only will be a better choice…
    But both will increase GH release 100%…

    Try not to eat for about 30 minutes after administering the following peptides as fat affects the GH pulsations
    Chris White
    Last edited by basskiller; 09-09-2014 at 11:44 PM.

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