CJC-1295 with DAC Research Information

Research-Product-CJC-1295-with-DAC-610x310

Product Description

CJC-1295 with DAC is a thirty amino acid based peptide, which is currently being researched for a variety of benefits, including the increase in metabolism. Invented by Canadian biotechnology company, Conjuchem, it has the ability to lengthen the half life of active agents, which has to do with a process called bioconjugation. During studies, it was discovered that, not only did CJC-1295 with DAC help in the water regulation and balance in the body, but it also gives relief from pain. Studies have also shown impressive results regarding the positive effects of this peptide on conditions such as indigestion and body pain. Here, we will discuss CJC-1295 with DAC in full detail by discussing them and the makeup of the peptide which results in providing a variety of benefits to the human being.

CJC-1295 with DAC Product Information

1.    Chemical Information

The peptide has a chemical formula of C152H252N44O42, and the molecular weight of this peptide is 3367.2.

2.    Systematic Name

CJC1295/DAC, CJC-1295 with DAC, CJC 1295

3.    Pharmacokinetic and other information

CJC-1925 with DAC is currently ‘unscheduled’ by the United States government meaning that it is not regulated by law.

CJC has a half-life, or the time taken for the compound to lose half of its potency value, is two hours.

CJC-1295 with DAC: The Biochemical Process

The mechanical dynamics of the CJC-1295 process present themselves primarily and directly to the central nervous system of the body. Specifically speaking, research involving living non human subjects, who were carefully given monitored dosages of the peptide showed GHRH1-29’s half-life by a major amount. This activation has led scientists to discover that the reaction itself actually takes control of or restricts the particular signals sent by the brain to the body. The signals, which are given, are quite specific, relating to the blood flow of the body and any areas of the body that are experiencing inflammation.Alternatively, when the switch to these receptors has been done, the brain is then able to successfully moderate the signals relating to these specific issues.

CJC-1295 with DAC and the Recovery from injury

The overall functionality of the CJC 1295 With DAC has led scientific study based on live animal test subjects to determine that CJC-1295 with DAC can be the source of a host of possible benefits.  Most of these advantages relate to an increase in the synthesis of proteins, which is directly correlated to the ability of the peptide to increase the half-life of GHRH1-29 by a major amount. Some of these advantages related to it include an increase in the density of the bones, a boost in the proliferation of the muscular tissue, a more efficient method of weight loss, and a faster way to recover from injury.It has also been determined that the functionality of the peptide can block programmed cell death, increase the bioactivity in the body, and also boost the rate of lipolysis.

Hemorrhagic Shock and GHRH1-29 Interaction

CJC-1295 with DAC, by design, motivates and stimulatesreflexes of the nerves within the brain and it regulates any organic flow of blood that may result in actual organ failure, which would result from genuine hemorrhagic shock. The shock, which is hemorrhagic, is the result of what is referred to as a ‘lower tissue perfusion’ or the administration of oxygen to the tissue manually through a variety of methods, which becomes worse invariably due to increased lack of oxygen to the region over time.

There are four classifications or types of hemorrhagic shock:

  • Septic (or ‘vasogenic’)
  • Cardiogenic
  • Hypovolemic
  • Neurogenic

Since science knows that no two individual cells show the same responses, as has been observed on the level of a cell, it is a bit difficult to deal with this condition.

Current related research and findings regarding CJC-1925 with DAC

While there has been a several research studies conducted in relation to CJC-1295 with DAC and its overall functionality, theorized benefits, and negative side effects, and operational mechanics, it needs to be emphasized that ALL of the research that has been conducted along with its resultant findings has been the product of studies on animals alone.  CJC-1295 with DAC is solely intended for the use of scientific study at this time. Therefore, any observations or findings relating to CJC-1295 with DAC’s overall functionality, theoretical benefits, mechanics, or negative side effects should only be contained to the restrictions of a strictly controlled environment such as a laboratory or a medical research facility.

Developmental information regarding CJC-1295 with DAC

CJC-1295 DAC and CJC-1295 (which is also known as Modified GRF 1-29) are both known as GHRH or Growth Hormone Releasing Hormones. They act on the body in a similar fashion, but the difference between the two peptides is based on the span of the half-life. Modified GRF 1-29 and Sermorelin or CJC-1295 with DAC has a short half-life of about half an hour, while CJC-1295 with DAC has a half-life that can last up to around eight days. Many scientists have said that the half life of Modified GRF 1-29 and Sermorelin is considered to be way more natural as they are said to produce a short pulse of Human Growth Hormone.

Despite the fact that plenty of research has been carried out on CJC-1295 with DAC in relation to how it functions and the benefits that it gives, it should be emphasized that CJC-1925 with DAC, at this point in time, is still just intended for scientific study. Because of this, any findings or observations relating to CJC-1295 with DAC should solely be the product of study performed in a medical research facility or a laboratory under strict conditions. Therefore, communicate with your health care provider before administering any supplement or medication at any time for your own safety, and make sure that you follow the instructions given by both your physician as well as the instructions mentioned on the cover of CJC-1295 with DAC.

TO PURCHASE

If you would like to purchase CJC-1295 with DAC for research, you can visit: https://peptidepros.net/product/cjc-1295-with-dac-2mg/

POSTING DISCLAIMER

The info provided herein is strictly for the advancement of research and disbursement of knowledge relating to CJC-1295 with DAC.  It is meant solely  for any qualified researchers looking to find potential applications or possible health benefits yet to be discovered for CJC-1295 with DAC.   This post is meant for informational use only and is in no way considered instructional, in fact, no dosage or other similar information is provided.  The facts contained herein have been gathered from various studies and tests conducted in sanctioned and/or controlled medical research facilities, Universities and laboratories, using in-vitro techniques or when approved animal and human subjects.  However, due to the fact that this peptide is not approved for human consumption, we emphatically state that you should gain the necessary legal approvals prior to conducting any research on animals or humans.  The following information is meant ONLY to share results from certified tests with other qualified researchers to further the understanding of this peptide.  This post is not to be construed as an advertisement or inducement to ingest this product.  Peptide Pros is opposed to  the use of peptides for recreational or cosmetic use unless otherwise approved by the FDA or a similar governing body designated to do so.

CJC-1295 NO DAC (Mod-grf 1-29) Research Information

Research-CJC-1295-no-DAC

Product Description

CJC-1295 No DAC is a thirty amino acid based peptide, which is currently being researched for a variety of benefits, including growth. Invented by Canadian biotechnology company, Conjuchem, it has the ability to lengthen the half life of active agents, which has to do with a process called bioconjugation. During studies, it was discovered that, not only did CJC-1295 without DAC help in the water regulation and balance in the body, but that it alsogives relief from pain. Studies have also shown impressive results regarding the positive effects of this peptide on conditions such as indigestion and body pain. Here, we will discuss CJC-1295 without DAC in full detail by discussing them and the makeup of the peptide which results in providing a variety of benefits to the human being.

GHRH1-29 (CJC-1295 no DAC) Product Information

1.    Chemical Information

The peptide has a chemical formula of C152H252N44O42, and the molecular weight of this peptide is 3367.2.

2.    Systematic Name

CJC1295/DAC, CJC-1295 without DAC, CJC 1295

3.    Pharmacokinetic and other information

CJC-1925 without DAC is currently ‘unscheduled’ by the United States government meaning that it is not regulated by law.

CJC has a half-life, or the time taken for the compound to lose half of its potency value, is two hours.

CJC-1295 without DAC: The Biochemical Process

The mechanical dynamics of the CJC-1295 process present themselves primarily and directly to the central nervous system of the body. Specifically speaking, research involving living non human subjects,who were carefully given monitored dosages of the peptide showed GHRH1-29’s half-life by a major amount. This activation has led scientists to discover that the reaction itself actually takes control of or restricts the particular signals sent by the brain to the body. The signals,which are given, are quite specific, relating to the blood flow of the body and any areas of the body that are experiencing inflammation. Alternatively, when the switch to these receptors has been done, the brain is then able to successfully moderate the signals relating to these specific issues.

CJC-1295 without DAC and the Synthesis of Proteins

One of the supposed benefits of CJC-1295 No DAC involves the boosting of the synthesis of proteins. Scientific studies have shown that the presence of CJC-1925 without DAC has a tendency to enhance the amount of proteins that an animal test subject can create through the blockage of the natural process of cellular degradation. Another advantage that it has been said to have revolves around the idea of lipolysis, and how the peptide shows an ability to speed up the process, in which the lipids in the bodyaresynthesized and broken down. This in turn allows the bodies of any subject to burn through fat more efficiently. The other benefits that can be possibly derived include a speedy rate of injury recovery, a more efficient process of muscular growth and an increase in bone density.

Hemorrhagic Shock and GHRH1-29Interaction

CJC-1295 no DAC, by design, motivates and stimulates the reflexes of the nerves within the brain and it regulates any organic flow of blood that may result in actual organ failure, which would result from genuine hemorrhagic shock. The shock, which is hemorrhagic, is the result of what is referred to as a ‘lower tissue perfusion’ or the administration of oxygen to the tissue manually through a variety of methods, which becomes worse invariably due to increased lack of oxygen to the region over time.

There are four classifications or types of hemorrhagic shock:

  • Septic (or ‘vasogenic’)
  • Cardiogenic
  • Hypovolemic
  • Neurogenic

Since science knows that no two individual cells show the same responses, as has been observed on the level of a cell, it is a bit difficult to deal with this condition.

Current related research and findings regarding CJC-1925 without DAC.

While there has been a several research studies conducted in relation to CJC-1295 without DAC and its overall functionality, theorized benefits, and negative side effects, and operational mechanics, it needs to be emphasized that ALL of the research that has been conducted along with its resultant findings hasbeen the product of studies on animals alone.  CJC-1295 no DAC is solely intended for the use of scientific study at this time. Therefore, any observations or findings relating to CJC-1295 No DAC’s overall functionality, theoretical benefits, mechanics, or negative side effects should only be contained to the restrictions of a strictly controlled environment such as a laboratory or a medical research facility.

Developmental information regarding CJC-1295 without DAC

CJC-1295 DAC and CJC-1295 (which is also known as Modified GRF 1-29) are both known as GHRH or Growth Hormone Releasing Hormones. They act on the body in a similar fashion, but the difference between the two peptides is based on the span of the half-life.Modified GRF 1-29 and Sermorelin or CJC-1295 without DAC has a short half-life of about half an hour, while CJC-1295 DAC has a half-life that can last up to aroundeight days. Many scientists have said that the half life of Modified GRF 1-29 and Sermorelin is considered to be way more natural as they are said to produce a short pulse of Human Growth Hormone.

Despite the fact that plenty of research has been carried out on CJC-1295 No DAC in relation to how it functions and the benefits that it gives, it should be emphasized that CJC-1925 without DAC, at this point in time, is still just intended for scientific study. Because of this, any findings or observations relating to CJC-1295 No DAC should solely be the product of study performed in a medical research facility or a laboratory under strict conditions.Therefore, communicatewith your health care provider before administering any supplement or medication at any time for your own safety, and make sure that you follow the instructions given by both your physician as well as the instructions mentioned on the cover of CJC-1295 without DAC.

 TO PURCHASE

If you would like to purchase CJC-1295 No DAC (Mod grf 1-29) for research, you can visit our store at: https://peptidepros.net/product/cjc-1295-no-dac-2mg/

IMPORTANT DISCLAIMER

The info provided herein is strictly for the advancement of research and disbursement of knowledge relating to CJC-1295 No DAC (Mod grf 1-29).  It is meant solely for any qualified researchers looking to find potential applications or possible health benefits yet to be discovered for CJC-1295 No DAC (Mod grf 1-29).   This post is meant for informational use only and is in no way considered instructional, in fact, no dosage or other similar information is provided.  The facts contained herein have been gathered from various studies and tests conducted in sanctioned and/or controlled medical research facilities, Universities and laboratories, using in-vitro techniques or when approved animal and human subjects.  However, due to the fact that this peptide is not approved for human consumption, we emphatically state that you should gain the necessary legal approvals prior to conducting any research on animals or humans.  The following information is meant ONLY to share results from certified tests with other qualified researchers to further the understanding of this peptide.  This post is not to be construed as an advertisement or inducement to ingest this product.  Peptide Pros is opposed to the use of peptides for recreational or cosmetic use unless otherwise approved by the FDA or a similar governing body designated to do so.

PT-141 (Bremelanotide) Research Information

PT-141-Bremelanotide-Product-Research

Product Description

Formerly known as PT-141, Bremelanotide is a recurrent peptide which is still being researched for a variety of benefits including female sexual dysfunction. Derived from the peptide hormone referred to as Melatonin II it was first created to be used for ‘sunless’ tanning. During studies it was discovered that, not only did Bremelanotide darken the skin but also stimulated sexual interest and arousal in women. Studies have also shown impressive results regarding the positive effects of this peptide on conditions such as reperfusion injury and hemorrhagic shock Here we will discuss Bremelanotide more extensively, discussing the details and makeup of the peptide which results in providing a variety of benefits to the human being.

PT-141 (Bremelanotide) Product Information

1.    Chemical InformationBremelanotide (PT 141) Molecular Structure

Bremelanotide contains a molecular mass of 1025.2 grams per mol. It’s chemical formula is C50H68N14O10.

2.    Systematic Name (IUPAC)

(3S 6S 9R 12S 15S)-15-[(N-acetyl-L-norleucyl)amino]- 9-bynzyl-6-{3-[(diaminomethylidine)amino]propyl}-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexaa zacyclotricosane-23-carboxylic acid

3.    Pharmacokinetic and other information

Bremelanotide is currently ‘unscheduled’ by the United States government meaning that PT-141 is not regulated by law.

Bremelanotide has a half-life, or the time it takes for the compound do lose half of its potency value, is 2 hours.

Bremelanotide: The Biochemical Process

The mechanical dynamics of the PT-141 process present themselves primarily and directly to the body’s central nervous system. Specifically speaking, research involving non-human living subjects which were administered carefully monitored dosages of the peptide showed a growth in the stimulation and ‘ignition’, if you will, of the MC-4R and MC-3R melanocortin receptors themselves. This activation has led science to discover that the reaction itself actually takes control of and/or constrains particular signals emitted by the brain to the body. The signals which are inhibited are quite specific, relating to the body’s blood flow and any areas of the body experiencing inflammation. In other words, when the switch to these receptors has been flipped the brain is able to successfully moderate the signals relating to these specific issues.

Bremelanotide and Reperfusion Shock

By definition ‘reperfusion damage’ is damage caused to organ tissue which has been cut off from its blood supply by any occurrence, say a stroke for example. The damage occurs when blood flow is restored to the tissue which has been with it for so long. When tissue is deprived of the oxygen and nutrients it needs the body kicks that area into a state which can result in oxidation if blood flow is ever restored, referred to as ‘oxidative stress’. This only occurs when the body has not been eased into the healthy state properly.

The smallest of these injuries are of great detriment to the individual, as they often lead to brain injuries such as strokes or heart attacks, and can even result in complete failure of all brain function. PT-141 works on an entirely neurological level, activating the receptors which stabilize the signals sent to empower the signals related to the restriction of blood flow, easing, if not completely stopping, the chances of reperfusion shock from occurring.

Hemorrhagic Shock and PT-141 Interaction

Bremelanotide, by design, stimulates and motivates the neural reflexes within the brain, thus regulating any organic flow of blood which may cause actual organ failure which would result from actual hemorrhagic shock. Hemorrhagic shock is the result of what is referred to as a ‘lower tissue perfusion’, or the administration of oxygen to the tissue manually through a variety of methods, which invariably worsens due to increased lack of oxygen to the area over time.

There are four types, or classifications, of hemorrhagic shock:

  • Septic (or ‘vasogenic’)
  • Neurogenic
  • Hypovolemic
  • Cardiogenic

It has been proven a bit difficult to deal with this particular condition as science knows that no two individual cells demonstrate the same responses, as observed on a cellular level.

Current related research and findings regarding PT-141 (Bremelanotide)

There are some important points which should be noted regarding the study of the peptide Bremelanotide, as this substance is still in the research phase. To date all findings, theories, and conclusions have been deduced through studies done on living, non-human subjects in a completely controlled and stabilized environment. It is vehemently recommended that ANY and ALL use of PT-141 be done on a fully controlled and supervised basis ONLY.

It should also be clearly noted that a study scheduled to begin in 2007 was postponed when rises in blood pressure were found to be another side-effect, which can be dangerous in many individual cases.

Developmental information regarding Bremelanotide

Bremelanotide (PT-141) is directly derived from the peptide hormone ‘Melanotan II’. As mentioned, it was developed with full intent of marketing the product as a sunless tanning compound as it directly affected the skin-tone.

Over the course of development it was discovered to have very effective female arousal properties as well as causing erections in males on a spontaneous basis. These side-effects were not anticipated, and occurred in 90% of male subjects in the study.

In 2012 a study was conducted which administered PT-141 to premenopausal female subjects, and high-level results were reported all the way around, showing effectiveness in the treatment of a number of menopausal symptoms which had manifest, lessening them significantly.

The effects of Bremelanotide on the libido of either sex has been found to work in completely different manner when compared to enhancement drugs such as Cialis or Viagra, both of which affect blood flow to the sex organs. Rather PT-141 has been proven to stimulate sexual desire by invigorating the areas of the brain which cause sexual desire, thereby enhancing libido and performance. To date Bremelanotide has continued to be closely studied and monitored, and is currently readily available for purchase for research only at this time since it is yet to be FDA approved. Administering any supplement or medication not FDA approved may be harmful and may cause serious illness.  Peptide Pros insist that none of their products be ingested for under any circumstances.

Source:

For research purposes PT-141 (Bremelanotide) may be purchased at the Peptide Pros Shop here: https://peptidepros.net/product/pt-141/

Oxytocin Research Information

Oxytocin Blog Post

Oxytocin Product Information

CHEMICAL MAKE UP

Oxitocin Molecule

Molecular Formula C43H66N12O12S2 
Molar Mass 1007.19 g/mol

OTHER NAMES

  • Its systematic name is cysteine-tyrosine-isoleucine-glutamine-asparagine-cysteine-proline-leucine-glycine-amide(cys – tyr – ile – gln – asn – cys – pro – leu – gly – NH2, or CYIQNCPLG-NH2).
  • oxytocin disulfide
  • oxytoceine

DISCOVERY

The word oxytocin was coined from the term oxytocic (used at least in the 1800s to refer to agents such as ergots that would cause uterine stimulation; Greekὀξύς, oxys, and τόκος, tokos, meaning “quick birth”) by chemists at Parke, Davis, and Company around 1927,[105] two decades after its uterine-contracting properties were discovered by British pharmacologist Sir Henry Hallett Dale in 1906.[106] The milk ejection property of oxytocin was described by Ott and Scott in 1910[107] and by Schafer and Mackenzie in 1911.[108] The nine amino acid sequence of oxytocin was elucidated by Vincent du Vigneaud et al. and by Tuppy in 1953[109] and synthesized biochemically soon after by du Vigneaud et al. in 1953.[110][111] Oxytocin was the first polypeptide hormone to be sequenced and synthesized.[112] Vigneaud was awarded the Nobel Prize in 1955 for his work.[113]

PROPOSED APPLICATIONS (CLINICAL TRIALS)

Oxytocin (/ˌɒksɨˈtoʊsɪn/; Oxt) is a mammalian neurohypophysial hormone. Produced by the hypothalamus and stored and secreted by the posterior pituitary gland, oxytocin acts primarily as a neuromodulator in the brain.
Oxytocin plays an important role in the neuroanatomy of intimacy, specifically in sexual reproduction of both sexes, in particular during and after childbirth; its name comes from Greek ὀξύς, oksys “swift” and τόκος, tokos “birth.” It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, maternal bonding, and, after stimulation of the nipples, lactation. Both childbirth and milk ejection result from positive feedback mechanisms.[3] Recent studies have begun to investigate oxytocin’s role in various behaviors, including orgasm, social recognition, pair bonding, anxiety, and maternal behaviors.[4] For this reason, it is sometimes referred to as the “bonding hormone”. There is some evidence that oxytocin promotes ethnocentric behavior, incorporating the trust and empathy of in-groups with their suspicion and rejection of outsiders.[5] Furthermore, genetic differences in the oxytocin receptor gene (OXTR) have been associated with maladaptive social traits such as aggressive behaviour.[6] It is on the World Health Organization’s List of Essential Medicines, a list of the most important medications needed in a basic health system.[7]

TO PURCHASE:

If you would like to purchase Oxytocin for research, you can visit: https://peptidepros.net/product/oxytocin-2mg/

POSTING DISCLAIMER

The info provided herein is strictly for the advancement of research and disbursement of knowledge relating to Oxytocin.  It is meant solely  for any qualified researchers looking to find potential applications or possible health benefits yet to be discovered for Oxytocin.   This post is meant for informational use only and is in no way considered instructional, in fact, no dosage or other similar information is provided.  The facts contained herein have been gathered from various studies and tests conducted in sanctioned and/or controlled medical research facilities, Universities and laboratories, using in-vitro techniques or when approved animal and human subjects.  However, due to the fact that this peptide is not approved for human consumption, we emphatically state that you should gain the necessary legal approvals prior to conducting any research on animals or humans.  The following information is meant ONLY to share results from certified tests with other qualified researchers to further the understanding of this peptide.  This post is not to be construed as an advertisement or inducement to ingest this product.  Peptide Pros is opposed to  the use of peptides for recreational or cosmetic use unless otherwise approved by the FDA or a similar governing body designated to do so.

Melanotan 2 (MT-2) Research Information

Melanotan-2-Research-610x310

CHEMICAL MAKE UP:

Molecular formula C50H69N15O9
Molar mass 1024.180

3D model of Melanotan-II

DISCOVERY

Very first found out at the University of Arizona as an endogenous hormone created to promote the body’s pigment tissues (melanin) through increasing or resembling the natural a-MSH produced in the physical body. They properly developed a peptide that was 1,000 times more powerful than the all-natural a-MSH in the physical body. Initially referred to as Melanotan, after that Melanotan 1, and also later on Melanotan 2. Researchers wanted to utilize this peptide to stop cancer malignancy (cancer) by lessening the system’s necessity for exposure to sun and also the damaging rays so as to get a tan. They likewise assumed it may assist individuals who’s actual skin is reasonable or lower in natural melanin, thereby potentially guarding them versus sunshine damage (sunburn/cancer).

PROPOSED APPLICATIONS (CLINICAL TRIALS)

An Pilot Stage I scientific test facilitated on three men by the College of Medicine, Pharmacology Division, University of Arizona in Tucson, Arizona released in 1996 stated that, “Melanotan II has tanning activity in humans given only 5 low doses every other day by subcutaneous injection” The negative effects stated were mild nausea as well as a “stretching and yawning complex” that associated with casual penile erections. [1.]

The Department of Pharmacology, University of Arizona University of Medication released a research in 1998 that involved ten men which had to deal with psychogenic erectile dysfunction. Their trial confirmed that, “Melanotan-II is a potent initiator of erections in men with psychogenic erectile dysfunction and has manageable side effects at a dose of 0.025 mg./kg.”[2.]

A clinical report released in 2000 of TWENTY guys along with psychogenic and natural erectile disorder conducted at the Segment of Urology of The University of Arizona College of Medicine ended, “that Melanotan II is a potent initiator of penile erection in men with erectile dysfunction.” [3.]

Melanotan 2 Clinical Trials

Research Scientist working with modern computer interface in Melanotan Clinical Studies

PROFESSIONAL TEST SOURCES

Dorr RT, Lines R, Levine N, et al. (1996). “Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study”. Life Sci.58 (20): 1777–84. doi:10.1016/0024-3205(96)00160-9. PMID 8637402.

Wessells H, Fuciarelli K, Hansen J, et al. (Aug 1998). “Synthetic melanotropic peptide initiates erections in men with psychogenic erectile dysfunction: double-blind, placebo controlled crossover study”. J Urol. 160 (2): 389–93. doi:10.1016/S0022-5347(01)62903-3. PMID 9679884.

Wessells H, Levine N, Hadley ME, Dorr R, Hruby V (Oct 2000). “Melanocortin receptor agonists, penile erection, and sexual motivation: human studies with Melanotan II”. Int J Impot Res. 12 (Suppl 4): S74–9. doi:10.1038/sj.ijir.3900582.PMID 11035391

ABSTRACT OF SIDE – EFFECTS POSITIVE AND NEGATIVE

In numerous case studies conducted involving animals (and when approved humans), the following occurrences were observed.  Increased libido in most test subjects (male and female), increased melanin and tan (thought to be protective against the sun’s harmful rays).

MELATONAN 2 AS WELL AS MELANOGENESIS

According to a medical report that has been based on animal test subjects, melanin release is typically started with the visibility of ultraviolet beams. When this select secretion takes place, this is chiefly introduced upon the skin. This is a procedure that is technically referred to as melanogenesis. When melanogensis takes place, it functions as an organic means of security from UV rays and its own inherent harmfulness.

When exposed to sunlight, the body starts producing more of alpha-MSH, but there are subjects who do not produce enough of this or whose melanocytes don’t attract enough of alpha-MSH, thus reducing the ability to handle the prolonged exposure to the sun. Typically during tanning, the melanocytes are activated by alpha-MSH and triggered to produce more melanin, which results in a darkened skin.

Initially, researchers injected the naturally occurring α-MSH into subjects and although the results were slightly positive, they found that its short half-life made it impractical to use; therefore the team had to search for a more stable alternative.

After a lot of hard work, researchers at the university found a peptide α-MSH that was a lot more powerful than the natural α-MSH (up to 1,000 times). They called this Melanotan 1 and a little later developed another analog—Melanotan II.

The research was perhaps prompted by a desire to increase the body defense against skin cancer. The knowledge that melanin when activated could produce as a byproduct a deeper tan without exposure to UV radiation, and that this could in theory reduce skin cancer rates, was the beginning of further studies.

Ultimately, the procedure works as a way of securing the laboratory test subjects from a wide array of skin afflictions as well as afflictions that may be caused by extended exposure to UV rays. Largely, this would indicate a defense mechanism from different forms of skin cancers cells. But scientific research study conducted on subjects examined has established that the fifty percent life of the α-MSH hormone is actually quick in its own attributes– it has been actually established to last only a few mins. Hence, the hormone’s ability to create melanin and also introduce the defensive procedures of melanogenesis is actually extremely short.

Having said that, these researchers have actually gone on to find out that Melatonan 2’s overall functions can trigger a stretching of the bodily hormone’s brief half-life. Scientific research study has actually kept in mind that the total performance relating to Melatonan 2 has been presented to become far more reliable when the existence of UV radiations has been more of an actual component of the study’s procedure.

MELATONAN 2 AND THE HYPOTHALAMUS

The primary feature of Melatonan 2 may be tied to the pituitary gland; the very small gland located below the hypothalamus gland at the foundation of the brain whose principal reason is to handle as well as moderate several of animal test subject’s bodily hormone system-related processes, featuring development, rate of metabolism, temperature control, and a lot more. Exclusively, technical reports that have been actually based on animal test subjects have established that Melatonan 2 works in combination along with a pituitary gland-based expression α-MSH, which is an abbreviation for alpha-melanocyte stimulating bodily hormone. Fundamentally, this articulation is actually charged with the requirement and also management of skin and also hair pigment; this procedure is actually done through the bodily hormone known as melanin.

TO PURCHASE

If you would like to purchase Melanotan 2 for research, you can visit our store at: https://peptidepros.net/product/melanotan-2-mt-2/

SOURCES:

IMPORTANT DISCLAIMER

The info provided herein is strictly for the advancement of research and disbursement of knowledge relating to Melanotan 2.  It is meant solely for any qualified researchers looking to find potential applications or possible health benefits yet to be discovered for Melanotan 2.   This post is meant for informational use only and is in no way considered instructional, in fact, no dosage or other similar information is provided.  The facts contained herein have been gathered from various studies and tests conducted in sanctioned and/or controlled medical research facilities, Universities and laboratories, using in-vitro techniques or when approved animal and human subjects.  However, due to the fact that this peptide is not approved for human consumption, we emphatically state that you should gain the necessary legal approvals prior to conducting any research on animals or humans.  The following information is meant ONLY to share results from certified tests with other qualified researchers to further the understanding of this peptide.  This post is not to be construed as an advertisement or inducement to ingest this product.  Peptide Pros is opposed to the use of peptides for recreational or cosmetic use unless otherwise approved by the FDA or a similar governing body designated to do so.