First Time Order Discount 15% (Code: BEST PEPTIDE)

Search

In Stock

DSIP 5mg

Delta-sleep-inducing-peptide, commonly known as DSIP, is a neuropeptide which affects different endocrine and physiological mechanisms within the central nervous system. It also exhibits antioxidative effect, as it can mitigate some oxidative stress.

 

Some research also shows that DSIP can modulate certain regulatory processes within the host’s body, processes such as GABAergic and glutamatergic, which enable nerve transmission.

$50.00

What Is DSIP (Delta Sleep-Inducing Peptide)?

Also known as Delta Sleep-Inducing Peptide, DSIP is a short, naturally produced neuropeptide, first discovered in the 70s. It was initially isolated from the brains of rabbits and gained its notoriety for inducing sleep during slow-wave sleep cycle.

Since the 70s, there’s been a lot of studies revolving around DSIP and its range of abilities seems to be spreading from inducing sleep all the way to affecting endocrine system, affecting stress levels and blood pressure, and altering pain perception.

DSIP Structure

  • Sequence: Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu
  • Molecular Formula: C35H48N10O15
  • Molecular Weight: 848.824 g/mol
  • PubChem CID: 68816
  • CAS Number: 62568-57-4
  • Synonyms: Emideltide, DSIP nonapeptide, Deltaran

DSIP And Sleep

Though initial studies revolved primarily around sleep (as the “sleep-inducing” part of the name suggests), the exact connection between DSIP and sleep is not yet as first as most researchers would have hoped. Why? Mostly because results were inconsistent and inconclusive… For example, one study might indicate a clear link between this peptide and sleep, while the second one might completely disprove it… the third one concludes there is no impact and the fourth one says it promotes sedation initially, but causes arousal later on.

DSIP Research and Chronic Pain

Chronic (and any other type of) pain is a state most researchers take very seriously and are always on the lookout for better, less addictive options of addressing it, and DSIP is no different. There was a pilot study done on monkeys with chronic pain episodes where it was concluded that this peptide reduced pain perception significantly (as compared to the placebo).

There were also some experiments with systemically administered morphine and amphetamine. These, and similar opioid drugs, act slowly (but surely) develop chronic addiction in rats with severe pain episodes. One study in rat models showed that, even though DSIP acts on the same receptors in the central nervous system, there was no evidence that it led to the same kind of addiction.

DSIP Research and Metabolism

Though DSIP was primarily investigated for its link with sleeping patterns and, as of late, pain relief potential, one of the more recent studies on its effects on rat lipid metabolism showed some interesting findings.

At the end of the study, researchers found that rats injected with DSIP experienced body weight reduction, total fat mass reduction as well as reduced serum lipids.

Since the results were so fascinating, there were many more similar studies aimed at digging deeper and figuring out this connection. One particular study explored DSIP’s influence on glucose metabolism in rats. To everyone’s surprise, DSIP application resulted in improved glucose tolerance and insulin sensitivity. But, even though the initial results were promising, it’s important to note that these were just some preliminary findings and that we’re missing large scale studies.

Depression, Chemical Imbalances, and DSIP

Though depression is a much more complicated condition, and cannot be reversed/addressed by changing/introducing one chemical into the patient’s body, scientists wanted to go down this path and see if DSIP affected it in any way.

So they designed a study around rats subjected to short-term hypoxic conditions. The findings showed that DSIP may have altered the mitochondrial activity in a hypoxic environment, which further suggested that this peptide can affect depressive states. And, since there is such a strong connection between sleeping cycles and depressive states, it appears that DSIP may affect depression.

However, there were no studies where DSIP application affected a patient’s depressive state so much it restored subjective normal feeling.

DSIP Research in Withdrawal and Addiction

One particular animal study showed that DSIP actually possesses an agonistic tendency towards opiate receptors. Which further confirmed researcher’s claims this peptide can potentially be used in the reduction of withdrawal symptoms from both opiates and alcohols.

DSIP Physiologic and Muscle-Building Effects

It’s interesting that DSIP was first identified in the brains of rabbits during deep sleep, but researchers still aren’t quite sure where this peptide is synthesized. Some suggest it’s produced outside of the central nervous system and does not affect sleep at all!

This allied the scientists to be a bit more creative in their research. And one such research gave birth to some speculations saying DSIP inhibits somatostatin; a protein produced in muscle cells that inhibits their growth. This action, in turn, contributes to the overall hypertrophy and hyperplasia of the skeletal muscles.

Since these findings contradict the original ones regarding sleep, some scientists are asking for the entire revising of DSIP and its complete research history. We’ll see what the future holds and which side will prevail in the end.

Reviews

There are no reviews yet.

Write a review

Your email address will not be published. Required fields are marked *

+ 19 = 24

Bestsellers

AICAR 50mg

$55.00
(0 Reviews)
AICAR (5-Aminoimidazole-4-carboxamide ribonucleoside) is one of the most commonly used pharmacological modulators of AMPK activity. AMPK is an enzyme that acts as a fuel gauge in high energy consumption situations. Of course, AICAR can also be synthesized in the lab, which is why it continues to be studied due to its potential in performance boost.

Tesamorelin

$70.00$125.00
(0 Reviews)
Tesamorelin is a synthetic growth hormone-releasing hormone (GHRH) analog. It was based on the 44 amino acids sequence of GHRH and contains a trans-3 hexenoic group to protect it from enzymatic degradation. These modifications allow it to be more stable and have a longer half-life.   Just like Sermorelin, Ipamorelin or GHRP-2, Tesamorelin is considered a growth hormone secretagogue (GHS) which stimulates the secretion of GH and increases the level of insulin-like growth factor (IGF-1). The importance of IGF-1 is it tends to be lower in patients with obesity, diabetes and especially in those with lipodystrophy. References: 
  1. Sinha DK, Balasubramanian A, Tatem AJ, Rivera-Mirabal J, Yu J, Kovac J, Pastuszak AW, Lipshultz LI. Beyond the androgen receptor: the role of growth hormone secretagogues in the modern management of body composition in hypogonadal males. Transl Androl Urol. 2020 Mar;9(Suppl 2):S149-S159. doi: 10.21037/tau.2019.11.30. PMID: 32257855; PMCID: PMC7108996.

GHRP 2 10mg

$50.00
(0 Reviews)
GHRP-2, also known as pralmorelin, is a synthetic growth hormone secretagogue, which specifically targets ghrelin (growth hormone receptor). The significance of targeting ghrelin becomes apparent when we see what are its two main effects – growth hormone secretion and meal initiation.   GHRP-2 was a pioneering growth hormone (GH) secretagogue and is currently used to evaluate GH deficiency and secondary adrenal failure.

Semaglutide

$105.00$190.00
(0 Reviews)
This is a synthetic peptide modeled after the naturally occurring hormone glucagon-like peptide-1 (GLP-1). GLP-1 is an incretin, a gut-derived peptide secreted in response to a meal, that regulates insulin secretion based on glucose levels in the blood. This GLP-1 agonist was developed specifically to have an extended half-life without losing potency. Since it falls under the category of glucagon-like peptide-1 receptor agonists, it acts to prompt the body to secrete more insulin and inhibit glucagon secretion. By allowing the body to secrete more insulin and inhibiting the secretion of glucagon, this joint effort brings blood glucose levels down.

KPV 10mg

$100.00
(0 Reviews)
KPV is one of several short peptide derivatives of alpha-melanocyte stimulating hormones, which originates from the C-terminal fragment of alpha-MSH.   Due to Lysine-proline-valine’s (KPV’s) potency, this peptide has been garnering more and more attention from the scientific community, and we are eager to see what the future lab research is going to show.

Melanotan 2 10mg

$55.00
(0 Reviews)
Melanotan 2 (MT-2) is a synthetic analogue of alpha-melanocyte-stimulating hormone, created in the 1980s. It has been found to act as a non-selective agonist of melanocortin receptors MC1, MC3, MC4 and MC5. It has been clinically documented that melanotan II activates MC1 receptor, which leads to melanogenesis, which is why this particular peptide was deemed “barbie drug.” References:
  1. https://pubmed.ncbi.nlm.nih.gov/8637402/
  2. https://www.sciencedirect.com/science/article/abs/pii/S0022354915495474
  3. https://www.sciencedirect.com/science/article/abs/pii/S2211266915000055

Thymosin Alpha 1 10mg

$120.00
(0 Reviews)
When speaking about thymosin alpha 1, we know that it’s a 28 amino acid peptide which naturally occurs in the thymus gland and has been known to modify and regulate the immune system via its action as a toll-like receptor and TLR-2 agonist.   Naturally present thymosin 1 in the body intensifies t-cell maturation and differentiation, the activity of natural killer cells, and also cytokine-mediated inflammation.
Back to Top
Product has been added to your cart