Pancragen

The Pancreatic Health Protector

Protect Pancreatic Health: Discover the Benefits of Pancragen

Pancragen peptide bioregulators are targeted at the pancreas. It is designed to consist of peptides, which are short chains of amino acids, that can potentially interact with pancreatic cells. In the case of the pancreas, the peptides might influence the production and regulation of enzymes and hormones like insulin, which are crucial for digestion and blood sugar regulation.

Potential Benefits Under Research

• Enhanced pancreatic function: May improve the pancreas’s ability to produce and regulate enzymes needed for digestion.
• Improved insulin regulation: Could potentially aid in the better production and effectiveness of insulin, which is crucial for blood sugar management.
• Cellular regeneration: Might support the repair and regeneration of pancreatic cells, contributing to overall organ health.
• Increased resilience to diseases: By boosting the health of the pancreas, these peptides could potentially help protect against diseases such as pancreatitis or even diabetes.
• Anti-aging effects: General claims around peptide bioregulators often include potential anti-aging effects on organs by supporting cellular function and health.

Overview

Pancragen is a naturally occurring tetrapeptide bioregulator that, as the name implies, has primary effects on the pancreas. Not to be confused with the DNA-based PancraGEN test, Pancragen has been shown to help control blood sugar, improve the endocrine function of the pancreas, regulate melatonin expression, and reduce the incidence and magnitude of metabolic syndrome. It has been investigated and is of interest in the treatment of both diabetes and the metabolic effects of aging. To some extent, Pancragen can be thought of as an anti-aging peptide for the pancreas. 

Structure

Amino Acid Sequence: Lys-Glu-Asp-Trp (KEDW)

Molecular Formula: C26H36N609 Molecular Weight: 576.25 g/mol PubChem CID: 68452887 Synonyms: SCHEMBL5491754 

Source: PepDraw

Pancragen and Aging 

Research on pancreatic cells shows that Pancragen stimulates the expression of a number of differentiation factors that control the growth of acinar and islet of Langerhans cells. The latter is responsible for insulin and glucagon. Though this may not seem like an anti-aging effect, it should be clear that restoration of improved growth and differentiation is a feature of young, healthy tissues. Improving these parameters, particularly in older tissues, is fundamentally an anti-aging effect. Throughout the rest of the sections of Pancragen, additional reasons for its classification as an anti­aging peptide will be manifest. In particular, its ability to change the epigenetic regulation of DNA to improve gene expression is one of the clearest indications that Pancragen can turn back the clock on DNA to promote function more in keeping with youth. 

Pancragen and Metabolic Disorders 

Further supporting the idea that Pancragen is an anti-aging peptide are its effects on metabolic disorders. Research shows that metabolic dysregulation in older people is at least partially caused by changes in melatonin secretion during sleep. This melatonin deficiency appears to be caused by changes in insulin levels, suggesting that loss of insulin function, both in disease and as a result of old age, may be responsible for changes in melatonin secretion, which is then responsible for some of the other symptoms of metabolic syndrome. 

Based on the above line of thought, it stands to reason that administration of Pancragen, which helps to normalize insulin secretion, could further reduce symptoms of metabolic syndrome by normalizing melatonin secretion. In fact, this is precisely what research reveals. Administration of Pancragen decreases glucose levels but also reduces plasma concentrations of insulin as well as the insulin resistance index which are strong indications that Pancragen is having a direct effect on melatonin signaling. 

Both exogenous and endogenous melatonin inhibit the pathophysiological mechanisms of metabolic syndrome and normalize metabolism. Research shows that melatonin receptors exist in the pancreas where they serve to modulate insulin and glucagon signaling in a diurnal (daylight-sensitive) fashion. There is a lot of new research focusing on how disruptions in melatonin signaling are linked to the development of type 2 diabetes and metabolic syndrome. 

If melatonin affects the pancreas, then it stands to reason that there is likely a feedback mechanism by which glucagon and insulin signal to the pineal gland whether to increase or decrease melatonin release. In fact, this feedback loop exists and, in type 2 diabetes, appears to be responsible for the additional metabolic effects that arise in this version of the disease that are less common in type 1 diabetes. This would explain why Pancragen’s ability to regulate insulin secretion in the pancreas also has beneficial effects on other symptoms of metabolic syndrome. 

Source: PubChem 

Pancragen and Diabetes 

Of course, the most obvious use for Pancragen is in the treatment of diabetes, hyperinsulinemia, and elevated blood glucose levels. Research in rhesus monkeys comparing Pancragen to glimepiride (a widely used drug for lowering blood sugar) reveals that while both compounds can reduce blood sugar levels to normal baselines, only Pancragen normalizes insulin levels and C-peptide levels. This would suggest that Pancragen is having a more physiologic effect, striking at the very heart of what causes elevated blood sugar and correcting the problem at a more fundamental level. 

Research in old monkeys shows that Pancragen normalizes plasma insulin, C-peptide, and glucose levels within 10 days and that the effect lasts, at least partially, for as long as 3 weeks. This suggests that Pancragen might be useful in restoring pancreatic function in elderly individuals or maintaining it as we age. This can help to normalize the metabolic system and reduce the impact of everything from osteoporosis to dementia. 

Additional research in cell cultures shows that Pancragen increases the expression of matrix metalloproteinases MMP2 and MMP9. It also increases the expression of serotonin, glycoprotein CD79alpha, and the anti-apoptotic protein MCl1 while decreasing levels of the pro-apoptotic protein p53. Additionally, levels of proliferation markers PCNA and Ki67 are increased. Vasili Ashapkin, author of the textbook DNA Methylation in Plants and collaborator with Vladimir Khavinson, points out that these findings collectively indicate that Pancragen activates the expression of signaling molecules associated with increased differentiation and functionality of pancreatic islet cells. These effects can only be accounted for by a broad functional mechanism such as direct alteration of DNA expression and condensation patterns. In other words, Pancragen is likely working at a very fundamental level within the DNA to alter the expression of multiple genes.

Pancragen and the Vascular System 

One of the most serious consequences of diabetes is on the function of small blood vessels called capillaries. Elevated glucose levels cause these capillaries to first become leak and then to die off as the cells that make them up, called endothelial cells, become dysfunctional and then die. Many of the long-term consequences of diabetes like heart disease, kidney disease, erectile dysfunction, and loss of limb result from damage to and loss of capillaries. 

Research on Pancragen shows that it helps to normalize the adhesion of mesenteric capillary endothelium. These findings suggest that Pancragen could protect the endothelium from some of the effects of diabetes, thus helping to stave off long-term consequences of the disease.

Article Author

The above literature was researched, edited and organized by Dr. Logan, M.D. Dr. Logan holds a doctorate degree from Case Western Reserve University School of Medicine and a B.S. in molecular biology. 

Scientific Journal Author 

Vladimir Khavinson is a Professor, resident of the European region of the International Association of Gerontology and Geriatrics; Member of the Russian and Ukrainian Academies of Medical Sciences; Main gerontologist of the Health Committee of the Government of Saint Petersburg, Russia; Director of the Saint Petersburg Institute of Bioregulation and Gerontology; Vice ­president of Gerontological Society of the Russian Academy of Sciences; Head of the Chair of Gerontology and Geriatrics of the North-Western State Medical University, St-Petersburg; Colonel of medical service (USSR, Russia), retired. Vladimir Khavinson is known for the discovery, experimental and clinical studies of new classes of peptide bioregulators as well as for the development of bioregulating peptide therapy. He is engaged in studying of the role of peptides in regulation of the mechanisms of ageing. His main field of actions is design, pre-clinical and clinical studies of new peptide geroprotectors. A 40-year­long investigation resulted in a multitude of methods of application of peptide bioregulators to slow down the process of aging and increase human life span. Six peptide-based pharmaceuticals and 64 peptide food supplements have been introduced into clinical practice by V. Khavinson. He is an author of 196 patents (Russian and international) as well as of 775 scientific publications. His major achievements are presented in two books: “Peptides and Ageing” (NEL, 2002) and “Gerontological aspects of genome peptide regulation” (Karger AG, 2005). Vladimir Khavinson introduced scientific specialty “Gerontology and Geriatrics” in the Russian Federation on the governmental level. Academic Council headed by V. Khavinson has oversighted over 200 Ph.D. and Doctorate theses from many different countries. 

Prof. Vladimir Khavinson is being referenced as one of the leading scientists involved in the research and development of Pancragen. In no way is this doctor/scientist endorsing or advocating the purchase, sale, or use of this product for any reason. There is no affiliation or relationship, implied or otherwise, between Guide to Peptide and this doctor. The purpose of citing the doctor is to acknowledge, recognize, and credit the exhaustive research and development efforts conducted by the scientists studying this peptide. 

Referenced Citations 

1. V. K. Khavinson et al., “Effects of pancragen on the differentiation of pancreatic cells during their ageinq,” Bull. Ex12,. Biol. Med., vol. 154, no. 4, Qp. 501-504, Feb. 2013, doi: 10.1007/s10517-013-1987-6. 
2. 0. V. Korkushko, V. K. Khavinson, V. B. Shatilo, I. A. AntonY.k-Sheglova, and E. V. Bondarenko, “Prospects of using pancragen for correction of metabolic disorders in elderly. people,” Bull. Ex12,. Biol. Med., vol. 151, no. 4, pp. 454-456, Aug. 2011, doi:
   10.1007 /s10517-011-1354-4. 
3. S. I. Rapoport, A. I. Molchanov, V. A. Golichenkov, 0. V. Burlakova, E. S. Suprunenko, and E. S. Savchenko, “[Metabolic syndrome and melatonin],” Klin. Med. (.Mask), vol. 91, no. 11, RP· 8-14, 2013.
4. E. Peschke, I. Bahr, and E. Muhlbauer, “Melatonin and pancreatic islets: interrelationships between melatonin, insulin and glucagon,” Int. J. Mo/. Sci., vol. 14, no. 4, pp. 6981-7015, Mar. 2013, doi: 10.3390/ijms14046981. 
5. N. D. Goncharova. L. G. lvanova, T. E. Oganyan, A. A. Vengerin, and V. K. Khavinson, “[Correction of impaired glucose tolerance using tetrapeptide (Pancragen) in old female rhesus monkeys],” Adv. Gerontol. Usepekhi Gerontol., vol. 28, no. 3,_pp. 579- 585, 2015. 
6. V. K. Khavinson, M. M.-G. Gapparov, N. E. Sharanova, A. V. Vasilyev, and G. A. Ryzhak, “Study of biological activity of Lys-Glu-Asp: Trp-NH2 endogenous tetrapeptide,” Bull. Exg_ Biol. Med., vol. 149, no. 3, pp. 351-353, Sep 2010, doi: 10.1007/s10517-010-0944-x. 
7. N. D. Goncharova. L. G. lvanova, T. E. Oganian, A. A. Vengerin, and V. K. Khavinson, “[Impact of tetrapeptide pancragen on endocrine function of the pancreas in old monkeys],” Adv. Gerontol. Use_ekhi Gerontol.1 vol. 27, no. 4, op. 662- 667, 2014. 
8. I. M. Kvetnoi, A. P. Ryzhak, I. N. Kostyuchek, and Y. A. Tafeev, “Effect of tetrapeptide pancragene on functional morphology of the pancreas in rats with experimental diabetes mellitus,” Bull. Exe_. Biol. Med., vol. 143, no. 3, pp. 368-371, Mar. 2007, doi:
   10.1007/s10517-007-0114-y.
9. V. K. Khavinson et al., “[Tetrapeptide stimulates functional activity of the pancreatic cells in aging).” Adv. Gerontol. Useekhi Gerontol., vol. 25, no. 4, J2p. 680-684, 2012. 
10. V. V. Ashapkin, N. S. Linkova, V. K. Khavinson, and B. F. Vanyushin, “EPigenetic mechanisms of peptidergic regulation of gene expression during aging of human cells,” Biochem. Biokhimiia, vol. 80, no. 3, pp. 310-322, Mar. 2015, doi: 10.1134IS0006297915030062. 
11. V. K. Khavinson, N. A. Gavrisheva, V. V. Malinin1 S. G. Chefu1 and E. L. Trofimov1
    “Effect of pancragen on blood glucose level, capillary permeability and adhesion in rats with experimental diabetes mellitus,” Bull. Exe. Biol. Med., vol. 144, no. 4,_pp. 559-562,. Oct. 2007, doi: 10.1007ls10517-007-0377-3.