Epitalon (Epithalon)
Epitalon (Epithalon)
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Contents: Epitalon
Form: Matrix: Powder
Purity: 99.0%
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Epithalon: Background and Applications
Epithalon, known alternately as Epitalon, Epithalone, or Epithalamin, signifies a diminutive man-made peptide famous for stimulating telomerase catalytic operation and advancing melatonin secretory output. Formulated initially in Russia throughout the 1980s period, scientific investigation concerning epithalon manifests effectiveness in postponing biological aging impacts on generative and immune system mechanisms while extending survival duration in murine laboratory organisms. Although its principal relevance concentrates within anti-aging investigation domains, epithalon demonstrates material benefits toward specific malignant pathologies, communicable conditions, and control of inherited material.
Epithalon Molecular Structure
Epithalon Research Findings
- Telomerase's Position in Epithalon's Longevity Mechanism
Preliminary scientific research conducted using cellular samples and tissue preparations revealed that cellular populations possess constrained replication capacity. During specified experimental settings, human cells and differentiated tissue cells show diminished multiplication capability dropping 40% throughout the third year and stop cellular division following roughly 60-80 successive multiplication cycles. This event, identified as cellular senescence, is ordinarily recognized as the Hayflick boundary.
Current scientific understanding indicates this observation might clarify the abbreviated lifespan demonstrated in biological systems. Post cellular degeneration, single cells lose multiplication competency, triggering tissue loss demonstrating senescence-related illnesses or capability impairment. The biochemical underpinnings of this occurrence continue incompletely grasped, yet telomere truncation functions as a key contributor toward aging effects. During hereditary material duplication, telomeres (protective chromosome terminations) experience steady reduction at every multiplication cycle, approaching a critical boundary where multiplication ceases. Telomerase enzyme performs the reverse function by restoring telomeric architecture, perhaps increasing cellular lifespan. Scientific investigation substantiates that epithalon strengthens telomerase enzymatic functioning via intensifying telomerase protein manufacturing, furnishing chromosome safeguarding and allowing increased cellular multiplication.
Epithalon and Genetic Reactivation
Analysis of epithalon's operational method demonstrates that therapy applied to mature cellular material reestablishes dormant transcriptional sequences. Analysis indicates epithalon rearranges genetic packaging molecules and reawakens genetic code sequences dynamic throughout growth plus those keeping protective immunity and cellular preservation. Examination performed with aging persons (between 60 plus 74 years) encompassing 266 contributors spanning numerous examinations display that subsequently to epithalon administration (delivered via 2-3 year schedules), constructive outcomes endured for a further three years following completion. The maintained advantageous impacts recommend that epithalon likely generates permanent rearrangement of hereditary substance handling in place of ephemeral variations, probably clarifying sustained advantages via renewal of translational operations, permanent epigenetic modifications together with supplementary cellular plus disease-stage phenomena.
Subsequent genetic elements impacted by epithalon include:
CER – heart endurance recovery capacity ER2 – strengthens ER2 production managing blood amino molecular compounds MAPK – escalates MAPK cascade action plus lessens inflammatory activity Twist1 – increases protein creation ZCREB1 – preserves daily biological cycles plus prevents programmed cellular exit Telomerase – augmented telomerase performance increases cell longevity
Epithalon's Impact on Neoplastic Development
A critical purpose throughout malignancy treatment focuses on suppressing uncontrolled cellular growth. Contemporary therapy options (incorporating pharmaceutical therapies plus radiotherapy) suppress cancerous cell expansion; nevertheless, this strategy demonstrates inadequate selectivity separating cancerous plus noncancerous cellular populations. This inadequate precision precipitates substantial detrimental impacts, pushing scientific attention toward focused healing techniques. Epithalon exhibits considerable guarantee within this context, as information shows that peptide administration minimizes tumor emergence from the pineal tissue. Scientific work using mature mice documents that continual epithalon usage (lasting numerous months) achieves 2.6-fold reduction in tumor appearance relative to untreated controls, plus 2.8-fold decline in colon tumor appearance together with 40% decrease in complete tumor frequency. These conclusions indicate that underneath both transient together with persistent treatment approaches, epithalon demonstrates cancer-fighting capacities via limiting uncontrolled cellular multiplication.
Extra confirmation supporting epithalon's merits originates from work on human cells. Scientific work confirms that epithalon administration rearranges genetic expression patterns plus might strengthen protective organism operation plus cellular vigor. For populations suffering compromised protected function, epithalon management (twice yearly), facilitates improved protection plus extended disease-free lifespans. An intriguing observation includes the probable role of regenerated circadian patterning, via epithalon's action on melatonin generation, in minimizing tumor emergence.
Epithalon's Function in Melatonin Generation
Sustaining diurnal biologic cycles stays elementary for upholding wellbeing. Multiple illness circumstances associate with disruptions in circadian patterning. Investigation in creature subjects indicates worsening pineal tissue operation plus lessening biochemical substance manufacture (enabling melatonin generation plus distribution) accompanies chronological aging. Throughout maturity, both circadian consistency and melatonin generation substantially diminish. Scientific examination confirms melatonin's value transcends slumber control encompassing immune defense, transcriptional processes, plus safeguarding versus tumor development.
Investigation indicates that epithalon stimulates pineal tissue to magnify biochemical substance manufacture plus enhance melatonin discharge. Documentation shows that PESI substance (pineal gland deceleration element), incorporating epithalon, restores melatonin generation subsequently to reduction in aging creature models together with magnifies existence duration. Scientific inquiry conducted spanning numerous countries validates epithalon's capacity for reestablishing biological periodicity plus increasing melatonin generation in aging creatures via direct modification of pineal tissue function. These investigations substantiate the supposition that biological periodicity restoration meaningfully participates in epithalon's longevity extension via magnified protective oversight, metabolic acceleration, plus amplified cellular activity.
Epithalon and Visual Acuity
Visual system decline develops via biological aging. The aging procedure correlates with amplified occurrence of eyesight ailments including cataracts. Epithalon presents favorable results addressing senescence-linked sight decline via multifaceted mechanisms inside ocular structures.
Analysis demonstrates that the substance augments blood circulation to eye tissue, potentially symbolizing one element in visual safeguarding. Throughout advancing years, eye vascular circulation declines markedly (approximately 40% lessening), together with lessened circulation precipitates malfunction. Via diminished vascular circulation, eye tissues experience weakened nutrient distribution plus diminished waste discharge, potentially producing cellular degradation together with sight reduction. By amplifying vascular circulation, epithalon possibly delivers protection versus progressive decrease.
Scientific Research Literature
Vladlen Khavinson functions as faculty, presides over the European segment of the International Association of Gerontology and Geriatrics (IAGG), plus heads the Saint Petersburg Institute of Bioregulation and Gerontology underneath management by the Health Division of the Russian Federation (Saint Petersburg, Russia). His scientific work in aging science, biophysical regulation, plus malignancy study commands worldwide prominence. Professor Khavinson presently manages chief editorial positions for construction of active medicinal substances. His investigative efforts encompass comprehensive studies regarding peptide use for enlarging wellness period via telomerase-based therapeutic approaches supporting existence extension. Contemporary research concentrates on practical execution of epithalon plus comparable peptide substances for practical healthcare advantage. Professor Khavinson preserves an extensive scientific record encompassing numerous papers on peptide biochemistry plus investigative utilization relative to aging plus linked conditions.
Prof. Vladlen Khavinson's research concentrates mainly on peptide substance implementation in aging domains plus stretches over thorough peptide research in his specialty. Beyond academic positions, backing originates from multiple organizations. This investigative work shows commitment to producing therapeutic value via peptide administration through human-based application. Transition of fundamental research information into therapeutic execution forms a principal objective, safeguarding realization through creation of substantiated medical accomplishment. Vladlen Khavinson is listed as Chief of FIT-RFI-FIT-14 ECR348 documented in the EUSPD documentation detailing distinct methods plus investigative structures.
Article Composer
The accompanying scientific evaluation was examined, changed, and methodically arranged by Dr. Logan, M.D. Dr. Logan maintains a doctoral degree obtained from Case Western Reserve University School of Medicine together with extra specialization in biological genetic science.
Research Literature References
V. Kh Khavinson, V. N. Anisimov, M. I. Zabezhinskii, I. G. Popovich, A. V. Zabezhinski, V. G. Morozov, I. M. Kvetnoi, and A. I. Yashin, "Effect of the pineal peptide preparation epithalamin on the life span and pineal and serum melatonin level in old rats." Ann. New York Acad. Sci., vol. 719, pp. 393-407, Jul. 1994. [PubMed].
V. Kh. Khavinson, G. M. Chalisova, N. Ashapkin, N. Shataeva, and A. Cartwright. "Mechanisms underlying the immunomodulatory actions of pineal peptides and their use in cancer control strategy." Biol. Today, vol. 8, pp. 13-20, 2012.
V. Kh Khavinson, V. G. Morozov, I. A. Abisheva, S. I. Semenchenko, and S. V. Vanyushin, "Effect of pineal peptide preparation epithalamin on the proliferation and the development of spontaneous tumors in old rodents." Front. Aging Neurosci., vol. 5, pp. 128, 2013.
V. Kh Khavinson, A. V. Malinin, "Gerontological aspects of genome peptide regulation: the role of short peptides." Biogerontology, vol. 6, no. 3, pp. 191-201, 2005. [PubMed].
V. Kh. Khavinson, I. V. Aliakina, G. A. Ryzhak, N. Muradian, V. Anisimov, and R. A. Suchkov. "Effect of epithalamin on the life span and hypothalamus resistance to aging." Adv. Gerontol., vol. 8, no. 2, pp. 109-14, 2005.
S. Dave, R. Kavanagh, J. Sheridan, A. Yu, S. Alrfi, P. Fournier, C. Van der Poorten, M. Lewin, D. Crawford, C. Patel, and K. G. Boutros. "The association between body mass index and tumor size in soft tissue sarcomas and GIST-soft tumors." Medicine (Kensington), vol. 29, no. 4, pp. 40-6, Aug 2016. [PubMed].
V. K. Khavinson, L. K. Shataeva, and K. A. Chalisova. "Effect of regulatory peptides on DNA synthesis in irradiated and non-irradiated splenocytes." Bull. Exp. Biol. Med., vol. 119, no. 1, pp. 79-81, Jan. 1995. [PubMed].
D. V. Kubanova et al. "Deconvolution effect of the pineal-gland peptide on the fatty acid cholesterol esters in the choroidal and ciliary body in albino rats and their correlation with degenerative processes." Tsitologiia., vol. 50, no. 9, pp. 779-82, Sep. 2008. [PubMed].
V. Khavinson, B. Goncharova, and N. Lapin. "Synthetic tetrapeptide epitalon restores disturbed neuroendocrine regulation in senescence accelerated OXYS rats." Neuroendocrinology Letters, vol. 22, no. 4, pp. 251-254, Aug. 2001. [PubMed].
N. I. Chalisova, M. E. Litivina, M. M. Shchukin, A. G. Drozdov, G. A. Ryzhak, and V. K. Khavinson. "Effect of peptide epitalon on microvascular reactions and their role in age-dependent reorganization of tissues." Bull. Exp. Biol. Med., vol. 141, no. 4, pp. 452-455, May 2006.
N. V. Linke and A. A. Pankova. "Peptide Regulation of Skin Fibroblast Functions during Aging in Vitro." Bull. Exp. Biol. Med., vol. 148, no. 1, pp. 151-155, July 2009. [PubMed].
I. V. Vinogradova, V. V. Ruslova, M. V. Zabezhinskii, V. A. Semenchenko, V. A. Yakovlev, T. S. Zavarykina, A. V. Arutinuyan, M. A. Karasik, A. N. Gorban, and V. Kh. Khavinson. "The Geroprotective Property of Epithalon and Metformin during Aging." Adv. Gerontol., vol. 143, no. 1, pp. 393-432, Dec. 2017. [PubMed].
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