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DragonHead Extract Supplement
DragonHead Extract Supplement
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Dragonhead extract
Anti-ageing
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48.00 €(52.18 US$) in stock
Description
DragonHead Extract is an anti-ageing supplement that mimics the effects of calorie restriction.
  • Produced from the leaves of the dragonhead plant (the most active part).
  • Helps replicate the effects of calorie restriction and increases longevity.
  • Helps improve the skin’s appearance (hydration, elasticity and density) and supports its regeneration.
  • Organic raw material.
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Hourglass and dragonhead plant

DragonHead Extract Supplement - 100% Organic Extract to Promote Longevity

DragonHead Extract is a supplement made from the dragonhead plant (Dracocephalum moldavica), sometimes called ‘Moldavian Melissa’, which is traditionally used in Uighur medicine for combatting the ageing process.

With its unique mode of action and high content in flavonoid glucuronides, it mimics the effects of calorie restriction, an action that significantly slows down the ageing process. In the short term, it produces benefits for the skin, while in the long term, it promotes longevity.

It has a similar action to that of the exceptional anti-ageing product Nicotinamide mononucleotide.

What benefits are offered by DragonHead Extract?

Aqueous extract of Dracocephalum moldavica is distinct in being able to mimic calorie restriction, and as a result, may be able to push back the limits of human life expectancy and reduce the risk of age-related diseases.

What exactly is calorie restriction and how does it affect ageing?

Calorie restriction is simply limiting one’s food intake to the minimum necessary. Until very recently, it was the only method known to increase longevity whilst improving general health (3-5).

Calorie restriction activates a cell protein called AMPK (6-7) which itself triggers the expression of a family of genes called sirtuins (8-9-20). These genes slow down the ageing process by acting on a number of cell mechanisms, such as DNA repair, resistance to oxidative stress and cell death. Studies also show that sirtuin activation increases insulin sensitivity and lipolysis, reduces levels of inflammation and plays a preventive role in neurodegenerative problems.

But just how many of us would be prepared to make such a huge sacrifice? A lifetime of drastically reduced calorie consumption in order to increase one’s life expectancy holds little appeal for most people (even if, in the past, such diets were undoubtedly responsible for the incredibly long life expectancy enjoyed by Japan’s Okinawa islanders).

Fortunately, researchers recently succeeded in isolating natural compounds capable of reproducing the beneficial effects of calorie restriction, with dragonhead emerging as one of the most impressive resources. When humans and other animals are given an extract of dragonhead, its flavonoid glucuronides activate AMPK in exactly the same way as calorie restriction. This brings about the same increase in activation of sirtuins, the genes that slow down ageing. This results in both general benefits and cellular ones, with effects ranging from a decrease in metabolic waste products, to a reduction in fat mass. Accordingly, one laboratory study showed that the compounds in DragonHead Extract led to an increase of 400% in AMPK activity, and of 300% in FOXO transcription factors which activate the sirtuin family. Perhaps most surprising is that the beneficial effects of this molecule are even observed in cases of overeating (which is common in Western countries).

With dragonhead’s ability to mimic calorie restriction, it’s therefore possible to have your cake (maximum life expectancy), and eat it too (normal calorie intake) and even have a cherry on top (a slim figure).

Additional benefits of DragonHead Extract

Through a domino effect, DragonHead Extract’s activation of sirtuins produces other health benefits too:

  • It improves the circulation(1).
  • It helps you slim down.
  • It supports regeneration of the skin and improves a number of visible markers (elasticity, density, hydration …). One study examined 32 women in their fifties with sun-damaged skin. Following daily administration of 200mg of DragonHead Extract for eight weeks, dermal imaging showed a 14% improvement in hydration, a 7% improvement in elasticity and an approximate 3% increase in skin density (2).

What exactly is Moldavian dragonhead?

It’s a plant that has recently been rediscovered and positively exploited for its high content in glucuronic flavonoids, the compounds responsible for its many properties. It is indigenous to central Asia where it plays a prominent part in Uighur medicine.

What is in DragonHead Extract capsules?

DragonHead Extract is produced from the aerial parts of Moldavian dragonhead which contain most of the active substances. The use of high-quality aqueous extraction produces an extract packed with active compounds such as flavonoids, terpenoids, steroids, glycosides and volatile components. Of all these ingredients, it is the flavonoids which are the most active. Several studies have shown the most important flavonoids to be tilianin, luteolin-7-O-glucuronides, apigenin and rosmarinic acid (15-17). But as in all plant extracts, it is really the synergy between the components which is key.

Pharmacological studies have demonstrated the biological activity of this exceptional synergy: researchers have observed antioxidant, anti-hypoxic, immune-modulatory, anti-microbial, and vasodilatory properties (the latter accounting for its traditional use in treating heart and blood pressure problems (18-19).

How should DragonHead Extract be taken?

The recommended dose is two 100mg capsules a day, to be taken in between meals.

Other anti-ageing supplements are available to buy from our catalogue including:

  1. Longevity Nutrients, an enhanced formulation for promoting longevity.
  2. Natural Dopamine Support 400 mg, a wild green oat extract.
  3. Natural Rapalogs, a natural ‘rapalog’ formulation for slowing down ageing.
  4. PQQ & Q10, a synergistic formulation for fighting cognitive impairment (PQQ and co-enzyme Q10).
Composition
Daily dose: 2 capsules
Number of doses per pack: 30
Amount per dose
DracoBelle™ (extract of dragonhead leaf - Dracocephalum moldavica) 200 mg
Other ingredients: white rice flour, acacia gum.

Each capsule contains 100mg of DracoBelle™. DracoBelle™, Mibelle, Switzerland.
Directions for use
Take 2 capsules a day.
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References
  1. Maimaitiyiming D, Hu G, Aikemu A. The treatment of Uygur medicine Dracocephalum moldavica L on chronic mountain sickness rat model. Pharmacoqnosy Magazine. 2014;10:477–82.
  2. DracoBelle™ Nu Key to skin’s beauty by mimicking caloric restriction, [https://haanspecialingredients.nl/framework/files/35/uploads/Brochure_DracoBelle_Nu_.pdf]
  3. Leanne M. Redman, Steven R. Smith, Jeffrey H. Burton, Corby K. Martin, Dora Il'yasova, Eric Ravussin. Metabolic Slowing and Reduced Oxidative Damage with Sustained Caloric Restriction Support the Rate of Living and Oxidative Damage Theories of Aging. Cell Metabolism, 2018; DOI: 10.1016/j.cmet.2018.02.019
  4. Heilbronn LK, de Jonge L, Frisard MI, DeLany JP, LarsonMeyer DE, Rood J, Nguyen T, Martin CK, Volaufova J, Most MM, Greenway FL, Smith SR, Deutsch WA, Williamson DA, Ravussin E (2006) Effect of 6-month calorie restriction on biomarkers of longevity, metabolic AGE (2011) 33:15–31 29 adaptation, and oxidative stress in overweight individuals: a randomized controlled trial. J Am Med Assoc 295 (21):2482–2482
  5. Blanc S, Schoeller D, Kemnitz J, Weindruch R, Colman R, Newton W, Wink K, Baum S, Ramsey J (2003) Energy expenditure of rhesus monkeys subjected to 11 years of dietary restriction. J Clin Endocrinol Metab 88(1):16–23
  6. Greer EL, Oskoui PR, Banko MR, et al. The energy sensor AMP-activated protein kinase directly regulates the mammalian FOXO3 transcription factor. J Biol Chem 2007 ; 282 : 30107–30119.
  7. Greer EL, Dowlatshahi D, Banko MR, et al. An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C. elegans. Curr Biol 2007 ; 17 : 1646–1656.
  8. Brunet A, Sweeney LB, Sturgill JF, et al. Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase. Science 2004 ; 303 : 2011–2015. [CrossRef] [PubMed] [Google Scholar]
  9. Motta MC, Divecha N, Lemieux M, et al. Mammalian SIRT1 represses forkhead transcription factors. Cell 2004 ; 116 : 551–563.
  10. Hwangbo DS, Gershman B, Tu MP, et al. Drosophila dFOXO controls lifespan and regulates insulin signalling in brain and fat body. Nature 2004 ; 429 : 562–566.
  11. Giannakou ME, Goss M, Junger MA, et al. Long-lived Drosophila with overexpressed dFOXO in adult fat body. Science 2004 ; 305 : 361.
  12. Henderson ST, Johnson TE. daf-16 integrates developmental and environmental inputs to mediate aging in the nematode Caenorhabditis elegans. Curr Biol 2001 ; 11 : 1975–1980.
  13. Willcox BJ, Donlon TA, He Q, et al. FOXO3A genotype is strongly associated with human longevity. Proc Natl Acad Sci USA 2008 ; 105 : 13987–13992
  14. Flachsbart F, Caliebe A, Kleindorp R, et al. Association of FOXO3A variation with human longevity confirmed in German centenarians. Proc Natl Acad Sci USA 2009 ; 106 : 2700–2705.
  15. Jiang W, He CH, Xing JG. Preparation technology of Dracocephalum moldevica total flavonoids pellets and its release mechanism. Chinese Traditional and Herbal Drugs. 2013;44:26–29.
  16. González-Trujano ME, Ponce-Muñoz H, Hidalgo-Figueroa S. Depressant effects of Agastache Mexicana methanol extract and one of major metabolites tilianin. Asian Pacific Journal of Tropical Medicine. 2015;8:185–90.
  17. Yang, L. N., Xing, J. G., He, C. H., Wu, T., The phenolic compounds from Dracocephalum moldavica L. Biochem. Syst. Ecol. 2014, 54, 19–22.
  18. Zeng, Q., Jin, H. Z., Qin, J. J., Fu, J. J., Hu, X. J., Liu, J. H., Yan, L., Chen, M., Zhang, W. D., Chemical constituents of plants from the genus Dracocephalum. Chem. Biodiv. 2010, 7, 1911–1929.
  19. Dastmalchi, K., Dorman, H. D., Laakso, I., Hiltunen, Raimo., Chemical composition and antioxidative activity of Moldavian balm (Dracocephalum moldavica L.) Food Sci. Technol. Int. 2007, 40, 1655– 1663.
  20. Michan S, Sinclair D. Sirtuins in mammals : Insights into their biological function. Biochem J 2007;404:1-13
  21. Bordone L, Cohen D, Robinson, et al. SIRT1 transgenic mice show phenotypes resembling calorie restriction. Aging Cell 2007;6:759-67

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