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Strona główna Kupuj przez tematyka zdrowotna Zwalczanie stanów zapalnych CBD 6% + Inflarelief
CBD 6% + Inflarelief
CBD 6% + Inflarelief CBD 6% + Inflarelief CBD 6% + Inflarelief
CBD 6% + Inflarelief
Zwalczanie stanów zapalnych Opinie klientów
62.00 €(69.27 US$) na stanie
Opis
Enhanced formulation for inflammation problems
  • Developed using the latest scientific advances.
  • Associated with an increase in the immune response.

CBD hemp oil standardised to 6.4% cannabidiol (CBD)

  • 5mg of CBD per softgel
  • Broad-spectrum dietary supplement: also contains all the non-psychotropic phytocannabinoids found in Cannabis sativa (cannabinol, cannabigerol, tetrahydrocannabivarin…)
  • Contains no psychotropic substances (THC)
  • CBD oil effects include relief of chronic pain, inflammation and inner restlessness (multiple benefits)
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Lista życzeń
CBD Oil 6 %

What is CBD?

Cannabidiol (CBD) is a phytocannabinoid molecule found in hemp (Cannabis sativa), just like the well-known psychotropic substance, tetrahydrocannabinol (THC). However unlike THC, CBD has no narcotic properties.

THC was the first psychoactive ingredient to be discovered in marijuana (1-3), but it was only in the 1990s that scientists identified the endogenous signalling system now known as the endocannabinoid system. This is a collection of endogenous messengers (endocannabinoids) and specific receptors located on external cell membranes (CB1 and CB2 receptors).

It works on a simple principle: when the body deems it necessary, endocannabinoid messengers are produced which bind to their corresponding receptors, triggering various cellular responses such as stimulation of appetite, limitation of synaptic transmission, anti-nociceptive effects (pain relief), hypothermia or reduction of spontaneous locomotion (4).

We know, for example, that endocannabinoids are effective at inhibiting the transmission of small diameter nociceptive fibres (which are involved in the pain process) and at reducing the release of neurotransmitters such as substance P, which are responsible for the transmission of pain. What’s less straightforward is how this system influences several complex mechanisms such as neuroplasticity, apoptosis, neuro-inflammation and traumatic memory.

It so happens that plants produce molecules that have a strong resemblance to endocannabinoids, so much so that they are able to bind to the same receptors (with varying degrees of affinity). Some of them, including THC, produce cellular responses which are very similar to – or even greater than - those triggered by endocannabinoids.

Cannabis contains more than 200 types of molecule that mimic endocannabinoids, including cannabidiol (CBD) which may account for up to 40% of the plant’s dry extract.

How does CBD work? What are its benefits?

The CB1 and CB2 receptors to which endocannabinoids and phytocannabinoids bind are not randomly located in the body. They’re primarily found on the surface of cells of the human brain, central nervous system and immune system tissues. The hippocampus (particularly the dentate gyrus) as well as the Globus pallidus which controls movements (5) have a very high concentration of CB1 receptors, whereas immune tissue has a higher density of CB2 receptors (6). Their specific siting suggests that cannabinoids are involved in modulating memory, emotion, pain (chronic, inflammatory and neuropathic) (7-8) and movements (9-10).

CBD binds more to CB2 receptors, and THC to CB1 receptors. When CBD binds to its receptors, it triggers a chain reaction which results in a decrease in the release of neurotransmitters.

The binding of CBD to CB2 receptors appears primarily to reduce the inflammatory response. This involves multiple cellular targets and leads to a rise in BDNF (a protein that encourages the growth and differentiation of new neurons), a reduction in microglial cells and a fall in pro-inflammatory mediators (11-13). It is this anti-inflammatory effect which makes CBD so useful for pain relief.

CBD thus helps lower the production of inflammatory cytokines, maintain cerebral circulation during ischaemic events and reduce neuro-inflammation (14). It also helps increase levels of adenosine in the brain which is associated with neuroprotection and decreased inflammation (15). In addition, it helps to activate PPARs (16), proteins that act as transcription factors of certain genes involved in inflammation and pain transmission.

Several studies have shown it to have additional benefits: it promotes vasodilation (17-18) and helps reduce reactive oxygen species (ROS) as well as lipid peroxidation (19-21). CBD is also involved in modulating receptors outside of the endocannabinoid system. For example, serotonin receptors also appear to play a part in CBD’s benefits and therapeutic properties.

CBD can reduce the intensity and impact of symptoms associated with chronic anxiety and stress (22-23). Human imaging has shown that CBD affects areas of the brain involved in the neurobiology of several psychiatric disorders. According to one study, a single dose of CBD administered orally to healthy volunteers altered resting activity in limbic and paralimbic regions of the brain (24-25).

Research has also shown a potential reduction in memory associated with traumatic experience.

The use of CBD oil for pain or anxiety is currently enjoying sustained popularity. Though media attention has played a substantial part in this, it is CBD’s properties and benefits, which are now well-documented, which are largely responsible for its success. Following is a summary of the properties variously demonstrated by in vitro, animal and clinical studies (26):

  • pain relief;
  • an effect on receptors in the brain, particularly serotonin, a neurotransmitter that regulates mood and social behaviour;
  • anti-inflammatory potential against cytokines;
  • neuroprotective benefits;
  • anxiolytic and stress-fighting properties;
  • anti-addiction benefits;
  • an effect on certain stress responses.

How is CBD Oil 6% produced?

Following extraction, CBD is diluted in hemp seed oil.

Ordinarily, hemp seed oil contains very little CBD (0.0025%). CBD is mostly found in the flowers of Cannabis sativa and, to a lesser degree, the leaves, but not in the seeds. CBD Oil 6% therefore contains hemp seed oil to which CBD extracted from hemp flowers has been added.

When cannabis grows, it produces THC-A and CBD-A, not THC or CBD. It is only when the two molecules are heated that they are decarboxylated into their active forms (27). The conversion of CBD-A into CBD can also be achieved more slowly by exposing the molecule to light, to heat (the temperature of gastric fluids is 37°C) or over time (28). CBD Oil 6% contains CBD and not CBD-A, as well as small amounts of a number of other phytocannabinoids. There is currently no product on the market offering greater CBD oil benefits.


Are there any CBD oil side-effects?

The hemp used in this product contains no THC. . It therefore has no narcotic effect and has an excellent safety profile in humans.

Once ingested, CBD is quickly distributed around the body. Its lipophilic nature means it rapidly crosses the blood-brain barrier to reach tissues in the brain. It does not alter the heart rate and affects neither blood pressure nor body temperature. The half-life of CBD is 9 hours, after which it is eliminated vie urine in a metabolised form.

Its softgel format and the fact that SuperSmart guarantees the purity of its ingredients means there are no particular contraindications associated with its use. To date, there have been no public health problems reported with the use of a THC-free hemp oil standardised in CBD.

What other steps can be combined with taking CBD Oil 6%?

CBD Oil 6% can be combined with InflaRelief Formula, an enhanced formulation for relief of inflammation problems, with Natural Pain Relief, a natural, universal painkiller, and with Posinol 50 mg, an extract of Apocynum venetum which promotes mental relaxation.

Notes

This product should not be used as a substitute for a varied, balanced diet and a healthy lifestyle. It’s important to follow the guidelines on how to take it and the recommended dose, and to use it by the ‘best before’ date. It is not recommended for women who are pregnant or breastfeeding, or for children under 15. Keep out of children’s reach. Store in a cool, dry place.

References

  1. Gaoni Y, Mechoulam R. Isolation structure and partial synthesis of an active constituent of hashish. J Am Chem Soc. 1964;86:1646–7.
  2. Mechoulam R, Braun P, Gaoni YA. Stereospecific synthesis of (-)-delta 1- and (-)-delta 1(6)-tetrahydrocannabinols. J Am Chem Soc. 1967;89:4552–4.
  3. Mechoulam R, Shvo Y, Hashish I. The structure of cannabidiol. Tetrahedron. 1963;19:2073–8.
  4. Venance L, Maldonado R, Manzoni O. Le système endocannabinoïde central. Med Sci (Paris) 2004 ; 20 : 45-53.
  5. Pertwee RG. The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: Δ9-tetrahydrocannabinol, cannabidiol and Δ9-tetrahydrocannabivarin. Br J Pharmacol. 2008;153:199–215.
  6. Pettit DAD, Harrison MP, Olson JM, Spencer RF, Cabral GA. Immunohistochemical localization of the neural cannabinoid receptor in rat brain. J. Neurosci Res. 1998;51:391–402
  7. Hill KP. Medical marijuana for treatment of chronic pain and other medical and psychiatric problems: A clinical review. JAMA. 2015;313:2474–83
  8. Rog DJ, Nurmikko TJ, Friede T, Young CA. Randomized, controlled trial of cannabis-based medicine in central pain in multiple sclerosis. Neurology. 2005;65:812–9
  9. Portella G, Laezza C, Laccetti P, De Petrocellis L, Di Marzo V, Bifulco M. Inhibitory effects of cannabinoid CB1 receptor stimulation on tumor growth and metastatic spreading: Actions on signals involved in angiogenesis and metastasis. FASEB J. 2003;17:1771–3
  10. Freund TF, Katona I, Piomelli D. Role of endogenous cannabinoids in synaptic signaling. Physiol Rev. 2003;83:1017–66.
  11. Nestler EJ, Barrot M, DiLeone RJ, Eisch AJ, Gold SJ, Monteggia LM. Neurobiology of depression. Neuron. 2002;34:13–25
  12. Wang Q, Shao F, Wang W. Maternal separation produces alterations of forebrain brain-derived neurotrophic factor expression in differently aged rats. Front Mol Neurosci. 2015;8:49
  13. Wee N, Kandiah N, Acharyya S, Chander RJ, Ng A, Au WL, et al. Depression and anxiety are co-morbid but dissociable in mild Parkinson's disease: A prospective longitudinal study of patterns and predictors. Parkinsonism Relat Disord. 2016;23:50–6
  14. Camposa AC, Fogac MV, Sonegoa AB, Guimarãesa FS. Cannabidiol, neuroprotection and neuropsychiatric disorders. Pharmacol Res. 2016;112:119–27
  15. Castillo A, Tolóna MR, Fernández-Ruizb, J, Romeroa J, Martinez-Orgadoa J. The neuroprotective effect of cannabidiol in an in vitro model of newborn hypoxic–ischemic brain damage in mice is mediated by CB2 and adenosine receptors. Neurobiol Dis. 2010;37:434–40.
  16. Esposito G, Scuderi C, Valenza M, Togna GI, Latina V, et al. Cannabidiol reduces ab-induced neuroinflammation and promotes hippocampal neurogenesis through PPARc involvement. PLoS One. 2011;6:e28668.
  17. Hillard CJ. Endocannabinoids and vascular function. J Pharmacol Exp Ther. 2000;294:27–32.
  18. Schultes RE. Hallucinogens of Plant Origin.Science. 1969;163:245–54.
  19. Esposito G, Scuderi C, Savani C, Steardo L, Jr, De Filippis D, Cottone P, et al. Cannabidiol in vivoblunts beta-amyloid induced neuroinflammation by suppressing IL-1ß and iNOS expression. Br J Pharmacol. 2007;151:1272–9.
  20. Hampson AJ, Grimaldi M, Axelrod J, Wink D. Cannabidiol and (-)Δ9-tetrahydrocannabinol are neuroprotective antioxidants. Proc Natl Acad Sci USA. 1998;95:8268–73.
  21. Iuvone T, Esposito G, Esposito R, Santamaria R, Di Rosa M, Izzo AA. Neuroprotective effect of cannabidiol, a non-psychoactive componentpCannabis sativa, on ß-amyloid-induced toxicity in PC12 cells. J Neurochem. 2004;89:134–41.
  22. Campos AC, Moreira FA, Gomes FV, Del Bel EA, Guimarães FS. Multiple mechanisms involved in the large-spectrum therapeutic potential of cannabidiol in psychiatric disorders. Philos Trans R Soc Lond B Biol Sci. 2012;367:3364–78.
  23. Bergamaschi MM, Queiroz RHC, Chagas MHN, de Oliveira DCG, De Martinis BS, Kapczinski F, et al. Cannabidiol reduces the anxiety induced by simulated public speaking in treatment-naive social phobia patients. Neuropsychopharmacology. 2011;36:1219–26.
  24. Crippa JA, Zuardi AW, Garrido GE, Wichert-Ana L, Guarnieri R, Ferrari L, et al. Effects of cannabidiol (CBD) on regional cerebral blood flow. Neuropsychopharmacology. 2004;29:417–26
  25. Fusar-Poli P, Crippa JA, Bhattacharyya S, Borgwardt SJ, Allen P, Martin-Santos R, et al. Distinct effects of Δ9-tetrahydrocannabinol and cannabidiol on neural activation during emotional processing. Arch Gen Psychiatry. 2009;66:95–105.
  26. Pisanti, S., et al., Cannabidiol: State of the art and new challenges for therapeutic applications. Pharmacol Ther, 2017. 175: p. 133-150
  27. Gowran A, Noonan J, Campbell VA. The multiplicity of action of cannabinoids: Implications for treating neurodegeneration. CNS Neurosci Ther. 2011;17:637–44.
  28. Russo, E.B., Cannabidiol Claims and Misconceptions.Trends in pharmacological sciences, 2017. 38(3): p. 198-201.
Informacje żywienioweCBD Oil 6 %
Daily dose: 2 softgels
Number of doses per pack: 15

Amount
per dose

Cannabidiol (CBD) from 156.25mg of non-psychotropic hemp oil standardised to 6.4% CBD 10mg
No RDA established. Other ingredients: organic olive oil.
Sposób stosowaniaCBD Oil 6 %
Adults. Take 2 softgels a day. Each softgel contains 78.125mg of hemp oil standardised to 6.4% cannabidiol (CBD), ie, 5mg of CBD.
This supplement contains no psychotropic substances.
InflaRelief FormulaTogether with oxidation and glycation, inflammation is one of the three basic mechanisms of ageing. Chronic inflammation is the source of many degenerative disorders and is characteristic of an ageing body. It is therefore a good idea to avoid it. Supplementation is a more effective option than drugs and does not have the latter’s side-effects

InflaRelief Formula, a supplement for inflammation problems

¤ New InflaRelief Formula combines even more natural and powerful nutrients (12 instead of 9) than before (with a higher daily dose). Together, they provide the body with an effective and polymorphic response to the inflammatory process in its many forms.

¤ Perluxan® is a standardised hop cone extract. Its alpha acids are powerful inhibitors of pain-inducing chemicals. Unlike the whole hop plant, this particular extract has no oestrogenic or sedative effects.

¤ Standardised nettle extract has scientifically-supported pain-relief and anti-inflammatory properties.

¤ Cat’s claw extract (Uncaria tomentosa), standardised in oxindole alkaloids, has regenerative and anti-inflammatory properties that benefit the joints in particular; it is also a potent stimulant of the immune system.

¤ "C3 Complex" curcuma extract contains 95% curcuminoids which are antioxidant, anti-inflammatory and Cox-2 inhibitors.

¤ Tulsi is a plant that has been used in Tibetan medicine for thousands of years. It has wide-ranging properties relating to anything from simple physical and mental weakness to acute stress, depression and many inflammation-related processes, both acute and chronic.

¤ Bromelain, a pineapple-derived proteolytic enzyme complex, is generally used for digestive inflammation problems and oedema, and to prevent blood clots which can affect the cardiovascular system.

¤ Ginger root extract, standardised in gingerols and shogaols, controls inflammation-mediators by inhibiting pro-inflammatory enzymes Cox 1 and 2 and lipoxygenase. This extract specifically benefits joints such as the hips and knees.

¤ Quercetin is a natural, antioxidant flavonol and polyvalent reliever, used particularly for respiratory and digestive allergies.

¤ Rutin, extracted from the aromatic shrub Ruta graveolens, has antioxidant and anti-inflammatory effects; it is vasoprotective and antithrombotic.

¤ Rosemary has rosmarinic acid with potent tissue-protective, antioxidant, anti-inflammatory and anti-allergy properties.

¤ 5-Loxin®, a specific extract of Boswellia serrata, provides 30% acetyl-keto-beta-boswellic acid (AKBA); a potent anti-inflammatory, it is as effective as some drugs, and is particularly good for degenerative joint disorders.

¤ Bioperine®, a black pepper extract standardised in piperine, has anti-inflammatory properties itself and also makes other ingredients more active enhancing their absorption and bioavailability.

With its combination of ingredients and wide spectrum action, InflaRelief Formula is an original, polyvalent and powerful supplement that effectively combats and neutralises the many mechanisms of inflammation - the ‘silent enemy’.
Informacje żywienioweInflaRelief Formula
Daily dose : 6 capsules
Number of doses per pack : 30
Amount per dose
Perluxan® (Extract of hop cone standardised to 30 % alpha and iso-alpha acids) 300 mg
Nettle extract 16:1 250 mg
Cat’s claw extract standardised to 3 % oxindole alkaloids 250 mg
Curcumin C3 Complex (35:1 extract of Curcuma longa standardised to 95 % curcuminoids) 250 mg
Tulsi dry extract (Ocimum sanctum L.) standardised to 2.5 % ursolic acid 250 mg
Bromelain 2400 GDU/g 250 mg
Ginger root extract standardised to 5 % gingerols and 1 % shogaols 250 mg
Quercetin 200 mg
Rutin 200 mg
Rosemary extract standardised to 6 % rosmarinic acid 150 mg
5-Loxin® (Boswellia serrata extract standardised to 30 % acetyl-11-keto-beta-boswellic acid) 100 mg
Bioperine® (Black pepper extract (Piper nigrum) standardised to 95 % piperine) 5 mg
Other ingredients : Acacia gum, rice flour.
Perluxan®, Pharmachem, USA. - Curcumin C3 Complex, Bioperine®, Sabinsa Corp, India - 5-Loxin®, Pl Thomas, USA.
Sposób stosowaniaInflaRelief Formula
Adults. Take 6 vegetarian capsules a day, spread over two or three doses or as advised by your therapist.

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Wszelkie prawa do powielania zastrzeżone
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