Untamed HIP & JOINT (Intensive Equine Joint Support)

 

Joint diseases like equine arthritis are caused by various degenerative factors, such as: inflammation, intensive training, genes, infection, injuries, weight, diet, heavy metals and chemicals.

Untamed HIP & JOINT (Equine) is scientifically formulated with a multi-functional approach to effectively target these factors and proactively promote your horse’s joint health. It provides the highest concentrations of anti-inflammatory and regenerative nutrients to help your Wild at Heart One keep enjoying a healthy and fulfilled life for as long as possible.

INDICATIONS
• 3X STRENGTH Natural Anti-inflammatory – HIGH POTENCY BOSWELLIA and TURMERIC EXTRACTS
• Effectively combats pain, swelling and degeneration in joints
• Promotes cellular regeneration of joint tissue
• Improves joint strength and flexibility for optimal mobility
• Regulates immune responses, supporting auto-immune related joint treatment
• It fights systemic inflammation and improves overall health, vitality & longevity.

Other Benefits
• Supports Natural Detoxification Processes
• Promotes Organ Health
• Supports Healthy Digestive Function
• Promotes Nerve Health & Emotional Well-being
• Enhances Immune Support
• Anti-oxidant & anti-inflammatory Support
• Rich in Plant-based mineral, vitamins, amino acids, and anti-oxidants

*None of these ingredients are listed in the FEI Equine Prohibited Substances Database
*Registered – Can be Claimed from Medical Aid Funds

 

R930.00R2,537.00

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Description

Joint deterioration in horses is a complex and progressive process that can result in severe pain, inflammation, and impaired mobility. This can manifest as irritability, limping, behavioural issues, and even early retirement from work or sports. In some unfortunate cases, it may even necessitate euthanasia. However, with proactive management strategies, horses can continue to live comfortably for many years following a joint disease diagnosis.

Joint diseases are caused by various degenerative factors like: inflammation, intensive training, genes, infection, injuries, weight, diet, heavy metals and chemicals. UNTAMED HIP & JOINT (Equine) is scientifically formulated with a multi-functional approach to target these factors and proactively promote your companion’s joint health.

UNTAMED HIP & JOINT(Equine) provides your horse with 3X strength natural anti-inflammatory action, with the added benefits of high-potency Boswellia and Curcumin extracts. Together with Glucosamine, these extracts are specifically selected for their proven safety and effectiveness in:
– Combatting pain, swelling & degeneration in joints
– Promoting regeneration of joint tissue including cartilage, bone, muscle, ligaments & tendons
– Promoting joint strength & flexibility for optimal mobility
– Regulating immune responses for auto-immune related joint treatment

To give your horse the most comprehensive natural equine arthritis treatment, UNTAMED HIP & JOINT (Equine) is further fortified with a nutrient-rich, and anti-inflammatory superfood, Spirulina. In synergy with Boswellia and Curcumin extracts, Spirulina enhances overall health, vitality, and longevity.By addressing not only the specific joint condition but also supporting the horse’s general well-being,you can help your horse feel and perform at their best.

Remember, protecting your horse’s joints from an early age is vital. Early intervention and treatment play a crucial role in increasing your companion’s longevity.

Product Info

• Glucosamine Potassium Sulfate 5000mg/10g
• Boswellia 65% extract 600mg/10g
• Turmeric/Curcumin 95% extract 600mg/10g
• Spirulina (Arthrospira platensis) 3800mg/10g
***NO artificial flavours, preservatives or additives! 

Loading (35 days):
Horses <500 kg:1 scoop 2x daily (20g)
Horses >500 kg:1.5 scoop 2x daily (30g)
Maintenance:
Horses <500 kg:1/2 scoop 2x daily (10g)
Horses >500 kg:1 scoop 2x daily (20g)

*Horses can be maintained on the loading phase if needed.
*Mix into feed, starting with small amounts.
*Can add coconut oil to supplement before mixing into feed. 

PLEASE NOTE
Do not use with anti-coagulant medication (like Warfarin or Heparin).  Not recommended for animals with cholelithiasis. Not for use during pregnancy or nursing. This product nor its information, is intended to substitute the professional advice or prescription of your veterinarian. Store at cool, dry temperatures. 

ANTI-INFLAMMATORY PROTECTION

Inflammation is a natural process by which the body promotes healing, and protects itself against damage caused by injury, infection, free radicals and foreign substances. There are however many risk factors, as those mentioned above, that induce chronic inflammation and promote infiltration of inflammatory agents into the joints. If not controlled, these agents cause constant swelling, pain, and eventually degeneration of joint tissue.  Consequently, arthritis sets in, with a debilitating effect on mobility and well-being.

CURCUMIN 95% extract (Curcuma longa) is a highly concentrated extract from turmeric, and one of the most researched, and effective anti-inflammatory plant extracts.  Curcumin reduces inflammation by multiple mechanisms like inhibiting pro-inflammatory signaling, inhibiting immune cell migration to the active site of inflammation, and reducing excessive existing inflammation by decreasing the activity of inflammatory enzymes1-7. Curcumin illustrates pronounced potential to reduce joint pain, enhance articular function, and improve quality of movement10-12.

BOSWELLIA (Boswellia serrata) is a powerful anti-inflammatory plant extract.  It demonstrates pronounced clinical efficiency in the treatment of painful inflammatory conditions like muscle injuries, arthritic diseases.    Boswellia’s mechanisms of action in arthritic treatment include: inhibition of inflammatory agents, improvement of blood circulation to the joints, alleviation of pain, and decreased joint swelling.  In contrast to non-steroidal anti-inflammatory drugs (NSAIDS) which disrupt glycosaminoglycan synthesis, Boswellia inhibits inflammation-induced degeneration of glycosaminoglycans levels, supporting the structural strength of the joints. 30,31 Research validates that Boswellia can significantly improve joint flexibility and mobility32.

SPIRULINA provides exceptional antioxidant activity against oxidative damage caused by physiological processes, heavy metals and toxic chemicals.  Oxidative stress causes cellular dysfunction and tissue degeneration, increasing the risk of various chronic diseases, including arthritis.  Spirulina activates antioxidant enzymes, inhibits fat oxidation and oxidative DNA damage, and scavenges inflammatory free radicals23. Its antioxidant properties in combination with its anti-inflammatory actions, may protect mobility by reducing exercise-induced oxidative muscle damage24, and alleviating arthritic symptoms like swelling, inflammation, cartilage degeneration, and liver stress29,55.

HEALTHY CARTILAGE and STRUCTURAL SUPPORT

During aging or reduced activity, muscle mass and strength declines, and body weight may unhealthily increase.  This predisposes the animal to decreased joint stability and misalignment.  Consequently, with increased mechanical stress, degenerative inflammation sets in, deteriorating cartilage and joins.

SPIRULINA:  UNTAMED HIP & JOINT – Equine is fortified with Spirulina, a complete and nutrient-rich protein source.  It is rich in amino acids, which inhibit muscle degeneration, and stimulate muscle protein synthesis, helping to maintain your horse’s lean muscle mass and strength. Enhancing the strength of the muscles surrounding the joints may improve structural joint support, and decrease the risk of joint injuries51,52 Protein also provides amino acids for proteoglycan and collagen production, which are essential building blocks in the extracellular matrix53. The extracellular matrix is present in all tissues, like the joints, muscles, tendons, cartilage, skin, and organs.  It provides structural support to the tissues and maintains proper hydration.  It is also responsible for vital biochemical and biomechanical processes involved in healthy tissue development.

CURCUMIN is well researched for its powerful anti-inflammatory actions.  And with its protective properties on cartilage8, it has exceptional medical value in the treatment of arthritic diseases. Research shows that highly concentrated curcumin extract stimulates the production of glycosaminoglycans, chondrocytes, and type II collagen which are involved in the formation and structural integrity of cartilage9.  It also inhibits inflammation-induced degeneration of cartilage and chondrocytes13,14.  Curcumin further inhibits joint inflammation and joint destruction by inhibiting bone resorption osteoclast cells, and blocking expression of genes, inflammatory enzymes like COX-2, and other inflammatory mediators that promotes joint degeneration25.

GLUCOSAMINE POTASSIUM SULPHATE is a superior form of glucosamine due to its enhanced bio-availability. It consists of a structural amino acid, glucosamine, which is abundantly found in joint cartilage, synovial fluid in the joints, and in the intervertebral discs.   It also contains Sulphur which is required by every cell in the body for efficient function.  Sulphur is a vital element for healthy connective tissues, it is utilized in detoxification of toxins, is involved in cellular respiration, promotes healing, and helps to relieve symptoms of arthritis. Research illustrates that Glucosamine Sulphate’s efficacy is superior to Chondroitin Sulphate in arthritic conditions. It has a growth-promoting effect on cartilage, and delays cartilage degeneration by various effective antioxidant and anti-inflammatory mechanisms. Studies conclude that long term supplementation with Glucosamine Sulphate clinically benefits arthritis sufferers by reducing pain, reducing arthritis progression, enhancing joint function and mobility, and decreasing the risk of total joint replacement15.  

IMMUNE MODULATION

The immune system is a complex defense system against foreign substances and pathogenic microorganisms.  The immune system produces antibodies from B lymphocytes (white blood cells), which bind to, and destroy invading organisms.  These antibodies are stored in the body to recognize, and destroy a recurring pathogen more effectively during follow up invasion.  T lymphocytes destroy invading pathogens by releasing toxic chemicals. They also release messenger chemicals to attract macrophagic white blood cells which engulf and kill pathogens.  T lymphocytes regulate immune responsiveness to specific agents, and can be divided into Th1 and Th2 cells.  Th1 cells are proposed to mostly mediate immune protection against intracellular viruses and certain bacteria, destroy cancerous cells, and activate delayed hypersensitivity skin reactions. Th2 cells mediate immune protection against extracellular bacteria, parasites, allergens, and toxins. Immune dysfunction and over expression of Th1 cells may result in a proinflammatory state and organ specific autoimmunity.  Overexpression of Th2 is indicated in systemic autoimmunity and chronic allergy related conditions. 

CURCUMIN regulates Th1 and Th2 immune responses, as well as production of inflammatory mediators.  By modulating immune function and inhibiting inflammation, Curcumin demonstrates marked clinical efficacy in the treatment of osteo- and rheumatoid arthritis26,27,49,50

SPIRULINA is well researched for its immune modulating activities.  It may enhance immune function by increasing cellular destruction of infectious agents, increasing antibody protection, and promoting production of other immune modulating chemicals.  Spirulina can also reduce immune system hyper-responsiveness as in the case of allergies, arthritis, and organ transplants54

SUPER FOOD Complex

UNTAMED HIP & JOINT – Equine is fortified with superfood, SPIRULINA, which functions in synergy with Curcumin and Boswellia to enhance health and restoration on various physiological levels.

SPIRULINA has exceptional nutritional properties with its rich composition of antioxidants, protein, fatty acids, fiber, vitamins and minerals. It serves as a prebiotic, supporting a healthy digestive environment, enhances physical performance 45,46, improves insulin sensitivity and blood glucose control42,44, supports immune function, protecting against allergies47, provides marked antioxidant protection, supports detoxification of toxic chemicals and heavy metals like fluoride, lead, cadmium, mercury and arsenic34-38, promotes liver health48, exerts neuroprotective effects, reducing the risk of cognitive decline, Alzheimer’s’ and Parkinson’s disease39-41, and reduces systemic degenerative inflammation.  Spirulina enhances overall health and well-being, and increases protection against various chronic disease like cardiovascular disease 42,43, skin conditions, allergies, cancer, liver disease, and joint disease 33.

Spirulina, is considered a complete protein source, containing all amino acids required for healthy physiological function.  Protein is an essential component of all living cells, and a substrate for a multitude of physiological processes.  As a protein, Spirulina has significant anti-inflammatory, antioxidant and immune modulating properties.  It enhances protection against toxins, viruses, and bacteria, reduces the risk of various cancers, promotes cardiovascular-, liver-, digestive- and hormonal health, maintains healthy skin and bone, supports healthy body weight, and promotes a sense of well-being.  Spirulina contains amino acids which form vital structural components in muscle cells, ligaments and tendons. Insufficient protein intake predisposes the animal to poor condition, muscle wasting, osteoporosis, impaired recovery after injury or training, and decreased mental ability. Protein rich diets promote a leaner and healthy body condition, and enhance muscle protein synthesis. Sufficient protein enables your horse to improve muscle composition and physical strength, especially when combined with regular exercise 56,57

Turmeric is a highly valued medicinal herb. Owing to CURCUMIN, its active constituent, it has been used for thousands of years for its remarkable medicinal benefits. Unfortunately, turmeric is not absorbed very well, and one has to take a large amount of turmeric powder to be of systemic benefit.  Hence the production of 95% Turmeric extract which provides pure curcumin, with higher medicinal significance in the body.  

Actions and health benefits of Curcumin 58-98

  • Antiallergenic: Turmeric is well known as an immunomodulatory herb. Curcumin alleviates symptoms associated with allergic immune responses by regulating Th-1(inflammatory) and Th-2 cytokine (autoimmunity/allergy) responses, inhibiting IgE levels, and inhibiting mast cell degranulation which releases histamine.  These properties give curcumin great potential for clinical management of allergic reactions like asthma, food allergies and allergy related skin conditions. 
  • Antimicrobial:  Curcumin provides broad-spectrum antimicrobial protection against bacteria like Staphylococcus epidermis, Staphylococcus aureus, Klebsiela pneumoniae, Helicobacter pylori,  Escherichia coli, Salmonella and many others; viruses like influenza viruses, herpes, coxsackie, hepatitis viruses, papilloma viruses, encephalitis viruses and many more; fungi like Cryptococcus neoformans, Candida albicans, and other skin fungi like T rubrum, T. mentagrophytes, E. floccosum and M. gypseum, and parasites Schistosomas, Toxocara canis, Eimeria species, Plasmodium, Trypanosoma, Giardia lamblia, Leishmania and Cryptosporidium. 
  • Powerful anti-inflammatory and antioxidant:  Curcumin reduces inflammation by multiple mechanisms like inhibiting pro-inflammatory signalling, inhibiting immune cell migration to the active site of inflammation, and reducing excessive existing inflammation by decreasing the activity of inflammatory enzymes.
  • Neuroprotective:  Curcumin can protect nerve cells against inflammation and degeneration caused by multiple pathological agents including toxins, stress related high cortisol levels, and age-related degenerative conditions like Alzheimer’s and Parkinson’s disease.
  • Protect against heart disease:  Curcumin provides protection against cardiac hypertrophy, inflammation, atherosclerosis, blood clot formation and high cholesterol.
  • Antidiabetic: Curcumin illustrates promising protection against insulin resistance, diabetes and its associated inflammatory pathways.
  • Antiarthritic:  Curcumin is well researched for its powerful anti-inflammatory actions which, in addition to its protective properties on cartilage, adds exceptional medical value to this plant extract for the treatment of arthritic diseases. Research shows that a highly-concentrated curcumin extract stimulates the production of glycosaminoglycans and chondrocytes, which are involved in the formation and structural integrity of cartilage.  Curcumin supplementation can reduce joint pain, enhance articular function, and improve quality of movement.
  • Anticancer:  Research illustrates that high dose of concentrated Curcumin extract can inhibit the growth of various cancers and enhance the anticancer effects of chemotherapy drugs and radiation.  Curcumin, may alleviate the risk of cancer by supporting the natural defense mechanisms of a mammal by increasing antioxidant protection, inhibiting inflammatory degeneration, enhancing liver detoxification by down-regulating Phase I and enhancing Phase II detoxification of cancer-causing agents like cigarette smoke, benzopyrene, and DMBA, and inhibiting cancer cell development and spreading.
  • Accelerates wound healing: Curcumin exerts a significant wound healing effect owing to its anti-oxidant, anti-inflammatory, anti-infectious, and immune-modulating characteristics. Curcumin targets various stages of wound healing. It promotes the removal of dead tissue from the site of injury, formation of new blood vessels in that area, granulation tissue, deposition of collagen for increased tissue strength and integrity, and wound closure.
  • Enhances skeletal muscle repair: Soft tissue injury is most often related to a sport injury.  The results are swelling, bruising, severe pain, and ultimately diminished muscle function & performance.  The repair process involves tissue degeneration, inflammation, regeneration, and scar tissue formation.  Curcumin promotes healthy muscle repair by supporting balanced and efficient anti-inflammatory-, immune- and anti-oxidant responses,which enhances muscle cell regeneration and accelerates recovery. By modulating inflammation, reducing lactate accumulation and reducing pain following intensive exercise, curcumin facilitates a faster return to training and increases the capacity for higher training intensity.
  • Supports healthy digestive function: Curcumin provides significant anti-inflammatory protection in the digestive tract, alleviating inflammatory damage, abdominal pain and gastric discomfort associated with IBS (irritable bowel syndrome), ulcerative colitis, Crohn’s disease and H. pylori- induced ulcers.

 BOSWELLIA

Boswellic acid, a constituent of Boswellia, has potent anti-inflammatory, expectorant, antiseptic, pain-relieving, antibacterial, anti-anxiety, and anti-neurotic properties.  Clinical studies indicate that Boswellic acids have the ability to modulate many mediators involved in disease progression. It exhibits clinical efficacy in the treatment of conditions like: arthritis, Alzheimer’s disease, asthma, various cancers and tumours, cognitive impairment, atherosclerosis, inflammatory bowel disease, ulcerative colitis, irritable bowel syndrome, bronchitis, sinusitis, diabetes, central nervous system disorders, and psoriasis.99-100

  1. Chun KS, et al Curcumin inhibits phorbol ester-induced expression of cyclooxygenase-2 in mouse skin through suppression of extracellular signal-regulated kinase activity and NF-kappaB activation. Carcinogenesis. 2003.
  2. Kunnumakkara AB, et al. Curcumin potentiates antitumor activity of gemcitabine in an orthotopic model of pancreatic cancer through suppression of proliferation, angiogenesis, and inhibition of nuclear factor-kappaB-regulated gene products. Cancer Res. 2007.
  3. Ponnurangam S, et al Urine and serum analysis of consumed curcuminoids using an IkappaB-luciferase surrogate marker assay. In Vivo. 2010.
  4. Aggarwal S, et al. Curcumin (diferuloylmethane) down-regulates expression of cell proliferation and antiapoptotic and metastatic gene products through suppression of IkappaBalpha kinase and Akt activation. Mol Pharmacol. 2006.
  5. Dileep KV, Tintu I, Sadasivan C Molecular docking studies of curcumin analogs with phospholipase A2. Interdiscip Sci. 2011.
  6. Binion DG, et al. Vascular cell adhesion molecule-1 expression in human intestinal microvascular endothelial cells is regulated by PI 3-kinase/Akt/MAPK/NF-kappaB: inhibitory role of curcumin. Am J Physiol Gastrointest Liver Physiol. 2009.
  7. Kumar A, et al Curcumin (Diferuloylmethane) inhibition of tumor necrosis factor (TNF)-mediated adhesion of monocytes to endothelial cells by suppression of cell surface expression of adhesion molecules and of nuclear factor-kappaB activation. Biochem Pharmacol. 1998.
  8. Henrotin Y, Priem F, Mobasheri A. Curcumin: a new paradigm and therapeutic opportunity for the treatment of osteoarthritis: curcumin for osteoarthritis management. Springerplus 2013; 2: 1-9.
  9. Jurenka JS. Anti-inflammatory properties of curcumin, a major constituent of Curcuma longa: a review of preclinical and clinical research. Altern Med Rev 2009; 14: 141-53.
  10. Belcaro G, Cesarone MR, Dugall M, et al. Efficacy and safety of Meriva, a Curcumin-phosphatidyl choline complex during extended administration in Osteoarthritis patients. Altern Med Rev 2010; 15: 337-44.
  11. Belcaro G, Cesarone MR, Dugall M, et al. Product evaluation registry of a curcumin phosphatidylcholine complex for the complementary management of osteoarthritis. Panminerva Med 2010; 52: 55-62.
  12. Clutterbuck AL, Mobasheri A, Shakibaei M, Allaway D, Harris P. Interleukin 1 beta induced extracellular matrix degradation and glycosaminoglycan release is inhibited by curcumin in an explant of cartilage inflammation. Ann NY Acad Sci 2009; 1171: 428-35.
  13. Shakibaei, M., Schulze-Tanzil, G., John, T. and Mobasheri, A. (2005) Curcumin protects human chondrocytes from IL-l1beta-induced inhibition of collagen type II and beta1-integrin expression and activation of caspase-3: an immunomorphological study. Ann Anat 187: 487–497
  14. Toegel, S., Wu, S.Q., Piana, C., Unger, F.M., Wirth, M., Goldring, M.B. et al. (2008) Comparison between chondroprotective effects of glucosamine, curcumin, and diacerein in IL-1beta-stimulated C-28/I2 chondrocytes. Osteoarthritis Cartilage 16: 1205–1212.
  15. Jerosch J. Effects of Glucosamine and Chondroitin Sulphate on Cartilage Metabolism in OA:  Outlook on Other Nutrient Partners Especially Omega-3 FattyAcids.  International Journal of Rheumatology, 2011; Vol 2011:1-11.
  16. Chun KS, et al Curcumin inhibits phorbol ester-induced expression of cyclooxygenase-2 in mouse skin through suppression of extracellular signal-regulated kinase activity and NF-kappaB activation. Carcinogenesis. 2003.
  17. Kunnumakkara AB, et al. Curcumin potentiates antitumor activity of gemcitabine in an orthotopic model of pancreatic cancer through suppression of proliferation, angiogenesis, and inhibition of nuclear factor-kappaB-regulated gene products. Cancer Res. 2007.
  18. Ponnurangam S, et al Urine and serum analysis of consumed curcuminoids using an IkappaB-luciferase surrogate marker assay. In Vivo. 2010.
  19. Aggarwal S, et al. Curcumin (diferuloylmethane) down-regulates expression of cell proliferation and antiapoptotic and metastatic gene products through suppression of IkappaBalpha kinase and Akt activation. Mol Pharmacol. 2006.
  20. Dileep KV, Tintu I, Sadasivan C Molecular docking studies of curcumin analogs with phospholipase A2. Interdiscip Sci. 2011.
  21. Binion DG, et al. Vascular cell adhesion molecule-1 expression in human intestinal microvascular endothelial cells is regulated by PI 3-kinase/Akt/MAPK/NF-kappaB: inhibitory role of curcumin. Am J Physiol Gastrointest Liver Physiol. 2009.
  22. Kumar A, et al Curcumin (Diferuloylmethane) inhibition of tumor necrosis factor (TNF)-mediated adhesion of monocytes to endothelial cells by suppression of cell surface expression of adhesion molecules and of nuclear factor-kappaB activation. Biochem Pharmacol. 1998.
  23. Abdelkhalek NK, Ghazy EW, Abdel-Daim MM (2015) Pharmacodynamic interaction of Spirulina platensis and deltamethrin in freshwater fish Nile tilapia, Oreochromis niloticus: impact on lipid peroxidation and oxidative stress. Environ Sci Pollut Res Int 22(4):3023–3031.
  24. Kalafati M, Jamurtas AZ, Nikolaidis MG et al (2010) Ergogenic and antioxidant effects of spirulina supplementation in humans. Med Sci Sports Exerc 2(1):142–151.
  25. Funk JL, Frye JB, Oyarzo JN, Kuscuoglu N, Wilson J, McCaffrey G, Stafford G, Chen G, Lantz RC, Jolad SD, Sólyom AM, Kiela PR, Timmermann BN.Efficacy and mechanism of action of turmeric supplements in the treatment of experimental arthritis. Arthritis Rheum. 2006 Nov;54(11):3452-64.
  26. Viswanath P. Kurup and Christy S. Barrios. Immunomodulatory effects of curcumin in allergy. September 2008; 52(9): 1031–1039.
  27. Shin HS, See HJ, Jung SY, Choi DW, Kwon DA, Bae MJ, Sung KS, Shon DH. Turmeric (Curcuma longa) attenuates food allergy symptoms by regulating type 1/type 2 helper T cells (Th1/Th2) balance in a mouse model of food allergy. J Ethnopharmacol. 2015 Dec 4; 175: 21-9.
  28. Funk JL, Frye JB, Oyarzo JN, Kuscuoglu N et al. Efficacy and mechanisms of action of turmeric supplements in the treatment of experimental arthritis. Arthritis Rheum. 2006; 54(11): 3452-64.
  29. Rasool M, Sabina EP, Lavanya B. Najwa Kisten. Anti-inflammatory effect of Spirulina fusiformis on adjuvant-induced arthritis in mice.  Biol Pharm Bull. 2006 Dec;29(12):2483-7.
  30. Siddiqui MZ. Boswellia Serrata, a potential antiinflammatory agent: an overview.  Indian J Pharm Sci.  2011 May-Jun; 73(3):  255-261.
  31. Kimmatkar N, Thawani V, Hingorani L, Khiyani R. Efficacy and tolerability of Boswellia serrata extract in treatment of osteoarthritis of knee–a randomized double-blind placebo-controlled trial. Phytomedicine. 2003 Jan;10(1):3-7.
  32. Kimmatkar N, Thawani V, Hingorani L, Khiyani REfficacy and tolerability of Boswellia serrata extract in treatment of osteoarthritis of knee–a randomized double-blind placebo-controlled trial. Phytomedicine. 2003 Jan; 10(1):3-7.
  33. Karkos PD, Leong SC, Karkos CD, Sivaji, N and Assimakopoulos DA. Review Article Spirulina in ClinicalPractice: Evidence-Based Human Applications Evidence-Based Complementary and Alternative Medicine Volume 2011, Article ID 531053, 4 pages.
  34. Solisio C, et al Cadmium biosorption on Spirulina platensis biomass . Bioresour Technol. (2008)
  35. Cain A, Vannela R, Woo LK. Cyanobacteria as a biosorbent for mercuric ion . Bioresour Technol. (2008).
  36. Saha SK, et al Effect of hexane extract of spirulina in the removal of arsenic from isolated liver tissues of rat . Mymensingh Med J. (2005)
  37. Banji D, et al Investigation on the role of Spirulina platensis in ameliorating behavioural changes, thyroid dysfunction and oxidative stress in offspring of pregnant rats exposed to fluoride . Food Chem. (2013)
  38. Gargouri M, et al Spirulina or dandelion-enriched diet of mothers alleviates lead-induced damages in brain and cerebellum of newborn rats . Food Chem Toxicol. (2012)
  39. Hwang JH, et al               Spirulina prevents memory dysfunction, reduces oxidative stress damage and augments antioxidant activity in senescence-accelerated mice . J Nutr Sci Vitaminol (Tokyo). (2011)
  40. Guo JP, Yu S, McGeer PL Simple in vitro assays to identify amyloid-beta aggregation blockers for Alzheimer’s disease therapy . J Alzheimers Dis. (2010)
  41. Pabon MM, et al A Spirulina-Enhanced Diet Provides Neuroprotection in an α-Synuclein Model of Parkinson’s Disease . PLoS One. (2012)
  42. Jarouliya U, et al             Alleviation of metabolic abnormalities induced by excessive fructose administration in Wistar rats by Spirulina maxima . Indian J Med Res. (2012)
  43. Rodríguez-Hernández A, et al Spirulina maxima prevents fatty liver formation in CD-1 male and female mice with experimental diabetes. Life Sci. (2001)
  44. Marcel AK, et al              The effect of Spirulina platensis versus soybean on insulin resistance in HIV-infected patients: a randomized pilot study . Nutrients. (2011)
  45. Lu HK, et al       Preventive effects of Spirulina platensis on skeletal muscle damage under exercise-induced oxidative stress . Eur J Appl Physiol. (2006)
  46. Jaspal Sandhu, Shweta Shenoy. Efficacy of Spirulina Supplementation on Isometric Strength and Isometric Endurance of Quadriceps in Trained and Untrained Individuals – a comparative study. Ibnosina Journal of Medicine and Biomedical Sciences.  Vol 2(2) (2010).
  47. Cingi C, et al The effects of spirulina on allergic rhinitis . Eur Arch Otorhinolaryngol. (2008)
  48. Yakoot M, Salem A. Spirulina platensis versus silymarin in the treatment of chronic hepatitis C virus infection. A pilot randomized, comparative clinical trial. BMC Gastroenterol. 2012 Apr 12;12:32.
  49. Bright JJ. Curcumin and autoimmune disease. Adv Exp Med Biol. 2007;595:425-51.
  50. Appelboom T, Maes N and Albert A. A New Curcuma Extract (Flexofytol®) in Osteoarthritis: Results from a Belgian Real-Life Experience. The Open Rheumatology Journal, 2014, 8, 77-81 77
  51. Hannah SS, Laflamme DP. Increased dietary protein spares lean body mass during weight loss in dogs. Proc 16th Annu Vet Med Forum: 714,1998. 
  52. Laflamme DP, Hannah SS. Effect of dietary protein on composition of weight loss in cats.  Proc Brit Small Anim Vet Ass: 277, 1998.
  53. Karsdal MA, Nielsen MJ, Sand JM, Henriksen K, Genovese F, Bay-Jensen A, Smith V, Adamkewicz JI, Christiansen C, Leeming DJ. Extracellular Matrix Remodeling: The Common Denominator in Connective Tissue Diseases. Possibilities for Evaluation and Current Understanding of the Matrix as More Than a Passive Architecture, but a Key Player in Tissue FailureAssay Drug Dev Technol. 2013 Mar; 11(2): 70–92.
  54. Ravi M, De SL, Azhuruddin S, Paul SFD. The beneficial effects of spirulina focusing on its immunomodulatory and antioxidant properties. Nutrition and Dietary Supplements. 2010; 2:73-83.
  55. Ali EAI, Barakat BM, Hassan R. Antioxidant and angiostatic effect of Spirulina platensis suspension in complete Freud’s Adjuvant-Induced arthritis in rats. PLOS One 10(4); 2015.
  56. Marco Antonio Hernández-Lepe et al. Effect of Arthrospira (Spirulina) maxima Supplementation and a Systematic Physical Exercise Program on the Body Composition and Cardiorespiratory Fitness of Overweight or Obese Subjects: A Double-Blind, Randomized, and Crossover Controlled Trial  Mar Drugs. 2018 Oct; 16(10): 364.
  57. Guillet C, Boirie Y, Walrand S. An integrative approach to in vivo protein synthesis measurement: from whole tissue to specific proteins. Curr Opin Clin Nutr Metab Care. 2004;7:531–538.
  58. Wang R, et al. Curcumin protects against glutamate excitotoxicity in rat cerebral cortical neurons by increasing brain-derived neurotrophic factor level and activating TrkB. Brain Res. 2008.
  59. Matteucci A, et al. Curcumin protects against NMDA-induced toxicity: a possible role for NR2A subunit. Invest Ophthalmol Vis Sci. 2011.
  60. Chen RW, et al. Regulation of c-Jun N-terminal kinase, p38 kinase and AP-1 DNA binding in cultured brain neurons: roles in glutamate excitotoxicity and lithium neuroprotection . J Neurochem. 2003.
  61. Xu Y, et al Curcumin reverses impaired cognition and neuronal plasticity induced by chronic stress. Neuropharmacology. 2009.
  62. Morimoto T, et al. The dietary compound curcumin inhibits p300 histone acetyltransferase activity and prevents heart failure in rats. J Clin Invest. 2008.
  63. DiSilvestro RA, et al Diverse effects of a low dose supplement of lipidated curcumin in healthy middle aged people. Nutr J. 2012.
  64. Pungcharoenkul K, Thongnopnua P. Effect of different curcuminoid supplement dosages on total in vivo antioxidant capacity and cholesterol levels of healthy human subjects. Phytother Res. 2011.
  65. Weisberg SP, Leibel R, Tortoriello DV. Dietary curcumin significantly improves obesity-associated inflammation and diabetes in mouse models of diabesity. Endocrinology. 2008.
  66. Yekollu SK, Thomas R, O’Sullivan B Targeting curcusomes to inflammatory dendritic cells inhibits NF-κB and improves insulin resistance in obese mice. Diabetes. 2011.
  67. Chun KS, et al Curcumin inhibits phorbol ester-induced expression of cyclooxygenase-2 in mouse skin through suppression of extracellular signal-regulated kinase activity and NF-kappaB activation. Carcinogenesis. 2003.
  68. Kunnumakkara AB, et al. Curcumin potentiates antitumor activity of gemcitabine in an orthotopic model of pancreatic cancer through suppression of proliferation, angiogenesis, and inhibition of nuclear factor-kappaB-regulated gene products. Cancer Res. 2007.
  69. Ponnurangam S, et al Urine and serum analysis of consumed curcuminoids using an IkappaB-luciferase surrogate marker assay. In Vivo. 2010.
  70. Aggarwal S, et al. Curcumin (diferuloylmethane) down-regulates expression of cell proliferation and antiapoptotic and metastatic gene products through suppression of IkappaBalpha kinase and Akt activation. Mol Pharmacol. 2006.
  71. Dileep KV, Tintu I, Sadasivan C Molecular docking studies of curcumin analogs with phospholipase A2. Interdiscip Sci. 2011.
  72. Binion DG, et al. Vascular cell adhesion molecule-1 expression in human intestinal microvascular endothelial cells is regulated by PI 3-kinase/Akt/MAPK/NF-kappaB: inhibitory role of curcumin. Am J Physiol Gastrointest Liver Physiol. 2009.
  73. Kumar A, et al Curcumin (Diferuloylmethane) inhibition of tumor necrosis factor (TNF)-mediated adhesion of monocytes to endothelial cells by suppression of cell surface expression of adhesion molecules and of nuclear factor-kappaB activation. Biochem Pharmacol. 1998.
  74. Henrotin Y, Priem F, Mobasheri A. Curcumin: a new paradigm and therapeutic opportunity for the treatment of osteoarthritis: curcumin for osteoarthritis management. Springerplus 2013; 2: 1-9.
  75. Jurenka JS. Anti-inflammatory properties of curcumin, a major constituent of Curcuma longa: a review of preclinical and clinical research. Altern Med Rev 2009; 14: 141-53.
  76. Belcaro G, Cesarone MR, Dugall M, et al. Efficacy and safety of Meriva, a Curcumin-phosphatidyl choline complex during extended administration in Osteoarthritis patients. Altern Med Rev 2010; 15: 337-44.
  77. Belcaro G, Cesarone MR, Dugall M, et al. Product evaluation registry of a curcumin phosphatidylcholine complex for the complementary management of osteoarthritis. Panminerva Med 2010; 52: 55-62.
  78. Clutterbuck AL, Mobasheri A, Shakibaei M, Allaway D, Harris P. Interleukin 1 beta induced extracellular matrix degradation and glycosaminoglycan release is inhibited by curcumin in an explant of cartilage inflammation. Ann NY Acad Sci 2009; 1171: 428-35.
  79. Srinivas L, Shalini VK, Turmerin: a water-soluble antioxidant peptide from turmeric [Curcuma longa]. Shylaja M.Arch Biochem Biophys. 1992 Feb 1; 292(2): 617-23.
  80. Nagabhushan M, Bhide SV. Nonmutagenicity of curcumin and its antimutagenic action versus chili and capsaicin. Nutr Cancer. 1986; 8(3): 201-10.
  81. Srivastava KC, Bordia A, Verma SK. Curcumin, a major component of food spice turmeric (Curcuma longa) inhibits aggregation and alters eicosanoid metabolism in human blood platelets. Prostaglandins Leukot Essent Fatty Acids. 1995 Apr; 52(4): 223-7.
  82. Srivastava R, Dikshit M, Srimal RC, Dhawan BN. Anti-thrombotic effect of curcumin. Thromb Res. 1985 Nov 1; 40(3): 413-7.
  83. Itokawa H, Shi Q, Akiyama T, Morris-Natschke SL, Lee KH. Recent advances in the investigation of curcuminoids. Chin Med. 2008 Sep 17; 3: 11.
  84. Soni KB, Rajan A, Kuttan R. Reversal of aflatoxin induced liver damage by turmeric and curcumin. Cancer Lett. 1992 Sep 30; 66(2): 115-21.
  85. He ZY, Shi CB, Wen H, Li FL, Wang BL, Wang J. Upregulation of p53 expression in patients with colorectal cancer by administration of curcumin. Cancer Invest. 2011 Mar; 29(3): 208-13.
  86. Carroll RE, Benya RV, Turgeon DK, Vareed S, Neuman M, Rodriguez L, Kakarala M, Carpenter PM, McLaren C, Meyskens FL Jr, Brenner DE. Phase IIa clinical trial of curcumin for the prevention of colorectal neoplasia. Cancer Prev Res (Phila). 2011 Mar; 4(3): 354-64.
  87. Golombick T, Diamond TH, Manoharan A, Ramakrishna R. Monoclonal gammopathy of undetermined significance, smoldering multiple myeloma, and curcumin: a randomized, double-blind placebo-controlled cross-over 4g study and an open-label 8g extension study. Am J Hematol. 2012 May; 87(5): 455-60.
  88. Holt PR, Katz S, Kirshoff R. Curcumin therapy in inflammatory bowel disease: a pilot study. Dig Dis Sci. 2005 Nov; 50(11): 2191-3.
  89. Prucksunand C, Indrasukhsri B, Leethochawalit M, Hungspreugs K. Phase II clinical trial on effect of the long turmeric (Curcuma longa Linn) on healing of peptic ulcer. Southeast Asian J Trop Med Public Health 2001; 32: 208-215.
  90. Bundy R, Walker AF, Middleton RW, Booth J. Turmeric extract may improve irritable bowel syndrome symptomology in otherwise healthy adults: a pilot study. J Altern Complement Med. 2004 Dec; 10(6): 1015-8.
  91. Viswanath P. Kurup and Christy S. Barrios. Immunomodulatory effects of curcumin in allergy. September 2008; 52(9): 1031–1039.
  92. Shin HS, See HJ, Jung SY, Choi DW, Kwon DA, Bae MJ, Sung KS, Shon DH. Turmeric (Curcuma longa) attenuates food allergy symptoms by regulating type 1/type 2 helper T cells (Th1/Th2) balance in a mouse model of food allergy. J Ethnopharmacol. 2015 Dec 4; 175: 21-9.
  93. Moghadamtousi SZ, Kadir HA, Hassandarvish P, Tajik H, Abudakar S, Zandi K. A review on antibacterial, antiviral, and antifungal activity of curcumin.  BioMed Research International 2014; Vol 2014.
  94. Shahiduzzaman Md and Daugschies A. Curcumin:  A natural herb extract with antiparasitic properties.  DOI:  1007/978-3-642-19382-8_6.
  95. Vikram Choudhary, H.G. Shivakumar. A review on curcumin: wound healing properties and biomarkers of wound healing. Int. Res. J. Pharm. 2018, 9 (9)
  96. Sen-Wei Tsai et al. (2019). Accelerated Muscle Recovery After In Vivo Curcumin Supplementation. Natural Product Communications Volume 15(1): 1–9
  97. Mark Davis et al. (2007) Curcumin effects on inflammation and performance recovery following eccentric exercise-induced muscle damage. Am J Physiol Regul Integr Comp Physiol 292: R2168–R2173
  98. Alistair R et al., (2021). Curcumin Improves Delayed Onset Muscle Soreness and Postexercise Lactate Accumulation. Jnl of Diet Sup. Vol 18(5):531-542
  99. Roy NK et al., (2019) An Update on Pharmacological Potential of Boswellic Acids against Chronic Diseases. Int J Mol Sci. 2019 Sep; 20(17): 4101.
  100. Ali Ridha Mustafa Al-Yasiry, Bożena Kiczorowska. Frankincense–therapeutic propertiesPostepy Hig Med Dosw (Online). 2016 Jan 4;70:380-91
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