Untamed REJUVENMAX (Comprehensive Equine Health & Performance Support)

 

    Untamed REJUVENMAX (Equine) provides 5 powerful natural extracts and equine superfoods, scientifically proven to:

  • Protect and regenerate nerve cells
  • Promote healthy liver-, kidney-, pancreatic-, and cardiovascular function
  • Promote natural detoxification processes, alleviating systemic inflammation
  • Support equine reproductive health and post-partum recovery
  • Balance and improve immunity with anti-fungal, anti-bacterial, and anti-viral action
  • Promote a healthy digestive system – assisting with inflammatory gut disorders like inflammatory bowel disease, gastric ulcers in horses, diarrhoea/constipation and irritable bowel syndrome
  • Enhance endurance & stamina in equine athletes & work horses
  • Speed and promote optimum recovery following pregnancy & lactation, illness, injury, surgery, intensive training, and malnutrition

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

R1,056.00R2,907.00

Or split into 4x interest-free payments Learn more
Description

Horses, regardless of their current health status, can derive significant benefits from natural health support. Harnessing the power of nature enables us to provide our beloved companions with the care they need to thrive, promoting their overall vitality and well-being through scientifically backed solutions.

Untamed Rejuvenmax (Equine), is a multi-functional equine health supplement, specifically designed to optimise the health and longevity of our cherished horses. Its unique formula incorporates a unique blend of natural extracts and nutrients that have undergone rigorous scientific scrutiny, demonstrating a wide range of health benefits.

Untamed Rejuvenmax (Equine) offers seven remarkable natural extracts and equine superfoods that have been scientifically proven to:
– protect & regenerate nerve cells
– promote healthy liver-, kidney-, pancreatic-, & cardiovascular function
– promote natural detoxification processes, alleviating systemic inflammation
– support reproductive health & post-partum recovery
– balance & improve immunity, with anti-fungal, anti-bacterial, anti-viral properties
– promote a healthy digestive system, assisting with inflammatory gut disorders, diarrhoea/constipation & IBS
– enhance physical & mental endurance & stamina
– improve physical condition
– promote speedy & optimum recovery following pregnancy & lactation, illness, injury, surgery, intensive training/ malnutrition

Untamed REJUVENMAX (Equine) may be used as an aid for:
– Infectious diseases like African Horse Sickness, Tetanus, Horse Influenza etc.
– Digestive conditions like colic, diarrhoea, IBS and Inflammatory Bowel Disease
– Conditions affecting the nervous system
– Liver, heart, pancreas and kidney support
– Laminitis
– Horse studding
– Performance Horses like race horses, show jumping horses, eventing-, dressage-, and vaulting horses
– Top health and condition

Whether you have a healthy performance horse, an aging horse, one with poor nutritional status, or a healthy, active horse, Untamed Rejuvenmax can be used to support their overall well-being and help them achieve top health and condition. By providing your horse with the care they need, you can help them perform at their best and enjoy a longer, healthier life.

(If your horse suffers from a chronic illness, please consult your vet before using Untamed Rejuvenmax. This product can be used to complement veterinary treatment during chronic illness, if approved by your vet.)

*None of the ingredients in Untamed REJUVENMAX (Equine) are listed in the FEI Equine Prohibited Substances Database

Product Info
  • Siberian ginseng 3000mg/10g
  • Astragalus extract 600mg/10g
  • Curcumin/Turmeric 95% extract 500mg/10g
  • Propolis concentrate 300mg/10g
  • Spirulina 5600mg/10g
    ***NO artificial flavours, preservatives or additives – 100% NATURAL EXTRACTS!

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

Maintenance:
Horses <500 kg:1/2 – 1 scoop 2x daily (10 – 20g)
Horses >500 kg:1 scoop 2x daily (20g)

*Can be used for acute or long-term treatment.
*Mix into feed, starting with small amounts. Slowly build up to suggested serving size in 7days.
*Can add coconut oil to supplement before mixing into feed.

PLEASE NOTE
Not for use during pregnancy or nursing. Not recommended for animals with cholelithiasis. This product nor its information, is intended to substitute the professional advice or prescription of your veterinarian. Store at cool, dry temperatures.

SIBERIAN GINSENG root is an exceptional adaptogen, and is valued as one of the highest esteemed medicinal plants. An adaptogen can be described as a substance which exhibits a non-specific enhancement in the body’s defence systems against external and internal stress factors.  It increases the body’s resistance to stress, fatigue and disease, and establishes biological homeostasis, with minimal side effects.

Actions and health benefits of Siberian ginseng:

  • Immune-modulating: Siberian ginseng has the ability to regulate immune function.  It can increase immune cell count and activity against pathogenic organisms, but also down-regulate immune cell hyper-responsiveness like histamine-mediated allergic reactions.  It also protects digestive health by enhancing intestinal immune defences, supporting healthy function of the gut lining, and protecting against inflammatory damage induced by pathogenic microorganisms and toxins112-114.
  • Antioxidant: Some of Siberian ginseng’s significant antioxidant mechanisms include: sparing of Vitamin E and increasing its tissue concentration, suppression of fat oxidation, increased antioxidant enzyme activity, and reduced accumulation of free radicals.115,116 Hereby Siberian ginseng enhances protection against toxin or chemical-induced liver damage, and inflammatory conditions including heart disease, atherosclerosis, arthritis, chronic inflammation, neurodegenerative diseases, cancer and aging, which are related to chronic oxidative stress.
  • Stress protection: Research show that Siberian ginseng exerts protective actions against various types of stressors, strengthens an organism’s resistance to such agents, and enhance non-specific defence mechanisms against stress-induced disease.  These stressors include damaging chemical and biological toxins, medication, radiation, and physical, mental and emotional stress117-121. Adaptogens like Siberian ginseng support homeostasis of the hormonal hypothalamic-pituitary-adrenal axis, and modulate intracellular communications involved in signalling pathways induced by stress. 
  • Antifatigue & performance enhancing: Siberian ginseng can reduce fatigue and enhance performance in spite of challenging circumstances. It has an ergogenic (improves exercise performance) effect during exhaustive exercise, and reduces exercise-induced cortisol elevation122.  Its performance enhancing effects can be attributed to its ability to: reduce muscle damage, inhibit elevation of blood urea nitrogen levels, and increase utilization of fats as energy source.  Siberian ginseng’s antifatigue effects may also be related to its antioxidant actions. 123,124
  • Neuroprotective: Extracts of Siberian ginseng demonstrate protective actions against amyloid beta-induced nerve cell death and loss of synapses, and support nerve cell restoration.  Siberian ginseng also alleviates neuronal inflammation, and subsequently displays significant potential in the treatment of nervous system disorders125-127.
  • Anti-depressant: At high concentrations, Siberian ginseng exerts antidepressant effects by increasing 5-HT, noradrenaline and dopamine concentrations127.
  • Bone density: Siberian ginseng has a protective effect against bone degeneration induced by corticosteroids132.
  • Cardioprotective: Siberian ginseng promotes cardiovascular health by regulating blood pressure, reducing LDL-cholesterol and improving the LDL/HDL cholesterol ratio, and providing antioxidant protection128,129.
  • Liver protective: Siberian ginseng protects liver cells against cell death caused by toxins like cadmium,130 and can reverse fatty liver disease associated with diabetes131.
  • Anticancer: Studies report that Siberian ginseng has the ability to inhibit chemical toxin-induced lung cancer, thyroid tumours, and leukaemia.  It also inhibits spontaneous leukaemia and mammary gland tumours, and reduce spreading of various tumours133,134.

Other health benefits: include increasing reproductive capacity and sperm count, stimulating DNA synthesis and cellular repair enzymes, protecting against radiation toxicity, increasing renal capacity in kidney infection, and being antiviral, antibacterial, and antifungal.

TURMERIC 95% extract/Curcumin

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 Turmeric extract (Curcumin)

  • 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 histamine82. These properties give curcumin great potential for clinical management of allergic reactions like asthma, food allergies and allergy related skin conditions83.
  • 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 Cryptosporidium84,85.
  • 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 enzymes58-64.
  • Neuroprotective: Curcumin can protect nerve cells against inflammation and degeneration caused by multiple pathological agents including toxins, stress related high cortisol levels49-52, 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 cholesterol53-55.
  • Antidiabetic: Curcumin illustrates promising protection against insulin resistance, diabetes and its associated inflammatory pathways56,57.
  • Antiarthritic: Curcumin is well researched for its powerful anti-inflammatory actions which, in addition to its protective properties on cartilage65, 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 cartilage66.  Curcumin supplementation can reduce joint pain, enhance articular function, and improve quality of movement67-69.
  • Anticancer: Research illustrates that high doses 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 defence 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 spreading70-78.
  • 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 ulcers79-81.

PROPOLIS CONCENTRATE

PROPOLIS is a natural substance produced by bees from plants.  It is mixed with beeswax and salivary enzymes and used as protection against pathogenic microorganisms, as thermal isolation, to repair damage, and in protecting the larvae from microbial infection.  These defence properties of Propolis, makes it an exceptionally valued natural product for the treatment of various medical conditions.

Actions and health benefits of Propolis:

  • Antioxidant: Propolis protects against free radical induced oxidative damage which causes various diseases like heart disease, arthritis, cancer, diabetes, Alzheimer’s and Parkinson’s disease, and liver disease.94-95
  • Anti-inflammatory: Some of the anti-inflammatory effects of Propolis include suppression of leukotrine and prostaglandin inflammatory mediators, and the lipoxygenase pathway in arachidonic metabolism.  Subsequently it may alleviate inflammatory symptoms like swelling, discomfort, and pain.96-98
  • Anti-bacterial: Propolis demonstrates significant antibacterial activity against Gram-positive bacteria like Staphylococcus, Enterococcos, Bacillus, Pseudomonas, Salmonella, Mycobacterium, and E. coli.89-91
  • Antifungal: Propolis inhibits the growth of multiple fungi like Candida species, Trichosporon and Rhodotorula species88 which infect areas like the skin, ears, eyes, digestive tract and lungs.
  • Anti-parasitic: Research demonstrates its anti-parasitic effect against Giardia lamblia, Toxoplasmas, Leishmania, and Trypanosoma species92,93.
  • Protects dental health: Propolis reduces the formation of dental plaque by blocking the attachment and accumulation of bacteria to the teeth, and can therefore be used in the treatment of dental caries87. It also inhibits fungi and viruses, and can be effectively used in treatment of wounds and ulcers in the mouth, gum disease, dental hypersensitivity, caries, and bad breath101-105. 
  • Liver protective: With its significant concentration of antioxidants, Propolis counteracts the toxic effects of various chemicals on the liver, like paracetamol and carbon tetrachloride (ingredients in solvents, cleaning products, aerosols, and refrigerants) 99,100. 
  • Immune-modulating: Propolis enhances immune function by increasing the activity of bactericidal immune cells, and increasing antibody production106,107.
  • Anti-allergenic: Propolis demonstrates anti-allergic activity by inhibiting histamine release, decreasing inflammatory mediators, inhibiting airway inflammation and hyper-responsiveness, and therefore reducing the occurrence of allergic asthma and rhinitis.110-111
  • Anticancer: Its anticancer activity is owed to its ability to inhibit DNA synthesis in tumour cells, induce cancer cell death, and activate macrophages to produce immune modulators and regulate immune cell activity.  Propolis also demonstrates benefit when used in combination of chemotherapy agents, by improving the efficiency of the drugs and reducing their side effects on immune cells, the liver, and kidneys108.

Other researched health benefits: anti-ulcer, wound healing, antidiabetic, cardioprotective, enhanced regeneration of cartilage, bone, and dental pulp, and growth stimulation in underdeveloped animals.109

ASTRAGALUS EXTRACT

ASTRAGALUS is an herbal root that has been used for hundreds of years to treat chronic illnesses, weakened immunity, cancer, and general weakness.

Actions and health benefits of Astragalus:

  • Immune-modulating: Astragalus improves various aspects of immunity, like increasing immune cell activity, enhancing thymus weight and immune cell production138.
  • Antimicrobial activity: Against bacteria like Shigella dysenteriae, Streptococcus hemolyticus, Diplococcus pneumonia, Staphylococcus aureus139. Virusses like avian influenza virus 141. Skin- and systemic fungal infections like Candida 140
  • Cardioprotective: Astragalus functions as a heart tonic.  It has a significant antioxidant effect on heart cells, alleviate the risk of blood clotting, strengthens left ventricular function, and may improve the symptoms of ischemic heart disease142-146.
  • Adjunct cancer treatment: Astragalus alleviates immune suppression induced by chemotherapy drugs whilst strengthening the immune function.  It also improves the efficacy of immunotherapy drugs in cancer treatment.  In combination with Ligusticum, research illustrates that Astragalus helps to enhance the activity of chemotherapy drugs, reduce recurrence of cancer, improve survival time, and reduce the toxic side effects of cancer medication 147-149.
  • Fertility: Sperm motility is stimulated by Astragalus, supporting male fertility150.
    Kidney tonic: Astragalus functions as a kidney tonic.  It has a diuretic action, and improves kidney function, and protein utilization in inflammatory kidney disorders151-152.

SPIRULINA

SPIRULINA is a nutrient-rich, blue-green algae, and is considered a super food.  It contains superior concentrations of protein and essential amino acids, carbohydrates, fatty acids, vitamins, minerals, multiple phyto-actives, and chlorophyll.

Actions and health benefits of Spirulina supplementation:

  • Protein-rich super food: supporting multiple body systems and general health1.
  • Anti-inflammatory and anti-allergic: 2,3,4, alleviating allergic symptoms like hay fever, rhinitis and hives10-13.
  • Antiparasitic activity against parasites like Demodex canis which causes inflammatory skin infection in dogs 9.
  • Antiviral activity against human enveloped viruses like Herpes simplex type I, cytomegalovirus, measles and mumps and influenza A5.
  • Reduces LDL-cholesterol, providing protection against cholesterol related cardiovascular disease6.
  • Supports systemic detoxification systems by promoting detoxification of toxic chemicals like pesticides, chemical drugs and heavy metals like lead, cadmium, mercury and arsenic, and protecting against liver damage caused by these toxins7,14-19. Spirulina therefore alleviates the risk of deleterious toxin-induced degeneration and chronic disease affecting the nervous system, immune function, hormone balance, genetic health, heart, kidneys, liver, bone and joints34-48.
  • Antioxidant and anticancer protection8: Spirulina is rich in anti-cancer nutraceuticals like beta-carotene and polysaccharides.  Research demonstrates that these constituents enhance protection against cancer by inhibiting cancer development, tumour size and spreading, and even reversing cancer. Some of its mechanisms include: antioxidant defence against free radical damage, inhibiting cancer cell signalling and cancer cell DNA synthesis, and inducing cancer cell death.  Many studies validate the significant benefit of Spirulina extracts in many cancers of the lungs, mouth, cervix, skin, blood, and liver174-180.
  • Neuroprotective: Spirulina protects against toxin induced degeneration of nerve cells and promotes growth and development of nerve tissue 20-24.  It therefore also demonstrates potential in protecting against age related cognitive decline, Parkinson’s and Alzheimer’s disease.
  • Antidiabetic: Spirulina improves insulin sensitivity and blood glucose control, alleviating the risk of diabetes25-26.
  • Enhances muscle performance and endurance capacity: Spirulina promotes muscle hypertrophy, enhances power output, and improves endurance capacity 27-30.
  • Liver protective: It protects against liver toxicity and supports liver regeneration31-33.
  • Enhance fertility and reproduction capacity: Spirulina enhances the fertility and reproductive capacity of healthy animals, diabetic animals, and animals with reduced fertility caused by chemical toxicity.  It increases testicular weight, sperm production and sperm quality 135-137.
  1. Karkos PD, Leong SC, Karkos CD, Sivaji N, and Assimakopoulo DA. Spirulina In Clinical Practice: Evidence-Based Human Applications. Evidence-Based Complementary and Alternative Medicine Volume 2011, Article ID 531053, 4 pages.
  2. Yang HN, Lee EH, and Kim HM. Spirulina platensis inhibits anaphaylactic reaction. Life Sciences, 1997; 61(13): 1237–1244.
  3. Kim HM, Lee EH, Cho HH, and Moon YH. Inhibitory effect of mast cell-mediated immediate-type allergic reactions in rats by Spirulina. Biochemical Pharmacology, 1998; 55(7): 1071–1076.
  4. Mao TK, van de Water J, and Gershwin ME. Effects of a Spirulina-based dietary supplement on cytokine production from allergic rhinitis patients. Journal of Medicinal Food, 2005; 8(1): 27–30.
  5. Ranjani Ramakrishnan. ANTIVIRAL PROPERTIES OF CYANOBACTERIUM, SPIRULINA PLATENSIS-A REVIEW. Pharmaceutical Sciences (IJMPS). 2013; 3(5): 1-10.
  6. Nakaya N, Homa Y, and Goto Y. Cholesterolloweringeffect of Spirulina.  Atherosclerosis, 1988; 37: 1329–1337.
  7. Misbahuddin M, Islam AZ, Khandker S, Al-Mahmud I, Islam N, and Anjumanara. Efficacy of spirulina extract plus zinc in patients of chronic arsenic poisoning: a randomized placebo-controlled study. Clinical Toxicology, 2006; 44(2): 135–141.
  8. Reddy MC, Subhashini J, Mahipal SVK et al. CPhycocyanin, a selective cyclooxygenase-2 inhibitor, induces apoptosis in lipopolysaccharide-stimulated RAW 264.7 macrophages. Biochemical and Biophysical Research Communications, 2003; 304(2): 385–392.
  9. Bezerra LF, de Souza AM, de Melo MA, de Lucena Wanderlei L & de Souza Mendes R. Use of Cyanobacterium Spirulina Associated with Amitraz to Treatment in Juvenile Generalized Canine Demodiciosis. Acta Scientiae Veterinariae, 2013. 41: 1124.
  10. Kim HM, Lee EH, Cho HH, et al. Inhibitory effect of mast cell-mediated immediate-type allergic reactions in rats by spirulina. Biochem Pharmacol. 1998; 55: 1071-1076.
  11. Yang HN, Lee EH, Kim HM. Spirulina platensis inhibits anaphylactic reaction. Life Sci. 1997; 61: 1237-1244.
  12. Mao TK, Water JV, Gershwin ME et al. Effects of a spirulina-based dietary supplement on cytokine production from allergic rhinitis patients. J Med Food. 2005; 8: 27-30.
  13. Cingi C, Conk-Dalay M, Cakli H, et al. The effects of spirulina on allergic rhinitis. Eur Arch Otorhinolaryngol. 2008 Mar 15.
  14. Torres-Duran PV, Miranda-Zamora R, Paredes-Carbajal MC, et al . Spirulina maxima prevents induction of fatty liver by carbon tetrachloride in the rat. Biochem Mol Biol Int. 1998; 44: 787-793.
  15. Vadiraja BB, Gaikwad NW, Madyastha KM . Hepatoprotective effect of C-phycocyanin: protection for carbon tetrachloride and R -(+)-pulegone-mediated hepatotoxicity in rats. Biochem Biophys Res Commun. 1998; 249: 428-431.
  16. 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)
  17. Paniagua-Castro N, et al Spirulina (Arthrospira) protects against cadmium-induced teratogenic damage in mice. J Med Food. (2011)
  18. El-Desoky GE, et al Improvement of Mercuric Chloride-Induced Testis Injuries and Sperm Quality Deteriorations by Spirulina platensis in Rats. PLoS One. (2013)
  19. Sharma MK, et al Evaluation of protective efficacy of Spirulina fusiformis against mercury induced nephrotoxicity in Swiss albino mice. Food Chem Toxicol. (2007)
  20. Chamorro G, et al Spirulina maxima pretreatment partially protects against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity. Nutr Neurosci. (2006)
  21. Thaakur SR, Jyothi B Effect of spirulina maxima on the haloperidol induced tardive dyskinesia and oxidative stress in rats. J Neural Transm. (2007)
  22. Bermejo-Bescós P, Piñero-Estrada E, Villar del Fresno AM Neuroprotection by Spirulina platensis protean extract and phycocyanin against iron-induced toxicity in SH-SY5Y neuroblastoma cells. Toxicol In Vitro. (2008)
  23. Pabon MM, et al A Spirulina-Enhanced Diet Provides Neuroprotection in an α-Synuclein Model of Parkinson's Disease. PLoS One. (2012)
  24. Spirulina Promotes Stem Cell Genesis and Protects against LPS Induced Declines in Neural Stem Cell Proliferation.
  25. Ou Y, et al Antidiabetic potential of phycocyanin: Effects on KKAy mice. Pharm Biol. (2013)
  26. Parikh P, Mani U, Iyer U Role of Spirulina in the Control of Glycemia and Lipidemia in Type 2 Diabetes Mellitus. J Med Food. (2001)
  27. Voltarelli FA, de Mello MA Spirulina enhanced the skeletal muscle protein in growing rats . Eur J Nutr. (2008)
  28. Efficacy of Spirulina Supplementation on Isometric Strength and Isometric Endurance of Quadriceps in Trained and Untrained Individuals – a comparative study
  29. Kalafati M, et al Ergogenic and antioxidant effects of spirulina supplementation in humans . Med Sci Sports Exerc. (2010)
  30. Lu HK, et al Preventive effects of Spirulina platensis on skeletal muscle damage under exercise-induced oxidative stress . Eur J Appl Physiol. (2006)
  31. Jarouliya U, et al. Alleviation of metabolic abnormalities induced by excessive fructose administration in Wistar rats by Spirulina maxima . Indian J Med Res. (2012)
  32. Pak W, et al Anti-oxidative and anti-inflammatory effects of spirulina on rat model of non-alcoholic steatohepatitis . J Clin Biochem Nutr. (2012)
  33. Bhattacharyya S, Mehta P The hepatoprotective potential of Spirulina and vitamin C supplemention in cisplatin toxicity . Food Funct. (2012)
  34. Thaakur SR, Jyothi B. Effect of Spirulina maxima on the haloperidol induced tardive dyskinesia and oxidative stress in rats. J Neural Transm. 2007; 114: 1217–1225.
  35. Kuhad A, Tirkey N, Pilkhwal S, Chopra K. Renoprotective effect of Spirulina fusiformis on cisplatin-induced oxidative stress and renal dysfunction in rats. Ren Fail. 2006; 28: 247–254.
  36. Remirez D, González R, Merino N, Rodriguez S, Ancheta O. Inhibitory effects of Spirulina in zymosan-induced arthritis in mice. Mediators Inflamm. 2002; 11: 75–79.
  37. Premkumar K, Pachiappan A, Abraham SK, Santhiya ST, Gopinath PM, Ramesh A. Effect of Spirulina fusiformis on cyclophosphamide and mitomycin-C induced genotoxicity and oxidative stress in mice. Fitoterapia. 2001; 72: 906–911.
  38. Upasani CD, Khera A, Balaraman R. Effect of lead with vitamin E, C, or Spirulina on malondialdehyde, conjugated dienes and hydroperoxides in rats. Indian J Exp Biol. 2001; 39: 70–74.
  39. Kumar N, Singh S, Patro N, Patro I. Evaluation of protective efficacy of Spirulina platensis against collagen-induced arthritis in rats. Inflammopharmacol. 2009; 17: 181–190.
  40. Karadeniz A, Cemek M, Simsek N. The effects of Panax ginseng and Spirulina platensis on hepatotoxicity induced by cadmium in rats. Ecotoxicol Environ Saf. 2009; 72: 231–235.
  41. Karadeniz A, Yildirim A, Simsek N, Kalkan Y, Celebi F. Spirulina platensis protects against gentamicin-induced nephrotoxicity in rats. Phytother Res. 2008; 22: 1506–1510.
  42. Torres-Dura´n PV, Paredes-Carbajal AMC, Mascher BD, Zamora-Gonza´lez BJ, Dı´az-Zagoya CJD, Jua´rez-Oropezaa AMA. Protective Effect of Arthrospira maxima on Fatty Acid Composition in Fatty Liver. Archives of Medical Research. 2006; 37: 479–483.
  43. Sharma MK, Sharma A, Kumar A, Kumar M. Spirulina fusiformis provides protection against mercuric chloride induced oxidative stress in Swiss albino mice. Food Chem Toxicol. 2007; 45: 2412–2419.
  44. Rasool M, Sabina EP, Lavanya B. Anti-inflammatory effect of Spirulina fusiformis on adjuvant-induced arthritis in mice. Biol Pharm Bull. 2006; 29: 2483–2487.
  45. Premkumar K, Abraham SK, Santhiya ST, Ramesh A. Protective effect of Spirulina fusiformis on chemical-induced genotoxicity in mice. Fitoterapia. 2004; 75: 24–31.
  46. Kim HM, Lee EH, Cho HH, Moon YH. Inhibitory effect of mast cell-mediated immediate-type allergic reactions in rats by Spirulina. Biochem Pharmacol. 1998; 55: 1071–1076.
  47. Khan M, Shobha JC, Mohan IK, Rao Naidu MU, Prayag A, Kutala VK. Spirulina attenuates cyclosporine-induced nephrotoxicity in rats. J Appl Toxicol. 2006; 26: 444–451.
  48. Chamorro G, Pérez-Albiter M, Serrano-García N, Mares-Sámano JJ, Rojas P. Spirulina maxima pretreatment partially protects against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity. Nutr Neurosci. 2006; 9: 207–212.
  49. 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.
  50. Matteucci A, et al. Curcumin protects against NMDA-induced toxicity: a possible role for NR2A subunit. Invest Ophthalmol Vis Sci. 2011.
  51. 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.
  52. Xu Y, et al Curcumin reverses impaired cognition and neuronal plasticity induced by chronic stress. Neuropharmacology. 2009.
  53. Morimoto T, et al. The dietary compound curcumin inhibits p300 histone acetyltransferase activity and prevents heart failure in rats. J Clin Invest. 2008.
  54. DiSilvestro RA, et al Diverse effects of a low dose supplement of lipidated curcumin in healthy middle aged people. Nutr J. 2012.
  55. 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.
  56. Weisberg SP, Leibel R, Tortoriello DV. Dietary curcumin significantly improves obesity-associated inflammation and diabetes in mouse models of diabesity. Endocrinology. 2008.
  57. 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.
  58. 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.
  59. 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.
  60. Ponnurangam S, et al Urine and serum analysis of consumed curcuminoids using an IkappaB-luciferase surrogate marker assay. In Vivo. 2010.
  61. 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.
  62. Dileep KV, Tintu I, Sadasivan C Molecular docking studies of curcumin analogs with phospholipase A2. Interdiscip Sci. 2011.
  63. 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.
  64. 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.
  65. 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.
  66. 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.
  67. 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.
  68. 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.
  69. 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.
  70. 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.
  71. Nagabhushan M, Bhide SV. Nonmutagenicity of curcumin and its antimutagenic action versus chili and capsaicin. Nutr Cancer. 1986; 8(3): 201-10.
  72. 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.
  73. Srivastava R, Dikshit M, Srimal RC, Dhawan BN. Anti-thrombotic effect of curcumin. Thromb Res. 1985 Nov 1; 40(3): 413-7.
  74. 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.
  75. 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.
  76. 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.
  77. 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.
  78. 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.
  79. Holt PR, Katz S, Kirshoff R. Curcumin therapy in inflammatory bowel disease: a pilot study. Dig Dis Sci. 2005 Nov; 50(11): 2191-3.
  80. 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.
  81. 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.
  82. Viswanath P. Kurup and Christy S. Barrios. Immunomodulatory effects of curcumin in allergy. September 2008; 52(9): 1031–1039.
  83. 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.
  84. 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.
  85. Shahiduzzaman Md and Daugschies A. Curcumin:  A natural herb extract with antiparasitic properties.  DOI:  1007/978-3-642-19382-8_6.
  86. Panossian A, Wikman G. Pharmacology of Schisandra chinensis Bail.  An overview of Russian research and uses in medicine.  J of Ethnopharmacology.  118(2):183-212.
  87. Selvan A, Singh R, and Prabhu D. Research article: antibacteria activity of bee propolis against clinical strains of Streptococcus mutants and synergism with chlorhexidine. International Journal Pharmaceutical Studies Research, vol. 2, pp.85–90,2011.
  88. Koc AN, Silici S, Kasap F, ¨ ormet-¨Oz HTH, MavusBuldu H, and Ercal BD. Antifungal activity of the honeybee products against Candida spp. and Trichosporon spp. Journal ofMedicinalFood,vol.14,no.1-2,pp.128–134,2011.
  89. Grange JM and Davey RW. Antibacterial properties of propolis (beeglue). Journal of the Royal Society of Medicine,vol. 83,no.3,pp.159–160,1990.
  90. Orsi RO, Sforcin JM, Rall VLM, Funari SRC, Barbosa L, and Fernandes A. Susceptibility profile of Salmonella against the antibacterial activity of propolis produced in two regions of Brazil. Journal of Venomous Animals and Toxins Including Tropical Diseases,vol.11,pp.109–116,2005.
  91. Benkovic V, Horvat Knezevic A, Dikic D et al. Radioprotective effects of propolis and quercetin in 𝛾-irradiated mice evaluated by the alkaline comet assay. Phytomedicine, vol. 15, no.10,pp.851–858,2008.
  92. De Castro SL, Salom˜ao K, DeSouza EM, Henriques-Pons A, and Barbosa HS. Brazilian green propolis: effects invitro and invivo on Trypanosoma cruzi. Evidence-Based Complementary and Alternative Medicine,vol.2011, Article ID185918, 11 pages, 2011.
  93. Torres D, Hollands I, and Palacios E. Effect of an alcoholic extract of propolis on the invitro growth of Giardia lamblia. JournalofVeterinaryScience,vol.21,no.1,pp.15–19,1990.
  94. Popeskovic D, Kepcija D, Dimitijevic D, and Stojanovic N. The antioxidative properties of propolis and some of its components. ActaVeterinaria,vol.30,pp.133–136,1980.
  95. Zhao JQ, Wen YF, Bhadauria M et al. Protective effects of propolis on inorganic mercury induced oxidative stress in mice. Indian Journal of Experimental Biology,vol.47,no.4,pp. 264–269,2009.
  96. Borrelli F, Maffia P, Pintoetal L. Phytochemical compounds involved in the anti-inflammatory effect of propolis extract. Fitoterapia,vol.73,no.1,pp.S53–S63,2002.
  97. DuToit K, Buthelezi S, and Bodenstein J. Anti-inflammatory and antibacterial profiles of selected compounds found in south african Propolis. South African Journal of Science,vol.105,no. 11-12,pp.470–472,2009.
  98. Mirzoevaand OK, Calder PC. The effect of propolis and its components on eicosanoid production during the inflammatory response. Prostaglandins Leukotrienes and Essential Fatty Acids,vol.55,no.6,pp.441–449,1996.
  99. Gonzalez R, Corcho I, Remirez D, Rodriguez S, Ancheta O, Merino N, Gonzalez A, Pascual C. (1995) Hepatoprotective effects of propolis extract on carbon tetrachloride-induced liver injury in rats 1073. Phytotherapy Research 9 (2): 114-117.
  100. Gonzalez R, Remirez D, Rodriguez S, Gonzalez A, Ancheta O, Merino N, Pascual C. (1994) Hepatoprotective effects of propolis extract on paracetamol-induced liver damage in mice 1074. Phytotherapy Research 8 (4): 229-232.
  101. Hayacibara MF, Koo H, Rosalen PL, Duarte S, Franco EM, Bown WH, Ikegaki M, Cury JA. (2005) In vitro and in vivo effects of isolated fractions of Brazilian propolis on caries development. Journal of Ethnopharmacology 101 (1-3): 110-115. ,
  102. Koo H, Cury JA, Rosalen PL, Ambrosano GMB, Ikegaki M, Park YK.(2002) Effect of a mouthrinse containing selected propolis on 3-day dental plaque accumulation and polysaccharide formation. Caries Research 36 (6): 445-448. ,
  103. Martinez SG, Gou GA, Ona TR, Palmer Oritz MC, Falcon Cuellar MA. (1988) [Preliminary study of the effects of propolis in the treatment of chronic gingivitis and oral ulceration]. Revista Cubana de Estomatologia 25 (3): 36-44. ,
  104. Oliveira AC, Murgo SS. (2006) Estidio da aplicacao da propolis ma odontologia (revisao de literatura) Application of propolis in odonotology, a review, X Encontro Latino Americano de Iniciação Científica e VI Encontro Latino Americano de Pós-Graduação – Universidade do Vale do Paraíba: pp 737-740
  105. Parolia A, Thomas M, Kundabala M, Mohan M.(2010) Propolis and its potential uses in oral health. Int J Med Med Sci 2: 210-215.
  106. Riou M, Guegnard F, Guegnard F.(2011) Flavonoids and Related Compounds in Parasitic Disease Control. Mini Rev Med Chem 8: 116-128.
  107. Sforsin JM. (2007) Propolis and the immune system: a review. Journal of Ethnopharmacology 113 (1): 1-14.
  108. Orsolic, N (2010) A review of propolis antitumour action in vivo and in vitro. JAAS 2 (1): 1-20.
  109. Bogdanov S. Propolis: Composition, Health, Medicine: A Review. 
  110. Sy LB, Wu YL, Chiang BL, Wang YH, and Wu WM. Propolis extracts exhibit an immunoregulatory activity in an OVA-sensitized airway inflammatory animal model. International Immunopharmacology, 6(7):1053–1060, 2006.
  111. Jung WK, Lee DY, Choietal YH. Caffeic acid phenethyl ester attenuates allergic airway inflammation and hyperresponsiveness in murine model of ovalbumin-induced asthma. Life Sciences,vol.82(13-14):797–805,2008.
  112. Barenboim GM, Sterlina AG, Bebyakova NV et al., 1986. Investigation of the pharmacokinetics and mechanism of action of Eleutherococcus glycosides. . Investigation of natural killer activation by the Eleutherococcus extract. Chem Pharm J, 20(8):914-917.
  113. Li W, Luo Q and Jin LH, 2013a. Acanthopanax senticosus extracts have a protective effect on Drosophila gut immunity. J Ethnopharmacol, 146(1):257-263.
  114. Wikman G, 1980. Research conducted on the effects of Eleutherococcus senticosus Maxim. Swedish Herbal Institute. Gothenburg, 9.
  115. Mikaelyan EM, Mkhitaryan VG, 1986. Antioxidant properties of Eleutherococcus. Biol Zh Arm, 39:593- 597.
  116. Hong JH, Cha YS and Rhee SJ, 2009. Effects of the cellcultured acanthopanax senticosus extract on antioxidative defense system and membrane fluidity in the liver of type 2 Diabetes mouse. J Clin Biochem Nutr, 45(1):101-109.
  117. Maianskii KA, 1962. The healing effect of combined Eleutherococcus/antibiotic treatment on experimentally induced chronic radiation sickness. In: Brekhman II, ed.The symposium on Eleutheroccocus and ginseng. Vladivostok, 26-28.
  118. Voskresensky ON, 1977. About connexion of adaptogenic and antioxydative action In: Adaptation and Adaptogens. Proceedings of the 2nd Symposium, May 1975, 91-96.
  119. Voskresensky ON, Devyatkina TA, Gumenyuk NA et al., 1986. The effect of Eleutherococcus and Ginseng on the development of free-radical pathology. In: New Data on Eleutherococcus: Proceedings of the 2nd International Symposium on Eleutherococcus, Moscow 1984. Vladivostok. 101-104.
  120. Collisson RJ, 1991. Siberian ginseng (Eleutherococcus senticosus Maxim). Brit J Phytother, 2(2):61-71.
  121. Yonezawa M et al., 1989. Radiation protection by Shigoka extract on split dose irradiation in mice. J Radiation Res, 30(3):247-254.
  122. Kimura Y, Sumiyoshi M, 2004. Effects of various Eleutherococcus senticosus cortex on swimming time, natural killer activity and corticosterone level in forced swimming stressed mice. J Ethnopharmacol, 95(2-3):447-453.
  123. Huang LZ, Huang BK, Liang J, Zheng CJ, Han T, Zhang QY and Qin LP, 2011b. Antifatigue activity of the liposoluble fraction from Acanthopanax senticosus. Phytother Res, 25(6):940-943.
  124. Huang LZ, Huang BK, Ye Q, Qin LP, 2011c. Bioactivity-guided fractionation for antifatique property of Acanthopanax senticosus. J Ethnopharmacol, 133(1):213-219.
  125. Tohda C, Ichimura M, Bai Y, Tanaka K, Zhu S, Komatsu K, 2008. Inhibitory effects of Eleutherococcus senticosus extracts on amyloid beta(25-35) induced neuritic atrophyand synaptic loss. J Pharmacol Sci, 107(3):329-339.
  126. Jin L, Wu F, Li X, Li H, Du C, Jiang Q, You J, Li S and Xu Y, 2013a. Anti-depressant Effects of Aqueous Extract from Acanthopanax senticosus in Mice. Phytother Res, 27(12):1829-1833.
  127. Jin ML, Park SY, Kim YH, Park G and Lee SJ, 2013b. Acanthopanax senticosus exertsneuroprotective effects through HO-1 signaling in hippocampal and microglialcells. Environ Toxicol Pharmacol, 35(2):335-346.
  128. Facchinetti F, Neri I, Tarbusi M, 2002. Eleutherococcus senticosus reduces cardiovascular stress response in healthy subjects: randomized, placebo-controled trial. Stress Health, 18:11-17.
  129. Lee YJ, Chung HY, Kwak HK, Yoon S, 2008. The effects of A. senticosus supplementation on serum lipid profiles, biomarkers of oxidative stress, and lymphocyte DNA damage in postmenopausal women. Biochem Biophys Res Commun, 375(1):44-48.
  130. Smalinskiene A, Lesauskaite V, Zitkevicius V, Savickiene N, Savickas A, Ryselis S,Sadauskiene I and Ivanov L, 2009. Estimation of the combined effect of Eleutherococcussenticosus extract and cadmium on liver cells. Ann N Y Acad Sci, 1171:314-320.
  131. Park SH, Lee SG, Kang SK, Chung SH, 2006. Acanthopanax senticosus reverses fatty liver disease and hyperglycemia in ob/ob mice. Arch Pharm Res, 29(9):768-776.
  132. Kropotov AV, Kolodnyak OL, Koldaev VM. Effects of Siberian ginseng extract and ipriflavone on the development of glucocorticoid-induced osteoporosis. Bull Exp Biol Med 2002;133:252-254.
  133. Davydov M, Krikorian AD. Eleutherococcus senticosus (Rupr. & Maxim) Maxim (Araliaceae) as adaptogen: a closer look. J Ethnopharmacol.  2000; 72: 345-393.
  134. Baranov AI. Medicinal uses of ginseng and related plants in the Soviet Union. Recent trends in Soviet literature.  J Ethnopharmacol 1982; 6: 339-353.
  135. Ross E, Dominy W. The nutritional value of dehydrated, blue-green algae (Spirulina platensis) for poultry. Poult Sci. 1990 May;69(5):794-800.
  136. Nah, W.H., I.K. Koh, H.S. Ahn, M.J. Kim, H.G. Kang, J.H. Jun and M.C. Gye, 2012. Effect of Spirulina maxima on spermatogenesis and steroidogenesis in streptozotocin-induced type I diabetic male rats. Food Chem., 134: 173-179.
  137. El-Desoky, G.E., S.A. Bashandy, I.M. Alhazza, Z.A. Al-Othman, M.A. Aboul-Soud and K. Yusuf, 2013. Improvement of mercuric chloride-induced testis injuries and sperm quality deteriorations by Spirulina platensis in rats. PLOS One, Vol. 8. 10.1371.
  138. Mills S, Bone K. Principles and Practice of Phytotherapy. Edinburgh, Scotland: Churchill Livingstone; 2000:273-279.
  139. Bensky D, Gamble A. Chinese Herbal Medicine: Materia Medica, Revised Edition. Seattle, WA: Eastland Press; 1993.
  140. MikaeiliI A, Karimi I, Shamspur L; Gholamine B, Modaresi M, Khanlari A. Anti-candidal activity of Astragalus verus in the in vitro and in vivo guinea pig models of cutaneous and systemic candidiasis. Rev. bras. farmacogn. vol.22 no.5 Curitiba Sept./Oct. 2012 Epub Mar 20, 2012
  141. Sanpha Kallon, Xiaorong Li, Jun Ji, Cuiying Chen, et al. Astragalus polysaccharide enhances immunity and inhibits H9N2 avian influenza virus in vitro and in vivo. Contributed equally. Journal of Animal Science and Biotechnology20134:22.
  142. Chen LX, Liao JZ, Guo WQ. Effects of Astragalus membranaceus on left ventricular function and oxygen free radical in acute myocardial infarction patients and mechanism of its cardiotonic action. Zhongguo Zhong Xi Yi Jie He Za Zhi 1995;15:141-143.
  143. Purmova J, Opletal L. Phytotherapeutic aspects of diseases of the cardiovascular system. 5. Saponins and possibilities of their use in prevention and therapy. Ceska Slov Farm 1995;44:246-251.
  144. Luo HM, Dai RH, Li Y. Nuclear cardiology study on effective ingredients of Astragalus membranaceus in treating heart failure. Zhongguo Zhong Xi Yi Jie He Za Zhi 1995;15:707-709.
  145. Li SQ, Yuan RX, Gao H. Clinical observation on the treatment of ischemic heart disease with Astragalus membranaceus. Zhongguo Zhong Xi Yi Jie He Za Zhi 1995;15:77-80.
  146. Lei ZY, Qin H, Liao JZ. Action of Astragalus membranaceus on left ventricular function of angina pectoris. Zhongguo Zhong Xi Yi Jie He Za Zhi 1994;14:199-202,195.
  147. Yoshida Y, Wang MQ, Liu JN, et al. Immunomodulating activity of Chinese medicinal herbs and Oldenlandia diffusa in particular. Int J Immunopharmacol 1997;19:359-370.
  148. Wang Y, Qian XJ, Hadley HR, Lau BH. Phytochemicals potentiate interleukin-2 generated lymphokine-activated killer cell cytotoxicity against murine renal cell carcinoma. Mol Biother 1992;4:143-146.
  149. Zee-Cheng RK. Shi-quan-da-bu-tang (ten significant tonic decoction), SQT. A potent Chinese biological response modifier in cancer immunotherapy, potentiation and detoxification of anticancer drugs. Methods Find Exp Clin Pharmacol 1992;14:725-736.
  150. Hong CY, Ku J, Wu P. Astragalus membranaceus stimulates human sperm motility in vitro. Am J Chin Med 1992;20:289294.
  151. Bensky D, Gamble A. Chinese Herbal Medicine: Materia Medica, Revised Edition. Seattle, WA: Eastland Press; 1993.
  152. Mills S, Bone K. Principles and Practice of Phytotherapy. Edinburgh, Scotland: Churchill Livingstone; 2000:273-279.
  153.  
  154. 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.
  155. Schwartz J, Shklar G, et al. Prevention of experimental oral cancer by extracts of spirulina- dunaliella algae. 1988. Harvard School of Dental Medicine. Pub. In Nutrition and Cancer 11, 127-134. 1988. USA.
  156. Lisheng, et al. Inhibitive effect and mechanism of polysaccharide of spirulina on transplanted tumor cells in mice. 1991. Pub. in Marine Sciences, Qingdao, N.5. pp 33-38. China.
  157. Qishen, P. et al. Enhancement of endonuclease activity and repair DNA synthesis by polysaccharide of spirulina. 1988. Pub. in Chinese Genetics Journal 15 (5) 374-381. China
  158. Ziegler, RG. 1989. A review of epidemiologic evidence that carotenoids reduce the risk of cancer. Journal of Nutrition, 119:116-122.
  159. Stahelin, HB, Gey KF, Eicholzer M, and Ludin E (1991). B-Carotene and cancer prevention: the Basel Study. American Journal of Clinical Nutrition, 53: 265S-9S.
  160. Prabhudas PR, Mikhail MS, Basu J, and Romney SL. (1992). BCarotene
    levels in exfoliated cervicovaginal epithelial cells in cervical intraepithelial neoplasia and cervical cancer. American Journal of Obstetrics and Gynecology, 167:1899-1903.
  161. Kornhauser, A, Wamer W, and Giles A, Jr. (1986). Protective effects of beta-carotene against psoralen phototoxicity: relevance to protection against carcinogenesis. Antimutagenesis and Anticarcinogenesis Mechanisms, edited by D. M. Shankel, P.E. Hartman, T. Kado Plenum Press.
  162. Martinotti, A; Ranzato E. (2015) Propolis: a new frontier for wound healing? Burns&Trauma 3:9.
  163. Vikram Choudhary, H.G. Shivakumar. A review on curcumin: wound healing properties and biomarkers of wound healing. Res. J. Pharm. 2018, 9 (9)
  164. Sen-Wei Tsai et al. (2019). Accelerated Muscle Recovery After In Vivo Curcumin Supplementation. Natural Product Communications Volume 15(1): 1–9
  165. 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
  166. Alistair R et al., (2021). Curcumin Improves Delayed Onset Muscle Soreness and Postexercise Lactate Accumulation. Jnl of Diet Sup. Vol 18(5):531-542
  167. Bingjiang Z et al.(2017) Wound healing effect of an Astragalus membranaceus polysaccharide and its mechanism. Molecular medicine reports 15: 4077-4083
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