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Cur-OST® is formulated using both Curcumin and Boswellia in addition to a host of other ingredients that work synergistically to: |
| • | Reduce inflammation by blocking enzyme pathways that are pro-inflammatory. |
| • | Rebuild cartilage and connective tissue that has been lost by aging, injury and normal wear and tear due to inflammation. |
| • | Restores lubrication and fluid to the joints, which may have been reduced to inflammation, helping to provide cushion as they move. |
Curcumin is one of the active ingredients extracted from Turmeric. Turmeric is composed primarily of Curcumin, desmethoxyCurcumin and bisdemethoxy Curcumin. Curcumin is considered the most active of the three Curcuminoids and composes about 2-4% of the total content of Turmeric. One of the most heavily cultivated Turmeric species is Curcuma longa, which is primarily grown in the southern and eastern parts of India.(1) Modern research has exploded regarding Curcumin over the past several decades. Curcumin acts at multiple targets and levels, affecting numerous transcription factors and cellular signaling pathways. Curcumin has been shown to benefit numerous chronic diseases by reducing inflammation. It is also an antioxidant, more powerful than vitamin E, which serves to quench oxygen and nitrogen free radicals. It has been termed a “complete anti-inflammatory”, affecting all processes and facets of inflammation including cytokines, chemokines, adhesion molecules, growth factors, transcription factors such as NF-kB and AP-1, as well as a large number of kinases such as p38 and JNK. (1) Curcumin’s biological activity is attributed to being both an anti-oxidant and anti-inflammatory, with both activities being complementary. Oxidative stress elicits an inflammatory response, so to be effective, the agent should quench free radicals as well as reduce inflammation. Most modern drugs fail to meet this standard and in most cases target to block COX-2, which is only a small piece of the inflammatory process. By blocking COX-2, there is then a reduction in the production of prostaglandin E2 (PGE-2) which is involved with pain signaling. All chronic diseases such as cardiovascular disease, cancer, diabetes, rheumatoid arthritis and Alzheimers have inflammation as a root component. COX-2 is also constitutively present in some tissues such as the brain and kidneys (2,3), as well as the gastrointestinal system (4). Thus, complete inhibition of COX-2 is not without possible negative consequences such as gastric ulceration and kidney damage. Most drugs exhibit a complete blockade or inhibition of a various pathways, which then impacts other pathways and leads to side effects. Curcumin does not exhibit complete blockade, but instead only down regulates the overactive pathway to basal or normal levels. |
| 1. | Curcumin Educational Material, Dolcas Laboraties, 2009 |
| 2. | Maslinska D, Kaliszek A, Operowska J et al, Constitutive Expression of Cyclooxygenase-2 in Developing Brain. A Charoid Plexus in Human Fetuses, Folia Neuropathol, 1999, 37; 287-91. |
| 3. | Komhoff, M et al. Cyclooxygenase-2 Selective Inhibitors Impair Glomerulogenesis and Renal Cortical Development, Kidney Int, 2000, 57: 414-22. |
| 4. | Kawai, S. Cyclooxygenase Selectivity and the Risk of Gastrointestinal Complications of Various Nonsteroidal Anti-Inflammatory Drugs: A Clinical Consideration. Inflamm Res, 1998, 47:S102-6. |
| Curcumin: Supporting Materials
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Research studies, in-vitro, indicate that boswellic acids are capable of inhibiting pro-inflammatory 5-lipoxygenase products which can contribute to bronchoconstriction, chemotaxis and increased vascular permeability. (1,2,3) The enzyme 5-lipoxygenase is one of the two key enzymes in the arachidonic acid cycle which contribute to inflammation. A Boswellia extract was compared to ketoprofen, a common non-steroidal anti-inflammatory, for effects on glycosaminoglycan metabolism in the joint cartilage. The Boswellia extract significantly reduced the degradation of glycosaminoglycans, while the ketoprofen group exhibited a decrease in tissue glycosaminoglycan content. (4) |
| 1. | Boswellia serrate Monograph, Alternative Medicine Review, vol. 13, no. 2, June 2008 |
| 2. | Ammon HP, Mack T, Singh GG, Safayhi H. Inhibition of leukotriene B4 formation in rat peritoneal neutrophils by an ethanolic extract of the gum resin exudate of Boswellia serrata. Planta Med, 1991; 57:203-207. |
| 3. | Robertson RP. Arachidonic acid metabolites relevant to medicine. In: Braunwald E, Isselbacher KJ, Petersdorf RG, et al, eds. Harrison’s Principles of Internal Medicine. 11th ed. New York , NY. McGraw-Hill: 1987:375. |
| 4. | Reddy GK, Chandrakasan G , Dhar SC. Studies on the metabolism of glycosaminoglycans under the influence of new herbal anti-inflammatory agents. Biochem Pharmacol. 1989;38:3527-3534. |
What does this mean for your pets aching joints? This premium Boswellia extract take a FAST EFFECT on your pet’s joints when they are aching and throbbing. |
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Oxidative Stress in a Small Population of TB Racehorses A Promising Natural Therapy for Equine Osteoarthritis |
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Navicular Disease |
Oxidative Stress |
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A revolutionary product for pets with joint pain and inflammation. Without the side effects like prescription products! LEARN MORE |
All natural ingredients utilizing powerful anti-inflammatory properties. We utilize the finest herbs, vitamins, and minerals. LEARN MORE |
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