» Articles » PMID: 19271029

Glucosamine/chondroitin/primorine Combination Therapy for Osteoarthritis

Overview
Specialty Pharmacology
Date 2009 Mar 10
PMID 19271029
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Osteoarthritis (OA) is the most common arthritis affecting the aging population. This degenerative disease can cause significant pain and functional disability in affected individuals. Despite advances in the retardation of rheumatoid arthritis with disease-modifying agents, comparable oral agents have been relatively unavailable for OA. The mainstays of therapy continue to be acetaminophen and nonsteroidal antiinflammatory medications to manage symptoms. Unfortunately, these medications can precipitate severe adverse events in some patients or may be contraindicated, leaving few choices remaining to control pain and suffering. Glucosamine sulfate and chondroitin sulfate have been evaluated in many studies as agents to relieve pain, improve functional activity, and slow disease progression in OA especially of the hip and knee. Studies have reported conflicting results regarding improvement in the pain and disability associated with OA with the use of glucosamine and chondroitin as single agents; however, when improvement has been demonstrated, the formulation has primarily been glucosamine sulfate combined with chondroitin sulfate. Recently, as a result of information implicating the role of reactive oxygen species and oxidative cellular stress reactions on the onset of neurodegenerative and inflammatory disorders, it has been theorized that medications that could control or alter these reactions might improve or prevent the onset of these conditions. Primorine is a combination of products thought to alter these biochemical oxidative byproducts. Based on current evidence, the use of a combination product of glucosamine sulfate and chondroitin sulfate seems to have the greatest potential as a therapeutic intervention for patients at increased risk from the adverse events of accepted current oral therapies. The use of primorine and its combination of products as an intervention in OA has theoretical advantages but its benefits are unproven. A new product, relamine, is a combination of these three formulations. While no studies have evaluated glucosamine sulfate, chondroitin sulfate and primorine in a single product, it may be an option for those who wish to try an alternate therapy for OA, as there appears to be a low risk for serious adverse events.

Citing Articles

Efficacy of Combination Therapy with Apigenin and Synovial Membrane-Derived Mesenchymal Stem Cells on Knee Joint Osteoarthritis in a Rat Model.

Estakhri F, Panjehshahin M, Tanideh N, Gheisari R, Azarpira N, Gholijani N Iran J Med Sci. 2021; 46(5):383-394.

PMID: 34539013 PMC: 8438345. DOI: 10.30476/IJMS.2020.83686.1301.


Shikonin inhibits inflammation and chondrocyte apoptosis by regulation of the PI3K/Akt signaling pathway in a rat model of osteoarthritis.

Fu D, Shang X, Ni Z, Shi G Exp Ther Med. 2016; 12(4):2735-2740.

PMID: 27703516 PMC: 5038895. DOI: 10.3892/etm.2016.3642.


The effects of different molecular weight chondroitin-4-sulfates in chondrocyte pellet culture.

Yang S, Peng S, Ko C, Chu I Cytotechnology. 2014; 68(3):371-9.

PMID: 25283267 PMC: 4846630. DOI: 10.1007/s10616-014-9788-y.


Down-regulation of IL-6, IL-8, TNF-α and IL-1β by glucosamine in HaCaT cells, but not in the presence of TNF-α.

Park K, Lee J, Cho H, Cho S, Cho J Oncol Lett. 2012; 1(2):289-292.

PMID: 22966296 PMC: 3436374. DOI: 10.3892/ol_00000051.


Intra-articular injections for the treatment of osteoarthritis: focus on the clinical use of hyaluronic acid.

Iannitti T, Lodi D, Palmieri B Drugs R D. 2010; 11(1):13-27.

PMID: 21142290 PMC: 3586124. DOI: 10.2165/11539760-000000000-00000.