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Inflammation rheumatoid arthritis

Aging (skin and other tissues), myocardial infarct or stroke, inflammation, rheumatoid arthritis, atherosclerosis, pulmonary disorders (asthma and chronic obstructive pulmonary diseases), radiation injury, organ transplant rejection, psoriasis, hypertension, AIDS, multiple types of cancer, neuro-degenerative diseases (Parkinson s), diabetes, muscular dystrophy... [Pg.62]

Chronic urinary tract infections Chronic inflammation Rheumatoid arthritis Systemic lupus erythematosus Rheumatoid (collagen vascular) diseases Inflammatory osteoarthritis Gout... [Pg.1822]

Phosphatidyl inositol signaling PI3K, AKT, PDK, PTEN, mTOR, GSK3/1, SHIP, PLC, PKC, SHC, GRB-2, SOS, Ras, Raf, Erk, Elkl, Fos Inflammation, Rheumatoid arthritis. Cancer, Respiratory diseases... [Pg.627]

Unfortunately steroids merely suppress the inflammation while the underlying cause of the disease remains. Another serious concern about steroids is that of toxicity. The abmpt withdrawal of glucocorticoid steroids results in acute adrenal insufficiency. Long term use may induce osteoporosis, peptidic ulcers, the retention of fluid, or an increased susceptibiUty to infections. Because of these problems, steroids are rarely the first line of treatment for any inflammatory condition, and their use in rheumatoid arthritis begins after more conservative therapies have failed. [Pg.388]

Selective AR agonists are undergoing clinical trials for cardiac arrhythmias and pain (Ai) cardiac imaging and inflammation (A2a) colon cancer, rheumatoid arthritis, psoriasis, and dry eye (A3). Selective AR antagonists are either in or advancing toward clinical trials for kidney disorders (Ax) Parkinson s disease (A2a) diabetes and asthma (A2B) cancer and glaucoma (A3). [Pg.27]

Human tumor necrosis factor (TNF) (Fig. 1) is a hormone-like proinflammatory peptide belonging to the group of cytokines. It is mainly produced by cells of the immune system in response to infection, inflammation, or cell damage. Disregulated TNF is an important factor in many pathological situations, like sqDsis, rheumatoid arthritis, inflammatory bowel disease (Crohn s disease), and Cachexia. The cytotoxic activity of TNF is of interest in development of new antitumoral strategies. [Pg.1247]

The corticosteroids may be used to treat rheumatic disorders such as ankylosing spondylitis, rheumatoid arthritis, gout, bursitis (inflammation of the bursa, usually the bursa of the shoulder), and osteoarthritis. [Pg.192]

Iron salts occasionally cause gastrointestinal irritation, nausea, vomiting, constipation, diarrhea, headache, backache, and allergic reactions. The stools usually appear darker (black). Iron dextran is given by the parenteral route Hypersensitivity reactions, including fatal anaphylactic reactions, have been reported with the use of this form of iron. Additional adverse reactions include soreness, inflammation, and sterile abscesses at the intramuscular (IM) injection site Intravenous (IV) administration may result in phlebitis at the injection site When iron is administered via the IM route, a brownish discoloration of tlie skin may occur. Fhtients with rheumatoid arthritis may experience an acute exacerbation of joint pain, and swelling may occur when iron dextran is administered. [Pg.434]

Tea extracts have been demonstrated to inhibit a wide range of inflammatory responses and may be useful in treating chronic inflammatory states. For example, rheumatoid arthritis is an inflammatory disease that causes pain, swelling, stiffness and loss of function in the joints. The antioxidants in green tea may prevent or reduce the severity of these symptoms by reducing inflammation and slowing cartilage breakdown (Adcocks et al, 2002 Haqqi et al, 1999). [Pg.136]

Although atherosclerosis and rheumatoid arthritis (RA) are distinct disease states, both disorders are chronic inflammatory conditions and may have common mechanisms of disease perpetuation. At sites of inflammation, such as the arterial intima undergoing atherogen-esis or the rheumatoid joint, oxygen radicals, in the presence of transition-metal ions, may initiate the peroxidation of low-density lipoprotein (LDL) to produce oxidatively modified LDL (ox-LDL). Ox-LDL has several pro-inflammatory properties and may contribute to the formation of arterial lesions (Steinberg et /., 1989). Increased levels of lipid peroxidation products have been detected in inflammatory synovial fluid (Rowley et /., 1984 Winyard et al., 1987a Merry et al., 1991 Selley et al., 1992 detailed below), but the potential pro-inflammatory role of ox-LDL in the rheumatoid joint has not been considered. We hypothesize that the oxidation of LDL within the inflamed rheumatoid joint plays a pro-inflammatory role just as ox-LDL has the identical capacity within the arterial intima in atherosclerosis. [Pg.98]

Pasquier, C., Mach, P.S., Raichuatg, D., Sar ti, G., Amor, B. and Delbarre, F. (1984). Mn-containing SOD deficiency in polymorphonuclear leucocytes of adults with rheumatoid arthritis. Inflammation 8, 27-32. [Pg.111]

Munthe, E., Kass, E. and Jellum, E. (1982). Evidence for enhanced radical scavenging prior to drug response in rheumatoid arthritis. In Advances in Inflammation Research (ed. S. Gorini) pp. 2II-2I8. Raven Press, New York. [Pg.260]

Rheumatoid arthritis (RA) is a complex systemic inflammatory condition manifesting initially as symmetric swollen and tender joints of the hands and/or feet. Some patients may experience mild articular disease, whereas others may present with aggressive disease and/or extraarticular manifestations. The systemic inflammation of RA leads to joint destruction, disability, and premature death. [Pg.867]

Choy EH, Panayi GS. Cytokine pathways and joint inflammation in rheumatoid arthritis. N Engl J Med 2001 344( 12) 907—916. Cronstein BN. Low-dose methotrexate A mainstay in the treatment of rheumatoid arthritis. Pharmcol Rev 2005 57(2) 163—172. [Pg.878]

In contrast with some other forms of arthritis (e.g., rheumatoid arthritis and gout), inflammation usually is absent and is mild and localized when present. [Pg.881]

Rheumatoid arthritis (RA) affects 1% of the US population, or 3 million people (1-3). Although women are 2.5 times more likely to get RA than men, some studies suggest the disease tends to be more severe in men. RA can affect people of all ages, but prevalence increases with age, approaching 5% in women over 55 years of age (1-3). RA is a chronic inflammatory disease characterized by synovial inflammation and hyperplasia, neovascularization, and progressive destruction of cartilage and bone (1,4,5). The cause(s) of RA remains poorly... [Pg.155]

Ellingsen T, Buus A, Stengaard-Pedersen K. Plasma monocyte chemoattractant protein 1 is a marker for joint inflammation in rheumatoid arthritis. J Rheumatol... [Pg.192]

Glycoproteins similar to the IDGFs are found in mammals and may constitute a novel class of cytokines, some of which are important in inflammation. The best characterized is the human glycoprotein HC gp-39 (= YKL40 16-23% identical to IDGFs), which accumulates in the synovial fluid of rheumatoid arthritis... [Pg.189]


See other pages where Inflammation rheumatoid arthritis is mentioned: [Pg.378]    [Pg.378]    [Pg.378]    [Pg.378]    [Pg.37]    [Pg.40]    [Pg.385]    [Pg.388]    [Pg.187]    [Pg.445]    [Pg.830]    [Pg.189]    [Pg.185]    [Pg.185]    [Pg.240]    [Pg.353]    [Pg.744]    [Pg.888]    [Pg.151]    [Pg.156]    [Pg.164]    [Pg.186]    [Pg.655]    [Pg.332]    [Pg.1023]    [Pg.155]    [Pg.28]    [Pg.135]    [Pg.200]    [Pg.306]    [Pg.102]    [Pg.199]    [Pg.575]    [Pg.101]    [Pg.600]   
See also in sourсe #XX -- [ Pg.173 , Pg.177 ]

See also in sourсe #XX -- [ Pg.600 ]




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