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Adjuvant arthritis as a model of inflammatory cachexia
R Roubenoff1, L M Freeman, D E Smith
1Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA.
Arthritis and Rheumatism
|March 1, 1997
Summary
Adjuvant arthritis in rats causes significant weight loss and decreased body cell mass, mirroring human rheumatoid arthritis. This inflammatory cachexia is linked to increased production of tumor necrosis factor alpha (TNF alpha) and interleukin-1 (IL-1).
Area of Science:
- Immunology and Rheumatology
- Animal Models of Disease
- Metabolic Research
Background:
- Rheumatoid arthritis (RA) is associated with changes in body composition and elevated inflammatory cytokines.
- Adjuvant arthritis (AA) in rats is a common model for studying inflammatory arthritis.
- The relationship between AA, body composition changes, and cytokine production requires further elucidation.
Purpose of the Study:
- To investigate if adjuvant arthritis (AA) in rats induces body composition and cytokine production changes similar to human rheumatoid arthritis (RA).
- To assess the role of anorexia versus inflammatory cachexia in AA-induced weight loss.
- To correlate weight loss with specific cytokine production in AA models.
Main Methods:
- Adjuvant arthritis (AA) was induced in Lewis rats using Freund's complete adjuvant.
- Body cell mass was quantified using 42K gavage to measure total exchangeable potassium.
- Splenocyte production of interleukin-1 (IL-1) and tumor necrosis factor alpha (TNF alpha) was assessed via bioassay; weight and food intake were also monitored.
Main Results:
- Animals with AA exhibited significant body weight loss (20% by day 28) and a 24.7% decrease in body cell mass.
- Anorexia alone did not account for the observed weight loss, as pair-fed controls showed significantly less weight reduction.
- Weight loss strongly correlated with TNF alpha production (r = 0.68, P < 0.007) and moderately with IL-1 production (r = 0.45, P < 0.04).
Conclusions:
- Adjuvant arthritis (AA) in rats serves as a valuable model for inflammatory cachexia, closely mimicking human rheumatoid arthritis pathophysiology.
- The findings support the hypothesis that cytokine-driven cachexia plays a significant role in chronic inflammatory arthritis.
- AA provides a robust platform for studying the mechanisms underlying inflammation-induced metabolic disturbances in arthritis.