Modulation of inflammation and oxidative stress in canine chondrocytes

被引:19
作者
Dycus, David L. [1 ,4 ]
Au, Angela Y. [2 ]
Grzanna, Mark W. [3 ]
Wardlaw, Jennifer L. [1 ]
Frondoza, Carmelita G. [1 ,3 ,5 ]
机构
[1] Mississippi State Univ, Coll Vet Med, Dept Clin Sci, Mississippi State, MS 39762 USA
[2] Syracuse Univ, Dept Biomed & Chem Engn, LC Smith Coll Engn & Comp Sci, Syracuse, NY 13244 USA
[3] Nutramax Labs Inc, Edgewood, MD 21040 USA
[4] Charleston Vet Referral Ctr, Dept Surg, Charleston, SC 29414 USA
[5] Johns Hopkins Univ, Sch Med, Dept Orthopaed Surg, Baltimore, MD 21239 USA
关键词
AVOCADO SOYBEAN UNSAPONIFIABLES; PROSTAGLANDIN E-2 PRODUCTION; GENE-EXPRESSION; NITRIC-OXIDE; ARTICULAR CHONDROCYTES; SYNOVIAL-FLUID; CYCLOOXYGENASE-2; EXPRESSION; SUPEROXIDE-DISMUTASE; REACTIVE NITROGEN; DOWN-REGULATION;
D O I
10.2460/ajvr.74.7.983
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective-To determine whether oxidative stress could be induced in canine chondrocytes in vitro. Sample-Chondrocytes obtained from healthy adult mixed-breed dogs. Procedures-Harvested chondrocytes were maintained at 37 degrees C with 5% CO2 for 24 hours. To assess induction of oxidative stress, 2 stimuli were used: hydrogen peroxide and a combination of interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha). To determine the effect of hydrogen peroxide, a set of chondrocyte-seeded plates was incubated with control medium alone or hydrogen peroxide (100, 200, or 300 mu M) for 24 hours. For inhibition of oxidative stress, cells were incubated for 24 hours with N-acetylcysteine (NAC; 10mM) before exposure to hydrogen peroxide. Another set of chondrocyte-seeded plates was incubated with control medium alone or with IL1 beta (10 ng/mL) and TNF-alpha (1 ng/mL) for 24 hours. Supernatants were obtained for measurement of prostaglandin E-2 production, and cell lysates were used for measurement of superoxide dismutase (SOD) activity and reduced-glutathione (GSH) concentration. Results-Chondrocytes responded to the oxidative stressor hydrogen peroxide with a decrease in SOD activity and GSH concentration. Exposure to the antioxidant NAC caused an increase in SOD activity in hydrogen peroxide-stressed chondrocytes to a degree comparable with that in chondrocytes not exposed to hydrogen peroxide. Similarly, NAC exposure induced significant increases in GSH concentration. Activation with IL-1 beta and TNF-alpha also led to a decrease in SOD activity and increase in prostaglandin E-2 production. Conclusions and Clinical Relevance-Canine chondrocytes responded to the oxidative stress caused by exposure to hydrogen peroxide and cytokines. Exposure to oxidative stress inducers could result in perturbation of chondrocyte and cartilage homeostasis and could contribute to the pathophysiology of osteoarthritis. Use of antioxidants, on the other hand, may be helpful in the treatment of arthritic dogs.
引用
收藏
页码:983 / 989
页数:7
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