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Polyunsaturated fatty acids influence inflammatory markers in a cellular model for canine osteoarthritis

花生四烯酸 多不饱和脂肪酸 六烯酸 二十碳五烯酸 一氧化氮 骨关节炎 化学 前列腺素E2 鱼油 一氧化氮合酶 脂肪酸 环氧合酶 生物化学 内分泌学 内科学 生物 医学 病理 渔业 替代医学
作者
Natalia S. Adler,Axel Schoeniger,Herbert Fuhrmann
出处
期刊:Journal of Animal Physiology and Animal Nutrition [Wiley]
卷期号:102 (2): e623-e632 被引量:41
标识
DOI:10.1111/jpn.12804
摘要

Summary Although it is well recognized that dietary supplementation with fish oil improves clinical symptoms in dogs suffering from osteoarthritis, the molecular basis for the dietary benefit is not yet completely resolved in dogs. This study was designed to further clarify how polyunsaturated fatty acids ( PUFA ) affect key factors of cartilage degeneration in a canine cell culture system mimicking osteoarthritis. Canine chondrocytes were incubated either without or with 10 μ m of eicosapentaenoic acid ( EPA ), docosahexaenoic acid ( DHA ), arachidonic acid ( AA ) or 3.6 μ m ibuprofen (Ibu) as positive control for 6 days. After the supplementation, cells were stimulated with 10 ng/ml interleukin‐1β ( IL ‐1β) for another 48 hr to induce osteoarthritic changes, or left unstimulated. We analysed fatty acid uptake via gas–liquid chromatography, nitric oxide ( NO ) production via Griess assay, prostaglandin E ( PGE ) production via ELISA and relative gene expression of several cartilage matrix proteinases, inducible nitric oxide synthase ( iNOS ) and cyclooxygenase‐2 via RT ‐ qPCR . After supplementation, the chondrocytes rapidly incorporated the PUFA into their fatty acid pools. The stimulation with IL ‐1β caused a marked increase of most of the inflammatory markers measured. N‐3 PUFA EPA reduced IL ‐induced gene expression of iNOS and corresponding production of NO . N‐6 PUFA AA also decreased iNOS and NO , but furthermore lowered gene expression of matrix metalloproteinase‐3. On the other hand, AA upregulated the aggrecanase ADAMTS ‐5 and augmented the release of PGE . The effect of n‐3 PUFA DHA turned out to be negligible. Our results reveal molecular mechanisms by which PUFA affect degenerative joint disease in dogs. Of particular importance is that not only EPA but also AA decreased several inflammatory markers in our model. Thus, we conclude that an appropriate balance of both n‐3 and n‐6 fatty acids deserves more attention in dietary interventions.
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