Effects of selective and non-selective COX inhibitors on antigen-induced release of prostanoid mediators and bronchoconstriction in the isolated perfused and ventilated guinea pig lung

• Published in: Prostaglandins, leukotrienes and essential fatty acids Vol. 78; no. 2; pp. 89 - 97
• Main Authors: Selg, Ewa, Låstbom, Lena, Ryrfeldt, Åke, Kumlin, Maria, Dahlén, Sven-Erik
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ltd 01.02.2008; Elsevier
• Subjects: Advanced Basic Science; Animals; Biological and medical sciences; Bronchoconstriction - immunology; Celecoxib; Cyclooxygenase 1 - metabolism; Cyclooxygenase 2 - metabolism; Cyclooxygenase Inhibitors - metabolism; Diclofenac - metabolism; Endocrinology & Metabolism; Flurbiprofen - metabolism; Fundamental and applied biological sciences. Psychology; Guinea Pigs; Humans; Leukotrienes - chemistry; Leukotrienes - immunology; Lung - immunology; Lung - physiology; Male; MEDICIN; MEDICINE; Ovalbumin - immunology; Piperazines - metabolism; Prostaglandins - immunology; Pyrazoles - metabolism; Sulfonamides - metabolism; Thiazoles - metabolism; Thromboxane A2 - immunology; Thromboxane B2 - immunology; Vertebrates: endocrinology; Antigen; Vertebrata; Mammalia; Guinea pig; Lung; Rodentia; Respiratory system; Release
• ISSN: 0952-3278; 1532-2823; 1532-2823
• DOI: 10.1016/j.plefa.2008.01.001

The contribution of cycloxygenase (COX)-1 and COX-2 in antigen-induced release of mediators and ensuing bronchoconstriction was investigated in the isolated perfused guinea pig lung (IPL). Antigen challenge with ovalbumin (OVA) of lungs from actively sensitised animals induced release of thromboxane (TX)A 2, prostaglandin (PG)D 2, PGF 2 α , PGI 2 and PGE 2, measured in the lung effluent as immunoreactive TXB 2, PGD 2-MOX, PGF 2 α , 6-keto PGF 1 α and PGE 2, respectively. This release was abolished by the non-selective COX inhibitor flurbiprofen (10 μM). In contrast, neither the selective COX-1 inhibitor FR122047 nor the selective COX-2 inhibitor celecoxib (10 μM each) significantly inhibited the OVA-induced bronchoconstriction or release of COX products, except for PGD 2. Another non-selecive COX inhibitor, diclofenac (10 μM) also significantly inhibited antigen-induced bronchoconstriction. The data suggest that both COX isoenzymes, COX-1 and COX-2 contribute to the immediate antigen-induced generation of prostanoids in IPL and that the COX-1 and COX-2 activities are not associated with different profiles of prostanoid end products.