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To clarify the role of NO in inflammation, we studied carrageenin-induced pleurisy in rats treated with an NO donor (NOC-18), a substrate for NO formation (L-arginine), and\/or an NO synthase inhibitor (S-(2-aminoethyl) isothiourea or -nitro-L-arginine). We assessed inflammatory cell migration, nitrite\/nitrate values, lipid peroxidation and pro-inflammatory mediators. NOC-18 and L-arginine reduced the migration of inflammatory cells and edema, lowered oxidative stress, and normalized antioxidant enzyme activities. NO synthase inhibitors increased the exudate formation and inflammatory cell number, contributed to oxidative stress, induced an oxidant\/antioxidant imbalance by maintaining high , and enhanced the production of pro-inflammatory mediators. L-arginine and NOC-18 reversed the proinflammatory effects of NO synthase inhibitors, perhaps by reducing the expression of adhesion molecules on endothelial cells. Thus, our results indicate that NO is involved in blunting\u2014not enhancing\u2014the inflammatory response.<\/jats:p>","DOI":"10.1155\/2010\/682879","type":"journal-article","created":{"date-parts":[[2010,6,2]],"date-time":"2010-06-02T14:35:18Z","timestamp":1275489318000},"page":"1-11","source":"Crossref","is-referenced-by-count":22,"title":["Involvement of Nitric Oxide in a Rat Model of Carrageenin-Induced Pleurisy"],"prefix":"10.1155","volume":"2010","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2257-0069","authenticated-orcid":true,"given":"Masahiro","family":"Iwata","sequence":"first","affiliation":[{"name":"Department of Rehabilitation, Faculty of Health Sciences, Nihon Fukushi University, 26-2 Higashihaemi-cho, Handa 475-0012, Japan"},{"name":"Department of Physical Therapy, Nagoya University School of Health Sciences, 1-1-20 Daikominami, Higashi-ku, Nagoya 461-8673, 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