{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T13:54:52Z","timestamp":1761918892545},"reference-count":34,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2006,10,9]],"date-time":"2006-10-09T00:00:00Z","timestamp":1160352000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Liver International"],"published-print":{"date-parts":[[2006,12]]},"abstract":"<jats:p><jats:bold>Abstract\n\t\t\t\t\tBackground\/Aims: <\/jats:bold> This study determined the roles of NAD(P)H oxidase, which generates reactive oxygen species (ROS), and of inducible nitric oxide synthase (iNOS), which generates nitric oxide (NO) on the development of hepatic fibrosis in mice.<\/jats:p><jats:p><jats:bold>Methods: <\/jats:bold> Hepatic fibrosis was produced by carbon tetrachloride administered for 12 weeks in wild\u2010type (WT) mice and in mice with knockout of either the gp91<jats:sup>phox<\/jats:sup> subunit of the NAD(P)H complex (gp91<jats:sup>phox\u2212\/\u2212<\/jats:sup>) or of iNOS (iNOS<jats:sup>\u2212\/\u2212<\/jats:sup>).<\/jats:p><jats:p><jats:bold>Results: <\/jats:bold> Liver fibrosis and hydroxyproline after carbon tetrachloride was lower in gp91<jats:sup>phox\u2212\/\u2212<\/jats:sup> and in iNOS<jats:sup>\u2212\/\u2212<\/jats:sup> mice than in WT mice. The increase in \u03b1<jats:sub>2<\/jats:sub>(I) collagen mRNA was absent in the gp91<jats:sup>phox\u2212\/\u2212<\/jats:sup> but not in the iNOS<jats:sup>\u2212\/\u2212<\/jats:sup> mice. Transformation growth factor \u03b2 (TGF\u2010\u03b2) mRNA was increased more in the gp91<jats:sup>phox\u2212\/\u2212<\/jats:sup> than in the WT mice, while in the iNOS<jats:sup>\u2212\/\u2212<\/jats:sup> mice there was no increase in TGF\u2010\u03b2 mRNA. 3\u2010Nitrotyrosine was similarly increased by carbon tetrachloride in gp91<jats:sup>phox\u2212\/\u2212<\/jats:sup> and WT mice, while there was no increase in the iNOS<jats:sup>\u2212\/\u2212<\/jats:sup> mice.<\/jats:p><jats:p><jats:bold>Conclusions:\n\t\t\t\t\t<\/jats:bold> Deficiencies in NAD(P)H oxidase and in iNOS separately reduce, but do not eliminate carbon tetrachloride\u2010induced liver fibrosis. Likely causes for this inhibitory effects are decreases in the production of ROS in NAD(P)H deficiency and of peroxinitrite radicals in iNOS deficiency.<\/jats:p>","DOI":"10.1111\/j.1478-3231.2006.01364.x","type":"journal-article","created":{"date-parts":[[2006,10,9]],"date-time":"2006-10-09T16:44:54Z","timestamp":1160412294000},"page":"1248-1257","source":"Crossref","is-referenced-by-count":16,"title":["Influences of reactive oxygen species and nitric oxide on hepatic fibrogenesis"],"prefix":"10.1111","volume":"26","author":[{"given":"Gennadiy","family":"Novitskiy","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James J.","family":"Potter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lan","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Esteban","family":"Mezey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2006,10,9]]},"reference":[{"key":"e_1_2_6_2_2","doi-asserted-by":"publisher","DOI":"10.1002\/hep.510300433"},{"key":"e_1_2_6_3_2","doi-asserted-by":"crossref","first-page":"16957","DOI":"10.1016\/S0021-9258(19)84800-7","article-title":"Stimulation of collagen gene expression by ascorbic acid in cultured human fibroblasts. 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