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  4. Enhanced inducible nitric oxide synthase expression and nitrotyrosine accumulation in experimental granulomatous hepatitis caused by Toxocara canis in mice
 
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Enhanced inducible nitric oxide synthase expression and nitrotyrosine accumulation in experimental granulomatous hepatitis caused by Toxocara canis in mice

Journal
Parasite Immunology
Journal Volume
26
Journal Issue
44354
Pages
273-281
Date Issued
2004
Author(s)
Fan C.-K.
Lin Y.-H.
CHIEN-CHING HUNG  
Chang S.-F.
Su K.-E.
DOI
10.1111/j.0141-9838.2004.00708.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-9644281805&doi=10.1111%2fj.0141-9838.2004.00708.x&partnerID=40&md5=39aa4f6c1bedcc9be48af319d3c64e88
https://scholars.lib.ntu.edu.tw/handle/123456789/588981
Abstract
The involvement of inducible nitric oxide synthase (iNOS) and nitrotyrosine (NT) in pathogenesis of toxocaral granulomatous hepatitis (TGH) in a murine host was quantitatively determined by biochemical, parasitological, pathological, and immunohistochemical assessments in a 42-week investigation. Mice were sacrificed for serum collection and histological processing as well as acid-pepsin digestion of the liver in a larval recovery study. Significantly increased levels of total serum NO were found in the trial, indirectly suggesting iNOS activation in the liver. iNOS reactivity was predominantly observed in infiltrating leucocytes in lesions and normal and apocrine-like cholangiocytes; in contrast, hepatocytes and multinucleated giant cells showed negative cytoplasmic staining in TGH. Strong iNOS-like reactivity was also detected on the body wall of larvae. The locations of NT reactivity were nearly identical to those of iNOS expression; infiltrating leucocytes or cholangiocytes stained for iNOS were also stained for NT in TGH. Enhanced iNOS expression, but not invading larvae (r = 0·256, P = 0·211), seemed to play a certain role in pathological damage in TGH due to a significant correlation between iNOS expression and serum alanine aminotransferase (ALT) levels (r = 0·593, P = 0·021) in the trial. Our present results indicate a potential therapeutic strategy for treatment of GH caused by other nematodes through manipulation of iNOS expression.
SDGs

[SDGs]SDG3

Other Subjects
3 nitrotyrosine; alanine aminotransferase; nitric oxide synthase; animal experiment; animal model; animal tissue; article; blood sampling; controlled study; giant cell; granulomatous hepatitis; histopathology; immunohistochemistry; leukocyte; liver cell; mouse; nonhuman; priority journal; protein expression; statistical analysis; Toxocara canis; Alanine Transaminase; Animals; Female; Giant Cells; Granuloma; Hepatitis, Animal; Hepatocytes; Larva; Leukocytes; Liver; Mice; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type II; Nitrites; Toxocara canis; Toxocariasis; Tyrosine; Animalia; Canis; Murinae; Nematoda; Toxocara canis
Type
journal article

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