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Acute glomerular upregulation of ornithine decarboxylase is not essential for mesangial cell proliferation and matrix expansion in anti-Thy-1-nephritis
Author(s) -
Markus Ketteler,
Ralf Westenfeld,
A Gawlik,
Emile de Heer,
A. Distler
Publication year - 2000
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/15.1.16
Subject(s) - ornithine decarboxylase , albuminuria , mesangial proliferative glomerulonephritis , endocrinology , medicine , mesangial cell , glomerulonephritis , mesangium , glomerulosclerosis , downregulation and upregulation , polyamine , kidney , biology , biochemistry , enzyme , proteinuria , gene
Pathways of L-arginine metabolism including nitric oxide, agmatine and polyamine synthesis are upregulated during glomerular inflammation in experimental glomerulonephritis. In anti-Thy-1-glomerulonephritis L-arginine-deficient diets ameliorate the disease course in this model. However, it is unclear which metabolic pathway is affected by this substrate depletion. Since polyamines are important proproliferative molecules, we studied the effect of specific polyamine synthesis blockade in vivo on mesangial cell proliferation and glomerular fibrosis in this model.

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