Ontology highlight
ABSTRACT: Aim
To examine the therapeutic effects and underlying mechanisms of DZ2002, a reversible S-adenosyl-L-homocysteine hydrolase (SAHH) inhibitor, on lupus-prone female NZB×NZW F1 (NZB/W F1) mice.Methods
Female NZB/W F1 mice were treated orally with DZ2002 (0.5 mg·kg(-1)·d(-1)) for 11 weeks, and the proteinuria level and body weight were monitored. After the mice ware euthanized, serum biochemical parameters and renal damage were determined. Splenocytes of NZB/W F1 mice were isolated for ex vivo study. Toll-like receptor (TLR)-stimulated human peripheral blood mononuclear cells (PBMCs) or murine bone marrow-derived dendritic cells (BMDCs) were used for in vitro study.Results
Treatment of the mice with DZ2002 significantly attenuated the progression of glomerulonephritis
SUBMITTER: He SJ
PROVIDER: S-EPMC4651227 | biostudies-literature | 2014 Feb
REPOSITORIES: biostudies-literature