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Amelioration of nephropathy with apoA-1 mimetic peptide in apoE-deficient mice
Author(s) -
Nosratola D. Vaziri,
Hwajin Kim,
Hamid Moradi,
Farbod Farmand,
Kaveh Navab,
Mohamad Navab,
Susan Hama,
Alan M. Fogelman,
Yasmir Quiroz,
Bernardo RodríguezIturbe
Publication year - 2010
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/gfq274
Subject(s) - oxidative stress , medicine , inflammation , apolipoprotein e , endocrinology , kidney disease , kidney , glomerulosclerosis , nephropathy , pathogenesis , proteinuria , immunology , diabetes mellitus , disease
There is mounting evidence that dyslipidaemia may contribute to development and progression of renal disease. For instance, hyperlipidaemia in apolipoprotein E-deficient (apoE(-/-)) mice is associated with glomerular inflammation, mesangial expansion and foam cell formation. ApoA-1 mimetic peptides are potent antioxidant and anti-inflammatory compounds which are highly effective in ameliorating atherosclerosis and inflammation in experimental animals. Given the central role of oxidative stress and inflammation in progression of renal disease, we hypothesized that apoA-1 mimetic peptide, D-4F, may attenuate renal lesions in apoE(-/-) mice.

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