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ABSTRACT: Background and purpose
The advanced glycation end products (AGEs) participate in the pathogenesis of diabetic nephropathy (DN) by promoting renal inflammation and injury. L-carnosine acts as a quencher of the AGE precursors reactive carbonyl species (RCS), but is rapidly inactivated by carnosinase. In this study, we evaluated the effect of FL-926-16, a carnosinase-resistant and bioavailable carnosine derivative, on the onset and progression of DN in db/db mice.Experimental approach
Adult male db/db mice and coeval db/m controls were left untreated or treated with FL-926-16 (30 mg·kg-1 body weight) from weeks 6 to 20 (prevention protocol) or from weeks 20 to 34 (regression protocol).Key results
In the prevention protocol, FL-926-16 significantly attenuated
SUBMITTER: Iacobini C
PROVIDER: S-EPMC5740255 | biostudies-literature | 2018 Jan
REPOSITORIES: biostudies-literature