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ABSTRACT: Objective
Type 1 diabetes leads to impairments in growth, function, and regenerative capacity of skeletal muscle; however, the underlying mechanisms have not been clearly defined.Research design and methods
With the use of Ins2(WT/C96Y) mice (model of adolescent-onset type 1 diabetes), muscle regeneration was characterized in terms of muscle mass, myofiber size (cross-sectional area), and protein expression. Blood plasma was analyzed for glucose, nonesterified fatty acids, insulin, and plasminogen activator inhibitor-1 (PAI-1). PAI-039, an effective inhibitor of PAI-1, was orally administered to determine if PAI-1 was attenuating muscle regeneration in Ins2(WT/C96Y) mice.Results
Ins2(WT/C96Y) mice exposed to 1 or 8 weeks of untreated type 1 diabetes before chemicall
SUBMITTER: Krause MP
PROVIDER: S-EPMC3121432 | biostudies-literature | 2011 Jul
REPOSITORIES: biostudies-literature