[HTML][HTML] Inhibition of protein kinase Cε prevents hepatic insulin resistance in nonalcoholic fatty liver disease

VT Samuel, ZX Liu, A Wang… - The Journal of …, 2007 - Am Soc Clin Investig
VT Samuel, ZX Liu, A Wang, SA Beddow, JG Geisler, M Kahn, X Zhang, BP Monia, S Bhanot…
The Journal of clinical investigation, 2007Am Soc Clin Investig
Nonalcoholic fatty liver disease is strongly associated with hepatic insulin resistance and
type 2 diabetes mellitus, but the molecular signals linking hepatic fat accumulation to hepatic
insulin resistance are unknown. Three days of high-fat feeding in rats results specifically in
hepatic steatosis and hepatic insulin resistance. In this setting, PKCε, but not other isoforms
of PKC, is activated. To determine whether PKCε plays a causal role in the pathogenesis of
hepatic insulin resistance, we treated rats with an antisense oligonucleotide against PKCε …
Nonalcoholic fatty liver disease is strongly associated with hepatic insulin resistance and type 2 diabetes mellitus, but the molecular signals linking hepatic fat accumulation to hepatic insulin resistance are unknown. Three days of high-fat feeding in rats results specifically in hepatic steatosis and hepatic insulin resistance. In this setting, PKCε, but not other isoforms of PKC, is activated. To determine whether PKCε plays a causal role in the pathogenesis of hepatic insulin resistance, we treated rats with an antisense oligonucleotide against PKCε and subjected them to 3 days of high-fat feeding. Knocking down PKCε expression protects rats from fat-induced hepatic insulin resistance and reverses fat-induced defects in hepatic insulin signaling. Furthermore, we show that PKCε associates with the insulin receptor in vivo and impairs insulin receptor kinase activity both in vivo and in vitro. These data support the hypothesis that PKCε plays a critical role in mediating fat-induced hepatic insulin resistance and represents a novel therapeutic target for type 2 diabetes.
The Journal of Clinical Investigation