Abstract

This study was aimed to confirm the hypothesis that Chronic intermittent hypobaric hypoxia (CIHH) could ameliorate inflammation of skeletal muscle in rats with metabolic syndrome (MS). Sprague-Dawley rats (male, 160-180 g) were randomly divided into 4 groups: control group (CON), fructose group (FRUC, 10% fructose in drinking water for 6 weeks), CIHH group (simulated 5,000 m altitude, 6 h per day for 6 weeks), and CIHH plus fructose groups (CIHH-F). Histopathology of skeletal muscle, systolic arterial pressure (SAP), blood biochemical, protein expression of TNFα, MCP-1 and NF-kappa B were measured. The SAP, body weight, and the plasma contents of glucose, insulin, insulin C peptide, triglyceride and total cholesterol were elevated in FRUC rats but not in CIHH-F rats. Meanwhile, the inflammatory response of skeletal muscle was presented in FRUC rats but not in CIHH-F rats, which was demonstrated by the infiltration of circulating mononuclear cells and the up-regulation of TNFα and MCP-1. Finally the protein expression of NF-kappa B in skeletal muscle was correspondingly up-regulated in FRUC rats, but such upregulation was not observed in CIHH-F rats. Our results suggest that CIHH prevents the inflammation of skeletal muscle in rats with MS via inhibiting NF-kappa B signaling. CIHH might be the new strategy for prevention and therapy of MS.

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