Omega-3 Multiple Effects Increasing Glucocorticoid-Induced Muscle Atrophy: Autophagic, Ampk And Ups Mechanisms

Alan Fappi,Juliana de C Neves, Karine A Kawasaki, Luana Bacelar, Leandro N Sanches,Felipe P da Silva, Rubens Larina-Neto,Gerson Chadi,Edmar Zanoteli

PHYSIOLOGICAL REPORTS(2019)

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摘要
Muscle atrophy occurs in many conditions, including use of glucocorticoids. N-3 (omega-3) is widely consumed due its healthy properties; however, concomitant use with glucocorticoids can increase its side effects. We evaluated the influences of N-3 on glucocorticoid atrophy considering IGF-1, Myostatin, MEK/ERK, AMPK pathways besides the ubiquitin-proteasome system (UPS) and autophagic/lysosomal systems. Sixty animals constituted six groups: CT, N-3 (EPA 100 mg/kg/day for 40 days), DEXA 1.25 (DEXA 1.25 mg/kg/day for 10 days), DEXA 1.25 + N3 (EPA for 40 days + DEXA 1.25 mg/kg/day for the last 10 days), DEXA 2.5 (DEXA 2.5 mg/kg/day for 10 days), and DEXA 2.5 + N3 (EPA for 40 days + DEXA 2.5 mg/kg/day for 10 days). Results: N-3 associated with DEXA increases atrophy (fibers 1 and 2A), FOXO3a, P-SMAD2/3, Atrogin-1/MAFbx (mRNA) expression, and autophagic protein markers (LC3II, LC3II/LC3I, LAMP-1 and acid phosphatase). Additionally, N-3 supplementation alone decreased P-FOXO3a, PGC1-alpha, and type 1 muscle fiber area. Conclusion: N-3 supplementation increases muscle atrophy caused by DEXA in an autophagic, AMPK and UPS process.
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关键词
autophagy, eicosapentaenoic acid, glucocorticoid, IGF-1 pathway, MEK/ERK pathway, muscle atrophy, Myostatin/Smad2/3 pathway, omega-3 fatty acid
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