Salicylate acutely stimulates 5'-AMP-activated protein kinase and insulin-independent glucose transport in rat skeletal muscles.

• Serizawa, Yasuhiro

• 大島, 里詠子

• Yoshida, Mitsuki

• Sakon, Ichika

• Kitani, Kazuto

• Goto, Ayumi

• Tsuda, Satoshi

• Hayashi, Tatsuya

抄録

Salicylate (SAL) has been recently implicated in the antidiabetic effect in humans. We assessed whether 5'-AMP-activated protein kinase (AMPK) in skeletal muscle is involved in the effect of SAL on glucose homeostasis. Rat fast-twitch epitrochlearis and slow-twitch soleus muscles were incubated in buffer containing SAL. Intracellular concentrations of SAL increased rapidly (<5min) in both skeletal muscles, and the Thr(172) phosphorylation of the α subunit of AMPK increased in a dose- and time-dependent manner. SAL increased both AMPKα1 and AMPKα2 activities. These increases in enzyme activity were accompanied by an increase in the activity of 3-O-methyl-d-glucose transport, and decreases in ATP, phosphocreatine, and glycogen contents. SAL did not change the phosphorylation of insulin receptor signaling including insulin receptor substrate 1, Akt, and p70 ribosomal protein S6 kinase. These results suggest that SAL may be transported into skeletal muscle and may stimulate AMPK and glucose transport via energy deprivation in multiple muscle types. Skeletal muscle AMPK might be part of the mechanism responsible for the metabolic improvement induced by SAL.

収録刊行物

• Biochemical and biophysical research communications

  Biochemical and biophysical research communications 453 (1), 81-85, 2014-10-10

  Elsevier Inc.

キーワード

• Salicylate
• 5′-AMP-activated protein kinase
• Glucose transport
• Insulin signaling
• Skeletal muscle
• Diabetes mellitus

詳細情報

• CRID: 1050845760729843840
• NII論文ID: 120005517911
• NII書誌ID: AA00564395
• ISSN: 0006291X
• HANDLE: 2433/192273
• 本文言語コード: en
• 資料種別: journal article
• データソース種別:
  • IRDB
  • CiNii Articles