4.6 Review

AMPK: mediating the metabolic effects of salicylate-based drugs?

Journal

TRENDS IN ENDOCRINOLOGY AND METABOLISM
Volume 24, Issue 10, Pages 481-487

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tem.2013.06.002

Keywords

AMPK; aspirin; salicylate; inflammation; diabetes; cancer

Funding

  1. Canada Research Chair in Metabolism and Obesity
  2. Canadian Institutes of Health Research
  3. Canadian Diabetes Association
  4. Wellcome Trust
  5. Cancer Research UK
  6. AstraZeneca
  7. Boehringer-Ingelheim
  8. GlaxoSmithKline
  9. Merck KgaA
  10. Janssen Pharmaceutica
  11. Pfizer
  12. Cancer Research UK [15101] Funding Source: researchfish

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Salicylates are among the oldest medicinal compounds known to humans, and have been used to reduce fever, pain, and inflammation. The major oral salicylates are aspirin and salsalate, both of which are rapidly metabolized to salicylate in vivo. Owing to its acetyl group, aspirin irreversibly inhibits cyclo-oxygenases and thus blocks platelet aggregation, whereas salsalate has been used for treatment of inflammatory diseases such as rheumatoid arthritis. Recently, beneficial effects of salicylates in type 2 diabetes and cancer have been proposed. This has led to renewed interest in understanding how these simple molecules have such diverse and multifaceted effects. Here we discuss the idea that AMP-activated protein kinase (AMPK) might mediate some effects of salicylate-based drugs, particularly by modulating cellular metabolism.

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