Biochemical Society Transactions

AMPK 2002: 2nd International Meeting on AMP-activated Protein Kinase

Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome

M.H. Gollob


The AMP-activated protein kinase (AMPK) system was first discovered 30 years ago. Since that time, knowledge of the diverse physiological functions of AMPK has grown rapidly and continues to evolve. Most recently, the observation that spontaneously occurring genetic mutations in the γ regulatory subunits of AMPK give rise to a skeletal and cardiac muscle disease emphasizes the critical importance of AMPK in the maintenance of health and disease. The cardiac phenotype observed in humans harbouring genetic mutations in the γ2 regulatory subunit (PRKAG2) of AMPK is consistent with abnormal glycogen accumulation in the heart. The perturbation of AMPK activity induced by genetic mutations in PRKAG2 and the resultant effect on muscle cell glucose metabolism may be relevant to the issue of targeting AMPK in drug development for insulin-resistant diabetes mellitus.

  • AMP-activated protein kinase
  • Wolff–Parkinson–White


  • AMPK 2002: 2nd International Meeting on AMP-activated Protein Kinase, a Biochemical Society-sponsored meeting held at University of Dundee, Scotland, 12–14 September 2002

  • Abbreviations used: AMPK, AMP-activated protein kinase; WPW, Wolff–Parkinson–White; HCM, hypertrophic cardiomyopathy.