digitonin and Obesity--Morbid

digitonin has been researched along with Obesity--Morbid* in 1 studies

Other Studies

1 other study(ies) available for digitonin and Obesity--Morbid

ArticleYear
Proteome analysis of skeletal muscle from obese and morbidly obese women.
    Diabetes, 2005, Volume: 54, Issue:5

    Obesity-related diseases such as the metabolic syndrome and type 2 diabetes originate, in part, from the progressive metabolic deterioration of skeletal muscle. A preliminary proteomic survey of rectus abdominus muscle detected a statistically significant increase in adenylate kinase (AK)1, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and aldolase A in obese/overweight and morbidly obese women relative to lean control subjects. AK1 is essential for the maintenance of cellular energy charge, and GAPDH and aldolase A are well known glycolytic enzymes. We found that muscle AK1 protein and enzymatic activity increased 2.9 and 90%, respectively, in obese women and 9.25 and 100%, respectively, in morbidly obese women. The total enzymatic activity of creatine kinase, which also regulates energy metabolism in muscle, was shown to increase 30% in obese/overweight women only. We propose that increased protein and enzymatic activity of AK1 is representative of a compensatory glycolytic drift to counteract reduced muscle mitochondrial function with the progression of obesity. This hypothesis is supported by increased abundance of the glycolytic enzymes GAPDH and aldolase A in obese and morbidly obese muscle. In summary, proteome analysis of muscle has helped us better describe the molecular etiology of obesity-related disease.

    Topics: Adenylate Kinase; Body Mass Index; Creatine Kinase; Digitonin; Electrophoresis, Gel, Two-Dimensional; Female; Humans; Middle Aged; Muscle Proteins; Obesity; Obesity, Morbid; Proteome; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

2005