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Deletion of myostatin improves vascular function in obese mice
Author(s) -
Qiu Shuiqing,
Mintz James,
Nernpermpisooth Nitirut,
Salet Christina,
Fulton David J,
Stepp David W
Publication year - 2013
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.27.1_supplement.918.6
Subject(s) - myostatin , medicine , endocrinology , vasodilation , mesenteric arteries , vascular smooth muscle , gastrocnemius muscle , lean body mass , adipose tissue , muscle hypertrophy , skeletal muscle , artery , body weight , smooth muscle
Exercise improves endothelial function in obese patients. Salutatory effects of exercise include increases in muscle size and quality, reduction in fat mass and alterations of the plasma milieu. The relationships between these changes and improvements in vascular function are poorly defined. Hypothesis Increasing muscle mass by deletion of muscle growth negative regulator myostatin, improves vascular function in mesenteric arteries from obese db/db mice. Myostatin deletion increases muscle mass in both lean (gastrocnemius 57.93%, gluteus maximus 60.95%, Triceps 57.64%) and obese mice (gastrocnemius 79.64%, gluteus maximus 112.32%, Triceps 103.61%). Myostatin deletion increases muscle fiber size in lean and obese mice (p< 0.05) but has no significant effects on adipocyte size in obese mice. Fasting glucose, HbA1c and glucose tolerance are improved in obese myostatin null mice. Obese mice demonstrate superoxide‐mediated impairment of ACh‐induced vasodilation compared to lean mice. Deletion of myostatin in obese mice improved ACh‐induced vasodilation in mesenteric arteries without effects in lean mice. This improvement was blunted by L‐NAME. PGI 2 and EDHF mediated vasodilation were preserved in obese mice, and unaffected by myostatin deletion. Taken together, these data suggested that increasing muscle mass by deletion of myostatin improves NO not PGI 2 or EDHF mediated vasodilation in obese mice.