کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3001586 1180651 2016 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Impaired glucose metabolism and exercise capacity with muscle-specific glycogen synthase 1 (gys1) deletion in adult mice
ترجمه فارسی عنوان
اختلال در متابولیسم گلوکز و ظرفیت تمرین با حذف گلیکوژن سنتاز 1 (gys1) در موش بالغ
کلمات کلیدی
gys1؛ تحمل گلوکز؛ حساسیت به انسولین؛ جذب گلوکز عضلانی؛ ظرفیت ورزش؛ موش های نابود کننده خاص (KO) قابل انعطاف است
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی سیستم های درون ریز و اتونومیک
چکیده انگلیسی


• Muscle-specific gys1 knockdown in adult mice results in 70% reduction in skeletal muscle glycogen levels.
• Muscle-specific gys1 knockdown leads to glucose intolerance and peripheral insulin resistance.
• Muscle glycogen depletion caused impaired performance, as well as fatigue development during exercise.

ObjectiveMuscle glucose storage and muscle glycogen synthase (gys1) defects have been associated with insulin resistance. As there are multiple mechanisms for insulin resistance, the specific role of glucose storage defects is not clear. The aim of this study was to examine the effects of muscle-specific gys1 deletion on glucose metabolism and exercise capacity.MethodsTamoxifen inducible and muscle specific gys-1 KO mice were generated using the Cre/loxP system. Mice were subjected to glucose tolerance tests, euglycemic/hyperinsulinemic clamps and exercise tests.Resultsgys1-KO mice showed ≥85% reduction in muscle gys1 mRNA and protein concentrations, 70% reduction in muscle glycogen levels, postprandial hyperglycaemia and hyperinsulinaemia and impaired glucose tolerance. Under insulin-stimulated conditions, gys1-KO mice displayed reduced glucose turnover and muscle glucose uptake, indicative of peripheral insulin resistance, as well as increased plasma and muscle lactate levels and reductions in muscle hexokinase II levels. gys1-KO mice also exhibited markedly reduced exercise and endurance capacity.ConclusionsThus, muscle-specific gys1 deletion in adult mice results in glucose intolerance due to insulin resistance and reduced muscle glucose uptake as well as impaired exercise and endurance capacity.In briefThis study demonstrates why the body prioritises muscle glycogen storage over liver glycogen storage despite the critical role of the liver in supplying glucose to the brain in the fasting state and shows that glycogen deficiency results in impaired glucose metabolism and reduced exercise capacity.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Metabolism - Volume 5, Issue 3, March 2016, Pages 221–232
نویسندگان
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