2002
DOI: 10.1053/meta.2002.34050
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Insulin and insulin-like growth factor-1 action on human skeletal muscle: Preferential effects of insulin-like growth factor-1 in type 2 diabetic subjects

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Cited by 22 publications
(15 citation statements)
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“…Insulin binding to IR has been reported to be normal [52] or impaired [53,54]. Furthermore, tyrosine phosphorylation and/or activity of the IR has been reported to be normal [51,53,[55][56][57] or impaired [50,54,58] in skeletal muscle from non-obese and obese Type 2 diabetic subjects, compared with nondiabetic subjects.…”
Section: Insulin Signaling Defects Are Associated With Type 2 Diabetesmentioning
confidence: 99%
“…Insulin binding to IR has been reported to be normal [52] or impaired [53,54]. Furthermore, tyrosine phosphorylation and/or activity of the IR has been reported to be normal [51,53,[55][56][57] or impaired [50,54,58] in skeletal muscle from non-obese and obese Type 2 diabetic subjects, compared with nondiabetic subjects.…”
Section: Insulin Signaling Defects Are Associated With Type 2 Diabetesmentioning
confidence: 99%
“…39 In skeletal muscle cells of type II diabetic patients, IGF-1 was found to be a more potent stimulant of glucose transport than insulin itself. 40 The administration of recombinant human IGF-1 to diabetic patients can reduce insulin dose requirement by 50% and serum glucose levels by 23% 41 while improving glucose tolerance, hyperinsulinemia, and hypertriglyceridemia. 42,43 Even in normal volunteers, Figure 1.…”
Section: Igf-1 and The Metabolic Syndromementioning
confidence: 99%
“…Low serum IGF1 levels are also associated with determinants of the metabolic syndrome including insulin resistance, serum leptin levels, waist-to-hip ratio, and type 2 diabetes mellitus (14)(15)(16)(17)(18). Moreover, low baseline levels of serum IGF1 predict an increased risk of fatal coronary events (19).…”
Section: Introductionmentioning
confidence: 99%