Initial hyperinsulinemia and subsequent β-cell dysfunction is associated with elevated palmitate levels

• Published in: Pediatric research Vol. 80; no. 2; pp. 267 - 274
• Main Authors: Staaf, Johan, Ubhayasekera, Sarojini J.K.A., Sargsyan, Ernest, Chowdhury, Azazul, Kristinsson, Hjalti, Manell, Hannes, Bergquist, Jonas, Forslund, Anders, Bergsten, Peter
• Format: Journal Article
• Language: English
• Published: New York Nature Publishing Group US 01.08.2016
• Subjects: 631/80; 692/308/3187; 692/308/575; Adolescent; Adult; Aged; Cells, Cultured; Child; Child, Preschool; Cross-Sectional Studies; Diabetes Complications - blood; Fatty Acids, Nonesterified - chemistry; Female; Glucose - pharmacology; Glucose Tolerance Test; Humans; Hyperinsulinism - blood; Insulin - metabolism; Insulin Secretion; Insulin-Secreting Cells - cytology; Male; Medicine & Public Health; Middle Aged; Obesity - blood; Obesity - complications; Palmitates - blood; Pediatric Obesity; Pediatric Surgery; Pediatrics; Time Factors; translational-investigation
• ISSN: 0031-3998; 1530-0447; 1530-0447
• DOI: 10.1038/pr.2016.80

Background: The prevalence of obesity-related diabetes in childhood is increasing and circulating levels of nonesterified fatty acids may constitute a link. Here, the association between palmitate and insulin secretion was investigated in vivo and in vitro . Methods: Obese and lean children and adolescents ( n = 80) were included. Palmitate was measured at fasting; insulin and glucose during an oral glucose tolerance test (OGTT). Human islets were cultured for 0 to 7 d in presence of 0.5 mmol/l palmitate. Glucose-stimulated insulin secretion (GSIS), insulin content and apoptosis were measured. Results: Obese subjects had fasting palmitate levels between 0.10 and 0.33 mmol/l, with higher average levels compared to lean subjects. While obese children with elevated palmitate (>0.20 mmol/l) had accentuated insulin levels during OGTT, obese adolescents with high palmitate had delayed first-phase insulin response. In human islets exposed to palmitate for 2 d GSIS was twofold enhanced, but after 7 d attenuated. Intracellular insulin content decreased time-dependently in islets cultured in the presence of palmitate and cleaved caspase 3 increased. Conclusion: The rapid accentuated and delayed insulin secretory responses observed in obese children and adolescents, respectively, with high palmitate levels may reflect changes in islet secretory activity and integrity induced by extended exposure to the fatty acid.