Altered Brain Response to Drinking Glucose and Fructose in Obese Adolescents

Author:

Jastreboff Ania M.12,Sinha Rajita34,Arora Jagriti5,Giannini Cosimo2,Kubat Jessica2,Malik Saima5,Van Name Michelle A.2,Santoro Nicola2,Savoye Mary2,Duran Elvira J.2,Pierpont Bridget2,Cline Gary1,Constable R. Todd5,Sherwin Robert S.1,Caprio Sonia2

Affiliation:

1. Division of Endocrinology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT

2. Division of Pediatric Endocrinology, Department of Pediatrics, Yale University School of Medicine, New Haven, CT

3. Department of Psychiatry, Yale Stress Center, Yale University School of Medicine, New Haven, CT

4. Child Study Center, Yale University School of Medicine, New Haven, CT

5. Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT

Abstract

Increased sugar-sweetened beverage consumption has been linked to higher rates of obesity. Using functional MRI, we assessed brain perfusion responses to drinking two commonly consumed monosaccharides, glucose and fructose, in obese and lean adolescents. Marked differences were observed. In response to drinking glucose, obese adolescents exhibited decreased brain perfusion in brain regions involved in executive function (prefrontal cortex [PFC]) and increased perfusion in homeostatic appetite regions of the brain (hypothalamus). Conversely, in response to drinking glucose, lean adolescents demonstrated increased PFC brain perfusion and no change in perfusion in the hypothalamus. In addition, obese adolescents demonstrated attenuated suppression of serum acyl-ghrelin and increased circulating insulin level after glucose ingestion; furthermore, the change in acyl-ghrelin and insulin levels after both glucose and fructose ingestion was associated with increased hypothalamic, thalamic, and hippocampal blood flow in obese relative to lean adolescents. Additionally, in all subjects there was greater perfusion in the ventral striatum with fructose relative to glucose ingestion. Finally, reduced connectivity between executive, homeostatic, and hedonic brain regions was observed in obese adolescents. These data demonstrate that obese adolescents have impaired prefrontal executive control responses to drinking glucose and fructose, while their homeostatic and hedonic responses appear to be heightened. Thus, obesity-related brain adaptations to glucose and fructose consumption in obese adolescents may contribute to excessive consumption of glucose and fructose, thereby promoting further weight gain.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

NIH

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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