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Altered Brain Response to Drinking Glucose and Fructose in Obese Adolescents.

Authors :
Jastreboff AM
Sinha R
Arora J
Giannini C
Kubat J
Malik S
Van Name MA
Santoro N
Savoye M
Duran EJ
Pierpont B
Cline G
Constable RT
Sherwin RS
Caprio S
Source :
Diabetes [Diabetes] 2016 Jul; Vol. 65 (7), pp. 1929-39. Date of Electronic Publication: 2016 Apr 05.
Publication Year :
2016

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.<br /> (© 2016 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.)

Details

Language :
English
ISSN :
1939-327X
Volume :
65
Issue :
7
Database :
MEDLINE
Journal :
Diabetes
Publication Type :
Academic Journal
Accession number :
27207544
Full Text :
https://doi.org/10.2337/db15-1216