Distinct Modulatory Effects of Satiety and Sibutramine on Brain Responses to Food Images in Humans: A Double Dissociation across Hypothalamus, Amygdala, and Ventral Striatum
- Paul C. Fletcher1,
- Antonella Napolitano2,
- Andrew Skeggs2,
- Sam R. Miller2,
- Bruno Delafont2,
- Victoria C. Cambridge1,
- Sanne de Wit3,
- Pradeep J. Nathan1,2,
- Allison Brooke2,
- Stephen O'Rahilly4,
- I. Sadaf Farooqi4, and
- Edward T. Bullmore1,2
- 1Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom,
- 2GlaxoSmithKline Clinical Unit Cambridge, Addenbrooke's Centre for Clinical Investigations, Addenbrooke's Hospital, Cambridge CB2 2QQ, United Kingdom,
- 3Amsterdam Center for the Study of Adaptive Control in Brain and Behavior, Department of Developmental Psychology, University of Amsterdam, 1018 WB Amsterdam, The Netherlands, and
- 4University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 2QQ, United Kingdom
- Correspondence should be addressed to either of the following: I. Sadaf Farooqi, University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK, isf20{at}cam.ac.uk; or Paul C. Fletcher, Department of Psychiatry, University of Cambridge, Herchel Smith Building for Brain and Mind Sciences, Cambridge CB2 0SZ, UK, E-mail: pcf22{at}cam.ac.uk
Abstract
We used functional magnetic resonance imaging to explore brain responses to food images in overweight humans, examining independently the impact of a prescan meal (“satiety”) and the anti-obesity drug sibutramine, a serotonin and noradrenaline reuptake inhibitor. We identified significantly different responses to these manipulations in amygdala, hypothalamus, and ventral striatum. Each region was specifically responsive to high-calorie compared to low-calorie food images. However, the ventral striatal response was attenuated by satiety (but unaffected by sibutramine), while the hypothalamic and amygdala responses were attenuated by drug but unaffected by satiety. Direct assessment of regional interactions confirmed the significance of this double dissociation. We explored the regional responses in greater detail by determining whether they were predictive of eating behavior and weight change. We observed that across the different regions, the individual-specific magnitude of drug- and satiety-induced modulation was associated with both variables: the sibutramine-induced modulation of the hypothalamic response was correlated with the drug's impact on both weight and subsequently measured ad libitum eating. The satiety-induced modulation of striatal response also correlated with subsequent ad libitum eating. These results suggest that hypothalamus and amygdala have roles in the control of food intake that are distinct from those of ventral striatum. Furthermore, they support a regionally specific effect on brain function through which sibutramine exerts its clinical effect.
- Copyright © 2010 the authors 0270-6474/10/3014346-10$15.00/0





