Cerebral Markers of the Serotonergic System in Rat Models of Obesity and After Roux‐en‐Y Gastric Bypass

• Published in: Obesity (Silver Spring, Md.) Md.), 2012-10, Vol.20 (10), p.2133-2141
• Main Authors: Ratner, Cecilia, Ettrup, Anders, Bueter, Marco, Haahr, Mette E., Compan, Valérie, Roux, Carel W., Levin, Barry, Hansen, Henrik H., Knudsen, Gitte M.
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers; Biomarkers - metabolism; Body Weight; Brain; Disease Models, Animal; Eating; Gastric Bypass; Gastrointestinal surgery; Life Sciences; Male; Neurobiology; Neurons and Cognition; Obesity; Obesity - metabolism; Obesity - surgery; Rats; Rats, Sprague-Dawley; Rats, Wistar; Receptor, Serotonin, 5-HT2A - metabolism; Receptors, Serotonin - metabolism; Receptors, Serotonin, 5-HT1 - metabolism; Rodents; Serotonin; Up-Regulation; Weight Loss
• ISSN: 1930-7381; 1930-739X
• DOI: 10.1038/oby.2012.75

Food intake and body weight are regulated by a complex system of neural and hormonal signals, of which the anorexigenic neurotransmitter serotonin (5‐hydroxytryptamine or 5‐HT) is central. In this study, rat models of obesity and weight loss intervention were compared with regard to several 5‐HT markers. Using receptor autoradiography, brain regional‐densities of the serotonin transporter (SERT) and the 5‐HT2A and 5‐HT4 receptors were measured in (i) selectively bred polygenic diet‐induced obese (pgDIO) rats, (ii) outbred DIO rats, and (iii) Roux‐en‐Y gastric bypass (RYGB)–operated rats. pgDIO rats had higher 5‐HT4 and 5‐HT2A receptor binding and lower SERT binding when compared to polygenic diet‐resistant (pgDR) rats. The most pronounced difference between pgDIO and pgDR rats was observed in the nucleus accumbens shell (NAcS), a brain region regulating reward aspects of feeding. No differences were found in the 5‐HT markers between DIO rats, chow‐fed control rats, and DIO rats experiencing a weight loss. The 5‐HT markers were also similar in RYGB and sham‐operated rats except for a downregulation of 5‐HT2A receptors in the NAcS. The higher receptor and lower SERT binding in pgDIO as compared to pgDR rats corresponds to what is reported in overweight humans and suggests that the dysfunctions of the 5‐HT system associated with overeating or propensity to become overweight are polygenically determined. Our results support that the obesity‐prone rat model has high translational value and suggests that susceptibility to develop obesity is associated with changed 5‐HT tone in the brain that may also regulate hedonic aspects of feeding.