Hajnal Andras, Margas Wojciech M, Covasa Mihai
Department of Neural and Behavioral Sciences, The Pennsylvania State University, College of Medicine, Hershey, PA 17033, USA.
Brain Res Bull. 2008 Jan 31;75(1):70-6. doi: 10.1016/j.brainresbull.2007.07.019. Epub 2007 Aug 8.
A decrease in D2-like receptor (D2R) binding in the striatum has been reported in obese individuals and drug addicts. Although natural and drug rewards share neural substrates, it is not clear whether such effects also contribute to overeating on palatable meals as an antecedent of dietary obesity. Therefore, we investigated receptor density and the effect of the D2R agonist quinpirole (0.05, 0.5 mg/kg, S.C.) on locomotor activity and sucrose intake in a rat model of diet-induced obesity, the CCK-1 receptor-deficient Otsuka Long Evans Tokushima Fatty (OLETF) rat. Compared to age-matched lean controls (LETO), OLETF rats expressed significantly lower [125I]-iodosulpride binding in the accumbens shell (-16%, p<0.02). Whereas the high dose of quinpirole increased motor activity in both strains equally, the low dose reduced activity more in OLETF. Both doses significantly reduced sucrose intake in OLETF but not LETO rats. These findings demonstrate an altered D2R signaling in obese OLETF rats similar to drug-induced sensitization and suggest a link between this effect and avidity for sucrose in this model.
据报道,肥胖个体和吸毒成瘾者纹状体中D2样受体(D2R)结合减少。尽管天然奖励和药物奖励共享神经底物,但尚不清楚这种效应是否也会导致对美味食物的过度进食,而美味食物是饮食性肥胖的一个先兆。因此,我们在饮食诱导肥胖的大鼠模型——胆囊收缩素-1受体缺陷型大冢长 Evans 德岛肥胖(OLETF)大鼠中,研究了受体密度以及D2R激动剂喹吡罗(0.05、0.5mg/kg,皮下注射)对运动活性和蔗糖摄入量的影响。与年龄匹配的瘦对照组(LETO)相比,OLETF大鼠伏隔核壳中的[125I] - 碘舒必利结合显著降低(-16%,p<0.02)。虽然高剂量的喹吡罗对两种品系的运动活性增加程度相同,但低剂量对OLETF大鼠运动活性的降低作用更大。两种剂量均显著降低了OLETF大鼠的蔗糖摄入量,但对LETO大鼠没有影响。这些发现表明,肥胖的OLETF大鼠中D2R信号传导发生改变,类似于药物诱导的致敏作用,并提示在该模型中这种效应与对蔗糖的偏好之间存在联系。