Gleiter C H, Linnoila M, Nutt D J
National Institute on Alcoholism and Alcohol Abuse, Bethesda.
Appetite. 1989 Apr;12(2):137-43. doi: 10.1016/0195-6663(89)90102-5.
It has been previously suggested that low affinity [3H]mazindol binding in the hypothalamus correlates with body weight and obesity. Low affinity [3H]mazindol binding in hypothalamic crude synaptosome preparations was carried out in normoglycemic obese mice (C57 B1/6J ob/ob) as well as in their lean littermates (C57 B1/6J +/?). NIH Swiss mice were used as additional controls. Furthermore the effect on this binding site of repeated electroconvulsive shock (ECS), a treatment known to change body weight gain, was studied in rats. Neither Bmax nor Kd were altered in obese mice compared with their lean littermates or NIH Swiss mice. The obese mice had a significantly greater body weight and weight gain than either control group. Once-daily ECS over 10 days (which significantly reduced weight gain in rats) did not change binding parameters for [3H]mazindol in hypothalami. The present data do not appear to support the hypothesis that this low affinity binding site has a physiological function in the control of body weight and obesity, at least in the examined paradigm.
此前有研究表明,下丘脑中低亲和力的[3H]马吲哚结合与体重及肥胖相关。在正常血糖的肥胖小鼠(C57 B1/6J ob/ob)及其瘦的同窝小鼠(C57 B1/6J +/?)的下丘脑粗制突触体标本中进行了低亲和力的[3H]马吲哚结合实验。NIH瑞士小鼠用作额外对照。此外,在大鼠中研究了重复电惊厥休克(ECS)这种已知会改变体重增加的治疗方法对该结合位点的影响。与瘦的同窝小鼠或NIH瑞士小鼠相比,肥胖小鼠的Bmax和Kd均未改变。肥胖小鼠的体重和体重增加显著高于任一对照组。连续10天每天一次的ECS(显著降低了大鼠的体重增加)并未改变下丘脑[3H]马吲哚的结合参数。目前的数据似乎不支持这一假说,即至少在所研究的范式中,这种低亲和力结合位点在体重和肥胖控制中具有生理功能。