Marcusson J, Bäckström I T, Ross S B
Department of Geriatric Medicine, University of Umeå, Sweden.
Psychopharmacology (Berl). 1988;94(2):193-6. doi: 10.1007/BF00176844.
Several reports have shown heterogeneity of [3H]imipramine binding to brain membranes. Recently, a high affinity and 5-HT sensitive [3H]imipramine binding site of protein nature, that was suggested to be identical to the substrate recognition site for 5-HT uptake, was demonstrated. Since most studies on the regulation of the [3H]imipramine binding sites by antidepressants have used desipramine displaceable binding, which is heterogenous in nature and contains binding not related to 5-HT uptake sites, the present report studies the possible effects of chronic (3 weeks) administration of imipramine or norzimeldine (10 mg/kg intraperitoneally twice daily) on 5-HT sensitive [3H]imipramine binding sites. For comparison, desipramine sensitive binding was also studied, as well as the physiological correlate 5-HT uptake. There were no changes in either [3H]imipramine binding or 5-HT uptake after the antidepressant treatment.
多项报告显示,[3H]丙咪嗪与脑膜的结合存在异质性。最近,发现了一种具有高亲和力且对5-羟色胺(5-HT)敏感的蛋白质性质的[3H]丙咪嗪结合位点,该位点被认为与5-HT摄取的底物识别位点相同。由于大多数关于抗抑郁药对[3H]丙咪嗪结合位点调节作用的研究都使用了地昔帕明可置换结合,而这种结合本质上是异质的,且包含与5-HT摄取位点无关的结合,因此本报告研究了丙咪嗪或去甲替林(10mg/kg,腹腔注射,每日两次,共3周)对5-HT敏感的[3H]丙咪嗪结合位点可能产生的影响。为作比较,还研究了地昔帕明敏感结合以及生理相关的5-HT摄取。抗抑郁药治疗后,[3H]丙咪嗪结合或5-HT摄取均无变化。