Olpe H R, Schellenberg A
J Neural Transm. 1981;51(3-4):233-44. doi: 10.1007/BF01248955.
The sensitivity of rostral and cingulate cortical neurons to microiontophoretically administered serotonin (5-HT) was compared in groups of rats treated either acutely or chronically for different periods with various drugs. The drugs used were: desipramine (10 mg/kg), clomipramine (10 mg/kg), CGP 6085 (10 mg/kg), clorgyline (0.3 mg/kg), and deprenyl (1 mg/kg). Serotonin and, in some instances, gamma-aminobutyric acid (GABA) were applied microiontophoretically over periods of 60 sec with various ejection currents to spontaneously active neurons in the rostral and cingulate cortex. Of all the compounds tested, only clorgyline produced a marked desensitization to 5-HT in both cortical areas. After prolonged treatment with all the other drugs, no change in the sensitivity to serotonin was observed. The desensitization to 5-HT induced by clorgyline developed after 4 to 10 days of treatment. The responsiveness of these cells to GABA was unchanged after chronic exposure to clorgyline. The present results are consistent with those biochemical studies showing that chronic treatment with 5-HT-uptake-blocking compounds has no effect on 5-HT-binding characteristics, as well as with the observation that prolonged treatment with the monoamine-oxidase A-type blocker clorgyline reduces the number of 5-HT-binding sites.
在分别用不同药物进行急性或慢性不同时期治疗的大鼠组中,比较了喙状皮质和扣带皮质神经元对微量离子导入给予的血清素(5-羟色胺,5-HT)的敏感性。所使用的药物有:去甲丙咪嗪(10毫克/千克)、氯丙咪嗪(10毫克/千克)、CGP 6085(10毫克/千克)、氯吉兰(0.3毫克/千克)和司来吉兰(1毫克/千克)。血清素,以及在某些情况下的γ-氨基丁酸(GABA),通过微量离子导入法,以不同的喷射电流在60秒内施加于喙状皮质和扣带皮质中自发活动的神经元上。在所有测试的化合物中,只有氯吉兰在两个皮质区域均对5-HT产生明显的脱敏作用。在用所有其他药物进行长期治疗后,未观察到对血清素敏感性的变化。氯吉兰诱导的对5-HT的脱敏作用在治疗4至10天后出现。在长期接触氯吉兰后,这些细胞对GABA的反应性未发生变化。目前的结果与那些生化研究一致,即显示用5-HT摄取阻断化合物进行慢性治疗对5-HT结合特性无影响,同时也与以下观察结果一致,即长期用单胺氧化酶A型阻滞剂氯吉兰治疗会减少5-HT结合位点的数量。