Wiener H L, Lajtha A, Sershen H
Center for Neurochemistry, Nathan S. Kline Institute for Psychiatric Research Ward's Island, New York, NY 10035.
Neuropharmacology. 1989 May;28(5):535-7. doi: 10.1016/0028-3908(89)90091-9.
The effect of nicotine on MPTP-induced changes in striatal dopamine receptors binding activity was investigated. Dopamine D1 and D2 receptors were labeled with [3H]SCH-23390 and [3H]spiperone respectively in BALB/cBy mice. With administration of only MPTP, which caused more than an 80% decrease in striatal dopamine level, binding of 0.15 nM [3H]spiperone was increased by 37%; whereas 0.3 nM [3H]SCH-23390 binding was unchanged. With chronic nicotine treatment (0.4 mg/kg twice daily for 7-9 days), [3H]SCH-23390 binding activity was increased by 27% and [3H]spiperone binding activity was unchanged. When nicotine was administered after MPTP, their separate effects could be seen in that both the D1 and D2 dopamine receptor ligand binding activities were increased and that nicotine elevated the ratio of D1/D2 receptor binding activities in MPTP-treated mice.
研究了尼古丁对MPTP诱导的纹状体多巴胺受体结合活性变化的影响。在BALB/cBy小鼠中,分别用[3H]SCH-23390和[3H]螺哌隆标记多巴胺D1和D2受体。仅给予MPTP时,纹状体多巴胺水平降低超过80%,0.15 nM [3H]螺哌隆的结合增加了37%;而0.3 nM [3H]SCH-23390的结合未发生变化。慢性尼古丁处理(0.4 mg/kg,每日两次,持续7 - 9天)后,[3H]SCH-23390结合活性增加了27%,[3H]螺哌隆结合活性未发生变化。当在MPTP后给予尼古丁时,可以看到它们各自的作用,即D1和D2多巴胺受体配体结合活性均增加,且尼古丁提高了MPTP处理小鼠中D1/D2受体结合活性的比值。