Das S, Matwyshyn G A, Bhargava H N
Gen Pharmacol. 1986;17(2):173-8. doi: 10.1016/0306-3623(86)90135-7.
The binding of [3H]quinuclidinyl benzilate (QNB) to various brain regions was determined in rats after acute or chronic treatment with morphine. Morphine and naloxone, in vitro, inhibited the binding of [3H]QNB to striatal membranes only at high concentrations. Thirty minutes after a single injection, morphine (5 or 40 mg/kg s.c.) did not alter the Bmax or Kd values for [3H]QNB binding to striatal receptors. The binding of [3H]QNB to membranes of different brain regions was not changed in morphine tolerant-dependent rats or rats undergoing abrupt or naloxone precipitated withdrawal. The results suggest that central cholinergic muscarinic receptors are unaffected by acute or chronic treatment with morphine, or during abstinence.
在大鼠经吗啡急性或慢性处理后,测定了[3H]东莨菪碱(QNB)与不同脑区的结合情况。吗啡和纳洛酮在体外仅在高浓度时抑制[3H]QNB与纹状体膜的结合。单次注射30分钟后,吗啡(5或40mg/kg皮下注射)未改变[3H]QNB与纹状体受体结合的Bmax或Kd值。在吗啡耐受-依赖大鼠或经历突然戒断或纳洛酮诱发戒断的大鼠中,[3H]QNB与不同脑区膜的结合未发生改变。结果表明,中枢胆碱能毒蕈碱受体不受吗啡急性或慢性处理或戒断期间的影响。