Duggan A W, Davies J, Hall J G
J Pharmacol Exp Ther. 1976 Jan;196(1):107-20.
Morphine, naloxone, nalorphine, levorphanol, dextrorphan and levallorphan were ejected electrophoretically from micropipettes near cholinoceptive and noncholinoceptive cells of the spinal cord, ventrobasal thalamus and cerebral cortex of decerebrate and barbiturate-anesthetized cats. Morphine excited those cells having nicotinic receptors for acetylcholine. Naloxone and nalorphine reduced the action of morphine and acetylcholine on these cells but not the effects of excitant amino acids. Levorphanol excited spinal neurons also excited by acetylcholine, an effect antagonized by naloxone, but also showed atropine-like activity when ejected for prolonged periods. Dextrorphan depressed the firing of both cholinoceptive and noncholinoceptive spinal neurons. Levallorphan reduced the effects of both acetylcholine and excitant amino acids on spinal neurons. The depressant effects of morphine and levorphanol on noncholinoceptive spinal neurons were not antagonized by naloxone.
在去大脑和巴比妥类麻醉的猫的脊髓、腹侧基底丘脑和大脑皮层的胆碱能感受性和非胆碱能感受性细胞附近,用微量移液器电泳法喷射吗啡、纳洛酮、烯丙吗啡、左啡诺、右啡烷和烯丙左吗喃。吗啡兴奋那些具有乙酰胆碱烟碱样受体的细胞。纳洛酮和烯丙吗啡降低吗啡和乙酰胆碱对这些细胞的作用,但不降低兴奋性氨基酸的作用。左啡诺兴奋的脊髓神经元也被乙酰胆碱兴奋,这种作用被纳洛酮拮抗,但长时间喷射时也表现出阿托品样活性。右啡烷抑制胆碱能感受性和非胆碱能感受性脊髓神经元的放电。烯丙左吗喃降低乙酰胆碱和兴奋性氨基酸对脊髓神经元的作用。吗啡和左啡诺对非胆碱能感受性脊髓神经元的抑制作用不被纳洛酮拮抗。