Narita M, Feng Y, Makimura M, Hoskins B, Ho I K
Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson 39216-4505.
Eur J Pharmacol. 1994 Dec 27;271(2-3):547-50. doi: 10.1016/0014-2999(94)90818-4.
Scatchard analysis of saturation binding data indicated that dissociation constant (KD) of [3H]phorbol 12,13-dibutyrate (PDB) binding to the membrane-bound protein kinase C of rat cortex and midbrain was significantly decreased following systemic repeated administration of morphine (mu-opioid receptor agonist) and butorphanol (mu/delta/kappa-mixed opioid receptor agonist). No change in the receptor density (Bmax) of [3H]PDB binding was found following repeated treatment with morphine and butorphanol. On the other hand, neither the Bmax nor KD values in pons/medulla were altered in these rats. These results suggest that systemic repeated opioid treatment, such as morphine and butorphanol leads to an increased affinity for phorbol ester binding to the membrane-bound protein kinase C in rat cortex and midbrain.
对饱和结合数据进行的Scatchard分析表明,在全身重复给予吗啡(μ-阿片受体激动剂)和布托啡诺(μ/δ/κ混合阿片受体激动剂)后,[3H]佛波醇12,13-二丁酸酯(PDB)与大鼠皮层和中脑膜结合蛋白激酶C的解离常数(KD)显著降低。重复给予吗啡和布托啡诺后,未发现[3H]PDB结合的受体密度(Bmax)有变化。另一方面,这些大鼠脑桥/延髓中的Bmax和KD值均未改变。这些结果表明,全身重复给予阿片类药物,如吗啡和布托啡诺,会导致佛波酯与大鼠皮层和中脑膜结合蛋白激酶C的结合亲和力增加。