Li J G, Li L Y, Ye C Y, Jin Y C, Yu X H, Liu M Q
Zhongguo Yao Li Xue Bao. 1989 Mar;10(2):97-100.
7 alpha-Bis (beta-chloroethyl)amino-methyl-6,14-endoethenotetrahydrooripavine (alpha-CAM) was found to bind to opioid receptors irreversibly and react directly with sulfhydryl (SH) groups in P2 preparations of rat brain. The P2 preparations were pretreated as follows: protection of the SH groups at the opioid receptor binding sites by morphine or etorphine, and inactivation of the SH groups outside the binding sites by N-ethylmaleimide (NEM), followed by removal of the morphine or etorphine by washing. alpha-CAM was still able to bind the pretreated P2 preparations in an irreversible manner. The results indicate that the formation of covalent bonds between alpha-CAM and the SH groups of opioid receptor binding sites is possibly one of the biochemical mechanisms of the irreversible action of alpha-CAM.
7α - 双(β - 氯乙基)氨基甲基 - 6,14 - 内乙烯基四氢奥里哌文(α - CAM)被发现可不可逆地结合阿片受体,并与大鼠脑P2制剂中的巯基(SH)基团直接反应。P2制剂的预处理如下:用吗啡或埃托啡保护阿片受体结合位点处的SH基团,并用N - 乙基马来酰亚胺(NEM)使结合位点外的SH基团失活,然后通过洗涤去除吗啡或埃托啡。α - CAM仍能够以不可逆的方式结合预处理过的P2制剂。结果表明,α - CAM与阿片受体结合位点的SH基团之间形成共价键可能是α - CAM不可逆作用的生化机制之一。