Rothman R B, Schumacher U K, Pert C B
J Neurochem. 1984 Oct;43(4):1197-200. doi: 10.1111/j.1471-4159.1984.tb12861.x.
beta-FNA, the beta-fumaramate methyl ester of naltrexone, has been shown to antagonize irreversibly the actions of morphine on the guinea pig ileum and mouse vas deferens bioassays but does not affect the actions of delta-receptor ligands on the mouse vas deferens bioassay, suggesting that the compound does not irreversibly bind to the delta receptor. In this paper we examine the effect of beta-FNA on the binding of the prototypic delta agonists, Leu-enkephalin and D-Ala2-D-Leu5-enkephalin, its metabolically stable analogue, and show that treatment of membranes with beta-FNA does lead to alterations in the in vitro properties of delta receptors.
β -FNA,即纳曲酮的β -富马酸甲酯,已被证明在豚鼠回肠和小鼠输精管生物测定中能不可逆地拮抗吗啡的作用,但在小鼠输精管生物测定中不影响δ受体配体的作用,这表明该化合物不会不可逆地结合到δ受体上。在本文中,我们研究了β -FNA对典型δ激动剂亮氨酸脑啡肽和D -丙氨酸2 - D -亮氨酸5 -脑啡肽及其代谢稳定类似物结合的影响,并表明用β -FNA处理膜确实会导致δ受体的体外特性发生改变。