Desaiah D, Ho I K
J Pharmacol Exp Ther. 1979 Jan;208(1):80-5.
The catecholamine-stimulated adenosine triphosphatase (ATP-ase) activities in mouse brain synaptosomes were inhibited by morphine both in vitro and in vivo. Morphine up to 10(-3) M had no effect on basal ATPase activities but at 10(-4) M significantly inhibited dopamine-sensitive ATPase activities in vitro. The morphine effect was antagonized by an opiate antagonist, naloxone. The catecholamine-sensitive ATPase activities were also inhibited by acute administration of morphine. The inhibition was dose-dependent. However, naloxone partially antagonized the morphine inhibition of depamine-sensitive ATPase activity but not norepinephrine-sensitive ATPase activity. A significant decrease in the sensitivity of synaptosomal ATPase to catecholamines was observed in mice rendered tolerant by morphine pellet implantation. The Na+,K+-ATPase was more affected by morphine as compared to Mg++-ATPase activity. The dopamine-sensitive Na+,K+-ATPase activity was restored by 50% in precipitated withdrawal mouse brain synaptosomes. Norepinephrine-sensitive ATPase activity was also restored partially in precipitated withdrawal animals. These results suggest that in mouse brain synaptosomes morphine may be interacting with ATPase at or near the catecholamine-active sites.
在体外和体内,吗啡均可抑制小鼠脑突触体中儿茶酚胺刺激的三磷酸腺苷酶(ATP酶)活性。高达10⁻³ M的吗啡对基础ATP酶活性无影响,但在体外,10⁻⁴ M的吗啡可显著抑制多巴胺敏感性ATP酶活性。吗啡的作用可被阿片拮抗剂纳洛酮拮抗。急性给予吗啡也可抑制儿茶酚胺敏感性ATP酶活性。这种抑制呈剂量依赖性。然而,纳洛酮可部分拮抗吗啡对多巴胺敏感性ATP酶活性的抑制,但对去甲肾上腺素敏感性ATP酶活性无拮抗作用。在通过植入吗啡丸粒产生耐受性的小鼠中,观察到突触体ATP酶对儿茶酚胺的敏感性显著降低。与Mg²⁺-ATP酶活性相比,Na⁺,K⁺-ATP酶受吗啡的影响更大。在戒断小鼠脑突触体中,多巴胺敏感性Na⁺,K⁺-ATP酶活性恢复了50%。在戒断动物中,去甲肾上腺素敏感性ATP酶活性也有部分恢复。这些结果表明,在小鼠脑突触体中,吗啡可能在儿茶酚胺活性位点或其附近与ATP酶相互作用。