Shavit Y, Depaulis A, Martin F C, Terman G W, Pechnick R N, Zane C J, Gale R P, Liebeskind J C
Proc Natl Acad Sci U S A. 1986 Sep;83(18):7114-7. doi: 10.1073/pnas.83.18.7114.
We previously reported that a single systemic injection of a high dose of morphine (greater than or equal to 20 mg/kg) transiently suppresses splenic natural killer cell cytotoxicity in rats. The present study examined the possibility that the immune-suppressive effect of morphine is mediated by opiate receptors in the brain. Supporting this hypothesis, we found that morphine (20 or 40 micrograms) injected into the lateral ventricle suppressed natural killer cell activity to the same degree as a systemic dose higher by three orders of magnitude. This effect was blocked by an opiate antagonist, naltrexone. Natural killer cell activity was unaffected by systemic administration of N-methyl morphine, a morphine analogue that does not cross the blood-brain barrier. These data implicate opiate receptors in the brain in morphine-induced suppression of natural killer cell cytotoxicity.
我们之前报道过,单次全身注射高剂量吗啡(大于或等于20毫克/千克)可短暂抑制大鼠脾脏自然杀伤细胞的细胞毒性。本研究探讨了吗啡的免疫抑制作用是否由大脑中的阿片受体介导。支持这一假设的是,我们发现注入侧脑室的吗啡(20或40微克)抑制自然杀伤细胞活性的程度与高三个数量级的全身剂量相同。这种作用被阿片拮抗剂纳曲酮阻断。自然杀伤细胞活性不受不能穿过血脑屏障的吗啡类似物N-甲基吗啡全身给药的影响。这些数据表明大脑中的阿片受体参与了吗啡诱导的自然杀伤细胞细胞毒性抑制作用。