Sawa A, Oka T
Jpn J Pharmacol. 1976 Oct;26(5):599-605. doi: 10.1254/jjp.26.599.
The effects of narcotic analgesics on the brain 5-hydroxytryptamine (5-Ht) and 5-hydroxyindoleacetic acid (5-HIAA) levels of rats and mice were investigated in relation to our preceding data on the effect of humoral modulatorents. The results suggest that morphine accelerates the release of brain 5-HT both in rats and mice, and that neither methadone nor pethidine alters the brain 5-HT and 5-HIAA levels in rats. The morphine-induced increase in brain 5-HT turnover is likely to be involved in the morphine-induced decrease in locomotor activity and hypothermia in rats. The activity-decreasing effects of methadone or pethidine, on the other hand, are mediated by mechanisms different from those which mediate the effects of morphine. In contrast, an increase in brain 5-HT turnover in mice apparently does not play an important role on activity-increasing effects of morphine but rather participates in other pharmacological effects of morphine.
结合我们之前关于体液调节剂作用的数据,研究了麻醉性镇痛药对大鼠和小鼠脑内5-羟色胺(5-Ht)和5-羟吲哚乙酸(5-HIAA)水平的影响。结果表明,吗啡能加速大鼠和小鼠脑内5-羟色胺(5-HT)的释放,而美沙酮和哌替啶均不改变大鼠脑内5-羟色胺(5-HT)和5-羟吲哚乙酸(5-HIAA)的水平。吗啡引起的脑内5-羟色胺(5-HT)周转增加可能与吗啡引起的大鼠运动活动减少和体温过低有关。另一方面,美沙酮或哌替啶的活动减少作用是由与介导吗啡作用的机制不同的机制介导的。相比之下,小鼠脑内5-羟色胺(5-HT)周转增加显然对吗啡的活动增加作用不起重要作用,而是参与吗啡的其他药理作用。