Carlsson K H, Jurna I
Neurosci Lett. 1987 Jun 26;77(3):339-43. doi: 10.1016/0304-3940(87)90524-6.
To study the question whether or not paracetamol produces a central analgesic effect, experiments were carried out on rats under urethane anaesthesia in which activity was elicited by supramaximal electrical stimulation of nociceptive afferents in the sural nerve and recorded from single neurones in the dorsomedial part of the ventral nucleus (VDM) of the thalamus. Paracetamol administered by intraperitoneal (i.p.) injection at doses of 50, 100 and 150 mg/kg reduced nociceptive evoked but not spontaneous activity. The amount of depression caused by the 3 doses and the time course of their effects was practically the same. suggesting that paracetamol is not capable to abolish nociceptive evoked activity in the thalamus but causes a maximum depression of the activity amounting to not more than about 60% of the controls. An intravenous (i.v.) injection of naloxone (1 mg/kg) did not diminish paracetamol-induced depression. The results present evidence for a central analgesic effect of paracetamol that is independent of endogenous opioids.
为研究对乙酰氨基酚是否产生中枢镇痛作用,在乌拉坦麻醉的大鼠身上进行了实验,通过对腓肠神经中的伤害性传入纤维进行超强电刺激来引发活动,并从丘脑腹侧核背内侧部分(VDM)的单个神经元记录活动。腹腔注射(i.p.)剂量为50、100和150mg/kg的对乙酰氨基酚可降低伤害性诱发活动,但不影响自发活动。这3种剂量引起的抑制量及其作用的时间进程基本相同,表明对乙酰氨基酚无法消除丘脑中的伤害性诱发活动,但可使活动最大程度抑制,抑制量不超过对照组的约60%。静脉注射(i.v.)纳洛酮(1mg/kg)并未减弱对乙酰氨基酚引起的抑制作用。这些结果为对乙酰氨基酚的中枢镇痛作用提供了证据,该作用独立于内源性阿片类物质。