Post C
Neurosci Lett. 1984 Oct 26;51(3):325-30. doi: 10.1016/0304-3940(84)90397-5.
When injected intrathecally in mice in a volume of 5 microliter, adenosine had no effect on tail-flick or hot-plate reaction latencies at dosages up to 1 mM concentration. There were no other behavioral effects observed either. Injecting 1 mM of the adenosine receptor agonist, 5'-N-ethylcarboxamide adenosine (NECA) caused both motor paralysis of the hind-legs with a duration of approximately 4 h and simultaneous antinociception. A slight weakness of the hindlegs, but a profound antinociceptive effect, was observed after the 100 microM dose only. After 10 microM, there was no effect on motor behavior but still a prolongation of the tail-flick and hot-plate reaction latencies. Pretreatment with the adenosine receptor antagonist theophylline attenuated the antinociceptive effect of NECA. Activation of spinal adenosine receptors thus appears to selectively elicit analgesia.
当以5微升的体积鞘内注射到小鼠体内时,腺苷在浓度高达1 mM的剂量下对甩尾或热板反应潜伏期没有影响。也未观察到其他行为影响。注射1 mM的腺苷受体激动剂5'-N-乙基羧酰胺腺苷(NECA)会导致后肢运动麻痹,持续时间约为4小时,同时产生抗伤害感受作用。仅在100 microM剂量后观察到后肢轻微无力,但有显著的抗伤害感受作用。在10 microM后,对运动行为没有影响,但甩尾和热板反应潜伏期仍延长。用腺苷受体拮抗剂茶碱预处理可减弱NECA的抗伤害感受作用。因此,脊髓腺苷受体的激活似乎选择性地引发镇痛作用。