Ossipov M H, Gebhart G F
Brain Res. 1983 Dec 19;289(1-2):349-54. doi: 10.1016/0006-8993(83)90040-9.
The antinociceptive efficacy of clonidine, St-91, tolazoline, phenylephrine or isoproterenol microinjected in the periaqueductal gray (PAG) in the rat was compared to that of morphine administered in the same site. Morphine (5 micrograms) was antinociceptive in all 3 analgesiometric tests employed (tail-flick, hot-plate and tail-shock vocalization). Clonidine (5-20 micrograms) did not significantly alter nociceptive thresholds, while St-91 (20 micrograms) produced a brief hyperalgesia in the tail-flick test. The alpha-2 antagonist tolazoline (20 micrograms) produced a brief antinociception in the tail-flick test. Phenylephrine and isoproterenol were without effect on nociceptive thresholds. It is suggested that the ventrolateral PAG, although a site of opiate-produced antinociception, is not involved in alpha-2-mediated antinociception.
将可乐定、St-91、妥拉唑啉、去氧肾上腺素或异丙肾上腺素微量注射到大鼠中脑导水管周围灰质(PAG)的抗伤害感受效能,与在同一部位注射吗啡的效能进行了比较。吗啡(5微克)在所有三种镇痛测定试验(甩尾、热板和尾部电击发声)中均具有抗伤害感受作用。可乐定(5 - 20微克)并未显著改变伤害感受阈值,而St-91(20微克)在甩尾试验中产生了短暂的痛觉过敏。α-2拮抗剂妥拉唑啉(20微克)在甩尾试验中产生了短暂的抗伤害感受作用。去氧肾上腺素和异丙肾上腺素对伤害感受阈值没有影响。提示腹外侧PAG虽然是阿片类药物产生抗伤害感受的部位,但不参与α-2介导的抗伤害感受作用。