Towett P K, Kanui T I
Department of Veterinary Physiology, University of Nairobi, Kenya.
Pharmacol Biochem Behav. 1993 May;45(1):153-9. doi: 10.1016/0091-3057(93)90099-f.
The antinociceptive and behavioral effects of pethidine (10, 20, or 30 mg/kg), acetylsalicylic acid (200, 400, or 600 mg/kg) and indomethacin (20, 40, or 50 mg/kg) in the naked mole-rat was studied in the hot-plate test. Instead of inducing analgesia, pethidine caused a dose-dependent reduction in response latency. Sensorimotor impairment and aggressive behavior were also observed following administration of pethidine (20 or 30 mg/kg). All animals receiving pethidine (30 mg/kg) died following fighting when kept in colony cages. Aggressive behavior and death was prevented by naloxone or by keeping animals in single cages. Acetylsalicylic acid (600 mg/kg) and indomethacin (40 or 50 mg/kg) caused a significant increase in response latency. It is concluded that in the mole-rat pethidine elicits aggression, sensorimotor impairment, and apparent hyperalgesia.
在热板试验中研究了哌替啶(10、20或30mg/kg)、乙酰水杨酸(200、400或600mg/kg)和吲哚美辛(20、40或50mg/kg)对裸鼹鼠的抗伤害感受和行为影响。哌替啶并未诱导镇痛,反而导致反应潜伏期呈剂量依赖性缩短。给予哌替啶(20或30mg/kg)后还观察到感觉运动障碍和攻击行为。所有接受哌替啶(30mg/kg)的动物在群居笼中饲养时打斗后死亡。纳洛酮或单独饲养动物可预防攻击行为和死亡。乙酰水杨酸(600mg/kg)和吲哚美辛(40或50mg/kg)使反应潜伏期显著延长。得出的结论是,在裸鼹鼠中,哌替啶引发攻击、感觉运动障碍和明显的痛觉过敏。