Wong C L
School of Pharmacy, University of Portsmouth, England.
Methods Find Exp Clin Pharmacol. 1992 Nov;14(9):695-700.
Restraint for a period from 15-60 min induced significant antinociceptive effect in both male and female mice. The restraint animals all showed an increase in response time to the hot plate test at 55 degrees C. The antinociceptive activity was still apparent one hour after restraint. In the male animals, prior administration of naloxone s.c. 15 min before restraint for 60 min did not affect the degree of antinociceptive activity induced by restraint. In addition, naloxone administered s.c. immediately after restraint for 60 min also did not affect the degree of antinociceptive activity in male mice. These findings indicate that in male animals the endogenous opioid mechanism is most likely not involved in the restraint-induced antinociception. However, for the female mice naloxone administered s.c. either before or immediately after restraint for 60 min dose-dependently suppressed the antinociceptive activity induced by restraint. It is concluded that restraint can induce antinociceptive activity in mice; however, different mechanisms may be involved in the antinociception observed. In male mice the endogenous opioid systems do not seem to play a significant role in restraint-induced antinociception, while for female animals blockade of opioid receptors would greatly diminish the antinociception observed after restraint.
对雄性和雌性小鼠进行15 - 60分钟的束缚可诱导出显著的抗伤害感受作用。受束缚的动物在55摄氏度热板试验中的反应时间均有所增加。束缚后一小时抗伤害感受活性仍然明显。在雄性动物中,在束缚60分钟前15分钟皮下注射纳洛酮并不影响束缚诱导的抗伤害感受活性程度。此外,在束缚60分钟后立即皮下注射纳洛酮也不影响雄性小鼠的抗伤害感受活性程度。这些发现表明,在雄性动物中,内源性阿片类机制很可能不参与束缚诱导的抗伤害感受。然而,对于雌性小鼠,在束缚60分钟前或后立即皮下注射纳洛酮会剂量依赖性地抑制束缚诱导的抗伤害感受活性。结论是,束缚可在小鼠中诱导抗伤害感受活性;然而,观察到的抗伤害感受可能涉及不同机制。在雄性小鼠中,内源性阿片系统似乎在束缚诱导的抗伤害感受中不发挥重要作用,而对于雌性动物,阿片受体的阻断会大大减弱束缚后观察到的抗伤害感受。