丙咪嗪对福尔马林试验吗啡耐受性的影响。

M R Zarrindast, S Shaverdian, M Sahebgharani
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引用次数: 4

摘要

本研究考察丙咪嗪对吗啡耐受和不耐受小鼠的抗痛感作用。在福尔马林试验的第一和第二阶段,皮下注射不同试验剂量的吗啡(3、6和9 mg/kg)和腹腔注射试验剂量的丙咪嗪(10、20和40 mg/kg)均对非耐受小鼠产生剂量依赖性的抗痛感。吗啡(1mg /kg)与丙咪嗪(10mg /kg)联合使用在第二阶段的试验中显示出增强的反应。单剂量吗啡(1.5 mg/kg)与低剂量丙咪嗪(2、4和8 mg/kg)联合使用未显示增强作用。阿片受体拮抗剂纳洛酮(2mg / kg)可降低吗啡或吗啡加丙咪嗪的抗感觉反应。为了诱导耐受性,小鼠皮下注射吗啡(50 mg/kg),每天1次,连续3天。第4天,评估吗啡或丙咪嗪的抗伤害感受作用。在试验的两个阶段观察到对吗啡(3、6和9 mg/kg)的耐受性,但对丙咪嗪(10、20和40 mg/kg)的耐受性不存在。在吗啡试验剂量(3,6和9mg /kg)之前给予低剂量丙咪嗪(4mg /kg)不能改变吗啡耐受的表达。当丙咪嗪在耐受性发展过程中使用时,无论是在第1天和第2天,还是在第2天和第3天,第二阶段试验的吗啡耐受性都降低了。结论阿片受体可能介导抗抑郁药诱导的抗痛觉,而丙咪嗪可能抑制吗啡耐受。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of imipramine on tolerance to morphine antinociception in the formalin test.

In this study, the effect of imipramine on morphine antinociception in tolerant and non-tolerant mice in the formalin test, was investigated. Subcutaneous administration of different test doses of morphine (3, 6 and 9 mg/kg) and intraperitoneal injection of test doses of imipramine (10, 20 and 40 mg/kg) induced a dose-dependent antinociception in non-tolerant mice, both in the first and second phases of the formalin test. The combination of morphine (1 mg/kg) with imipramine (10 mg/kg) showed a potentiated response in the second phase of the test. Combination of a single dose of morphine (1.5 mg/kg) with lower doses of imipramine (2, 4 and 8 mg/kg) did not show potentiation. The antinociceptive response of either morphine or morphine plus imipramine was reduced by the opioid receptor antagonist naloxone (2 mg/ kg). In order to induce tolerance, mice were treated subcutaneously with morphine (50 mg/kg) once daily for 3 days. On day 4, the antinociceptive effect of test doses of morphine or imipramine were assessed. Tolerance to the responses of test doses of morphine (3, 6 and 9 mg/kg), but not imipramine (10, 20 and 40 mg/kg) in both phases of the test was observed. Administration of lower dose of imipramine (4 mg/kg) before the test doses of morphine (3, 6 and 9 mg/kg) was not able to alter the expression of morphine tolerance. When imipramine was used during development of tolerance, either on days 1 and 2 or on days 2 and 3, the morphine tolerance in the second phase of the test was reduced. It is concluded that opioid receptor mechanism(s) may mediate the antidepressant-induced antinociception, however, imipramine may be useful in inhibiting morphine tolerance.

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