Chu Chin-Chen, Shieh Ja-Ping, Shui Hao-Ai, Chen Jen-Yin, Hsing Chung-Hsi, Tzeng Jann-Inn, Wang Jhi-Joung, Ho Shung-Tai
Department of Anesthesiology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Behav Pharmacol. 2010 Sep;21(5-6):523-9. doi: 10.1097/FBP.0b013e32833db7d4.
Long-term use of morphine can cause neuronal dystrophic changes in specific areas of the brain. These changes may underlie the mechanism for developing morphine antinociceptive tolerance and physical dependence. We evaluated the effect of tianeptine, an antidepressant with prominent neuroprotective and neuroplastic properties, on the development of morphine antinociceptive tolerance and physical dependence. Male C57BL/6 mice were rendered tolerant to or dependent on morphine by subcutaneously injecting them with morphine (10 mg/kg) and intraperitoneally with saline or tianeptine (1, 3, or 5 mg/kg) twice daily for 6 days. The mice were given a daily tail-flick test 1 h after the first morphine injection to evaluate the development of their tolerance to morphine antinociception. To evaluate their physical dependence on morphine, 3 h after the final morphine injection on day 6, naloxone-HCl-precipitated (2 mg/kg, intraperitoneally) withdrawal symptoms were counted for 30 min, and body weight was checked 1 h after the naloxone injection. Tianeptine per se produced no antinociception, neither did it modify the antinociception produced by morphine, nor did it evoke the behavioral responses different from those in the saline controls. The combination of tianeptine with morphine significantly reduced the development of morphine antinociceptive tolerance and suppressed the incidence of naloxone-precipitated withdrawal symptoms. We conclude that tianeptine is an effective inhibitor of morphine-induced antinociceptive tolerance and physical dependence in mice. Our results would imply that comedication with tianeptine and morphine might benefit those who need long-term morphine treatment.
长期使用吗啡可导致大脑特定区域的神经元营养不良性改变。这些改变可能是吗啡抗伤害感受耐受性和身体依赖性形成机制的基础。我们评估了噻奈普汀(一种具有显著神经保护和神经可塑性特性的抗抑郁药)对吗啡抗伤害感受耐受性和身体依赖性形成的影响。通过每天两次皮下注射吗啡(10毫克/千克)并腹腔注射生理盐水或噻奈普汀(1、3或5毫克/千克),连续6天,使雄性C57BL/6小鼠对吗啡产生耐受性或依赖性。在首次注射吗啡1小时后,每天对小鼠进行一次甩尾试验,以评估其对吗啡抗伤害感受耐受性的形成情况。为了评估它们对吗啡的身体依赖性,在第6天最后一次注射吗啡3小时后,腹腔注射盐酸纳洛酮(2毫克/千克)诱发戒断症状30分钟,并在注射纳洛酮1小时后检查体重。噻奈普汀本身没有产生抗伤害感受作用,既没有改变吗啡产生的抗伤害感受作用,也没有引发与生理盐水对照组不同的行为反应。噻奈普汀与吗啡联合使用显著降低了吗啡抗伤害感受耐受性的形成,并抑制了纳洛酮诱发的戒断症状的发生率。我们得出结论,噻奈普汀是小鼠吗啡诱导的抗伤害感受耐受性和身体依赖性的有效抑制剂。我们的结果表明,噻奈普汀与吗啡联合用药可能对需要长期吗啡治疗的患者有益。