哌醋甲酯、美沙酮与不同抗抑郁药物对小鼠抗痛觉的相互作用及其可能的临床意义

S. Schreiber, M. Bader, V. Rubovitch, C. Pick
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引用次数: 6

摘要

摘要目的:哌醋甲酯(MPH)是一种用于治疗注意缺陷多动障碍(ADHD)的精神兴奋剂,被广泛用于抗抑郁药和美沙酮维持治疗(MMT)的患者。临床前研究表明,MPH单独或与吗啡联合使用均能发挥镇痛作用。方法:采用热板法,研究急性剂量美沙酮与亚阈值剂量美沙酮及不同抗抑郁药物的相互作用以及增加剂量美沙酮与慢性美沙酮的相互作用。结果:在MPH中添加亚阈剂量的文拉法辛、地西帕明和氯丙帕明均能显著增强MPH的抗痛感(P < 0.05)。在艾司西酞普兰和急性美沙酮之间没有发现这种相互作用。然而,在使用ALZET渗透性微型泵给药2周的慢性美沙酮的基础上加入增加剂量的MPH,仅在高剂量MPH (7.5 mg/kg)下,慢性美沙酮的抗伤害性作用增强。结论:这些发现可能意味着需要对MMT患者的MPH管理给予过度关注。MPH与艾司西酞普兰之间未发现相互作用,这可能提示MPH与选择性5 -羟色胺再摄取抑制剂(SSRIs)合用对抑郁症ADHD患者可能是安全的。为了验证这些可能的临床意义,需要进一步的研究。
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Interaction between methylphenidate, methadone and different antidepressant drugs on antinociception in mice, and possible clinical implications
Abstract Objectives: Methylphenidate (MPH), a psychostimulant used for treatment of attention deficit hyperactivity disorder (ADHD), is widely used by patients on antidepressants and methadone maintenance treatment (MMT). Preclinical studies showed MPH to exert analgesic effects when given alone or with morphine. Methods: Using the hotplate assay on mice, we studied the interaction of acute doses of MPH with sub-threshold doses of methadone and different antidepressant medications and the interaction of increasing doses of MPH with chronic methadone. Results: Adding a sub-threshold dose of venlafaxine, desipramine or clomipramine to MPH produced significant augmentation of MPH antinociception with each medication (P < 0.05). No such interactions were found between escitalopram and acute methadone. However, addition of increasing doses of MPH to chronic methadone given for 2 weeks using ALZET osmotic mini pumps induced augmentation of the antinociceptive effect of chronic methadone exclusively at high dose of MPH (7.5 mg/kg). Conclusions: These findings may implicate the need of an excessive attention to the administration of MPH to MMT patients. The no interaction found between MPH and escitalopram may hint to the possibly safe co-administration of MPH and selective serotonin reuptake inhibitors (SSRIs) to depressed ADHD patients. Further studies are needed in order to validate these possible clinical implications.
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