Walters A S, Hening A
Dept. of Neurology, UMDNJ-Robert Wood Johnson Medical School, New Brunswick 08903-0019.
Med Hypotheses. 1989 Jan;28(1):1-2. doi: 10.1016/0306-9877(89)90145-x.
Patients who are on neuroleptics with acute akathisia improve more with opioid therapy than patients who are off neuroleptics with tardive akathisia. Since tardive akathisia usually occurs after long term neuroleptic exposure, we propose that this difference in therapeutic response is due to permanent changes in receptor sensitivity that arise from such prolonged exposure. We have previously described a patient with severe acute akathisia whose motor restlessness was totally suppressed by opioid therapy. This improvement was rapidly reversed by the opiate receptor blocker naloxone. This suggests that the endogenous opiate system is involved in the pathogenesis of neuroleptic-induced akathisia.
正在服用抗精神病药物且患有急性静坐不能的患者,与停用抗精神病药物且患有迟发性静坐不能的患者相比,使用阿片类药物治疗时改善更为明显。由于迟发性静坐不能通常在长期使用抗精神病药物后出现,我们认为这种治疗反应的差异是由于长期暴露导致受体敏感性发生了永久性变化。我们之前描述过一名患有严重急性静坐不能的患者,其运动不安通过阿片类药物治疗得到了完全抑制。阿片受体阻滞剂纳洛酮迅速逆转了这种改善。这表明内源性阿片系统参与了抗精神病药物所致静坐不能的发病机制。