Lipinski J F, Mallya G, Zimmerman P, Pope H G
Laboratory for Psychiatric Research, McLean Hospital, Belmont, Mass 02178.
J Clin Psychiatry. 1989 Sep;50(9):339-42.
Five patients receiving fluoxetine for the treatment of obsessive compulsive disorder or major depression developed akathisia. The typical fluoxetine-induced symptoms of restlessness, constant pacing, purposeless movements of the feet and legs, and marked anxiety were indistinguishable from those of neuroleptic-induced akathisia. Three patients who had experienced neuroleptic-induced akathisia in the past reported that the symptoms of fluoxetine-induced akathisia were identical, although somewhat milder. Akathisia appeared to be a common side effect of fluoxetine and generally responded well to treatment with the beta-adrenergic antagonist propranolol, dose reduction, or both. The authors suggest that fluoxetine-induced akathisia may be caused by serotonergically mediated inhibition of dopaminergic neurotransmission and that the pathophysiology of fluoxetine-induced akathisia and tricyclic antidepressant-induced "jitteriness" may be identical.
五名接受氟西汀治疗强迫症或重度抑郁症的患者出现了静坐不能。典型的氟西汀诱发症状,如坐立不安、持续踱步、双脚和腿部无目的运动以及明显焦虑,与抗精神病药物诱发的静坐不能症状难以区分。三名过去曾经历过抗精神病药物诱发静坐不能的患者报告称,氟西汀诱发的静坐不能症状相同,尽管症状稍轻。静坐不能似乎是氟西汀的常见副作用,通常对β-肾上腺素能拮抗剂普萘洛尔治疗、减少剂量或两者联合治疗反应良好。作者认为,氟西汀诱发的静坐不能可能是由5-羟色胺介导的多巴胺能神经传递抑制引起的,氟西汀诱发的静坐不能和三环类抗抑郁药诱发的“神经过敏”的病理生理学可能相同。