Benfield P, Heel R C, Lewis S P
Drugs. 1986 Dec;32(6):481-508. doi: 10.2165/00003495-198632060-00002.
Fluoxetine is a new antidepressant which enhances serotoninergic neurotransmission through potent and selective inhibition of neuronal reuptake of serotonin. Metabolism by N-desmethylation occurs in man yielding desmethylfluoxetine, which also inhibits serotonin reuptake. Both the parent compound and metabolite possess elimination half-lives of several days facilitating the maintenance of steady-state plasma concentrations during long term treatment. Fluoxetine has overall therapeutic efficacy comparable with imipramine, amitriptyline and doxepin in patients with unipolar depression treated for 5 to 6 weeks, although it may be less effective than tricyclic antidepressants in relieving sleep disorders in depressed patients. Geriatric patients also responded as well to fluoxetine as to doxepin. The symptomatic improvement in patients with unipolar depression during short term fluoxetine treatment has been satisfactorily maintained when therapy was extended for at least 6 months: the relapse rate was low and similar to that of imipramine. Preliminary data have shown that patients with bipolar depression gained similar therapeutic benefit from fluoxetine or imipramine. Other preliminary trials have indicated that fluoxetine may be useful in obsessive-compulsive disorders. Usual doses of fluoxetine cause significantly fewer anticholinergic-type side effects than tricyclic antidepressants. Nausea, nervousness and insomnia are the most frequently reported fluoxetine-related adverse effects, but these have usually not been severe. Therapeutic doses of fluoxetine do not affect cardiac conduction intervals in patients without pre-existing cardiovascular disease and fluoxetine has been relatively safe in the small number of patients who have taken overdoses. It has not been clearly established whether some types of depression may respond more readily to fluoxetine than other antidepressants, and its overall therapeutic efficacy has not been compared with other second generation antidepressants. Thus, with its different and perhaps improved side effect profile compared with older tricyclic antidepressants, fluoxetine offers properties that could be used to advantage in many patients with depression.
氟西汀是一种新型抗抑郁药,它通过强效且选择性地抑制神经元对血清素的再摄取来增强血清素能神经传递。在人体内,通过N-去甲基化进行代谢,生成去甲氟西汀,它也能抑制血清素再摄取。母体化合物和代谢产物的消除半衰期均为几天,这有利于在长期治疗期间维持稳态血药浓度。在对单相抑郁症患者进行5至6周的治疗时,氟西汀的总体治疗效果与丙咪嗪、阿米替林和多塞平相当,不过在缓解抑郁症患者的睡眠障碍方面,它可能不如三环类抗抑郁药有效。老年患者对氟西汀的反应与对多塞平的反应一样好。当将氟西汀治疗至少延长6个月时,单相抑郁症患者在短期治疗期间的症状改善得到了令人满意的维持:复发率较低,与丙咪嗪相似。初步数据表明,双相抑郁症患者从氟西汀或丙咪嗪中获得了相似的治疗益处。其他初步试验表明,氟西汀可能对强迫症有用。氟西汀的常用剂量引起的抗胆碱能类副作用明显少于三环类抗抑郁药。恶心、紧张和失眠是最常报告的与氟西汀相关的不良反应,但这些通常并不严重。治疗剂量的氟西汀对没有预先存在心血管疾病的患者的心脏传导间期没有影响,并且在少数过量服用的患者中,氟西汀相对安全。目前尚未明确确定某些类型的抑郁症是否比其他抗抑郁药对氟西汀的反应更敏感,并且其总体治疗效果尚未与其他第二代抗抑郁药进行比较。因此,与较老的三环类抗抑郁药相比,氟西汀具有不同且可能更好的副作用谱,它具有的特性可在许多抑郁症患者中发挥优势。