Smeraldi E, Benedetti F, Barbini B, Campori E, Colombo C
Istituto Scientifico Ospedale San Raffaele, Department of Neuropsychiatric Sciences, University of Milan, School of Medicine, Italy.
Neuropsychopharmacology. 1999 Apr;20(4):380-5. doi: 10.1016/S0893-133X(98)00129-8.
Total sleep deprivation (TSD) shows powerful but transient clinical effects in patients affected by bipolar depression. Pindolol blocks the serotonergic 5-HT1A autoreceptor, thus improving the antidepressant effect of selective serotonin reuptake inhibitors. We evaluated the interaction of TSD and pindolol in the treatment of acute episodes of bipolar depression. Forty bipolar depressed inpatients were randomized to receive pindolol 7.5 mg/day or placebo for nine days in combination with three consecutive TSD cycles. Pindolol significantly improved the antidepressant effect of TSD, and prevented the short-term relapse after treatment. The response rate (HDRS scores < 8) at the end of treatment was 15/20 for pindolol, and 3/20 for placebo. Coadministration of pindolol and TSD resulted in a complete response, which could be sustained for six months with lithium salts alone, in 65% of cases. This results suggest a major role for serotonergic transmission in the mechanism of action of TSD, and makes TSD treatment more effective in the treatment of bipolar depression.
完全睡眠剥夺(TSD)在双相抑郁症患者中显示出强大但短暂的临床效果。吲哚洛尔可阻断5-羟色胺能5-HT1A自身受体,从而增强选择性5-羟色胺再摄取抑制剂的抗抑郁作用。我们评估了TSD与吲哚洛尔在双相抑郁症急性发作治疗中的相互作用。40例双相抑郁住院患者被随机分为两组,一组接受7.5毫克/天的吲哚洛尔或安慰剂,为期九天,并结合三个连续的TSD周期。吲哚洛尔显著增强了TSD的抗抑郁作用,并预防了治疗后的短期复发。治疗结束时,吲哚洛尔组的缓解率(汉密尔顿抑郁量表评分<8)为15/20,安慰剂组为3/20。在65%的病例中,吲哚洛尔与TSD联合使用产生了完全缓解,且仅用锂盐即可维持六个月。这些结果表明5-羟色胺能传递在TSD作用机制中起主要作用,并使TSD治疗在双相抑郁症治疗中更有效。