Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, USA.
Am J Psychiatry. 2012 Sep;169(9):974-81. doi: 10.1176/appi.ajp.2012.11081289.
The α7 nicotinic acetylcholine receptor (nAChR) is associated with cognitive and P50 auditory gating deficits in schizophrenia, and α7 nAChR agonists can potentially reverse these deficits. The authors examined multiple dosages of tropisetron, a partial agonist at the nAChR, for short-term effects on cognition and P50 deficits in schizophrenia.
In a randomized double-blind design, 40 nonsmoking patients with schizophrenia who had P50 ratios greater than 0.5 and were stabilized on 3-6 mg/day of risperidone were randomly assigned to receive placebo (N=10) or oral tropisetron at 5 mg/day (N=10), 10 mg/day (N=10), or 20 mg/day (N=10). The authors measured P50 inhibitory gating and administered the Chinese-language version of the Repeatable Battery for the Assessment of Neuropsychological Status at baseline and after 10 days of treatment.
After 10 days of treatment, all three daily doses of tropisetron significantly improved overall cognitive deficits, with 10 mg showing the greatest improvement for the immediate memory index score and 20 mg for the delayed memory index score on the cognitive battery. The P50 deficits were also improved, and that improvement was significantly correlated with cognitive improvement. Two patients in the 20 mg/day group dropped out because of adverse effects, but the other dosages were well tolerated.
The improvement of cognition with tropisetron appeared to be associated with normalization in P50 deficits. Thus, α7 nAChR agonists appear to be a promising therapeutic approach for the treatment of cognitive deficits that are related to abnormal P50 suppression in schizophrenia.
α7 型烟碱型乙酰胆碱受体(nAChR)与精神分裂症的认知和 P50 听觉门控缺陷有关,α7 nAChR 激动剂可能逆转这些缺陷。作者研究了托吡酯(nAChR 的部分激动剂)的多种剂量对精神分裂症患者认知和 P50 缺陷的短期影响。
采用随机双盲设计,将 40 名未吸烟的精神分裂症患者纳入研究,这些患者的 P50 比值大于 0.5 ,并且稳定服用利培酮 3-6mg/天,他们被随机分为安慰剂组(N=10)或托吡酯 5mg/天组(N=10)、10mg/天组(N=10)或 20mg/天组(N=10)。作者测量了 P50 抑制门控,并在基线和治疗 10 天后进行了汉语版重复认知评估电池测试。
治疗 10 天后,托吡酯的三种日剂量均显著改善了整体认知缺陷,其中 10mg 组对即时记忆指数评分的改善最大,20mg 组对延迟记忆指数评分的改善最大。P50 缺陷也得到了改善,这种改善与认知改善显著相关。20mg/天组的 2 名患者因不良反应退出,但其他剂量均耐受良好。
托吡酯改善认知似乎与 P50 缺陷的正常化有关。因此,α7 nAChR 激动剂似乎是一种有前途的治疗方法,可用于治疗与精神分裂症中异常 P50 抑制相关的认知缺陷。