University Department of Psychiatry, Neurosciences Building, Warneford Hospital, Oxford, UK.
J Psychopharmacol. 2012 Jan;26(1):125-32. doi: 10.1177/0269881111400649. Epub 2011 Mar 15.
Rimonabant is a cannabinoid type 1 receptor (CB1) antagonist formerly used to treat obesity, but which was withdrawn from the market in late 2008 because of its association with psychiatric adverse effects such as depression and anxiety. Previously, we showed that a single dose of rimonabant produced a negative bias on an emotional word memory task, in the absence of subjective mood effects. The present study investigated whether a similar effect on emotional processing could be seen after 7 days' daily treatment with rimonabant 20 mg, using a randomized, placebo-controlled, between-subjects design in healthy volunteers (final n = 21). In comparison with placebo, rimonabant induced a negative bias on a memory recognition task without producing a change in subjective mood. This raises the possibility that the depressogenic effects of rimonabant may be linked to emotional memory biases, and that such biases may be detectable in the absence of subjective mood changes. Investigating such effects could be useful in detecting adverse psychiatric effects of novel treatments.
利莫那班是一种大麻素 1 型受体(CB1)拮抗剂,以前用于治疗肥胖症,但由于其与抑郁和焦虑等精神不良影响有关,已于 2008 年底从市场上撤出。此前,我们发现单次剂量的利莫那班在情绪单词记忆任务中产生了负面偏差,而没有主观情绪影响。本研究使用健康志愿者的随机、安慰剂对照、组间设计(最终 n = 21),调查了在 7 天的每日利莫那班 20 毫克治疗后,是否会出现类似的情绪处理效果。与安慰剂相比,利莫那班在记忆识别任务中引起了负面偏差,而没有引起主观情绪变化。这表明利莫那班的致抑郁作用可能与情绪记忆偏差有关,并且在没有主观情绪变化的情况下可能可以检测到这种偏差。研究这种影响可能有助于检测新型治疗方法的不良精神副作用。