Bai Y M, Lin C C, Chen J Y, Liu W C
Department of Psychiatry, Yu-Li Veterans Hospital, Hua-Lien, Taiwan.
J Clin Psychopharmacol. 2001 Dec;21(6):608-11. doi: 10.1097/00004714-200112000-00012.
The objective of this study was to investigate the efficacy of pirenzepine in the treatment of clozapine-induced hypersalivation. Pirenzepine is reported to counteract hypersalivation by its selective antagonistic activity on the M4-muscarinic receptor, which is stimulated by clozapine. Twenty patients with clozapine-induced hypersalivation underwent a random-order, double-blind, placebo-controlled, cross-over trial which lasted 8 weeks each for the pirenzepine and placebo investigations, with a 4-week washout period in between. The severity of hypersalivation was assessed using an objective measure: saliva production monitored through the diameter of wetted surface on tissue paper placed over the patient's pillow. Our study showed that pirenzepine had no significant therapeutic effect on hypersalivation compared with placebo, suggesting that hypersalivation induced by clozapine might have a neurobiological basis other than the M4-muscarinic receptor.
本研究的目的是探讨哌仑西平治疗氯氮平引起的流涎过多的疗效。据报道,哌仑西平通过对M4毒蕈碱受体的选择性拮抗活性来对抗流涎过多,而氯氮平会刺激该受体。20例氯氮平引起流涎过多的患者进行了一项随机顺序、双盲、安慰剂对照的交叉试验,哌仑西平和安慰剂研究各持续8周,中间有4周的洗脱期。使用客观指标评估流涎过多的严重程度:通过放置在患者枕头上方的纸巾上湿润表面的直径来监测唾液分泌量。我们的研究表明,与安慰剂相比,哌仑西平对流涎过多没有显著的治疗效果,这表明氯氮平引起的流涎过多可能有除M4毒蕈碱受体以外的神经生物学基础。