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抗精神病药对大鼠膀胱平滑肌乙酰胆碱收缩反应的抑制作用。

Inhibitory Effects of Antipsychotics on the Contractile Response to Acetylcholine in Rat Urinary Bladder Smooth Muscles.

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Toho University.

Department of Pharmacy, Faculty of Pharmacy, Musashino University.

出版信息

Biol Pharm Bull. 2021;44(8):1140-1150. doi: 10.1248/bpb.b21-00363.

Abstract

The clinical applications of antipsychotics for symptoms unrelated to schizophrenia, such as behavioral and psychological symptoms, in patients with Alzheimer's disease, and the likelihood of doctors prescribing antipsychotics for elderly people are increasing. In elderly people, drug-induced and aging-associated urinary disorders are likely to occur. The most significant factor causing drug-induced urinary disorders is a decrease in urinary bladder smooth muscle (UBSM) contraction induced by the anticholinergic action of therapeutics. However, the anticholinergic action-associated inhibitory effects of antipsychotics on UBSM contraction have not been sufficiently assessed. In this study, we examined 26 clinically available antipsychotics to determine the extent to which they inhibit acetylcholine (ACh)-induced contraction in rat UBSM to predict the drugs that should not be used by elderly people to avoid urinary disorders. Of the 26 antipsychotics, six (chlorpromazine, levomepromazine (phenothiazines), zotepine (a thiepine), olanzapine, quetiapine, clozapine (multi-acting receptor targeted antipsychotics (MARTAs))) competitively inhibited ACh-induced contractions at concentrations corresponding to clinically significant doses. Further, 11 antipsychotics (perphenazine, fluphenazine, prochlorperazine (phenothiazines), haloperidol, bromperidol, timiperone, spiperone (butyrophenones), pimozide (a diphenylbutylpiperidine), perospirone, blonanserin (serotonin-dopamine antagonists; SDAs), and asenapine (a MARTA)) significantly suppressed ACh-induced contraction; however, suppression occurred at concentrations substantially exceeding clinically achievable blood levels. The remaining nine antipsychotics (pipamperone (a butyrophenone), sulpiride, sultopride, tiapride, nemonapride (benzamides), risperidone, paliperidone (SDAs), aripiprazole, and brexpiprazole (dopamine partial agonists)) did not inhibit ACh-induced contractions at concentrations up to 10 M. These findings suggest that chlorpromazine, levomepromazine, zotepine, olanzapine, quetiapine, and clozapine should be avoided by elderly people with urinary disorders.

摘要

抗精神病药物在阿尔茨海默病患者中用于治疗与精神分裂症无关的症状(如行为和心理症状)的临床应用以及医生为老年人开抗精神病药物的可能性正在增加。在老年人中,药物引起的和与衰老相关的尿失禁很可能发生。引起药物性尿失禁的最重要因素是治疗药物的抗胆碱能作用导致的膀胱平滑肌(UBSM)收缩减少。然而,抗精神病药物对 UBSM 收缩的抗胆碱能作用相关抑制作用尚未得到充分评估。在这项研究中,我们检查了 26 种临床可用的抗精神病药物,以确定它们在多大程度上抑制了大鼠 UBSM 中乙酰胆碱(ACh)诱导的收缩,以预测老年人不应使用的药物,以避免尿失禁。在 26 种抗精神病药物中,有 6 种(氯丙嗪、左美丙嗪(吩噻嗪类)、佐替平(噻嗪类)、奥氮平、喹硫平、氯氮平(多作用受体靶向抗精神病药(MARTAs)))在对应于临床显著剂量的浓度下竞争性抑制 ACh 诱导的收缩。此外,11 种抗精神病药物(奋乃静、氟奋乃静、丙氯拉嗪(吩噻嗪类)、氟哌啶醇、溴哌利多、替哌隆、螺哌隆(丁酰苯类)、匹莫齐德(二苯丁基哌啶)、哌泊噻嗪、博兰西林(血清素-多巴胺拮抗剂;SDAs)和阿立哌唑)显著抑制 ACh 诱导的收缩;然而,抑制作用发生在大大超过临床可达到的血药水平的浓度下。其余 9 种抗精神病药物(哌泊噻嗪(丁酰苯类)、舒必利、舒托必利、齐拉西酮、奈莫必利(苯甲酰胺类)、利培酮、帕利哌酮(SDAs)、阿立哌唑和布瑞哌唑(多巴胺部分激动剂))在高达 10 μM 的浓度下不抑制 ACh 诱导的收缩。这些发现表明,氯丙嗪、左美丙嗪、佐替平、奥氮平、喹硫平和氯氮平应避免在有尿失禁的老年人中使用。

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