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

机译:抗精神病药对大鼠膀胱平滑肌乙酰胆碱收缩响应的抑制作用

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摘要

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(-5) M. These findings suggest that chlorpromazine, levomepromazine, zotepine, olanzapine, quetiapine, and clozapine should be avoided by elderly people with urinary disorders.
机译:抗精神病药对与精神分裂症无关的症状的临床应用,例如Alzheimer疾病患者的行为和心理症状,以及患者抗精神病人的医生对老年人的可能性增加。在老年人中,可能发生药物诱导和衰老相关的尿障碍。导致药物诱导的尿紊乱的最重要因素是通过治疗剂的抗胆碱能作用诱导的尿膀胱平滑肌(UBSM)收缩减少。然而,抗精神病药物对UBSM收缩的抗胆碱能动作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,以确定它们抑制乙酰胆碱(ACH)的程度 - 诱导大鼠UBSM的收缩,以预测老年人不应使用的药物以避免尿紊乱。在26例抗精神病药中,六个(氯丙嗪,LevomeProdazines(吩噻嗪),Zotepine(A Thiepine),奥氮平,喹喔啉,氯氮平(多效受体靶向抗精神病药(Martas))竞争地抑制对应于临床显着剂量的浓度的ACH引起的收缩。此外,11抗抗精神病药(Perphenazine,Fluphenazine,Prochorsazine(吩噻唑),氟哌啶醇,溴吡咯,Timipherone,Spiperne(丁基核糖酮),Pimozide(二苯基丁基哌啶),Perospirone,Blonanserin(血清素 - 多巴胺拮抗剂; SDAS)和aseNapine(玛莎))显着抑制了ach引起的收缩;然而,抑制在基本上超过临床可实现的血液水平的浓度发生。剩余的九种抗精神病药(吡酰蛋白(丁苯酮),硫吡啶,索华啶,Tiapride,Nemonapride(苯甲酰胺),丙基吡啶酮,Paliperidone(SDAS),AripiPrazole和Bresprazole(多巴胺部分激动剂))不抑制浓度的ACH引起的收缩这些研究结果表明,泌尿疾病的老年人应避免氯丙嗪,氯丙嗪,Levomepromazine,Zotepine,Olanzapine,喹喔啉和氯氮平。

著录项

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  • 作者单位

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Clin Pharm 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Clin Pharm 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

    Toho Univ Fac Pharmaceut Sci Dept Chem Pharmacol 2-2-1 Miyama Funabashi Chiba 2748510 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

    antipsychotics; rat urinary bladder smooth muscle; anticholinergic effect; urinary disorder;

    机译:抗精神病药;大鼠膀胱平滑肌;抗胆碱能作用;泌尿障碍;

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