...
首页> 外文期刊>Life sciences >TIOTROPIUM BROMIDE (BA 679 BR), A NOVEL LONG-ACTING MUSCARINIC ANTAGONIST FOR THE TREATMENT OF OBSTRUCTIVE AIRWAYS DISEASE
【24h】

TIOTROPIUM BROMIDE (BA 679 BR), A NOVEL LONG-ACTING MUSCARINIC ANTAGONIST FOR THE TREATMENT OF OBSTRUCTIVE AIRWAYS DISEASE

机译:噻托溴铵(BA 679 BR),一种新型长效抗真菌药,用于治疗阻塞性气道疾病。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Tiotropium bromide (Ba 679 BR) is a novel potent and long-lasting muscarinic antagonist that has been developed for the treatment of chronic obstructive airways disease (COPD). Binding studies with [H-3]tiotropium bromide in human lung have confirmed that this is a potent muscarinic antagonist with equal affinity for M(1)- M(2)- and M(3)-receptors and is approximately 10-fold more potent than ipratropium bromide. Tiotropium bromide dissociates very slowly from lung muscarinic receptors compared with ipratropium bromide. In vitro tiotropium bromide has a potent inhibitory effect against cholinergic nerve-induced contraction of guinea-pig and human airways, that has a slower onset than atropine or ipratropium bromide. After washout, however, tiotropium bromide dissociates extremely slowly compared with the dissociation of atropine and ipratropium bromide. Measurement of acetylcholine (ACh) release from guinea-pig trachea shows that tiotropium bromide, ipratropium bromide and atropine all increase ACh release on neural stimulation and that this effect is washed out equally quickly for the three antagonists. This confirms binding studies to transfected human muscarinic receptors which suggested that tiotropium bromide dissociates slowly from M(3)-receptors (on airway smooth muscle) but rapidly from M(2) autoreceptors (on cholinergic nerve terminals). Clinical studies with Inhaled tiotropium bromide confirm that it is a potent and long-lasting bronchodilator in COPD and asthma. Furthermore, it protects against cholinergic bronchoconstriction for >24 h. This suggests that tiotropium bromide will be a useful bronchodilator, particularly in patients with COPD, and may be suitable for daily dosing. The selectivity for M(3)- Over M(2)-receptors may also confer a clinical advantage. [References: 47]
机译:噻托溴铵(Ba 679 BR)是一种新型有效且长效的毒蕈碱拮抗剂,已被开发用于治疗慢性阻塞性气道疾病(COPD)。与[H-3]噻托溴铵在人肺中的结合研究已证实,这是一种有效的毒蕈碱拮抗剂,对M(1)-M(2)-和M(3)-受体具有相同的亲和力,并且约高10倍比异丙托溴铵更有效。与异丙托溴铵相比,噻托溴铵与肺毒蕈碱受体的解离非常缓慢。体外噻托溴铵对胆碱能神经引起的豚鼠和人呼吸道收缩具有有效的抑制作用,其起效慢于阿托品或异丙托溴铵。然而,与阿托品和异丙托溴铵的解离相比,洗出后噻托溴铵的解离非常缓慢。对豚鼠气管中乙酰胆碱(ACh)释放的测量表明,噻托溴铵,异丙托溴铵和阿托品在神经刺激下均会增加ACh的释放,并且对于三种拮抗剂,这种作用会很快被冲掉。这证实了对转染的人类毒蕈碱受体的结合研究,这表明噻托溴铵从M(3)-受体(在气道平滑肌上)缓慢解离,但从M(2)自体受体(在胆碱能神经末梢)上迅速解离。吸入噻托溴铵的临床研究证实,它在COPD和哮喘中是一种有效且持久的支气管扩张药。此外,它还可以防止胆碱能支气管收缩超过24小时。这表明噻托溴铵将是一种有用的支气管扩张药,尤其是在患有COPD的患者中,并且可能适合于日常给药。 M(3)-超过M(2)-受体的选择性也可能赋予临床优势。 [参考:47]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号