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通过脊髓损毁大鼠的心率反应研究了扎莫特罗(ICI 118,587)的部分激动剂活性。

The partial agonist activity of xamoterol (ICI 118,587) studied by heart rate response in pithed rats.

作者信息

Hashimoto T, Kondo K, Shiina A, Toyo-Oka T, Kawasaki K, Kimura K, Hosoda S

机构信息

Department of Cardiology and Internal Medicine, Jichi Medical School, Tochigi, Japan.

出版信息

Jpn Circ J. 1988 Jan;52(1):60-5. doi: 10.1253/jcj.52.60.

Abstract

The partial agonist activity of xamoterol was evaluated by measuring changes in heart rate (HR) in pithed rats. Xamoterol showed dose-dependent positive chronotropic effects in catecholamine-depleted pithed rats (HR: 199 +/- 6 beats/min) and dose-dependent negative chronotropic effects in sympathetic nerve-stimulated pithed rats (HR: 325 +/- 16 beats/min). In contrast, isoproterenol exerted dose-dependent positive chronotropic effects in either condition (HR: 189 +/- 7 and 332 +/- 5 beats/min) and propranolol exerted dose-dependent negative chronotropic effects in either condition (HR: 209 +/- 5 and 344 +/- 19 beats/min). When exogenous noradrenaline was continuously infused into catecholamine-depleted pithed rats, xamoterol showed dose-related positive chronotropic effects with noradrenaline at 0.5 micrograms/(kg min) (HR: 235 +/- 4 beats/min), virtually no effects at 1.5 micrograms/(kg min) (HR: 297 +/- 11 beats/min) and dose-related negative chronotropic effects at 5 micrograms/(kg min) (HR: 330 +/- 5 beats/min). During continuous infusion of xamoterol [100 ng/(kg min)] into pithed rats, the control HR before stimulation was increased and the maximum increase produced by the sympathetic nerve stimuli at 0.25 to 4 Hz decreased. The maximum increase in HR brought about by xamoterol was about 71% of that induced by isoproterenol, and those by pindolol and practolol were about 40% and 21% respectively. It is concluded that xamoterol is a partial agonist with a strong agonist action.

摘要

通过测量脊髓横断大鼠的心率(HR)变化来评估昔莫罗尔的部分激动剂活性。昔莫罗尔在去甲肾上腺素耗竭的脊髓横断大鼠中呈现剂量依赖性的正性变时作用(HR:199±6次/分钟),而在交感神经刺激的脊髓横断大鼠中呈现剂量依赖性的负性变时作用(HR:325±16次/分钟)。相比之下,异丙肾上腺素在两种情况下均呈现剂量依赖性的正性变时作用(HR:189±7次/分钟和332±5次/分钟),普萘洛尔在两种情况下均呈现剂量依赖性的负性变时作用(HR:209±5次/分钟和344±19次/分钟)。当向去甲肾上腺素耗竭的脊髓横断大鼠持续输注外源性去甲肾上腺素时,昔莫罗尔在去甲肾上腺素剂量为0.5微克/(千克·分钟)时呈现与剂量相关的正性变时作用(HR:235±4次/分钟),在1.5微克/(千克·分钟)时几乎无作用(HR:297±11次/分钟),在5微克/(千克·分钟)时呈现与剂量相关的负性变时作用(HR:330±5次/分钟)。在向脊髓横断大鼠持续输注昔莫罗尔[100纳克/(千克·分钟)]期间,刺激前的对照心率升高,交感神经在0.25至4赫兹刺激产生的最大心率增加降低。昔莫罗尔引起的心率最大增加约为异丙肾上腺素诱导值的71%,吲哚洛尔和普拉洛尔引起的心率最大增加分别约为40%和21%。结论是昔莫罗尔是一种具有强激动剂作用的部分激动剂。

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