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Interactions between domperidone and ropinirole, a novel dopamine D2-receptor agonist.

机译:多潘立酮与一种新的多巴胺D2受体激动剂罗匹尼罗之间的相互作用。

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摘要

1. Ropinirole, SK&F 101468 has been characterized preclinically as a specific dopamine D2-receptor agonist. Nine male healthy subjects were investigated for the effects on supine and erect heart rate and blood pressure, catecholamines and prolactin, of a single dose of 800 micrograms ropinirole preceded by a single dose of 20 mg domperidone or domperidone-placebo, and those of a single dose of domperidone followed by ropinirole-placebo. 2. Single doses of 800 micrograms ropinirole did not cause clinically significant changes in supine resting heart rate and blood pressure. However, they caused postural faintness on 3 min immobile upright standing on 10/26 occasions. 3. Pretreatment with 20 mg domperidone 1 h before administration of ropinirole prevented the postural symptoms in all but one subject. It did not alter ropinirole's plasma pharmacokinetics. 4. Ropinirole did not alter supine or standing catecholamine concentrations. 5. Domperidone increased the plasma concentrations of prolactin whereas ropinirole administered alone reduced them. A single dose of 800 micrograms ropinirole did not attenuate the prolactin increase induced by a single dose of 20 mg domperidone administered 1 h earlier.
机译:1. Ropinirole,SK&F 101468在临床上已被表征为一种特定的多巴胺D2受体激动剂。研究了9名男性健康受试者,研究了单剂量800毫克罗哌尼洛,单剂量20毫克多潘立酮或多潘立酮-安慰剂以及单次服用安慰剂对仰卧和直立心率,血压,儿茶酚胺和催乳激素的影响。剂量的多潘立酮,然后使用罗匹尼罗-安慰剂。 2.单剂800微克罗匹尼罗不会引起仰卧静息心率和血压的临床显着变化。但是,他们在10/26次站立3分钟的静止不动时导致姿势昏厥。 3.在服用罗匹尼罗前1小时用20 mg多潘立酮进行预处理可预防除一名受试者外的所有体位症状。它没有改变罗匹尼罗的血浆药代动力学。 4.罗匹尼罗不会改变仰卧位或儿茶酚胺的浓度。 5.多潘立酮可增加血浆催乳素的浓度,而单独服用罗匹尼罗可降低血浆中的催乳素浓度。一次服用800微克罗匹尼罗不会减弱1小时前服用一次20毫克多潘立酮所引起的催乳素增加。

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