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Z1046:一种新型特异性外周多巴胺能化合物。

Z1046: a new specific peripheral dopaminergic compound.

作者信息

Ferlenga P, Zanzottera D, Biasini I, Marchini F, Semeraro C

机构信息

Zambon Group, Bresso, Milan, Italy.

出版信息

Acta Physiol Hung. 1996;84(3):283-4.

PMID:9219608
Abstract

It is well established that peripheral dopamine receptors activation evokes vasodilation and neurohormonal modulation. Z1046 is a potent mixed dopaminergic agonist and is highly selective over adrenergic and serotoninergic (5-HT2) activities. In contrast, dopamine had agonist activities on all adrenergic receptors while it is known that dopexamine has a beta 2 agonist activity and is an inhibitor of the neuronal uptake. As far as fenoldopam is concerned, selective stimulation of D1-like receptors leads to an increase of renin release. In conclusion, Z1046 is a potent and specific drug for dopamine receptors. This profile makes Z1046 different from other dopaminergic agents.

摘要

外周多巴胺受体激活可引起血管舒张和神经激素调节,这一点已得到充分证实。Z1046是一种强效的混合多巴胺能激动剂,对肾上腺素能和血清素能(5-HT2)活性具有高度选择性。相比之下,多巴胺对所有肾上腺素能受体均有激动活性,而多培沙明具有β2激动活性且是神经元摄取的抑制剂。就非诺多泮而言,对D1样受体的选择性刺激会导致肾素释放增加。总之,Z1046是一种强效且特异性的多巴胺受体药物。这种特性使Z1046有别于其他多巴胺能药物。

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