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α-肾上腺素能药物。3. 2-氨基四氢萘的行为效应。

alpha-Adrenergic agents. 3. Behavioral effects of 2-aminotetralins.

作者信息

Holz W C, Hieble J P, Gill C A, DeMarinis R M, Pendleton R G

出版信息

Psychopharmacology (Berl). 1982;77(3):259-67. doi: 10.1007/BF00464577.

Abstract

Studies with 5-substituted-8-methoxy-2-amino-tetralin compounds suggest that some are alpha 1-adrenoceptor agonists, which readily penetrate the blood-brain barrier. They potentiate the locomotor activity that is induced by apomorphine (AP) in reserpinized mice, an effect that has been suggested to result from activation of central alpha-receptors. This effect is selectively blocked by the preferential alpha 1-antagonist phenoxybenzamine, but not by drugs that block other types of receptors. The effect is also produced by the centrally administered alpha 1-agonists phenylephrine and methoxamine, but not by various types of standard CNS stimulants. When administered in high doses, some of the aminotetralin compounds induce locomotor activity in reserpinized mice without AP, an effect also found with high doses of centrally administered phenylephrine and methoxamine. This effect is blocked by a series of drugs at doses that correspond to their alpha 1-antagonist potencies.

摘要

对5-取代-8-甲氧基-2-氨基四氢萘化合物的研究表明,其中一些是α1肾上腺素能受体激动剂,它们能够轻易穿透血脑屏障。它们能增强利血平化小鼠中由阿扑吗啡(AP)诱导的运动活性,这种效应被认为是由中枢α受体的激活所导致。这种效应被选择性α1拮抗剂酚苄明选择性阻断,但不会被阻断其他类型受体的药物所阻断。中枢给予α1激动剂去氧肾上腺素和甲氧明也会产生这种效应,但各种标准的中枢神经系统兴奋剂则不会。当高剂量给药时,一些氨基四氢萘化合物在没有AP的情况下也能诱导利血平化小鼠的运动活性,高剂量的中枢给予去氧肾上腺素和甲氧明也会出现这种效应。这种效应在与它们的α1拮抗效力相对应的剂量下会被一系列药物阻断。

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