Barr G A, Gibbons J L, Bridger W H
Pharmacol Biochem Behav. 1979 Oct;11(4):419-22. doi: 10.1016/0091-3057(79)90118-7.
beta-Phenylethylamine (PEA) is an endogenous amine that in some instances acts biochemically and behaviorally like amphetamine. In the present experiments, the effects of PEA on mouse killing by rats were compared and constrasted with the effects of d-amphetamine on this behavior. When given acutely to experienced mouse killing rats, PEA (16 and 32 mg/kg) inhibited killing in a direct dose dependent manner. This is similar to the dose dependent inhibition of killing by amphetamine reported previously. However, d-amphetamine but not PEA showed physiologic tolerance following 8 days of twice daily administration. Cross tolerance between the two drugs only occurred when d-amphetamine was administered subacutely. It was concluded that PEA and d-amphetamine have sililar acute effects but differed when given subacutely since PEA did not show tolerance and there was not bidirectional cross-tolerance. These data suggest that these drugs have different pharmacologic actions when given repeatedly. One possible difference may be the duration of action.
β-苯乙胺(PEA)是一种内源性胺类物质,在某些情况下,其生化和行为作用类似于苯丙胺。在本实验中,将PEA对大鼠捕杀小鼠行为的影响与d-苯丙胺对该行为的影响进行了比较和对比。当对有捕杀小鼠经验的大鼠急性给予PEA(16和32毫克/千克)时,它以直接的剂量依赖性方式抑制捕杀行为。这与先前报道的苯丙胺对捕杀行为的剂量依赖性抑制相似。然而,在每日两次给药8天后,d-苯丙胺表现出生理耐受性,而PEA则没有。只有当亚急性给予d-苯丙胺时,两种药物之间才会出现交叉耐受性。得出的结论是,PEA和d-苯丙胺具有相似的急性效应,但亚急性给药时有所不同,因为PEA没有表现出耐受性,也不存在双向交叉耐受性。这些数据表明,反复给药时这些药物具有不同的药理作用。一个可能的差异可能在于作用持续时间。