Bulach C, Doaré L, Massari B, Simon P
J Pharmacol. 1984 Jan-Mar;15(1):1-15.
Norepinephrine (NE), octopamine (OA) and phenethylamine (PEA) are easily destroyed by M.A.O. but we could show, even injected intraperitoneally that they are active upon tests used generally to reveal an "antidepressant" effect. This effect is especially studied by using antagonism of apomorphine, reserpine, oxotremorine-induced hypothermia. The psychopharmacological spectra of NE and OA are close to the one of salbutamol and the observed effects correspond to alpha- and beta-adrenergic stimulations. The PEA spectrum is similar to the one of amphetamine and the observed effects correspond to adrenergic stimulations and to a dopaminergic stimulation. The mechanisms involved in the tests realized to show an "antidepressant" effect could reflect an activity not only through endogeneous NA but also possibly through endogeneous OA and PEA.
去甲肾上腺素(NE)、章鱼胺(OA)和苯乙胺(PEA)很容易被单胺氧化酶(M.A.O.)破坏,但我们能够证明,即使通过腹腔注射,它们在通常用于揭示“抗抑郁”作用的测试中也具有活性。这种作用尤其通过使用阿扑吗啡、利血平、氧化震颤素诱导的体温过低的拮抗作用来研究。NE和OA的精神药理学谱与沙丁胺醇的谱相近,观察到的作用对应于α-和β-肾上腺素能刺激。PEA的谱与苯丙胺的谱相似,观察到的作用对应于肾上腺素能刺激和多巴胺能刺激。为显示“抗抑郁”作用而进行的测试所涉及的机制可能不仅反映了内源性去甲肾上腺素的活性,还可能反映了内源性OA和PEA的活性。