麦角酸二乙胺(LSD-25)的研究。3试图用神经体液阻滞剂预处理来减弱lsd在人体内的反应。

H. Isbell, C. R. Logan, E. J. Miner
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引用次数: 24

摘要

人们对中枢神经系统中脉冲可能的化学传递越来越感兴趣。涉及的神经体液包括乙酰胆碱、1,2去甲肾上腺素、2-4和血清素。4-6这些中枢化学突触传递理论反过来又导致了一些假设,这些假设认为麦角酸二乙胺(LSD-25)和其他拟精神药物引起的精神病是由于与一种或另一种神经体液的竞争导致中枢神经系统功能紊乱,或者相反,是由于拟精神药物加重了神经体液的作用。最大的兴趣集中在血清素和LSD可能的相互作用上。Woolley, Shaw和Gaddum独立地提出了一种假说,认为LSD精神病是LSD和血清素在神经元上或神经元内对受体位置的竞争。这一假说可能被称为血清素缺乏理论,它部分基于以下证据:血清素存在于大脑中
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Studies on lysergic acid diethylamide (LSD-25). III. Attempts to attenuate the LSD-reaction in man by pretreatment with neurohumoral blocking agents.
Interest in possible chemical transmission of impulses in the central nervous system has been increasing. The neurohumors involved include acetylcholine, 1,2 norepinephrine, 2-4 and serotonin. 4-6 These theories of central chemical synaptic transmission have led, in turn, to hypotheses which ascribe the psychosis induced by lysergic acid diethylamide (LSD-25) and other psychotomimetic drugs to derangements in central nervous system function because of competition with one or another of the neurohumors or, on the contrary, to accentuation of the effects of the neurohumors by the psychotomimetic agents. The greatest interest has centered on possible interactions of serotonin and LSD. Woolley and Shaw 5 and Gaddum 6 independently evolved a hypothesis which ascribes the LSD psychosis to competition between LSD and serotonin for receptor sites on or in neurons. This hypothesis, which might be termed the serotonin-deficiency theory, is based in part on the following evidence: Serotonin is found in brain, 6,7
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