Effects of 5-hydroxytryptamine, LSD and related compounds on electrical activities evokedin vitro in thin sections from the superior colliculus

N. Kawai, C. Yamamoto
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引用次数: 51

Abstract

Effects of 5-hydroxytryptamine (5-HT), lysergic acid diethylamide (LSD) and other psychotomimetics upon the potentials induced in thin sections from the superior colliculus of the guinea pig were studiedin vitro. The postsynaptic field potential (PSR) evoked by optic tract stimulation was suppressed by 5-HT in concentrations of 10−7–10−6M. Single neuron discharges induced by optic tract stimulation were also suppressed by 5-HT but spontaneous cell firings were not affected. By higher concentrations of 5-HT (more than 10−4M) PSR was once suppressed but gradually recovered. LSD, lysergic acid ethylamide (LAE) and other related compounds potentiated the 5-HT suppressing action in relatively low concentrations but blocked it in higher ones. Morphine and 2-bromolysergic acid ethylamide (BOL) did not antagonize the 5-HT action. When two shocks were delivered to the optic tract at short intervals and the time course of suppression of the second PSR was studied, it was found that LSD and related compounds accelerated the recovery of the test PSR. Physiological roles of 5-HT in the superior colliculus are discussed.

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5-羟色胺、LSD及相关化合物对上丘离体薄切片电活性的影响
体外研究了5-羟色胺(5-HT)、麦角酸二乙胺(LSD)等拟精神药物对豚鼠上丘薄片电位的影响。5-羟色胺在10−7 ~ 10−6M浓度下可抑制视束刺激引起的突触后场电位(PSR)。视神经束刺激引起的单个神经元放电也被5-HT抑制,但自发细胞放电不受影响。当5-HT浓度高于10−4M时,PSR一度被抑制,但逐渐恢复。LSD、麦角酸乙胺(LAE)等相关化合物在较低浓度时增强了5-HT的抑制作用,而在较高浓度时则阻断了其抑制作用。吗啡和2-溴化麦角酸乙胺(BOL)对5-羟色胺无拮抗作用。在短时间间隔两次冲击视神经束时,研究第二次PSR抑制的时间过程,发现LSD及相关化合物加速了测试PSR的恢复。讨论了5-羟色胺在上丘中的生理作用。
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