Kameyama T, Nagasaka M
Neuropharmacology. 1983 Jul;22(7):813-7. doi: 10.1016/0028-3908(83)90125-9.
Rats exhibited a marked suppression of motor activity when placed in the same chamber where they had been given electric shocks. Administration of apomorphine-HCl (0.1, 0.5 and 1.0 mg/kg, i.p.) attenuated the conditioned suppression, dose-dependently, but did not facilitate motor activity of control (i.e. non-shocked) rats. Methamphetamine-HCl (0.1, 0.5 and 1 mg/kg, i.p.) increased motor activity of both the shocked and non-shocked rats, in a dose-related manner. Haloperidol (0.3 and 1 mg/kg, i.p.), but not chlorpromazine-HCl (5 mg/kg, i.p.), enhanced the conditioned-suppression response. Atropine-sulfate (5 and 10 mg/kg, i.p.), p-chlorophenylalanine (300 mg/kg, i.p.) and alpha-methyl-p-tyrosine (100 mg/kg, i.p.) were slightly effective in reducing the conditioned-suppression response. Apomorphine- and methamphetamine-induced reduction of the conditioned-suppression response was inhibited by pretreatment with haloperidol. When catecholamine-synthesizing processes in rats were inhibited by pretreatment with alpha-methyl-p-tyrosine, or alpha-adrenergic receptor sites were blocked by pretreatment with phenoxybenzamine, the effect of methamphetamine, but not that of apomorphine, was reduced. Therefore, enhancement of dopaminergic neurotransmission may be responsible for attenuation of the conditioned-suppression response.
当大鼠被放置在曾遭受电击的同一实验箱中时,其运动活动表现出明显的抑制。腹腔注射盐酸阿扑吗啡(0.1、0.5和1.0毫克/千克)可剂量依赖性地减轻条件性抑制,但对对照组(即未受电击)大鼠的运动活动无促进作用。腹腔注射盐酸甲基苯丙胺(0.1、0.5和1毫克/千克)可使受电击和未受电击的大鼠的运动活动均呈剂量相关地增加。氟哌啶醇(0.3和1毫克/千克,腹腔注射)可增强条件性抑制反应,而盐酸氯丙嗪(5毫克/千克,腹腔注射)则无此作用。硫酸阿托品(5和10毫克/千克,腹腔注射)、对氯苯丙氨酸(300毫克/千克,腹腔注射)和α-甲基对酪氨酸(100毫克/千克,腹腔注射)在减轻条件性抑制反应方面略有效果。预先给予氟哌啶醇可抑制阿扑吗啡和甲基苯丙胺诱导的条件性抑制反应的减轻。当用α-甲基对酪氨酸预处理抑制大鼠儿茶酚胺合成过程,或用苯氧苄胺预处理阻断α-肾上腺素能受体位点时,甲基苯丙胺的作用减弱,但阿扑吗啡的作用未受影响。因此,多巴胺能神经传递的增强可能是条件性抑制反应减轻的原因。