Handley S L, Thomas K V
Psychopharmacology (Berl). 1978 Jul 19;58(3):283-8. doi: 10.1007/BF00427392.
In the mouse, central noradrenaline receptor stimulation by clonidine, or intracerebroventricular injection of noradrenaline or alpha-methylnoradrenaline, caused marked enhancement of the locomotor stimulant effects of dexamphetamine in doses that were without effect when given alone. A minimally locomotor-stimulant dose of apomorphine reduced the effect of dexamphetamine. Pimozide and phenoxybenzamine each virtually abolished locomotor stimulation after dexamphetamine, while FLA63 caused significant reduction. Phenoxybenzamine also abolished the enhancement by clonidine. The intensity of the dexamphetamine effect was dose-related, while in the case of apomorphine the duration rather than the intensity was related to the dose administered. Clonidine potentiated apomorphine locomotor stimulation; following this drug combination, the nature of the movements more closely resembled those seen after dexamphetamine. The results suggest the involvement of both noradrenaline and dopamine in the dexamphetamine response.
在小鼠中,可乐定对中枢去甲肾上腺素受体的刺激,或脑室内注射去甲肾上腺素或α-甲基去甲肾上腺素,可显著增强右旋苯丙胺的运动兴奋作用,而单独给予这些药物时则无此效应。最小运动兴奋剂量的阿扑吗啡可降低右旋苯丙胺的作用。匹莫齐特和酚苄明几乎都消除了右旋苯丙胺后的运动兴奋,而FLA63则导致显著降低。酚苄明也消除了可乐定的增强作用。右旋苯丙胺作用的强度与剂量相关,而对于阿扑吗啡,持续时间而非强度与给药剂量有关。可乐定增强了阿扑吗啡的运动兴奋作用;使用这种药物组合后,运动的性质更类似于右旋苯丙胺后的运动。结果表明去甲肾上腺素和多巴胺都参与了右旋苯丙胺反应。