Vaupel D B, Nozaki M, Martin W R, Bright L D
Eur J Pharmacol. 1978 Apr 15;48(4):431-7. doi: 10.1016/0014-2999(78)90171-1.
The effects of beta-phenethylamine (PEA), d-amphetamine and LSD were studied on spinal reflexes, autonomic signs, and behavior in the non-tolerant and LSD tolerant (30 microgram/kg/day) chronic spinal dog. LSD (10 microgram/kg) facilitated the flexor reflex, produced the stepping reflex, increased respiration, pulse rate and temperature, slightly dilated pupils and produced whining, tracking and restlessness. Direct tolerance developed to all of these effects except temperature. PEA (0.8 mg/kg/min infused for 12 min) and amphetamine (3.2 mg/kg) facilitated the flexor reflex, increased respiration, temperature and the skin twitch reflex latency, caused a marked mydriasis, retracted the nictitating membrane and produced restlessness and stereotypic head movements. PEA but not amphetamine elicited stepping, and only amphetamine consistently slowed heart rate. No cross tolerance to the physiologic or behavioral effects of amphetamine was observed. Partial tolerance developed only to the actions of PEA on the stepping reflex and the nictitating membrane. The single dose effects and the lack of cross tolerance to amphetamine and PEA suggest modes of action different from LSD. PEA has some actions which differ from those of amphetamine.
研究了β-苯乙胺(PEA)、右旋苯丙胺和麦角酸二乙酰胺(LSD)对未产生耐受性以及对LSD产生耐受性(30微克/千克/天)的慢性脊髓犬的脊髓反射、自主神经体征和行为的影响。LSD(10微克/千克)可促进屈肌反射、产生踏步反射、增加呼吸、脉搏率和体温,使瞳孔略有散大,并引起哀鸣、追踪和不安。除体温外,对所有这些效应均产生了直接耐受性。PEA(以0.8毫克/千克/分钟的速度输注12分钟)和苯丙胺(3.2毫克/千克)可促进屈肌反射、增加呼吸、体温和皮肤抽搐反射潜伏期,引起明显的瞳孔散大,使瞬膜退缩,并产生不安和刻板的头部运动。PEA可引起踏步,但苯丙胺不会,且只有苯丙胺能持续减慢心率。未观察到对苯丙胺的生理或行为效应产生交叉耐受性。仅对PEA对踏步反射和瞬膜的作用产生了部分耐受性。单剂量效应以及对苯丙胺和PEA缺乏交叉耐受性表明其作用方式与LSD不同。PEA的一些作用与苯丙胺不同。