Wagner G C, Preston K, Ricaurte G A, Schuster C R, Seiden L S
Drug Alcohol Depend. 1982 Aug;9(4):279-84. doi: 10.1016/0376-8716(82)90067-9.
Cathinone, the principal alkaloid of Khat, was compared to the psychomotor stimulant d-amphetamine on a number of neurochemical measures. Like d-amphetamine, d,l-cathinone released and blocked the uptake of tritiated dopamine (DA) in synaptosomal preparations. In addition, repeated high doses of d,l-cathinone produced long-lasting DA depletions in various rat brain regions and decreased the number of synaptosomal DA uptake sites in a manner similar to that seen after repeated d-amphetamine administration. Importantly, this DA neurotoxic effect of d,l-cathinone, like that of d-amphetamine, is selective since regional brain levels of norepinephrine (NE) or serotonin (5-HT) are not altered on a long-term basis by repeated administration of d,l-cathinone. These findings are discussed with reference to the current practice of Khat leaf chewing by people in north-eastern Africa.
将阿拉伯茶的主要生物碱卡西酮与精神运动兴奋剂d-苯丙胺在多项神经化学指标上进行了比较。与d-苯丙胺一样,消旋卡西酮在突触体标本中释放并阻断了氚标记多巴胺(DA)的摄取。此外,重复给予高剂量的消旋卡西酮会在大鼠不同脑区产生持久的DA耗竭,并以类似于重复给予d-苯丙胺后观察到的方式减少突触体DA摄取位点的数量。重要的是,消旋卡西酮的这种DA神经毒性作用与d-苯丙胺一样具有选择性,因为重复给予消旋卡西酮不会长期改变去甲肾上腺素(NE)或5-羟色胺(5-HT)的脑区水平。结合非洲东北部人们目前咀嚼阿拉伯茶叶的习惯对这些发现进行了讨论。