Niddam R, Arbilla S, Baud P, Langer S Z
Eur J Pharmacol. 1985 Mar 26;110(1):121-4. doi: 10.1016/0014-2999(85)90037-8.
Perfused rat striatal slices were prelabelled with either 3H-amphetamine or [3H] beta-phenylethylamine. Electrical stimulation released a significant amount of radioactivity only from the slices prelabelled with [3H] beta-phenylethylamine. The electrically evoked release of radioactivity from slices labelled with [3H] beta-phenylethylamine was entirely calcium-dependent and was abolished after pretreatment with reserpine (5 mg/kg s.c., 24 h). In addition, S-sulpiride (1 microM), which facilitates the electrically evoked release of radioactivity from slices labelled with [3H]DA by blocking dopamine autoreceptors, also induced an increase of the radioactivity released by electrical stimulation from slices labelled with [3H] beta-phenylethylamine. Our results indicate that, in spite of the structural similarities between AMPH and PEA, only the latter which is the naturally occurring analog of AMPH can be released by electrical stimulation in a calcium-dependent manner.
灌注的大鼠纹状体切片预先用3H-苯丙胺或[3H]β-苯乙胺标记。电刺激仅从预先用[3H]β-苯乙胺标记的切片中释放出大量放射性。用[3H]β-苯乙胺标记的切片中放射性的电诱发释放完全依赖于钙,在用利血平(5mg/kg皮下注射,24小时)预处理后被消除。此外,S-舒必利(1μM)通过阻断多巴胺自身受体促进用[3H]多巴胺标记的切片中放射性的电诱发释放,它也诱导用[3H]β-苯乙胺标记的切片中电刺激释放的放射性增加。我们的结果表明,尽管苯丙胺和苯乙胺在结构上相似,但只有后者(苯丙胺的天然类似物)可以通过电刺激以钙依赖的方式释放。