Ungar F, Mosnaim A D, Ungar B, Wolf M E
Biol Psychiatry. 1977 Oct;12(5):661-8.
Incubation of p-tyramine (TRM) with rat midbrain plus corpus striatum (MB+ CS) crude synaptosomal preparations, under conditions which reduce to a minimum amine uptake, results in appreciable binding of this amine by synaptosomes. This process is inhibited by preincubation with a number of drugs active in the CNS, e.g., chlorpromazine, desipramine, d-amphetamine, and diphenhydramine. Morphine, however, does not affect this binding. The Ki for each one of these compounds, as well as the K association constant and concentration of the binding sites of TRM, were determined. These results suggest a role for TRM in synaptic transmission mechanisms occurring in the nigrostriatal system, a function which could be regulated by a number of substances representing some of the major chemical classes of centrally active drugs (CD).
在将胺摄取降至最低的条件下,用大鼠中脑加纹状体(MB + CS)粗制突触体制剂孵育对酪胺(TRM),会导致该胺与突触体有明显的结合。该过程会被与多种中枢神经系统活性药物(如氯丙嗪、地昔帕明、右旋苯丙胺和苯海拉明)预孵育所抑制。然而,吗啡并不影响这种结合。测定了这些化合物各自的Ki以及TRM结合位点的缔合常数K和浓度。这些结果表明TRM在黑质纹状体系统中发生的突触传递机制中起作用,这一功能可能受代表一些主要中枢活性药物化学类别的多种物质调节。