Prado M A, Santos T M, Gomez M V
Departamento de Bioquimica e Imunologia, Instituto de Ciencias Biologicas-UFMG, Belo Horizonte, Minas Gerais, Brasil.
Neurosci Lett. 1990 Mar 26;111(1-2):195-200. doi: 10.1016/0304-3940(90)90367-i.
The effect of vesicular acetylcholine (ACh) transport blocker 2-(4-phenylpiperidino)cyclohexanol (AH-5183) on the subcellular storage and release of ACh was studied in rat brain cortical slices. AH-5183 reduced the release of ACh from cortical slices stimulated by tityustoxin and ouabain. Tissue stimulated in the presence of AH-5183 contained more ACh in both the nerve terminal synaptic vesicles and cytoplasmic fraction than did tissue stimulated in drug's absence. Thus, AH-5183 blocked the tityustoxin and ouabain induced release of ACh from both cytoplasmic and vesicular pools. AH-5183 also depressed the spontaneous release of ACh from incubated slices and, in this condition, the drug had no effect in the subcellular distribution of ACh. It is suggested that AH-5183 interferes with the process of ACh release independent of its blocking action on ACh transport into the synaptic vesicles.
在大鼠脑皮质切片中研究了囊泡乙酰胆碱(ACh)转运阻滞剂2-(4-苯基哌啶基)环己醇(AH-5183)对ACh亚细胞储存和释放的影响。AH-5183减少了由替尤斯毒素和哇巴因刺激的皮质切片中ACh的释放。在AH-5183存在下刺激的组织,其神经末梢突触小泡和细胞质部分中的ACh含量均高于在无药物情况下刺激的组织。因此,AH-5183阻断了替尤斯毒素和哇巴因诱导的细胞质和囊泡池中ACh的释放。AH-5183还抑制了孵育切片中ACh的自发释放,在这种情况下,该药物对ACh的亚细胞分布没有影响。提示AH-5183干扰ACh释放过程,与其对ACh转运到突触小泡的阻断作用无关。