Girbe F, Ramassamy C, Piton C, Costentin J
Unité de Neuropsychopharmacologie, CNRS URA 1170, Faculté de Médecine et Pharmacie de Rouen, Saint-Etienne du Rouvray, France.
Neuroreport. 1994 May 9;5(9):1027-9. doi: 10.1097/00001756-199405000-00002.
On synaptosomes prepared from striata of mice, increasing concentrations of ascorbic acid (from 0.01 mM to 0.5 mM) did not modify the 3H-dopamine uptake. However, at the 0.1 mM concentration, ascorbic acid increased the potassium-induced release of 3H-dopamine by synaptosomes previously loaded with the amine. This effect was dependent on the presence of Ca2+ in the superfusion medium and was not shared by dehydroascorbic acid (from 1 mM to 0.01 mM). This effect of ascorbic acid, which occurs in the range of its endogenous concentrations, suggests that it is a putative modulator of dopaminergic transmission.
在从小鼠纹状体制备的突触体上,抗坏血酸浓度增加(从0.01 mM至0.5 mM)并不会改变3H-多巴胺的摄取。然而,在0.1 mM浓度时,抗坏血酸会增加预先加载了该胺类的突触体中钾离子诱导的3H-多巴胺释放。这种效应依赖于灌流介质中Ca2+的存在,脱氢抗坏血酸(从1 mM至0.01 mM)则没有这种作用。抗坏血酸在其内源性浓度范围内产生的这种效应表明,它可能是多巴胺能传递的一种调节剂。