Okada M, Hirano T, Mizuno K, Chiba T, Kawata Y, Kiryu K, Wada K, Tasaki H, Kaneko S
Department of Neuropsychiatry, Hirosaki University, Japan.
Epilepsy Res. 1997 Sep;28(2):143-53. doi: 10.1016/s0920-1211(97)00042-9.
To clarify the effects of carbamazepine (CBZ) on dopamine (DA) release and their metabolism, the extracellular and total levels of DA, its metabolites (DOPAC and HVA) and precursor, 3,4-dihydroxyphenylalanine (DOPA) in the striatum and hippocampus were studied. DA re-uptake and DOPA accumulation in the striatum and hippocampus, and monoamine oxidase (MAO) activities were also determined. After acute and chronic administrations of CBZ, the plasma concentration of CBZ associated with therapeutic activity increased the extracellular and total levels of all substances determined, whereas supratherapeutic concentration of CBZ decreased extracellular and total levels of all substances. Neither therapeutic nor supratherapeutic concentrations of CBZ affected MAO-A nor -B activities, nor DA re-uptake. DOPA accumulation caused by NSD1015 was inhibited by therapeutic and supratherapeutic concentrations of CBZ. These results suggest that a therapeutic concentration of CBZ enhances DA turnover, whereas a supratherapeutic concentration of CBZ inhibits DA turnover. These effects of CBZ on dopaminergic systems may be, at least partially, involved in the mechanisms of action of CBZ.
为阐明卡马西平(CBZ)对多巴胺(DA)释放及其代谢的影响,研究了纹状体和海马中DA的细胞外水平和总水平、其代谢产物(3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA))以及前体3,4-二羟基苯丙氨酸(DOPA)。还测定了纹状体和海马中DA的再摄取、DOPA的积累以及单胺氧化酶(MAO)的活性。急性和慢性给予CBZ后,与治疗活性相关的CBZ血浆浓度增加了所有测定物质的细胞外水平和总水平,而超治疗浓度的CBZ则降低了所有物质的细胞外水平和总水平。治疗浓度和超治疗浓度的CBZ均未影响MAO-A或 -B的活性,也未影响DA的再摄取。治疗浓度和超治疗浓度的CBZ抑制了NSD1015引起的DOPA积累。这些结果表明,治疗浓度的CBZ可增强DA的周转,而超治疗浓度的CBZ则抑制DA的周转。CBZ对多巴胺能系统的这些作用可能至少部分参与了CBZ的作用机制。