Sved A F, Baker H A, Reis D J
Brain Res. 1984 Jun 15;303(2):261-6. doi: 10.1016/0006-8993(84)91212-5.
BALB/cJ and CBA/J mice have been shown to have different numbers of dopamine (DA) neurons in the central nervous system, with BALB/cJ mice having 20-50% more DA neurons in each dopaminergic cell group which is reflected in a difference in tyrosine hydroxylase activity in these cell groups. The present study compared the levels of DA and the rate of DA synthesis between these two inbred mouse strains. Three measures were used to reflect the rate of DA synthesis: the levels of DA metabolites (DOPAC and HVA) in the striatum, the rate of disappearance of DA following inhibition of tyrosine hydroxylase with alpha-methyl-P-tyrosine, and the rate of accumulation of DOPA following inhibition of aromatic amino acid decarboxylase with NSD-1015. Striatal DA levels were slightly higher in CBA/J mice than BALB/cJ mice. The rate of DA synthesis in the striatum, as estimated from the accumulation of DOPA following NSD-1015 injection or from the decline of DA levels following alpha-methyl-p-tyrosine injection, was from 30-50% greater in the BALB/cJ mice compared to the CBA/J mice. In striatum, DOPAC levels were higher, HVA levels lower, and DOPAC plus HVA levels equal in CBA/J mice compared to BALB/cJ mice. The results show that BALB/cJ mice, with more DA neurons than CBA mice, also synthesize more DA. In addition, the data suggest that DA levels do not necessarily reflect numbers of DA neurons, and that catecholamine metabolite levels are not a good measure for comparing catecholamine synthesis between inbred animal strains.
已证明BALB/cJ和CBA/J小鼠中枢神经系统中多巴胺(DA)神经元数量不同,BALB/cJ小鼠每个多巴胺能细胞组中的DA神经元多20 - 50%,这反映在这些细胞组中酪氨酸羟化酶活性的差异上。本研究比较了这两种近交系小鼠之间的DA水平和DA合成速率。采用了三种方法来反映DA合成速率:纹状体中DA代谢物(DOPAC和HVA)的水平、用α-甲基-P-酪氨酸抑制酪氨酸羟化酶后DA的消失速率,以及用NSD - 1015抑制芳香族氨基酸脱羧酶后多巴的积累速率。CBA/J小鼠纹状体中的DA水平略高于BALB/cJ小鼠。根据NSD - 1015注射后多巴的积累或α-甲基-对-酪氨酸注射后DA水平的下降估计,BALB/cJ小鼠纹状体中的DA合成速率比CBA/J小鼠高30 - 50%。与BALB/cJ小鼠相比,CBA/J小鼠纹状体中的DOPAC水平较高,HVA水平较低,DOPAC加HVA水平相等。结果表明,DA神经元比CBA小鼠多的BALB/cJ小鼠合成的DA也更多。此外,数据表明DA水平不一定反映DA神经元的数量,并且儿茶酚胺代谢物水平不是比较近交动物品系间儿茶酚胺合成的良好指标。