Jarvis J A, Magos L
Naunyn Schmiedebergs Arch Pharmacol. 1976;292(3):295-8. doi: 10.1007/BF00517392.
500 mg/kg sodium diethyldithiocarbamate (DDC) and trace quantities of uniformly labelled 14C-tyrosine were administered simultaneously to male albino rats of Porton-Wistar strain of approximately 210 g body weight. Thirty minutes later total radioactivity, the concentration and the specific activity of free tyrosine were increased both in plasma and in the brain by 40% compared with rats untreated with DDC. The incorporation of 14C from 14C-tyrosine into the fraction corresponding to the elution of glutamine-glutamate from the amberlite resin column was 80% less in the brain 30 min after DDC. The exhalation of 14CO2 was depressed by 80% in the first hour after DDC. When 14C-tyrosine was given 3.5 h after DDC the only differences between experimental and control rats were the increased incorporation of 14C into the glutamine-glutamate and aspartate fractions and the increased exhalation of 14CO2 which became significiant in the third and fourth half hour periods after the injection of 14C-tyrosine. From the experiments it is concluded that DDC, an inhibitor of dopamine-beta-hydroxylase, also interferes with the major catabolic pathway of tyrosine.
将500毫克/千克二乙氨基二硫代甲酸钠(DDC)和微量均匀标记的14C-酪氨酸同时给予体重约210克的Porton-Wistar品系雄性白化大鼠。30分钟后,与未用DDC处理的大鼠相比,血浆和脑中游离酪氨酸的总放射性、浓度和比活性均增加了40%。DDC处理30分钟后,脑中从14C-酪氨酸掺入对应于从琥珀酸树脂柱洗脱谷氨酰胺-谷氨酸的级分中的14C减少了80%。DDC给药后第一小时,14CO2的呼出量降低了80%。当在DDC给药3.5小时后给予14C-酪氨酸时,实验大鼠和对照大鼠之间的唯一差异是14C掺入谷氨酰胺-谷氨酸和天冬氨酸级分中的量增加,以及14CO2的呼出量增加,这在注射14C-酪氨酸后的第三和第四个半小时期间变得显著。从实验得出结论,多巴胺-β-羟化酶的抑制剂DDC也干扰酪氨酸的主要分解代谢途径。