Shaliapina V G, Milusheva Ts B
Probl Endokrinol (Mosk). 1977 Jul-Aug;23(4):94-9.
L-DOPA uptake by the brain and synthesis of dophamine and noradrenaline from it was studied in experiments on rats. L-DOPA (catecholamine precursor) was injected in a dose of 5 mg per 100 g of weight intraperitoneally simultaneously with hydrocortisone or 3 hours after its three-fold administration. Hydrocortisone at first intensified the uptake of L-DOPA by the brain, and, correspondingly, the dophamine synthesis. But three-fold administration of the hormone was followed by a fall of the L-DOPA and catecholamine content in the brain due to decreased L-DOPA diffusion from the blood. Oxidative catecholamine deamination was enhanced under the effect of hydrocortisone; it was prevented by prescription of nuredal, a MAO inhibitor.
在大鼠实验中研究了脑对左旋多巴的摄取以及由其合成多巴胺和去甲肾上腺素的过程。将左旋多巴(儿茶酚胺前体)以每100克体重5毫克的剂量腹腔注射,同时注射氢化可的松,或在氢化可的松三次给药后3小时注射。氢化可的松起初增强了脑对左旋多巴的摄取,相应地也增强了多巴胺的合成。但在该激素三次给药后,由于左旋多巴从血液中的扩散减少,脑内左旋多巴和儿茶酚胺含量下降。在氢化可的松的作用下,儿茶酚胺的氧化脱氨基作用增强;单胺氧化酶抑制剂优降宁可防止这种情况发生。