Kim Do-Hoon, Moon Yoo-Sun, Jung Jun-Sub, Suh Hong-Won, Song Dong-Keun
Department of Psychiatry, College of Medicine, Institute of Natural Medicine, Hallym University, Kangwon-Do, 200-702, Chunchon, Republic of Korea.
Prog Neuropsychopharmacol Biol Psychiatry. 2003 Sep;27(6):1055-8. doi: 10.1016/S0278-5846(03)00147-7.
A non-N-methyl-D-aspartate (non-NMDA) receptor antagonist, 6-cyano-7-nitro-quinoxaline-2,3-dione (CNQX), administered intracerebroventricularly (0.1-0.5 microg), significantly inhibited the immobilization stress-induced plasma corticosterone levels in a dose-dependent manner. However, CNQX administered intraperitoneally (1-10 mg/kg) showed a dose-dependent increase of basal plasma corticosterone levels in nonstressed mice and an additive increase of plasma corticosterone levels at the dose of 10 mg/kg in 1 h immobilization-stressed mice. The results suggest that the central and peripheral non-NMDA receptors may be differently involved in the regulation of plasma corticosterone levels in non- and immobilization-stressed mice.
一种非N-甲基-D-天冬氨酸(非NMDA)受体拮抗剂,6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX),脑室内给药(0.1 - 0.5微克),以剂量依赖方式显著抑制固定应激诱导的血浆皮质酮水平。然而,腹腔注射CNQX(1 - 10毫克/千克)在非应激小鼠中显示基础血浆皮质酮水平呈剂量依赖性增加,在固定应激1小时的小鼠中,10毫克/千克剂量时血浆皮质酮水平呈相加性增加。结果表明,中枢和外周非NMDA受体可能在非应激和固定应激小鼠血浆皮质酮水平的调节中发挥不同作用。