Lodge D, Anis N A, Burton N R
Neurosci Lett. 1982 Apr 26;29(3):281-6. doi: 10.1016/0304-3940(82)90330-5.
The (+) isomer of ketamine was approximately 3 and 1.5 times as potent as the (-) isomer in reducing excitation of rat and cat Renshaw cells by N-methylaspartate (NMA) and acetylcholine (ACh) respectively. The potency ratio of the two isomers of ketamine as NMA antagonists was similar to that obtained in anaesthetic and analgesic tests [16, 19, 25].
氯胺酮的(+)异构体在分别降低N-甲基天冬氨酸(NMA)和乙酰胆碱(ACh)对大鼠和猫Renshaw细胞的兴奋作用方面,效力约为(-)异构体的3倍和1.5倍。氯胺酮两种异构体作为NMA拮抗剂的效价比与在麻醉和镇痛试验中得到的结果相似[16,19,25]。