Daló N L, Larson A A
University of Minnesota, Department of Veterinary Biology, St. Paul 55108.
Eur J Pharmacol. 1990 Aug 2;184(1):173-7. doi: 10.1016/0014-2999(90)90679-z.
Urethane and ketamine were tested for their ability to alter the caudally directed binding and scratching response elicited by the intrathecal (i.t.) injection of excitatory amino acids (EAAs) or substance P (SP). EAAs, such as N-methyl-D-aspartate (NMDA), kainate acid and quisqualic acid, but not SP, were inhibited by subanesthetic doses of urethane. In contrast, SP was more sensitive than NMDA to the inhibitory effect of (+)-ketamine. (-)-Ketamine produced much less inhibition of the SP-induced behaviors than the (+)isomer. These results have important implications regarding the use of urethane and ketamine as anesthetics for studies in which these excitatory compounds are potential mediators.
对氨基甲酸乙酯和氯胺酮改变鞘内注射兴奋性氨基酸(EAA)或P物质(SP)所引发的尾部定向性黏附及抓挠反应的能力进行了测试。亚麻醉剂量的氨基甲酸乙酯可抑制EAA(如N-甲基-D-天冬氨酸(NMDA)、海人酸和喹啉酸)引发的反应,但对SP无抑制作用。相比之下,SP比NMDA对(+)-氯胺酮的抑制作用更敏感。(-)-氯胺酮对SP诱导行为的抑制作用远低于(+)异构体。这些结果对于在兴奋性化合物可能作为潜在介质的研究中使用氨基甲酸乙酯和氯胺酮作为麻醉剂具有重要意义。