Lasoń W, Przewłocka B, Przewłocki R
Neuropeptides Research Department, Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Brain Res Mol Brain Res. 1992 Jan;12(1-3):243-7. doi: 10.1016/0169-328x(92)90090-x.
Injection of N-methyl-D-aspartate (NMDA, 7.5 micrograms) kainate (1 microgram) or quisqualate (2 micrograms) into the rat dorsal hippocampus induced wet-dog shakes and convulsions. As shown by an in situ immunohistochemical analysis, 3 h after the excitatory amino acids injections the rats displayed a bilateral profound elevation of the proenkephalin and prodynorphin mRNA levels in dentate gyrus granule cells (2-3 or 1.5-2 fold higher than control levels, respectively). Pretreatment of rats with D-amino-phosphonovalerate (D-APV, 10 micrograms), a selective antagonist of NMDA receptor, prevented the behavioral and biochemical changes evoked by NMDA. The changes in the behavior and gene expression evoked by kainate or quisqualate were diminished in rats which received 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX, 2 micrograms), a putative antagonist of quisqualate and kainate receptors. The study demonstrated that activation of NMDA, quisqualate or kainate receptors in the hippocampus induced seizures associated with a marked increase in the proenkephalin (PENK) and the prodynorphin (PDYN) gene expression in the rat dentate gyrus.
向大鼠背侧海马注射N-甲基-D-天冬氨酸(NMDA,7.5微克)、海人藻酸(1微克)或quisqualate(2微克)可诱发湿狗样抖动和惊厥。原位免疫组化分析显示,注射兴奋性氨基酸3小时后,大鼠齿状回颗粒细胞中前脑啡肽和前强啡肽mRNA水平出现双侧显著升高(分别比对照水平高2 - 3倍或1.5 - 2倍)。用NMDA受体的选择性拮抗剂D-氨基磷酸戊酸(D-APV,10微克)预处理大鼠,可预防由NMDA诱发的行为和生化变化。在接受quisqualate和海人藻酸受体的假定拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,2微克)的大鼠中,由海人藻酸或quisqualate诱发的行为和基因表达变化有所减弱。该研究表明,海马中NMDA、quisqualate或海人藻酸受体的激活诱发了癫痫发作,同时大鼠齿状回中前脑啡肽(PENK)和前强啡肽(PDYN)基因表达显著增加。