Jang C G, Oh S, Ho I K
Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson 39216-4505, USA.
Neurochem Res. 1998 Nov;23(11):1371-7. doi: 10.1023/a:1020746505854.
Little is known about the functional modulation of NMDA receptor subunits at the molecular level. Therefore, a series of experiments were conducted to elucidate more fully the role of NMDA receptor subtypes in pentobarbital tolerance and withdrawal. We investigated the influence of centrally administered pentobarbital on the regulation of mRNA levels of the family of NMDA receptor 2 (NR2) subtypes (NR2A, NR2B, and NR2C) by in situ hybridization histochemistry in rat brain. Animals were rendered tolerant by continuous intracerebroventricular (i.c.v.) infusion with pentobarbital (300 microg/10 microl/hr for 6 days) through pre-implanted cannulae connected to osmotic mini-pumps, and dependent, by abrupt withdrawal from pentobarbital. The NR2A subunit mRNA was increased in cortical areas in pentobarbital tolerant and withdrawal rats. In contrast, the NR2B mRNA was decreased in parietal cortex and hippocampus in both tolerance and withdrawal rats. The level of NR2C mRNA was increased in withdrawal rats, while there was no change in tolerant rats. These results indicate that continuous i.c.v. infusion with pentobarbital alters NR2 subunit mRNA expression in the rat brain, suggesting that NR2 subunits may play an important role in the development of tolerance to and withdrawal from pentobarbital.
关于NMDA受体亚基在分子水平上的功能调节,目前所知甚少。因此,我们进行了一系列实验,以更全面地阐明NMDA受体亚型在戊巴比妥耐受性和戒断中的作用。我们通过原位杂交组织化学研究了脑室内注射戊巴比妥对大鼠脑中NMDA受体2(NR2)亚型家族(NR2A、NR2B和NR2C)mRNA水平调节的影响。通过预先植入的与渗透微型泵相连的套管,对动物进行连续脑室内(i.c.v.)输注戊巴比妥(300微克/10微升/小时,持续6天)使其产生耐受性,并通过突然停用戊巴比妥使其产生依赖性。在戊巴比妥耐受和戒断的大鼠中,皮质区域的NR2A亚基mRNA增加。相比之下,在耐受和戒断的大鼠中,顶叶皮质和海马中的NR2B mRNA均减少。戒断大鼠中NR2C mRNA水平增加,而耐受大鼠中则无变化。这些结果表明,连续脑室内输注戊巴比妥会改变大鼠脑中NR2亚基mRNA的表达,提示NR2亚基可能在戊巴比妥耐受性和戒断的发展中起重要作用。