Liu Jin-bian, Yao Yong-xing, Jiang Wei
Department of Anesthesiology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, China.
Neurosci Lett. 2009 Mar 20;452(3):268-72. doi: 10.1016/j.neulet.2009.01.073. Epub 2009 Feb 4.
N-methyl-D-aspartate receptor (NMDAR) and Group I metabotropic glutamate receptors (mGluRs) are involved in the process of morphine tolerance. Previous studies have shown that Group I mGluRs can modulate NMDAR functions in the central nervous system. The aim of the present study was to examine the influence of Group I mGluRs antagonists on the expression of NMDA receptor NR1 subunit (NR1) in the rat spinal cord. Morphine tolerance was induced in rats by repeated administration of 10 microg morphine (intrathecal, i.t.) twice a day for 7 consecutive days. Tail flick test was used to assess the effect of Group I mGluRs antagonist, AIDA ((RS)-1-Aminoindan-1,5 dicarboxylic acid) or mGluR5 antagonist, MPEP (2-methyl-6-(phenylethynyl)pyridine) on morphine antinociceptive tolerance. The expression of NR1 was measured by immunofluorescence and Western blot. Behavioral tests revealed that both AIDA and MPEP attenuated the development of morphine tolerance. The expression of NR1 was upregulated in the dorsal horn of spinal cord after chronic morphine treatment. AIDA or MPEP co-administered with morphine attenuated morphine induced upregulation of NR1. These findings suggest that the development of morphine tolerance partly prevented by Group I mGluRs antagonists may due to its inhibitory effect on the expression of NR1 subunit.
N-甲基-D-天冬氨酸受体(NMDAR)和I组代谢型谷氨酸受体(mGluRs)参与吗啡耐受过程。先前的研究表明,I组mGluRs可调节中枢神经系统中的NMDAR功能。本研究的目的是检测I组mGluRs拮抗剂对大鼠脊髓中NMDA受体NR1亚基(NR1)表达的影响。通过连续7天每天两次鞘内注射10微克吗啡诱导大鼠产生吗啡耐受。采用甩尾试验评估I组mGluRs拮抗剂AIDA((RS)-1-氨基茚满-1,5-二羧酸)或mGluR5拮抗剂MPEP(2-甲基-6-(苯乙炔基)吡啶)对吗啡镇痛耐受的影响。通过免疫荧光和蛋白质印迹法检测NR1的表达。行为学试验显示,AIDA和MPEP均减弱了吗啡耐受的发展。慢性吗啡处理后脊髓背角中NR1的表达上调。与吗啡联合给药的AIDA或MPEP减弱了吗啡诱导的NR1上调。这些发现表明,I组mGluRs拮抗剂部分预防吗啡耐受的发展可能是由于其对NR1亚基表达的抑制作用。