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NMDA受体通道参与大鼠脊髓背角C纤维诱发电位LTP的表达
引用本文:张红梅,周利君,胡能伟,张彤,刘先国.NMDA受体通道参与大鼠脊髓背角C纤维诱发电位LTP的表达[J].生物化学与生物物理进展,2006,33(12):1183-1189.
作者姓名:张红梅  周利君  胡能伟  张彤  刘先国
作者单位:中山大学中山医学院生理学教研室,广州,510089
基金项目:国家自然科学基金;中华医学基金会资助项目
摘    要:以往研究表明,激动NMDA受体是引起海马长时程增强(LTP)的必备条件,而LTP的表达主要与AMPA受体的磷酸化及其受体组装到突触后膜有关.但是,近年来有研究表明NMDA受体通道也参与了LTP的表达.为探讨NMDA受体通道是否参与了脊髓背角C纤维诱发电位LTP的表达,诱导LTP后,分别静脉或脊髓局部给予NMDA受体拮抗剂MK801或APV,观察其作用.发现静脉注射非竞争性NMDA受体MK801(0.1mg/kg)对脊髓LTP无影响,注射0.5mg/kg显著抑制LTP,但是当剂量增高到1.0mg/kg时,抑制作用并未进一步增大.脊髓局部给予MK801也能抑制脊髓背角LTP.为验证上述结果,使用了竞争性NMDA受体拮抗剂APⅤ.结果显示,脊髓局部给予50μmol/LAPⅤ对LTP无影响,100μmol/L对LTP有显著的抑制作用,当浓度升至200μmol/L时,抑制作用并未见进一步增强.因此认为,NMDA受体通道部分地参与了脊髓背角C纤维诱发电位LTP的表达.

关 键 词:长时程增强  NMDA受体  痛觉过敏  脊髓背角
收稿时间:4/23/2006 4:18:04 PM
修稿时间:9/1/2006 4:15:00 PM

NMDA Receptor Channels Are Involved in The Expression of Long-term Potentiation of C-fiber Evoked Field Potentials in Rat Spinal Dorsal Horn
ZHANG Hong-Mei,ZHOU Li-Jun,HU Neng-Wei,ZHANG Tong and LIU Xian-Guo.NMDA Receptor Channels Are Involved in The Expression of Long-term Potentiation of C-fiber Evoked Field Potentials in Rat Spinal Dorsal Horn[J].Progress In Biochemistry and Biophysics,2006,33(12):1183-1189.
Authors:ZHANG Hong-Mei  ZHOU Li-Jun  HU Neng-Wei  ZHANG Tong and LIU Xian-Guo
Institution:Pain Research Center, Department of Physiology, Zhongshan Medical School of Sun Yat-sen University, Guangzhou 510089, China;Pain Research Center, Department of Physiology, Zhongshan Medical School of Sun Yat-sen University, Guangzhou 510089, China;Pain Research Center, Department of Physiology, Zhongshan Medical School of Sun Yat-sen University, Guangzhou 510089, China;Pain Research Center, Department of Physiology, Zhongshan Medical School of Sun Yat-sen University, Guangzhou 510089, China;Pain Research Center, Department of Physiology, Zhongshan Medical School of Sun Yat-sen University, Guangzhou 510089, China
Abstract:In hippocampus, numerous studies have shown that N-methyl-D-aspartate (NMDA) receptors are essential for the initiation of long-term potentiation (LTP), whereas the expression of LTP is primarily mediated by the phosphorylation of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors and the increased insertion of postsynaptic AMPA receptors. However, in recent years there is also evidence that NMDA receptor channels contribute to the expression of LTP under physiological conditions. It was examined whether NMDA receptor channels contributed to the expression of LTP of C-fiber evoked field potentials in rat spinal dorsal horn by intravenous or spinal application of NMDA receptor antagonists after the establishment of LTP. It was found that MK 801 (a non-competitive NMDA receptor antagonist) at dose of 0.1 mg/kg (iv) had no effect on the spinal LTP and at the dose of 0.5 mg/kg depressed the LTP significantly. However, the inhibitory effect of MK 801 at higher dose (1.0 mg/kg)was not different from that produced by the dose of 0.5 mg/kg. The similar inhibitory effect on spinal LTP was also observed, when MK 801 was applied locally at the recording segments of spinal cord. To confirm the above results, a competitive NMDA receptor antagonist AP V was tested. Spinal application of AP V at a concentration of 100 μmol/L produced a stronger depression than at 50 μmol/L. When the concentration of AP V increased to 200 μmol/L, no further depression was observed. These results indicate that NMDA receptor channels are involved in the expression of LTP of C-fiber evoked field potentials in the rat spinal dorsal horn.
Keywords:long-term potentiation  NMDA receptor  hyperalgesia  spinal cord
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