期刊文献+

应用^1H—MRS和LCModel研究鼻喷酒石酸布托啡诺对猪脑代谢物的影响及谷氨酸复合物的绝对定量 被引量:4

Absolute quantification of swine brain glutamate compounds concentration using MR spectroscopy and LCModel after nasal spraying butorphanol tartrate
下载PDF
导出
摘要 目的通过氢质子磁共振波谱(1H-MRS)技术,研究鼻喷给药途径下中枢性镇痛药物对脑代谢物的影响,探讨鼻腔给药途径下1H-MRS及LCModel的应用价值。方法本实验选取9头健康2周龄乳猪(3.612±0.371)kg,行单体素PRESS序列扫描,获得鼻喷给药前后脑代谢物的波谱分析数据,用LCModel软件自动、客观地对波谱图进行线性拟合和基线校正。结果鼻喷酒石酸布托啡诺前1H-MRS测定动物脑谷氨酸复合物(Glx)浓度为(9.276±0.542)mmol/kg,鼻喷给药后Glx浓度为(7.283±0.540)mmol/kg。给药前后Glx浓度差异有统计学意义(t=2.826,P=0.022),而氮-乙酰天门冬氨酸(NAA)、胆碱(Cho)浓度改变无统计学意义,鼻喷给药前后NAA、Cho浓度分别为(6.094±0.384)mmol/kg∶(5.530±0.346)mmol/kg(t=1.270,P=0.240)和(1.547±0.114)mmol/kg∶(1.255±0.079)mmol/kg(t=1.800,P=0.110)。结论用1H-MRS技术及LCModel软件证明了Glx可能是中枢性止痛剂作用的重要神经递质。 Objective The purpose of this study was to investigate whether the central nervous system (CNS) analgesics affect the metaholites of swine brain by nasal spraying. Methods Single voxel proton magnetic resonance spectroscopy (^1H-MRS) was performed on 9 swine. The data were post-processed using LCModel software. Results Before nasal spraying butorphanol tartrate, the mean Glutamate compounds (GLxs) concentration was (9.276±0.542) mmol/kg. After nasal spraying, the mean Glx concentration was (7.283±0.540) mmol/kg. Using paired sample t-test we found that swine brain Glx level was significantly decreased after using nasal spray analgesic (t=2.826, P=0.022). However, there were no significant differences in mean NAA and Choline (Cho) concentrations before and after nasal spraying[(6.094±0.384)mmol/kg vs. (5.530±0.346)mmol/kg (t=1.270,P=0.240) and (1.547±0.114) mmol/kg vs. (1.255±0.079) mmol/kg (t=1.800,P=0.110), respectively). Conclusion Our results imply that Glxs are nociceptive neurotransmitters and play an important role in the analgesia.
出处 《国外医学(临床放射学分册)》 2008年第4期217-220,共4页
基金 国家自然科学基金项目(30470515)
关键词 磁共振波谱学 鼻腔给药 LCMODEL 谷氨酸复合物 绝对定量 Proton magnetic resonance spectroscopy Nasal spraying LCModel Glutamate/Glutamine Absolute quantification
  • 相关文献

参考文献23

  • 1Frey WH. Intranasal delivery: bypassing the blood-brain barrier to deliver therapeutic agents to brain and spinal cord [J]. Drug Deliv Tech, 2002, 2(5): 46-49.
  • 2Msthison S, Nagilla R, Kompella UB. Nasal route for direct delivery of solutes to the central nervous system: fact or fiction [J]. J Drug Target, 1998, 5(6): 415- 441.
  • 3相小强,陶涛,陈庆华.透血脑屏障制剂的研究进展[J].中国新药杂志,2002,11(7):519-523. 被引量:15
  • 4Illum L. Nasal drug delivery: new development and strategies [J]. Drug Discov Today, 2002, 7 (23): 1184-1189.
  • 5Illum L. Transport of drugs from the nasal cavity to the central nervous systerms [J].Eur J Pharm Sci, 2000, 11(1): 1-18.
  • 6Bodnar RJ, Hadjimarkou MM, Krzanowska EK, et al. Differential dose-dependent effects of central morphine treatment upon food intake in male and female rats receiving neonatal hormone manipulations [J]. Neurosci, 2003, 6( 1 ): 53-57.
  • 7Honey G, Bullmore E.Human pharmacological MRI[J]. Trends Pharmacol Sci, 2004, 25(7): 366-374.
  • 8Rogers R, Wise RG, Painter DJ, et al. An investigation to dissociate the analgesic and anesthetic properties of ketamine using functional magnetic resonance imaging [J]. Anesthesiology, 2004, 100 (2): 292-301.
  • 9Jin YH, Nishioka H, Wakabayashi K, et al. Effect of morphine on the release of excitatory amino acids in the rat hind instep: pain is modulated by the interaction between the peripheral opioid and glutamate systems[J].Neuroscience, 2006, 138(4): 1329-1339.
  • 10Tartaglia MC, Narayanan S, De Stefano N, et al. Choline is increased in pre-lesional normal appearing white matter in multiple sclerosis[J].J Neurol, 2002, 249(10): 1382-1390.

二级参考文献3

共引文献14

同被引文献22

引证文献4

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部