期刊文献+

关节炎大鼠吗啡耐受模型的建立 被引量:12

Establishment of morphine tolerance model with arthritis in rat
下载PDF
导出
摘要 目的:建立一种以慢性炎症为基础的吗啡耐受模型。方法:将32只健康雄性SD大鼠随机分为4组,关节炎鞘内给予吗啡组(A组),关节炎腹腔给予吗啡组(B组),单纯鞘内给予吗啡组(C组),单纯腹腔给予吗啡组(D组)。A组与C组鞘内给予10μg/kg吗啡1日2次,B组与D组经腹腔给予同样剂量的吗啡。以热板法缩爪潜伏期和50%缩爪阈值作为行为学指标进行观察。结果:给药后第7天,A组大鼠的行为学指标较B、C、D组有统计学差异,C组与B、D两组相比有统计学差异,而B、D两组间无统计学差异。结论:可以在慢性炎症的基础上经鞘内给药制作出吗啡耐受的大鼠模型,而且本模型较以前的模型更加接近于实际。 Objective: To establish a morphine tolerance model with chronic arthritis in rat. Methods: The 32 SD rats were randomly derided into four groups. Group A: administered morphine intrathecally in rats with arthritis. Group B: administered morphine intraperitoneally in rats with arthritis Group C: administered morphine intrathecally in rats without arthritis Group D:administered morphine intraperitoneally in rats without arthritis.The group A and group C were intrathecally administered morphine 10 p.g/kg two times a day and the group B and group D were intraperitoneally administered the same dose of morphine. The thermal withdral latency (TWL) and mechanical withdrawl threshold (MWT) of rats were used to evaluate its behaviour. Results: Compared with the B,C,D groups, the TWL and MWT in group A has the statistic significance after 7 days administering drugs. Compared with the B,D groups, the TWL and MWT in group C has the statistic significance. There no statistic significance between Bgroup and D group. Conclusion: The morphine tolerance model with chronic arthritis of rat can be established and it is more practicable than the previous model.
作者 石钊 王国林
出处 《天津医科大学学报》 2007年第4期482-484,共3页 Journal of Tianjin Medical University
基金 天津自然科学基金资助项目(06YFJMJC08600) 天津市卫生局基金资助项目(06KY51)
关键词 吗啡耐受 大鼠 关节炎 Morphine tolerance Rats Arthritis
  • 相关文献

参考文献10

  • 1Mao J, Sung B, Ji RR, et al. Chronic morphine induces downregulation of spinal glutamate transporters: implications in morphine tolerance and abnormal pain sensitivity [J]. Neuroscience, 2002, 22 (18):8312.
  • 2Yaksh TL, Rudy TA. Chronic catheterization of the spinal subarachoid space [J]. Physiol Behav, 1976, 17(6):1031.
  • 3Butler SH, Godefroy F, Besson JM ,et al. A limited arthritic model for chronic pain studies in the rat [J]. Pain, 1992, 48( 1 ):73.
  • 4ChaPlan SR, Bach FW , Pogrel JW , et al.Quantitative assessment of tactile allodynia in the rat paw [J] .Neurosci Methods,1994, 53 ( 1 ) : 55.
  • 5Guitart X, Nestler EJ. 2nd messenger and protein phosphorylation mechanisms underlying opiate addiction:studies in the rat locus coeruleus [J]. Neurochem Res, 1993, 18 ( 1 ):5.
  • 6Jensen MK, Thomsen AB , Hoisted J.10-year follow-up of chronic nonmalignant pain patients: opioid use, health related quality of life and health care utilization [J]. Eur pain, 2006, 10(5):423.
  • 7Chu LF, Clark D J, Angst MS. Opioid tolerance and hyperalgesia in chronic pain patients after one month of oral morphine therapy: a preliminary prospective study [J ]. Pain, 2006, 7( 1):43.
  • 8Liang DY, Guo T, Liao G, et al. Chronic pain and genetic background interact and influence opioid analgesia, tolerance, and physical dependence [J]. pain, 2006, 121 (3):232.
  • 9Fernandez-Duenas V, Pol O, Garcia-Nogales P, et al. Tolerance to the antinociceptive and anti-exudative effects of morphine in a murine model of peripheral inflammation [J] . Pharmaeol Exp Ther, 2007, 322 ( 1 ) :360.
  • 10Gardell LR, King T, Ossipov MH, et al. Opioid receptor-mediated hyperalgesia and antinociceptive tolerance induced by sustained opi- ate delivery [J]. Neurosci Lett, 2006, 396 (1):44.

同被引文献94

引证文献12

二级引证文献28

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