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作 者:付华[1] 王颖[1] 杨胜男[1] 李聪[1] 王学斌[2]
机构地区:[1]长春师范大学,长春130032 [2]山东临沂大学生命科学学院,临沂276005
出 处:《中国免疫学杂志》2014年第4期449-453,共5页Chinese Journal of Immunology
基 金:吉林省科技厅自然科学基金项目(20130101125JC);吉林省教育厅"十二五"重点基金项目(2013第246号);山东省自然科学基金项目(No.ZR2011CM030)
摘 要:目的:探讨外侧缰核注射不同浓度的降钙素基因相关肽(Calcitonin gene-related peptide,CGRP)对大鼠痛觉调节的影响。方法:对大鼠的外侧缰核分别微量注射浓度为0.875、1.75、3.5和7 nmol/μl CGRP,采用热板和压板测试,分别测量大鼠5、10、15、20、30、45和60 min的后爪缩爪反应潜伏期(Hindpaw Withdrawal Latency,HWL),观察CGRP对大鼠的镇痛效果,并与注射生理盐水的对照组大鼠作比较。结果:注射CGRP以后,大鼠的后爪缩爪反应潜伏期与对照组相比明显延长,其中浓度为0.875 nmol/μl CGRP对大鼠左爪热刺激HWL有差异(P<0.05),对大鼠右爪热刺激HWL差异显著(P<0.001),对大鼠左爪机械刺激HWL有显著差异(P<0.001),而对大鼠右爪机械刺激HWL差异不明显(P>0.05);浓度为1.75、3.5和7 nmol/μl CGRP对大鼠左、右爪热刺激、机械刺激HWL均有显著性差异(P<0.001)。CGRP对正常大鼠的镇痛作用具有剂量依赖性,且在20 min时效果最为明显。结论:CGRP在外侧缰核内明显延长大鼠的HWL,即CGRP在外侧缰核具有镇痛作用。Objective:To observe the analgesic effect of the CGRP on the model rats of chronic pain. Methods: Saline and 4 different gradients of mixture(0. 875,1.75,3.5 and 7.0 nmal/μl) would be injected into the Lateral habenular complex. Using the Hot-plate Test and Randall Selitto Test to measure Hindpaw Withdrawal Lateneies that caused by harmful heat and mechanical stimula- tion representing the value of pain in 5,10,15,20,30,45,60 rain. The HWL was used as a basic value, compared with the group which injected into saline. Results: Compared with the NS control group, There were different in 0. 875 nmol/μl CGRP of left rats foot ther- mal stimulus HWL( P 〈 0.05 ), right foot hot stimulation of rat HWL significant difference ( P 〈 0.001 ), left foot mechanical stimulation on rats HWL has significant difference(P 〈 0. 001 ) , But the right foot mechanical stimulation of rat HWL difference was not obvious ( P 〉 0.05 ) ; The concentration of 1.75, 3.5 and 7 nmol/μl CGRP to rats with left and right foot hot stimulation, Each of them gets the best pharmacodynamic in 20 minutes. Conclusion: Caleitonin gene related peptide significantly prolong rats in the lateral rein nuclear HWL. The calcitonin gene related peptide in the lateral rein nuclear has analgesic action.
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