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CGRP对辣椒素致痛大鼠热刺激缩足反射潜伏期的影响
引用本文:曹莹莹,李丽,成洪聚,马克涛,赵磊,司军强.CGRP对辣椒素致痛大鼠热刺激缩足反射潜伏期的影响[J].农垦医学,2009,31(2):110-113.
作者姓名:曹莹莹  李丽  成洪聚  马克涛  赵磊  司军强
作者单位:石河子大学医学院新疆地方与民族高发病教育部重点实验室/石河子大学医学院生理教研室,新疆石河子,832002
摘    要:目的:通过测大鼠的PWTL,探讨CGRP对辣椒素致痛大鼠热痛觉过敏的影响。方法:雌性SD大鼠48只,体重200—220g,随机分为6组,每组都为8只,A组:正常对照组;B组:生理盐水组;C组:大腿背侧坐骨神经干周围注射辣椒素组;D组:腹腔注射生理盐水+大腿背侧坐骨神经干周围注射辣椒素组;E组:腹腔注射CGRP+大腿背侧坐骨神经干周围注射辣椒素组;F组:腹腔注射CGRP8-37大腿背侧坐骨神经千周围注射辣椒素组。分别在注射前及注射后10、20、30、40、50、60min进行热板实验。结果:辣椒素组,大鼠的PWTL比实验前明显缩短(P〈0.05),给予CGRP干预后,大鼠的PWTL与实验前和单独注射辣椒素组相比明显缩短(P〈0.05),给予CGRP受体竞争性拮抗剂CGRP8-37干预后,发现大鼠的PWTL较GGRP干预组明显延长,差异有统计学意义(P〈0.05)。结论:CGRP能促进辣椒素致痛大鼠痛阈降低、痛觉过敏,而CGRP8-37能对抗这种伤害效应。

关 键 词:CGRP  辣椒素  CGRP8-37  痛觉过敏  热刺激缩足反射潜伏期

The effect of CGRP on paw withdraw thermal latency on capsaicin-induced pain rats
Cao Yingying,Li li,Cheng Hongju,Ma Ketao,Zhao Lei,Si Jungqiang.The effect of CGRP on paw withdraw thermal latency on capsaicin-induced pain rats[J].Agricultural Reclamation Medicine,2009,31(2):110-113.
Authors:Cao Yingying  Li li  Cheng Hongju  Ma Ketao  Zhao Lei  Si Jungqiang
Institution:Cao Yingying,Li li, Cheng Hongju, Ma Ketao, Zhao Lei, Si Jungqiang ( Laboratory of Xin jiang Endemic and EtDisease, Shihezi University School of medicine, Physiology of Medicine Department of Shihezi University,Xinjiang Shihezi ,832002)
Abstract:Objective: Through the measurement of thermally stimulated rat withdrawal reflex latency ( paw withdraw thermal latency, PWTL) , to explore the impact of calcitonin gene-related peptide (CGRP) on capsaicin-indueed pain in rats. Methods : forty eight female SD rats weighing 200 - 220g were randomly divided into six groups, each group has eight animals, Group A : normal control group ; Group B : saline group ; Group C : dorsal thigh sciatic nerve injection of capsaicin group luck around ; Group D : intraperitoneal injection saline + thigh dorsal do around the sciatic nerve injection of capsaicin group; Group E: intraperitoneal injection of CGRP + thigh dorsal do around the sciatic nerve injection of capsaicin group; Group F: intraperitoneal injection CGRP8-37 + thigh dorsal do around the sciatic nerve injection of capsaicin group. Separately in injection before and after injection 10,20,30,40,50,60 miu for hot-plate test. Results:The eapsaicin group PWTL rats was significantly shorter than before the experiment ( P 〈 0.05 ). CGRP given after the intervention and PWTL
rats before the experiment and the capsaicin group was significantly shorter ( P 〈 0.05 ). Given the competitive CGRP receptor antagonist CGRP8-37 after the intervention and found that PWTL rats was longer than the CGRP group( P 〈 0.05 ). Conclusion:CGRP can promote capsaicin-induced pain in rats, reduce pain threshold and improving hyperalgesia, and CGRP8-37 can combat the effects of the injury.
Keywords:CGRP  CGRP8-37
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