间隔联合应用BAM8-22增强慢性吗啡抑制c-Fos表达的作用  

Intermittent Co-administration of BAM8-22 Enhances the Inhibition of Chronic Morphine on Formalin-evoked c-Fos Expression

在线阅读下载全文

作  者:江剑平[1] 付艳[1,2] 胡粉娟[1] 

机构地区:[1]福建师范大学生命科学学院福建省发育和神经生物学重点实验室,福建福州350117 [2]大秦家畜牧兽医站,山东招远265408

出  处:《福建师范大学学报(自然科学版)》2015年第4期82-86,共5页Journal of Fujian Normal University:Natural Science Edition

基  金:福建省自然科学基金资助项目(2014J01305);福建省教育厅重点项目(JA14072)

摘  要:通过观察腰段脊髓背角c-Fos阳性神经元数量变化,探讨鞘内间隔联合应用牛肾上腺髓质8-22肽(bovine adrenal medulla 8-22,BAM8-22)在福尔马林引起的持续性痛中对吗啡耐受的影响.结果显示,连续6 d应用吗啡导致耐受(吗啡耐受组)后,福尔马林诱发的c-Fos阳性神经元数量明显增加,与吗啡组相比,其脊髓Ⅰ-Ⅱ、Ⅲ-Ⅳ和Ⅴ-Ⅵ层c-Fos阳性神经元分别增加了164.9%、131.5%和125.3%(P〈0.05~0.01);但隔天给予BAM8-22(吗啡+BAM8-22组)则能明显增强慢性吗啡抑制c-Fos阳性神经元的表达,与吗啡耐受组相比,其脊髓Ⅰ-Ⅱ和Ⅴ-Ⅵ层c-Fos阳性神经元数量分别下降了66.6%和48.8%(P〈0.05~0.01).在福尔马林引起的持续性痛中,BAM8-22延缓吗啡耐受是通过抑制脊髓背角伤害性神经元的活性来实现的。The present study was designed to investigate the effects of intermittent co-administration of bovine adrenal medulla 8-22( BAM8-22) on morphine tolerance through examining the expression of c-Fos in the lumbar spinal cord in formalin test. The results showed that formalin-evoked c-Fos positive neurons were remarkably increased in morphine tolerance when morphine was administrated daily for 6 days. The number of c-Fos positive neurons increased by 164. 9%,131. 5% and125. 3% in laminae Ⅰ- Ⅱ、Ⅲ- Ⅳ and Ⅴ- Ⅵ,respectively,compared with morphine group( P 0. 05 ~ 0. 01). Intermittent co-administration of BAM8-22( morphine plus BAM8-22 group)remarkably enhanced the inhibition of chronic morphine on formalin-evoked c-Fos expression,the number of c-Fos positive neurons decreased by 66. 6% and 48. 8% in laminae Ⅰ- Ⅱ and Ⅴ- Ⅵ,respectively,compared with morphine in tolerant group( P 0. 05 ~ 0. 01). The present study provided evidence at a cellular level showing that BAM8-22 attenuate morphine tolerance by inhibiting the activation of nociceptive neurons in the spinal dorsal horn in formalin-induced persistent pain.

关 键 词:牛肾上腺髓质8-22肽(BAM8-22) 吗啡耐受 持续性痛 福尔马林实验 c-Fos阳性神经元 

分 类 号:Q426[生物学—神经生物学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象