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[切口痛-瑞芬太尼诱发痛觉过敏大鼠脊髓神经元中糖原合酶激酶-3β及其磷酸化的变化]

[Changes of glycogen synthase kinase-3β and its phosphorylation in spinal cord neurons in rats with incisional pain-remifentanil-induced hyperalgesia].

作者信息

Yuan Yuan, Wang Jing-Yao, Yuan Fang, Yu Yong-Hao, Wang Guo-Lin

机构信息

Department of Anesthesiology, Tianjin Medical University General Hospital, Tianjin, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2012 Feb 21;92(7):435-9. doi: 10.3760/cma.j.issn.00376-2491-2012.07.002.

DOI:10.3760/cma.j.issn.00376-2491-2012.07.002
PMID:22490960
Abstract

OBJECTIVE

To investigate the change in glycogen synthase kinase-3β (GSK-3β) in spinal cord neurons in rats with incisional pain (IP)-remifentanil-induced hyperalgesia.

METHODS

32 SD male rats (240 - 260 g) were randomly divided into 4 groups (n = 8 each): group R, group I, group R + I and group C. IP was established as Brennan's description. Paw withdrawal threshold (PWT) and paw withdrawal latency (PWL) were measured 24h before anesthesia and 2, 6, 24, 48 h after anesthesia. The rats were sacrificed after the last threshold measurement. The expressions of GSK-3β mRNA in rats' spinal cord neurons were determined by real-time PCR. The expressions of GSK-3β and pGSK-3β in rats' spinal cord neurons were determined by Western blot.

RESULTS

Remifentanil-induced hyperalgesia developed in group R, I and R + I. The expression of GSK-3β mRNA and the expression of GSK-3β in rats' spinal cord neurons were highest in group R + I. In addition, the ratio of pGSK-3β/GSK-3β was smallest in group R + I.

CONCLUSION

These data indicate that the increased GSK-3β activity in rats spinal cord neurons is involved in remifentanil-induced hyperalgesia.

摘要

目的

探讨切口痛(IP)-瑞芬太尼诱导的痛觉过敏大鼠脊髓神经元中糖原合酶激酶-3β(GSK-3β)的变化。

方法

将32只SD雄性大鼠(240 - 260 g)随机分为4组(每组n = 8):R组、I组、R + I组和C组。按照Brennan的描述建立IP模型。在麻醉前24小时以及麻醉后2、6、24、48小时测量 paw withdrawal threshold(PWT)和 paw withdrawal latency(PWL)。在最后一次阈值测量后处死大鼠。通过实时PCR测定大鼠脊髓神经元中GSK-3β mRNA的表达。通过蛋白质免疫印迹法测定大鼠脊髓神经元中GSK-3β和pGSK-3β的表达。

结果

R组、I组和R + I组出现瑞芬太尼诱导的痛觉过敏。大鼠脊髓神经元中GSK-3β mRNA的表达以及GSK-3β的表达在R + I组中最高。此外,pGSK-3β/GSK-3β的比值在R + I组中最小。

结论

这些数据表明大鼠脊髓神经元中GSK-3β活性增加与瑞芬太尼诱导的痛觉过敏有关。

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