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脑室内注射D-丝氨酸对福尔马林诱导疼痛的抗伤害感受作用。

Antinociceptive effect of intracerebroventricular administration of D-serine on formalin-induced pain.

作者信息

Ito Miho, Yoshikawa Masanobu, Ito Kenji, Matsuda Mitsumasa, Jin Xing Lu, Takahashi Shigeru, Kobayashi Hiroyuki, Suzuki Toshiyasu

机构信息

Department of Anesthesiology, Tokai University School of Medicine, Isehara, Kanagawa, 259-1193, Japan,

出版信息

J Anesth. 2014 Apr;28(2):228-34. doi: 10.1007/s00540-013-1708-3. Epub 2013 Sep 19.

Abstract

PURPOSE

In a previous study using the tail-flick test, we found that intracerebroventricular administration of D-serine, an endogenous co-agonist at the glycine sites of N-methyl-D-aspartate (NMDA) receptors, elicited an antinociceptive effect on thermal nociception. The purpose of the present study was to evaluate the effect of intracerebroventricular administration of D-serine on nociception induced by tissue damage or inflammation using the formalin test.

METHODS

Infusion of drugs into the third ventricle in rat was performed via indwelling cannulae. Drugs were infused at a volume of 10 μl over 2 min, and the infusion cannula was left in place for 2 min before removal. The formalin test was performed 10 min after drug administration.

RESULTS

Intracerebroventricular administration of D-serine significantly and dose-dependently decreased the number of flinches in both the early and late phases in the formalin test. This antinociceptive effect was antagonized by intracerebroventricular administration of L-701,324, a selective antagonist at the glycine sites of NMDA receptors.

CONCLUSION

The present data suggest that activation of NMDA receptors via glycine sites at the supraspinal level induces an antinociceptive effect on both acute and tonic pain.

摘要

目的

在先前一项使用甩尾试验的研究中,我们发现,脑室内注射D-丝氨酸(N-甲基-D-天冬氨酸(NMDA)受体甘氨酸位点的内源性协同激动剂)可对热痛觉产生抗伤害感受作用。本研究的目的是使用福尔马林试验评估脑室内注射D-丝氨酸对组织损伤或炎症诱导的痛觉的影响。

方法

通过留置套管将药物注入大鼠第三脑室。以10μl的体积在2分钟内注入药物,注入套管在移除前留置2分钟。给药10分钟后进行福尔马林试验。

结果

脑室内注射D-丝氨酸在福尔马林试验的早期和晚期均显著且剂量依赖性地减少了退缩次数。这种抗伤害感受作用被脑室内注射L-701,324(NMDA受体甘氨酸位点的选择性拮抗剂)所拮抗。

结论

目前的数据表明,脊髓上水平通过甘氨酸位点激活NMDA受体可对急性和持续性疼痛产生抗伤害感受作用。

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