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电针对完全弗氏佐剂诱导的大鼠炎性疼痛模型的影响:增强抗伤害感受作用并加速耐受性形成。

Electroacupuncture effects in a rat model of complete Freund's adjuvant-induced inflammatory pain: antinociceptive effects enhanced and tolerance development accelerated.

作者信息

Huang Cheng, Huang Zhi-Qin, Hu Zhi-Ping, Jiang Shao-Zu, Li Han-Ting, Han Ji-Sheng, Wan You

机构信息

Department of Physiology, Gannan Medical University, 1 Yixueyuan Road, Ganzhou 341000, Jiang-Xi Province, China.

出版信息

Neurochem Res. 2008 Oct;33(10):2107-11. doi: 10.1007/s11064-008-9721-x. Epub 2008 May 7.

Abstract

We have previously shown that electroacupuncture (EA) produced antinociception through the release of endogenous opioid peptides to activate opioid receptors during acute nociception. EA produced tolerance after its prolonged application. It has reported that 100 Hz EA could reduce mechanical hyperalgesia in complete Freund's adjuvant (CFA)-induced inflammatory nociception rats. The present study aims to investigate the antinociceptive effect of EA and the development of EA tolerance in chronic inflammatory nociception rats with CFA injection into the hind paw plantar. The results showed that the antinociceptive effect of 100 Hz EA was significantly enhanced in CFA-induced inflammatory nociception rats. Naloxone at 20 mg/kg could significantly block this antinociceptive effect. Chronic tolerance to EA was developed faster in CFA-induced inflammatory nociception rats than in normal rats. Therefore, 100 Hz EA could enhance antinociceptive effects and accelerate tolerance development in CFA-induced inflammatory nociception rats. The enhancement of EA antinociceptive effect in CFA-induced inflammatory nociception rats might involve the endogenous opioid peptides such as dynorphin.

摘要

我们之前已经表明,在急性伤害感受过程中,电针(EA)通过释放内源性阿片肽激活阿片受体产生抗伤害感受作用。EA长期应用后会产生耐受性。据报道,100Hz的EA可减轻完全弗氏佐剂(CFA)诱导的炎性伤害感受大鼠的机械性痛觉过敏。本研究旨在探讨电针对后足跖注射CFA的慢性炎性伤害感受大鼠的抗伤害感受作用及电针耐受性的产生。结果显示,在CFA诱导的炎性伤害感受大鼠中,100Hz EA的抗伤害感受作用显著增强。20mg/kg的纳洛酮可显著阻断这种抗伤害感受作用。CFA诱导的炎性伤害感受大鼠比正常大鼠更快产生对EA的慢性耐受性。因此,100Hz EA可增强CFA诱导的炎性伤害感受大鼠的抗伤害感受作用并加速耐受性的产生。CFA诱导的炎性伤害感受大鼠中EA抗伤害感受作用的增强可能涉及强啡肽等内源性阿片肽。

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