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电针对角叉菜胶诱导的炎症大鼠模型脊髓磷酸肌醇 3-激酶/蛋白激酶 B 磷酸化的抑制作用。

Electroacupuncture inhibits phosphorylation of spinal phosphatidylinositol 3-kinase/Akt in a carrageenan-induced inflammatory rat model.

机构信息

Division of Meridian and Structural Medicine, School of Korean Medicine, Pusan National University, Yangsan 626-870, Republic of Korea.

出版信息

Brain Res Bull. 2012 Feb 10;87(2-3):199-204. doi: 10.1016/j.brainresbull.2011.11.010. Epub 2011 Nov 25.

Abstract

We investigated the changes of pain-related spinal signaling pathway after electroacupuncture (EA) stimulation in a carrageenan-induced rat model. EA stimulation (2Hz, 1mA) was needle-delivered for 30 min at acupoints corresponding to Zusanli and Sanyinjiao 3 h after carrageenan injection. Thermal and mechanical sensitivity of the hindpaw induced by carrageenan was strongly inhibited by EA stimulation. Phosphorylation of extracellular signal-regulated kinase, phosphatidylinositol 3-kinase (PI3K), Akt, and cAMP response element-binding protein (CREB) were examined in the L4-5 segments of the spinal cord by Western blot analysis 4h and 5h after carrageenan injection. Phosphorylation of Akt and especially PI3K were significantly induced by carrageenan-induction, but these expressions were markedly inhibited by EA stimulation. CREB phosphorylation showed a similar, but insignificant, pattern as like PI3k/Akt. Immunohistochemical analyses confirmed that phosphorylation of PI3K and Akt showed a similar pattern as Western blotting and were observed in most neurons and a few astrocytes. EA and PI3K inhibitor synergistically inhibited carrageenan-induced hyperalgesia. These results reveal that both neuronal PI3K and Akt may play an important role in EA-induced antinociception via inactivation in an inflammatory pain model.

摘要

我们研究了电针(EA)刺激在角叉菜胶诱导的大鼠模型中对疼痛相关脊髓信号通路的变化。在角叉菜胶注射后 3 小时,在对应于足三里和三阴交的穴位上进行 2Hz、1mA 的 EA 刺激 30 分钟。EA 刺激强烈抑制了由角叉菜胶引起的后足热和机械敏感性。通过 Western blot 分析,在角叉菜胶注射后 4h 和 5h 检查 L4-5 节段脊髓中的细胞外信号调节激酶、磷脂酰肌醇 3-激酶(PI3K)、Akt 和 cAMP 反应元件结合蛋白(CREB)的磷酸化。PI3K/Akt 的磷酸化明显受角叉菜胶诱导,而这些表达明显受 EA 刺激抑制。CREB 磷酸化表现出类似但不显著的模式,如 PI3k/Akt。免疫组织化学分析证实,PI3K 和 Akt 的磷酸化表现出与 Western blot 相似的模式,在大多数神经元和少数星形胶质细胞中观察到。EA 和 PI3K 抑制剂协同抑制角叉菜胶诱导的痛觉过敏。这些结果表明,神经元 PI3K 和 Akt 可能在炎症性疼痛模型中通过失活在 EA 诱导的镇痛中发挥重要作用。

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