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[细胞外信号调节蛋白激酶在大鼠皮下筋膜中的表达及其针刺后的变化]

[Expression of extracellular signal-regulated protein kinases in the subcutaneous fascia of rats and their changes after acupuncture].

作者信息

Jiang Xue-mei, Yang Chun, Yuan Lin, Diao Jian-xin, Zhang Xue-quan, Huang Yong, Dai Jing-xing, Qiu Xiao-zhong, Yu Lei

机构信息

School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2009 Apr;29(4):623-6.

Abstract

OBJECTIVE

To observe the effect of acupuncture on the expression of extracellular signal-regulated protein kinases 1/2 (ERK1/2) in the subcutaneous fascia of SD rats.

METHODS

Eighteen SD rats were randomly divided into 6 groups (n=3) including 5 acupuncture groups and a control group. The rats in the 5 acupuncture groups received electro-acupuncture therapy in the regions of the inguinal groove, and at 0, 1, 6, 12, and 36 h after the last therapy, the superfacial fascia surrounding the acupuncture point (about 1.5 cm in diameter) were collected. The fascia tissues at the corresponding sites and at the acupoint Zusanli (ST36) were obtained from the control rats. The expression of ERK1/2 and phosphorylated ERK1/2 (p-ERK1/2) in the tissues were detected by Western blotting.

RESULTS

ERK1/2 and p-ERK1/2 expressions were detected in the tissues harvested from both the acupoint and the non-acupoint in the control rats with similar expression intensities. In the rats of each acupuncture group, ERK1/2 expression was significantly increased on the acupuncture side in comparison with the control side.

CONCLUSION

The normal loose connective tissue may participate in tissue proliferation and differentiation possibly via phosphorylation of ERK. Acupuncture can promote the signal transduction pathway of ERK, which can be a possible mechanism for the effect of acupuncture in modulating the physiopathological conditions.

摘要

目的

观察针刺对SD大鼠皮下筋膜中细胞外信号调节蛋白激酶1/2(ERK1/2)表达的影响。

方法

将18只SD大鼠随机分为6组(n = 3),包括5个针刺组和1个对照组。5个针刺组大鼠在腹股沟沟区域接受电针治疗,在最后一次治疗后0、1、6、12和36小时,收集针刺点周围的浅筋膜(直径约1.5 cm)。从对照大鼠获取相应部位及足三里穴(ST36)处的筋膜组织。采用蛋白质免疫印迹法检测组织中ERK1/2和磷酸化ERK1/2(p-ERK1/2)的表达。

结果

对照组大鼠穴位和非穴位采集的组织中均检测到ERK1/2和p-ERK1/2表达,表达强度相似。各针刺组大鼠针刺侧的ERK1/2表达较对照侧显著增加。

结论

正常疏松结缔组织可能通过ERK磷酸化参与组织增殖和分化。针刺可促进ERK信号转导通路,这可能是针刺调节生理病理状态作用的一种机制。

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