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[阻断p38信号通路可降低创伤性脑损伤大鼠的基质金属蛋白酶-9表达并减轻脑水肿]

[Blocking p38 signal pathway lowers MMP-9 expression and reduces brain edema in rats with traumatic brain injury].

作者信息

Tang Zhaohua, Liao Zhengbu, Shi Quanhong, Xie Yanfeng, He Zhaohui, Zhan Yan

机构信息

Department of Neurosurgery, First Affiliated Hospital of Chongqing Medical University, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2012 Jun;32(7):928-31.

Abstract

OBJECTIVE

To explore the role of p38 signal pathway in regulating matrix metalloproteinase-9 (MMP-9) expression and brain edema formation in a rat model of traumatic brain injury (TBI).

METHODS

A total of 130 adult male Sprague Dawley rats were randomly divided into 4 groups, namely the normal group (n=10), sham-operated group (n=40), TBI (induced by Feeney free falling methods) group (n=40), and SB group with intraperitoneal SB203580 treatment (10 µmol/L) 15 min before TBI (n=40). The rats were sacrificed 2 h and 2 days after TBI. The expressions of p38, p-p38, and MMP-9 mRNA and protein were detected by RT-PCR and Western blotting. The blood brain barrier permeability was detected by Evans Blue (EB) test, and the brain water content (BWC) was determined using a gravimetric technique.

RESULTS

The expression of p-p38 protein increased markedly 2 h after TBI (P<0.05), and was suppressed by SB203580 treatment (P<0.05). MMP-9 mRNA and protein showed no obvious increase at 2 h after TBI, but significantly increased at 2 days as compared with those in the sham-operated group (P<0.05). MMP-9 mRNA and protein were much lower in SB group than in TBI group 2 days after TBI (P<0.05). The blood brain barrier permeability significantly increased 2 h after TBI (P<0.05) and kept increasing until 2 days (P<0.05), but was reduced significantly by SB203580 (P<0.05). BWC increased obviously 2 days after TBI (P<0.05) and was lessened by SB203580 (P<0.05).

CONCLUSION

Blocking p38 signal pathway can attenuate MMP-9 upregulation and brain edema after TBI, suggesting the important role of p38 in regulating MMP-9 expression to affect traumatic brain edema.

摘要

目的

探讨p38信号通路在创伤性脑损伤(TBI)大鼠模型中调节基质金属蛋白酶-9(MMP-9)表达及脑水肿形成中的作用。

方法

将130只成年雄性Sprague Dawley大鼠随机分为4组,即正常组(n = 10)、假手术组(n = 40)、TBI组(采用Feeney自由落体法诱导)(n = 40)和SB组(在TBI前15分钟腹腔注射SB203580(10 μmol/L))(n = 40)。在TBI后2小时和2天处死大鼠。通过逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测p38、磷酸化p38(p-p38)以及MMP-9的mRNA和蛋白表达。通过伊文思蓝(EB)试验检测血脑屏障通透性,采用重量法测定脑含水量(BWC)。

结果

TBI后2小时p-p38蛋白表达显著增加(P < 0.05),而SB203580治疗可抑制其表达(P < 0.05)。TBI后2小时MMP-9的mRNA和蛋白无明显增加,但与假手术组相比,2天时显著增加(P < 0.05)。TBI后2天,SB组的MMP-9 mRNA和蛋白水平明显低于TBI组(P < 0.05)。TBI后2小时血脑屏障通透性显著增加(P < 0.05),并持续增加至2天(P < 0.05),但SB203580可使其显著降低(P < 0.05)。TBI后2天BWC明显增加(P < 0.05),SB203580可使其减轻(P < 0.05)。

结论

阻断p38信号通路可减轻TBI后MMP-9的上调及脑水肿,提示p38在调节MMP-9表达以影响创伤性脑水肿中起重要作用。

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