Adams J, Collaço-Moraes Y, de Belleroche J
Department of Biochemistry, Charing Cross and Westminster Medical School, London, England.
J Neurochem. 1996 Jan;66(1):6-13. doi: 10.1046/j.1471-4159.1996.66010006.x.
We have characterised the induction of the mitogen-inducible form of cyclooxygenase, COX-2, in the rat cerebral cortex in response to excitotoxin injection into the nucleus basalis. This model is associated with intense stimulation of the ascending pathway to the cerebral cortex, seizure activity, and subsequent ipsilateral cortical induction of various immediate early genes (IEGs), including c-fos, c-jun, and zif268, and ornithine decarboxylase enzyme activity and mRNA, all of which processes are sensitive to treatment with the N-methyl-D-aspartate (NMDA) receptor antagonist MK-801. In this study we show that excitotoxin injection also causes a marked induction of COX-2 mRNA in ipsilateral cortex detectable at 1 h and peaking at 4 h, where COX-2 mRNA levels were 19 times those in unoperated animals. Levels of COX-2 mRNA remained significantly elevated at 24 h. The early induction of COX-2 at 1 h was also seen in sham-operated animals, but at 4 h the COX-2 mRNA level was significantly increased (4.4-fold) in animals injected with excitotoxin compared with sham-operated animals. The induction at this time point (4 h) was explored pharmacologically and found to be significantly attenuated by treatment with MK-801 (1.5 mg/kg), lamotrigine (10 mg/kg), which prevents presynaptic glutamate release by blocking voltage-sensitive Na+ channels, and the glucocorticoid dexamethasone (3 mg/kg), which has an indirect inhibitory effect on phospholipase A2 and COX activity.(ABSTRACT TRUNCATED AT 250 WORDS)
我们已经对大鼠大脑皮质中丝裂原诱导型环氧化酶COX - 2的诱导情况进行了表征,该诱导是对向基底核注射兴奋性毒素的反应。此模型与大脑皮质上行通路的强烈刺激、癫痫活动以及随后同侧皮质中各种即刻早期基因(IEGs)的诱导有关,这些基因包括c - fos、c - jun和zif268,还有鸟氨酸脱羧酶的酶活性和mRNA,所有这些过程都对N - 甲基 - D - 天冬氨酸(NMDA)受体拮抗剂MK - 801的治疗敏感。在本研究中,我们表明注射兴奋性毒素还会导致同侧皮质中COX - 2 mRNA显著诱导,在1小时可检测到,4小时达到峰值,此时COX - 2 mRNA水平是未手术动物的19倍。COX - 2 mRNA水平在24小时仍显著升高。在假手术动物中也可见到1小时时COX - 2的早期诱导,但在4小时时,与假手术动物相比,注射兴奋性毒素的动物中COX - 2 mRNA水平显著增加(4.4倍)。对该时间点(4小时)的诱导进行了药理学研究,发现用MK - 801(1.5毫克/千克)、拉莫三嗪(10毫克/千克,通过阻断电压敏感性钠通道来阻止突触前谷氨酸释放)和糖皮质激素地塞米松(3毫克/千克,对磷脂酶A2和COX活性有间接抑制作用)治疗后,诱导明显减弱。(摘要截断于250字)