Key Laboratory of Cerebrovascular Pharmacology of Jiangxi Province, Department of Pharmacology, Gannan Medical College, Ganzhou, People's Republic of China.
Cell Mol Neurobiol. 2013 Jul;33(5):715-22. doi: 10.1007/s10571-013-9939-2. Epub 2013 Apr 26.
We previously found that xanthotoxol, one of the major active ingredients in Cnidium monnieri (L.) Cusson, exerts protective effects in a rat model of focal cerebral ischemia/reperfusion injury by alleviating brain edema, inhibiting the neutrophil infiltration, and decreasing the expression of intercellular adhesion molecule-1 (ICAM-1) and E-selectin. The present study was designed to further determine the possible mechanisms of action of neuroprotective properties of xanthotoxol after cerebral ischemia. Transient focal cerebral ischemia/reperfusion model in male Sprague-Dawley rats was induced by 2-h middle cerebral artery occlusion followed by 24-h reperfusion. Xanthotoxol (5 and 10 mg/kg) or vehicle were administered intraperitoneally at 1 and 12 h after the onset of ischemia. At 24 h after reperfusion, we assessed the effect of xanthotoxol on the blood-brain barrier (BBB) permeability, the production of pro-inflammatory mediators such as interleukin (IL)-1β, tumor necrosis factor (TNF)-α, IL-8, nitric oxide (NO), inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and the p65 subunit of the transcription factor, nuclear factor-κB (NF-κB) in the cortex after ischemic insult. The results showed that xanthotoxol treatment significantly attenuated BBB disruption, reduced the IL-1β, TNF-α, IL-8 and NO level, and attenuated the iNOS activity compared with vehicle-treated animals. Further, xanthotoxol treatment also significantly prevented the ischemia/reperfusion-induced increase in the protein expression of iNOS, COX-2, and the nuclear NF-κB p65. These results, taken together with those of our previous study, suggest that the neuroprotection may be attributed to the ability of xanthotoxol to attenuate the expression of pro-inflammatory mediators and thereby inhibit the inflammatory response after cerebral ischemia.
我们之前发现,蛇床子素是蛇床子(Cnidium monnieri(L.)Cusson)的主要活性成分之一,通过减轻脑水肿、抑制中性粒细胞浸润以及降低细胞间黏附分子-1(ICAM-1)和 E-选择素的表达,对大鼠局灶性脑缺血再灌注损伤模型发挥保护作用。本研究旨在进一步确定蛇床子素在脑缺血后的神经保护作用的可能作用机制。通过 2 小时大脑中动脉闭塞后再灌注 24 小时,诱导雄性 Sprague-Dawley 大鼠短暂性局灶性脑缺血/再灌注模型。在缺血后 1 小时和 12 小时,通过腹腔内给予蛇床子素(5 和 10 mg/kg)或载体。在再灌注 24 小时后,评估蛇床子素对血脑屏障(BBB)通透性的影响,以及缺血后皮质中促炎介质(如白细胞介素(IL)-1β、肿瘤坏死因子(TNF)-α、IL-8、一氧化氮(NO)、诱导型一氧化氮合酶(iNOS)、环氧化酶-2(COX-2)和转录因子核因子-κB(NF-κB)p65 亚单位的产生。结果表明,与载体处理的动物相比,蛇床子素治疗显著减轻了 BBB 破坏,降低了 IL-1β、TNF-α、IL-8 和 NO 水平,并减弱了 iNOS 活性。此外,蛇床子素治疗还显著防止了缺血/再灌注诱导的 iNOS、COX-2 和核 NF-κB p65 蛋白表达增加。这些结果与我们之前的研究结果一起表明,神经保护作用可能归因于蛇床子素减轻促炎介质表达的能力,从而抑制脑缺血后的炎症反应。