首页> 外文期刊>European Journal of Pharmacology: An International Journal >Protective effect of hydroxysafflor yellow A alone or in combination with acetylglutamine on cerebral ischemia reperfusion injury in rat: A PET study using F-18-fuorodeoxyglucose
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Protective effect of hydroxysafflor yellow A alone or in combination with acetylglutamine on cerebral ischemia reperfusion injury in rat: A PET study using F-18-fuorodeoxyglucose

机译:羟基烷烃黄色的保护作用单独或与乙酰谷氨酰胺组合在大鼠脑缺血再灌注损伤中:使用F-18-FuorodoOx亚葡萄糖的PET研究

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摘要

Hydroxysafflor yellow A (HSYA) and acetylglutamine (NAG) are extensively applied in the treatment of brain injury. In this study, we investigated the neuroprotective effect and underlying mechanism of HSYA alone or together with NAG using a rat model of cerebral ischemia reperfusion injury. Male Sprague-Dawley (SD) rats (n=5) were intraperitoneally injected with 5, 10, 20 mg/kg HSYA, 300 mg/kg NAG and 10 mg/kg HSYA + 300 mg/kg NAG after the onset of reperfusion and once each day for the following 7 days. After assessing the neurological deficit and infarct volume, we used 18F-FDG-PET to evaluate the regional cerebral metabolic rate of glucose consumption, immunohistochemical analysis to detect the expression of GFAP, NGF, Bcl-2, Bax, caspase-3 and ICAM-1 in brain tissue at day 7 after cerebral I/R injury. Meanwhile, the mRNA levels of ICAM-1, IL-1 beta, TNF-alpha and NF-kappa B were determined by qRT-PCR, the protein levels of Bcl-2, Bax and caspase-3 were detected by western blot. The results indicated that HSYA significantly up-regulated glucose metabolism, improved neurological function, decreased cerebral infarction volume. HSYA alone or together with NAG attenuated apoptosis and inflammation by up-regulating GFAP, NGF and Bcl-2 expression, suppressing the expression of Bax, caspase-3 and ICAM-1, IL-1, TNF-alpha and NF-kappa B. These finding suggested that HSYA exerted neuroprotection against cerebral I/R injury by modulating inflammation and apoptosis process, and HSYA in combination with NAG possessed a synergetic effect on protecting cerebral I/R brain injury.
机译:羟基烷烃黄色A(HSYA)和乙酰戊胺(NAG)广泛应用于脑损伤的治疗。在这项研究中,我们研究了使用大鼠脑缺血再灌注损伤的大鼠模型单独或与NAG一起单独的神经保护作用和底层机制。雄性Sprague-Dawley(SD)大鼠(n = 5)腹膜内注射5,10,20mg / kg HSYA,300mg / kg NAG和10mg / kg HSYA + 300 mg / kg唠叨,然后再灌注每天一次进行一次7天。在评估神经缺陷和梗塞体积后,我们使用18F-FDG-PET评估葡萄糖消耗的区域脑代谢率,免疫组化分析,检测GFAP,NGF,BCL-2,BAX,Caspase-3和ICAM的表达。 1在脑I / R损伤后第7天脑组织中的1。同时,通过QRT-PCR测定ICAM-1,IL-1β,TNF-α和NF-Kappa B的mRNA水平,通过Western印迹检测到Bcl-2,Bax和Caspase-3的蛋白质水平。结果表明,HSYA明显上调葡萄糖代谢,改善神经功能,脑梗死量减少。 HSYA单独或通过NAG衰减细胞凋亡和炎症通过上调GFAP,NGF和BCL-2表达,抑制Bax,Caspase-3和ICAM-1,IL-1,TNF-α和NF-Kappa B的表达。这些发现表明,HSYA通过调节炎症和凋亡过程来施加对脑I / R损伤的神经保护作用,HSYA与NAG联合的HSSYA对保护脑I / R脑损伤具有协同作用。

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