首页> 外文期刊>Journal of Venomous Animals and Toxins including Tropical Diseases >Immunohistochemical investigation of neuronal injury in cerebral cortex of cobra-envenomed rats
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Immunohistochemical investigation of neuronal injury in cerebral cortex of cobra-envenomed rats

机译:眼镜蛇毒大鼠大脑皮质神经元损伤的免疫组织化学研究

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The immunohistochemical expression of neuron-specific enolase, NSE (a cytoplasmic glycolytic enzyme of the neurons), synaptophysin, SYN (a major membrane glycoprotein of synaptic vesicles), and Bcl-2 (anti-apoptotic protein) were determined in cerebral cortex of rats envenomed with neurotoxic venom from Egyptian cobra. Male rats were intramuscularly (IM) injected with a single injection of either physiological saline solution or ? LD50 or LD50 of cobra venom and sacrificed 24, 48, or 72 hr after envenoming. Formalin-fixed paraffin sections were immunohistochemically studied by avidin-biotin-peroxidase complex method. Neuron histological structure and isolation of genomic DNA were also detected. The results showed a dose and time-dependent increase in NSE and SYN immunoreactivity in cerebral cortex of envenomed rats except in 72 hr high dose envenoming, where decreased SYN was observed. On the other hand, low dose venom induced high Bcl-2 expression 24 hr after envenoming, while the high dose decreased Bcl-2 protein expression. Temporal and spatial Bcl-2 expression was accompanied by DNA fragmentation in cerebral cortex of all envenomed rats, although no serious histological alterations were noticed. These results suggest that cobra venom may lead to neuronal injury and impairment of axonal transport as ascertained by alterations in NSE and SYN immunoreactivity. It could also indicate that venom alters the molecular machinery of apoptosis by inhibiting Bcl-2 expression; however, some vulnerable cells have the ability to overcome this by increasing Bcl-2 protein. These immunohistochemical investigations can be used as tools for detecting neuronal abnormalities even before the occurrence of any histological alterations in case of cerebral cortex neurotoxicity.
机译:确定了大鼠大脑皮层中神经元特异性烯醇化酶,NSE(神经元的胞质糖酵解酶),突触素,SYN(突触小泡的主要膜糖蛋白)和Bcl-2(抗凋亡蛋白)的免疫组织化学表达。充满埃及眼镜蛇的神经毒性毒液。雄性大鼠肌肉注射(IM)一次注射生理盐水溶液或生理盐水。眼镜蛇毒的LD50或LD50,在麻醉后24、48或72小时处死。用抗生物素蛋白-生物素-过氧化物酶复合物方法对福尔马林固定的石蜡切片进行免疫组织化学研究。还检测了神经元的组织学结构和基因组DNA的分离。结果显示,除72小时高剂量毒蛇毒(观察到SYN降低)外,毒蛇鼠大脑皮层的NSE和SYN免疫反应性呈剂量和时间依赖性增加。另一方面,低剂量毒液在麻醉后24小时诱导Bcl-2高表达,而高剂量降低Bcl-2蛋白表达。尽管没有观察到严重的组织学改变,但所有被灌胃的大鼠的大脑皮层中的时空Bcl-2表达均伴随着DNA断裂。这些结果表明,眼镜蛇毒可导致神经元损伤和轴突运输受损,这可通过改变NSE和SYN免疫反应性来确定。这也可能表明毒液通过抑制Bcl-2表达来改变细胞凋亡的分子机制。但是,一些易受伤害的细胞有能力通过增加Bcl-2蛋白来克服这一问题。这些免疫组织化学研究甚至可以在脑皮质神经毒性发生任何组织学改变之前用作检测神经元异常的工具。

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