首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Polyunsaturated fatty acids induce ischemic and epileptic tolerance.
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Polyunsaturated fatty acids induce ischemic and epileptic tolerance.

机译:多不饱和脂肪酸诱导缺血性和癫痫耐受性。

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摘要

The findings reported in this work show that pretreatment with polyunsaturated fatty acids, particularly linolenic acid, present in vegetable oils, can provide a potent tolerance against neurodegeneration in two models of neuronal death-generating treatments such as kainic acid injection and global ischemia. Rats were injected i.v. with 500 nmol/kg of linolenic acid as long as 3 days prior to 6 min global ischemia or received an injection of linolenic acid as long as 3 days prior to a dose of 7.5 mg/kg kainic acid. Neuronal degeneration, assessed by analysis of neuronal density on Cresyl Violet-stained hippocampal sections, was significantly reduced in linolenic acid-treated rats (94-85% of cell survival in the ischemic model and 99-79% of cell survival in the epileptic model in respective CA1 and CA3 subfields). The neuroprotection observed following the injection of linolenic acid 3 days prior to induction of a severe ischemic or epileptic challenge was associated with the induction of the neuroprotective HSP70 heat shock protein within the time window of protection. The injection of 500 nmol/kg of linolenic acid induced a maximal HSP70 expression of 387% at 72 h. In contrast, the overexpression of one well-known protein inducer of neuronal cell death, Bax, which is induced by both ischemic and kainic acid-induced epileptic insults, was prevented by linolenic acid in the 3-day window of protection.These results strengthen the idea of an interesting potential therapeutical value of polyunsaturated fatty acids in neuronal protection.
机译:这项工作中报告的发现表明,用植物油中存在的多不饱和脂肪酸(尤其是亚麻酸)进行预处理,可以在两种神经元致死性治疗模型(例如海藻酸注射液和全脑缺血)中提供有效的抗神经变性的能力。大鼠静脉内注射。在6分钟的局部缺血前3天服用500 nmol / kg的亚麻酸,或在服用7.5 mg / kg海藻酸之前3天服用亚麻酸。通过对Cresyl紫染色海马切片的神经元密度进行分析评估,神经元变性在亚麻酸处理的大鼠中明显减少(缺血模型中细胞存活率为94-85%,癫痫模型中细胞存活率为99-79%在相应的CA1和CA3子字段中)。诱导严重缺血或癫痫发作前三天注射亚麻酸后观察到的神经保护作用与在保护时间内诱导神经保护性HSP70热休克蛋白有关。注射500 nmol / kg的亚麻酸在72 h时诱导HSP70的最大表达达387%。相比之下,在3天的保护期中,亚麻酸阻止了一种众所周知的神经元细胞死亡的蛋白诱导剂Bax的过表达,而Bax是由缺血性和卡因酸诱导的癫痫性损伤所诱导的。多不饱和脂肪酸在神经元保护中的潜在潜在治疗价值的想法。

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