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首页> 外文期刊>Inflammation research: Official journal of the European Histamine Research Society >Evaluation of neuroprotective effects of insulin on immuno-inflammatory and systemic disorders induced by kaliotoxin, a Kv1.3 channel blocker
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Evaluation of neuroprotective effects of insulin on immuno-inflammatory and systemic disorders induced by kaliotoxin, a Kv1.3 channel blocker

机译:胰岛素对kaliotoxin诱导的免疫炎症和全身疾病的评价,Kv1.3通道阻滞剂

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摘要

Objective Kaliotoxin2 (KTX2) is a highly selective blocker of voltage-dependent potassium channels Kv1.3 containing 37 amino acid residues. It is purified from Androctonus australis scorpion venom. The binding of KTX2 to its targets is able to alter the neuronal excitability leading to neurological disorders, accompanied by an inflammatory response. In brain, activation of insulin receptor signaling pathway by insulin induces current suppression and concomitant tyrosine phosphorylation of Kv1.3 channel. The aim of this study is to evaluate the effect of insulin injected by i.c.v. route on the neuro-pathophysiological and systemic disorders induced by KTX2. Materials and methods Tissue damage, inflammatory response and oxidative stress biomarkers were assessed in NMRI mice at 24?h after co-injection of KTX2 and insulin by intracerebroventricular route. Results Obtained results revealed that the central administration of insulin prevents cerebral cortex injury, brain edema and blood–brain barrier alteration induced by KTX2, these are accompanied by significant decrease of systemic disorders including serum cytokines, inflammatory and oxidative stress markers and tissue damage. Conclusion These results indicate that insulin is able to reduce neuro-immunological effects and systemic disorders induced by KTX2. The neuroprotective effect of insulin may be due to its crucial role in the regulation of inflammation response and its properties to modulate the activity of Kv1.3 channels in brain.
机译:目标Kaliotoxin2(KTX2)是含有37个氨基酸残基的电压依赖性钾通道Kv1.3的高选择性阻滞剂。它纯化来自Androctonus澳大利亚蝎子毒液。 KTX2对其靶标的结合能够改变导致神经元疾病的神经元兴奋性,伴随着炎症反应。在脑中,胰岛素激活胰岛素受体信号传导途径诱导KV1.3通道的电流抑制和伴随酪氨酸磷酸化。本研究的目的是评估I.C.V注射胰岛素的效果。 ktx2诱导的神经病理生理学和全身疾病的途径。通过脑室内途径共注入KTX2和胰岛素后,在24μm中在NMRI小鼠中评估材料和方法组织损伤,炎症反应和氧化应激生物标志物。结果获得的结果表明,胰岛素的中央施用阻止了KTX2诱导的脑皮质损伤,脑水肿和血脑屏障变化,这些患者伴有全身性疾病的显着降低,包括血清细胞因子,炎症和氧化应激标记物和组织损伤。结论这些结果表明,胰岛素能够减少KTX2诱导的神经免疫效应和全身疾病。胰岛素的神经保护作用可能是由于其在调节炎症反应的关键作用及其调节脑中KV1.3通道活性的性质。

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