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首页> 外文期刊>Neurological Research >Effect of neutralization of rat interleukin 6 bioactivity on inducible nitric oxide synthase up-regulation and cerebral ischemic damage
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Effect of neutralization of rat interleukin 6 bioactivity on inducible nitric oxide synthase up-regulation and cerebral ischemic damage

机译:中和大鼠白介素6的生物活性对诱导型一氧化氮合酶上调和脑缺血损伤的影响

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摘要

Objectives: Our aim was to investigate whether neutralization of rat interleukin 6 (IL-6) bioactivity attenuates inducible nitric oxide synthase (iNOS) up-regulation and ameliorates cerebral ischemic damage in a model of focal central nervous system (CNS) ischemia.Methods: Seventy rats were randomly allocated to groups: Group I (n=10) consisted of normal controls; Group II (n=20) underwent surgical exposure of the middle cerebral artery but no cauterization; the remaining 40 rats were subjected to middle cerebral artery occlusion. Immediately after occlusion, each of these 40 rats was randomly assigned to either the occlusion-only group (Group III, n=20) or the occlusion plus IL-6 antibody treatment group (Group IV, n=20). Half of the rats from each of Groups II, III and IV were eternized at 24 hours and the other half at 72 hours. The samples were used for iNOS immunohistochemistry and structural analysis.Results: A single dose of the antibody had no effect on structural changes and iNOS at 24 hours after occlusion. However, administering three doses of the antibody resulted in markedly decreased quantitative and qualitative levels of iNOS-positive stained cells and milder subcellular damage compared with the findings in the occlusion-only group at 72 hours after occlusion.Discussion: Our findings prove that IL-6 bioactivity is one of the pathological events that trigger the induction of iNOS in the process of CNS ischemic injury. It appears that there may be therapeutic value in neutralization of IL-6 bioactivity to attenuate iNOS up-regulation and ameliorate cerebral ischemic damage in long-term recovery.
机译:目的:我们的目的是研究在中枢神经系统(CNS)缺血模型中中和大鼠白介素6(IL-6)生物活性是否能减弱诱导型一氧化氮合酶(iNOS)的上调并减轻脑缺血性损伤。 70只大鼠随机分为各组:第一组(n = 10)由正常对照组组成;第二组(n = 20)接受了大脑中动脉的手术暴露,但未进行烧灼;其余40只大鼠进行大脑中动脉闭塞。闭塞后,立即将这40只大鼠中的每只随机分为仅闭塞组(III组,n = 20)或闭塞加IL-6抗体治疗组(IV组,n = 20)。 II组,III组和IV组中的每只大鼠的一半在24小时时灭绝,另一半在72小时时灭绝。结果:单剂量抗体对闭塞后24小时的结构变化和iNOS没有影响。然而,与仅闭塞组在闭塞后72小时的发现相比,施用三剂抗体导致iNOS阳性染色细胞的定量和定性水平显着降低,亚细胞损伤更轻。讨论:我们的发现证明IL- 6生物活性是在CNS缺血性损伤过程中触发iNOS诱导的病理事件之一。似乎在中和IL-6的生物活性方面可能具有治疗价值,以减轻iNOS的上调并减轻长期恢复中的脑缺血损伤。

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  • 来源
    《Neurological Research》 |2009年第7期|714-720|共7页
  • 作者单位

    Department of Neurosurgery, ?ukurova University School of Medicine, Adana, Turkey;

    Department of Neurosurgery, ?ukurova University School of Medicine, Adana, Turkey;

    Department of Neurosurgery, ?ukurova University School of Medicine, Adana, Turkey;

    Department of Neurosurgery, ?ukurova University School of Medicine, Adana, Turkey;

    Department of Histology, ?ukurova University School of Medicine, Adana, Turkey;

    Department of Histology, ?ukurova University School of Medicine, Adana, Turkey;

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