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首页> 外文期刊>Bali Medical Journal >THE ROLE OF RECOMBINANT IL-10 ON THE SERUM LEVEL OF TNF-α, ONE HOUR POST TRAUMATIC BRAIN INJURY OF THE WISTAR RAT
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THE ROLE OF RECOMBINANT IL-10 ON THE SERUM LEVEL OF TNF-α, ONE HOUR POST TRAUMATIC BRAIN INJURY OF THE WISTAR RAT

机译:重组IL-10对WISTAR大鼠一小时创伤性脑损伤血清TNF-α水平的作用。

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摘要

Background: Brain injury often occurs not only primary brain injury, but often also occur secondary brain injury. Inflammation is a process that occurs immediately after trauma characterized by activation of the mediator substance. TNF-α is a major cytokinee involved in the inflammatory processes that have adverse effects if the serum level are excessive. There needs to be a balance of the inflammatory process in the brain injury so things that harm does not occur. As anti-inflammatory IL-10 plays an important role in maintaining the balance. The objective of this study is to determine the effect of IL-10 intervention as an anti-inflammatory will decrease the serum level of TNF-α in traumatic brain injury. Material And Method: Experimental Study in the Rattus Wistar ?rats, post test control group design, male, aged 3-4 months, with body weight (BW) 300-400g, were obtained from the Laboratory Animal Faculty of Medicine, University of Hasanuddin as much as 24 tails, which is the result of breeding. Subjects were divided into four groups, each group of six rats, treated with controlled cortical impact model (Feeney’s weight-drop) of traumatic brain injury. Blood taken with capillary tube in retro-orbita plexus or sinus.This study has approved by ethical clearance for research. Results: Levels of TNF-α group of rats 1 hour post-trauma without administration of recombinant IL-10 (28.58 ± 7.28) pg / mL; was significantly higher (p <0.05) than the levels of TNF-α rats without kraniektomi group (22.06 ± 3.34) pg / mL and group kraniektomi rats without brain injury (23.07 ± 2.51) pg / mL. Levels of TNF-α group of rats 1 hour post-trauma by administration of recombinant IL-10 (23.39 ± 6.30) pg / mL; significantly lower (p 0.05) in the group without craniectomy or craniectomy group without head injury. Conclusions: ?Intervention of recombinant IL-10 decreases levels of TNF-α serum soon after traumatic brain injury in rats.
机译:背景:脑损伤不仅经常发生于原发性脑损伤,而且还经常发生于继发性脑损伤。炎症是在创伤后立即发生的过程,其特征在于介质物质的活化。 TNF-α是参与炎症过程的主要细胞因子,如果血清水平过高,则会产生不利影响。脑损伤中需要平衡炎症过程,以免发生伤害。由于抗炎性IL-10在维持平衡中起着重要作用。这项研究的目的是确定IL-10干预的效果,因为抗炎剂会降低颅脑外伤后血清TNF-α的水平。材料和方法:在Rattus Wistar大鼠上进行的实验研究,试验后对照组的设计,男性,年龄3-4个月,体重(BW)300-400g,来自Hasanuddin大学的实验动物医学院多达24条尾巴,这是繁殖的结果。将受试者分为四组,每组六只大鼠,分别用创伤性脑损伤的受控皮质撞击模型(Feeney的体重减轻)进行治疗。眼眶后神经丛或鼻窦毛细血管抽取的血液。这项研究已获伦理学许可进行研究。结果:创伤后1小时未给予重组IL-10(28.58±7.28)pg / mL的大鼠TNF-α水平;明显高于没有kraniektomi组的TNF-α大鼠(22.06±3.34)pg / mL和没有脑损伤的kraniektomi组(23.07±2.51)pg / mL(p <0.05)。创伤后1小时通过给予重组IL-10(23.39±6.30)pg / mL,使大鼠TNF-α水平升高;不进行颅骨切除术的组或未发生颅脑损伤的颅骨切除术组的患病率显着降低(p 0.05)。结论:?重组IL-10的干预可在大鼠脑外伤后立即降低TNF-α血清水平。

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