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肿瘤坏死因子α阻滞剂阿达木单抗在实验性脊髓损伤中的作用

Effects of tumor necrosis factor alpha blocker adalimumab in experimental spinal cord injury.

作者信息

Börcek Alp Özgün, Çivi Soner, Öcal Özgür, Gülbahar Özlem

机构信息

Department of Neurosurgery, Gazi University Faculty of Medicine, Ankara, Turkey.

Department of Neurosurgery, Medicana Private Hospital, Konya, Turkey.

出版信息

J Korean Neurosurg Soc. 2015 Feb;57(2):73-6. doi: 10.3340/jkns.2015.57.2.73. Epub 2015 Feb 26.

Abstract

OBJECTIVE

Tumor necrosis factor alpha (TNF-α) have proven effects in pathogenesis of neuroinflammation after spinal cord injury (SCI). Current study is designed to evaluate the effects of an anti-TNF-α agent, adalimumab, on spinal cord clip compression injury in rats.

METHODS

Thirty two male adult Wistar rats were divided into four groups (sham, trauma, infliximab, and adalimumab groups) and SCI was introduced using an aneurysm clip. Animals in treatment groups received 5 mg/kg subcutaneous adalimumab and infliximab right after the trauma. Malondialdehyde (MDA) levels were studied in traumatized spinal cord tissues 72 hours after the injury as a marker of lipid peroxidation.

RESULTS

Animals that received anti-TNF-α agents are found to have significantly decreased MDA levels. MDA levels were significantly different between the trauma and infliximab groups (p<0.01) and trauma and adalimumab groups (p=0.022). There was no significant difference in neurological evaluation of the rats using Tarlov scale.

CONCLUSION

These results suggest that, like infliximab, adalimumab has favorable effects on lipid peroxidation induced by spinal cord trauma in rats.

摘要

目的

肿瘤坏死因子α(TNF-α)已被证实在脊髓损伤(SCI)后神经炎症的发病机制中起作用。本研究旨在评估抗TNF-α药物阿达木单抗对大鼠脊髓夹闭压迫损伤的影响。

方法

将32只成年雄性Wistar大鼠分为四组(假手术组、创伤组、英夫利昔单抗组和阿达木单抗组),使用动脉瘤夹造成脊髓损伤。治疗组动物在创伤后立即皮下注射5mg/kg阿达木单抗和英夫利昔单抗。在损伤后72小时,研究创伤脊髓组织中的丙二醛(MDA)水平,作为脂质过氧化的标志物。

结果

发现接受抗TNF-α药物的动物MDA水平显著降低。创伤组与英夫利昔单抗组(p<0.01)以及创伤组与阿达木单抗组(p=0.022)之间的MDA水平存在显著差异。使用Tarlov量表对大鼠进行神经学评估时没有显著差异。

结论

这些结果表明,与英夫利昔单抗一样,阿达木单抗对大鼠脊髓创伤诱导的脂质过氧化具有有利影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8186/4345196/bbfae605ff9a/jkns-57-73-g001.jpg

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