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考克斯-2选择性抑制剂帕瑞昔布对大鼠脊髓损伤影响的研究

The Investigation of the Cox-2 Selective Inhibitor Parecoxib Effects in Spinal Cord Injury in Rat.

作者信息

Yuksel Ulas, Bakar Bulent, Dincel Gungor Cagdas, Budak Yildiran Fatma Azize, Ogden Mustafa, Kisa Ucler

机构信息

a Department of Neurosurgery, Sanliurfa Training and Research Hospital , Sanliurfa , Turkey.

b Department of Neurosurgery, Faculty of Medicine, Kirikkale University , Kirikkale , Turkey.

出版信息

J Invest Surg. 2019 Aug;32(5):402-413. doi: 10.1080/08941939.2017.1423423. Epub 2018 Jan 22.

DOI:10.1080/08941939.2017.1423423
PMID:29355394
Abstract

: Today, spinal cord injury (SCI) can be rehabilitated but cannot be treated adequately. This experimental study was conducted to investigate possible beneficial effects of methylprednisolone and parecoxib in treatment of SCI. : Forty-eight male Wistar albino rats were assigned into CONTROL, acute (MP-A, PX-A, and PXMP-A), and subacute (MP-S, PX-S, and PXMP-S) stage groups. Then, to induce SCI, a temporary aneurysm clip was applied to the spinal cord following T7-8 laminectomy, except in the CONTROL group. Four hours later parecoxib, methylprednisolone, or their combination was administered to rats intraperitoneally except CONTROL, SHAM-A, and SHAM-S groups. Rats in the acute stage group were sacrificed 72 h later, and whereas rats in the subacute stage were sacrificed 7 days later for histopathological and biochemical investigation and for gene-expression analyses. : Parecoxib and methylprednisolone and their combination could not improve histopathological grades in any stage. They also could not decrease malondialdehyde or caspase-3, myeloperoxidase levels in any stage. Parecoxib and methylprednisolone could decrease the TNF-α gene expression in subacute stage. Methylprednisolone could increase TGF-1β gene-expression level in acute stage. : Neither of the experimental drugs, either alone or in combination, did not show any beneficial effects in SCI model in rats.

摘要

如今,脊髓损伤(SCI)虽可康复但无法得到充分治疗。本实验研究旨在探讨甲基强的松龙和帕瑞昔布在治疗脊髓损伤方面可能的有益作用。

48只雄性Wistar白化大鼠被分为对照组、急性阶段组(MP - A、PX - A和PXMP - A)以及亚急性阶段组(MP - S、PX - S和PXMP - S)。然后,除对照组外,在T7 - 8椎板切除术后,用临时动脉瘤夹夹闭脊髓以诱导脊髓损伤。4小时后,除对照组、假手术急性组(SHAM - A)和假手术亚急性组(SHAM - S)外,给大鼠腹腔注射帕瑞昔布、甲基强的松龙或它们的组合。急性阶段组的大鼠在72小时后处死,而亚急性阶段的大鼠在7天后处死,用于组织病理学和生化研究以及基因表达分析。

帕瑞昔布、甲基强的松龙及其组合在任何阶段均不能改善组织病理学分级。它们在任何阶段也不能降低丙二醛、半胱天冬酶 - 3、髓过氧化物酶水平。帕瑞昔布和甲基强的松龙可降低亚急性阶段肿瘤坏死因子 - α(TNF - α)的基因表达。甲基强的松龙可提高急性阶段转化生长因子 - 1β(TGF - Ⅰβ)的基因表达水平。

无论是单独使用还是联合使用,这两种实验药物在大鼠脊髓损伤模型中均未显示出任何有益作用。

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