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组织因子途径抑制剂可保护缺血性脊髓。

Tissue factor pathway inhibitor protects the ischemic spinal cord.

作者信息

Koudsi B, Chatman D M, Ballinger B A, Ferguson E W, Kraemer B A, Miller G A, Wun T C, Farr G, Money S R

机构信息

Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Surg Res. 1996 Jun;63(1):174-8. doi: 10.1006/jsre.1996.0243.

Abstract

Tissue factor pathway inhibitor (TFPI) is a novel agent that binds to tissue factor/VIIa complex and factor-Xa, thereby reducing the effect of tissue factor (TF) on inflammation and the extrinsic pathway of coagulation. We hypothesize that systemic treatment with TFPI may limit ischemia-reperfusion (IR) injury. Our experiment was designed to evaluate the effects of TFPI on IR in the spinal cord. Twenty-three adult New Zealand white rabbits had snare occlusion devices placed circumferentially around the aorta and tunneled to a subcutaneous position. Forty-eight hours later, in the fully awake state, the animals were treated with either TFPI (1 mg/kg bolus followed by a 1-hr infusion of 20 microgram/kg/min), or heparin (100 U/kg bolus) followed by a 1-hr infusion of 10 ml/kg/hr of PBS while controls received phosphate buffered saline (20 ml followed by a 1-hr infusion of 10 ml/kg/hr). The infrarenal aorta was occluded for 21 min in all groups via the snare device. Animals were observed for 3 days and neurologic recovery was graded by the Tarlov criteria. Results were evaluated as percent of animals with hindlimb recovery (Tarlov 3 and 4). At 24 hr postocclusion, 88% of the TFPI-treated animals had recovered neurologic function versus only 20% of heparin-treated animals and 10% of the phosphate buffered saline group (P=0.031 and 0.009, respectively). At 72 hr, 63% of the TFPI animals retained neurologic function versus 20% of heparin-treated animals and 10% of phosphate buffered saline-treated animals (P=0.032, TFPI versus phosphate buffered saline). The mechanism of action of TFPI is not completely understood, yet this drug may hold promise in the prevention of IR injury of the spinal cord.

摘要

组织因子途径抑制剂(TFPI)是一种新型药物,它可与组织因子/Ⅶa复合物及因子Ⅹa结合,从而降低组织因子(TF)对炎症及凝血外源性途径的作用。我们推测,TFPI全身治疗可能会限制缺血再灌注(IR)损伤。我们设计了本实验来评估TFPI对脊髓IR的影响。23只成年新西兰白兔在主动脉周围环形放置圈套闭塞装置,并将其引入皮下位置。48小时后,在完全清醒状态下,动物分别接受TFPI(1mg/kg静脉推注,随后以20μg/kg/min的速度输注1小时)或肝素(100U/kg静脉推注),随后以10ml/kg/hr的速度输注1小时的PBS,而对照组接受磷酸盐缓冲盐水(20ml,随后以10ml/kg/hr的速度输注1小时)。所有组均通过圈套装置将肾下主动脉闭塞21分钟。观察动物3天,并根据塔尔洛夫标准对神经功能恢复情况进行分级。结果以出现后肢恢复(塔尔洛夫3级和4级)的动物百分比来评估。闭塞后24小时,接受TFPI治疗的动物中有88%恢复了神经功能,而接受肝素治疗的动物仅为20%,磷酸盐缓冲盐水组为10%(P分别为0.031和0.009)。72小时时,63%接受TFPI治疗的动物保留了神经功能,而接受肝素治疗的动物为20%,接受磷酸盐缓冲盐水治疗的动物为10%(TFPI与磷酸盐缓冲盐水相比,P = 0.032)。TFPI的作用机制尚未完全明确,但这种药物在预防脊髓IR损伤方面可能具有前景。

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