氨甲环酸对大鼠椎板切除术后硬膜外纤维化的剂量依赖性实验研究。

Alican Baris, Esra Circi, Emre Ozmen, Hazal Izol Ozmen, Serdar Yuksel, Ozan Beytemur
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引用次数: 0

摘要

目的:本研究旨在评估氨甲环酸(TXA)在大鼠椎板切除术模型中预防硬膜外纤维化的剂量依赖性效果,并探讨其作为脊髓手术术后纤维化治疗干预措施的潜力。方法:将32只雌性Wistar-Albino大鼠随机分为4组(对照组、10 mg/kg TXA、30 mg/kg TXA、100 mg/kg TXA);N =8 /组)。在标准化椎板切除术后,术前通过尾静脉静脉给予TXA作为负荷剂量。术后第4周处死大鼠,整体切除腰椎,组织学观察硬膜外纤维化、炎症细胞密度、成纤维细胞密度。结果:与对照组(p=0.004)、10 mg/kg (p=0.002)和30 mg/kg TXA组(p=0.03)相比,高剂量TXA (100 mg/kg)显著减少硬膜外纤维化。虽然与对照组相比,30 mg/kg组的硬膜外纤维化等级较低,但差异无统计学意义。各组间炎症细胞或成纤维细胞密度无显著差异。结论:大剂量TXA (100 mg/kg)以剂量依赖的方式有效减少硬膜外纤维化,显示出作为改善脊柱手术术后预后的全身治疗选择的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The dose-dependent effect of tranexamic acid on epidural fibrosis after laminectomy: an experimental study on rats.

Objective: This study aimed to evaluate the dose-dependent efficacy of tranexamic acid (TXA) in preventing epidural fibrosis in a rat laminectomy model and explore its potential as a therapeutic intervention for postoperative fibrosis in spinal surgery. Methods: In this experimental animal study, 32 female Wistar-Albino rats were randomized into four groups (control, 10 mg/kg TXA, 30 mg/kg TXA, and 100 mg/kg TXA; n=8 per group). Following a standardized laminectomy procedure, TXA was administered intravenously as a loading dose through the tail vein prior to surgery. The rats were sacrificed at the 4th-week post-surgery, the lumbar vertebrae were excised en bloc, and epidural fibrosis, inflammatory cell density, and fibroblast density were assessed histologically. Results: High-dose TXA (100 mg/kg) significantly reduced epidural fibrosis compared to the control (p=0.004), 10 mg/kg (p=0.002), and 30 mg/kg TXA groups (p=0.03). While the 30 mg/kg group showed lower epidural fibrosis grades compared to the control, the difference was not statistically significant. No significant differences were observed in inflammatory or fibroblast densities across groups. Conclusion: High-dose TXA (100 mg/kg) effectively reduced epidural fibrosis in a dose-dependent manner, demonstrating potential as a systemic therapeutic option to improve postoperative outcomes in spinal surgery.

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