首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Effects of iloprost on vasospasm after experimental spinal cord injury: an electron and light microscopic study.
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Effects of iloprost on vasospasm after experimental spinal cord injury: an electron and light microscopic study.

机译:伊洛前列素对实验性脊髓损伤后血管痉挛的影响:电子和光显微镜研究。

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摘要

It has been increasingly reported that traumatic and ischemic insults to the spinal cord may produce tissue damage through both direct and indirect mechanisms. In spite of many theories about post-traumatic spinal cord injury, there is still no satisfactory account of the exact mechanism. Vasospasm may be related to the trauma and release of vasoconstrictor or vasoactive amines. This study aims at studying the possible protective mechanisms of iloprost, a stable analogue of prostacyclin, after spinal cord injury on the rabbit. Forty-two adult male rabbits (New Zealand albino) were inflicted injuries by epidural application of an aneurysm clip to the spinal cord. Twenty-one rabbits received an i.v. infusion of 25 microg kg(-1) x h(-1) iloprost. The remaining twenty-one rabbits received an i.v. infusion of saline as the control group. Intravenous treatment started immediately after the infliction of the spinal cord injury and lasted for 1 h. Iloprost treatment had no side effects on the general physiological parameters in the rabbits. Control and iloprost treatment groups were divided into three sub-groups. The first group of animals was deeply anesthetized and spinal cords were removed 15 min after treatment. Second and third group animals were sacrificed in the 3rd and 24th hours respectively. All spinal cords were removed for light and electron microscopic examination. The width of anteriolar smooth muscle cells and the ultrastructural analysis of sulcal arterioles and venules in the ventral median fissure of spinal cords treated by iloprost revealed less thickening in all groups especially on the 24th hour group (p < 0.01), but less thickening was observed on the 3rd hour group. Iloprost-treated groups had limited edema and moderate protection of myelin and axons. These results suggest that iloprost treatment after spinal cord injury has a highly protective effect, and the possible protective effect of iloprost is resolution of vasospasm due to spinal cord injury.
机译:越来越多的报道称,脊髓的创伤性和缺血性损伤可能通过直接和间接机制产生组织损伤。尽管有许多关于创伤后脊髓损伤的理论,但仍然没有令人满意的确切机制。血管痉挛可能与血管收缩剂或血管活性胺的创伤和释放有关。本研究旨在研究伊洛前列素(一种前列环素的稳定类似物)在兔子脊髓损伤后的可能保护机制。42 只成年雄性兔子(新西兰白化病兔)因硬膜外应用动脉瘤夹到脊髓而受伤。21 只兔子接受静脉输注 25 μg kg(-1) x h(-1) 伊洛前列素。其余21只兔子作为对照组接受静脉输注生理盐水。脊髓损伤后立即开始静脉治疗,持续1小时。伊洛前列素治疗对兔子的一般生理参数没有副作用。对照组和伊洛前列素治疗组分为三个亚组。第一组动物深度麻醉,治疗后15分钟切除脊髓。第二组和第三组动物分别在第 3 小时和第 24 小时处死。取出所有脊髓进行光学和电子显微镜检查。伊洛前列素治疗脊髓腹正中裂前平滑肌细胞的宽度和脑沟小动脉和小静脉的超微结构分析显示,所有组的增厚程度均较低,尤其是第 24 小时组 (p < 0.01),但第 3 小时组观察到的增厚较少。伊洛前列素治疗组的水肿有限,髓鞘和轴突保护中度。这些结果表明,脊髓损伤后伊洛前列素治疗具有高度的保护作用,伊洛前列素可能的保护作用是缓解脊髓损伤引起的血管痉挛。

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