Conditioned Medium Derived from the Human Amniotic Membrane Prevents Brain Damage against Cerebral Ischemia/Reperfusion in Three Phases, Subacute, Acute, and Chronic in a Stroke Model in Rats

Seyyed Mohammad Taghi Razavi-Toosi, Yasin Asadi, N. Aboutaleb, Masoumeh Faezi
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Abstract

Introduction: Stem cells isolated from amniotic membrane can produce and freedom substances that have the ability to regenerate damaged tissues and contain proteins and other factors that apply via numerous major and minor mechanisms leading to increasing angiogenesis and tissue survival. The research was conducted to prove the defensive characteristics of the secretome in the face of temporary focal cerebral ischemia in mouse stroke models. Methods: Cerebral ischemia protocol in a specific area was implemented in rats with middle cerebral artery occlusion for 60 minutes and then reperfusion was given for 6, 20 and 30 minutes. Within 30 minutes after the start of reperfusion, conditioned medium derived from human amniotic membrane (AMSC-CM) was poured into the right ventricle (ICV) with a dose of 0.5 microliters. Finally, the volume of the injury, cerebral tissue water, sensorimotor activity and the strength of the blood-brain barrier integrity were evaluated 24 hours after drug injection. Results: ICV injection of conditioned medium at the start of reperfusion phase considerably decrease the volume of the injury in 6, 20, and 30 hours after reperfusion compared MCAO operated group (p < 0.01), cerebral tissue water in the treatment group decreased considerably after intervention in comparison with the MCAO group in core and penumbral area not in the subcortical area (p < 0.05), Also, the Evans Blue penetration rate in all times in the core and penumbral area in AMSC-CM group considerably decreased paralleled with the MCAO group (p < 0.05). Conclusion: The results show that treatment with AMSC-CM during 6-30 h after ischemia-reperfusion insult exerts some beneficial effects against ischemia-reperfusion injury. These findings provide an important vision for more complementary research and treatment of stroke.
从人羊膜中提取的条件培养基可在亚急性、急性和慢性三个阶段预防脑缺血/再灌注对大鼠中风模型造成的脑损伤
导言:从羊膜中分离出的干细胞可产生和自由释放具有再生受损组织能力的物质,其中含有的蛋白质和其他因子可通过许多主要和次要机制应用于增加血管生成和组织存活。本研究旨在证明在小鼠中风模型中,分泌组在面对暂时性局灶性脑缺血时的防御特性。研究方法对特定区域的大鼠实施脑缺血方案,大脑中动脉闭塞 60 分钟,然后再灌注 6、20 和 30 分钟。再灌注开始后 30 分钟内,向右心室注入 0.5 微升的人羊膜条件培养基(AMSC-CM)。最后,在注射药物 24 小时后评估损伤体积、脑组织水分、感觉运动活动和血脑屏障完整性的强度。结果与 MCAO 手术组相比,再灌注开始时 ICV 注射条件培养基可显著减少再灌注后 6、20 和 30 小时的损伤体积(P < 0.01),与 MCAO 组相比,治疗组干预后核心区和半影区的脑组织水分显著减少,而皮层下区没有减少(P < 0.05),而且 AMSC-CM 组核心区和半影区各时间段的 Evans Blue 穿透率与 MCAO 组相比显著下降(P < 0.05)。结论结果表明,缺血再灌注损伤后6-30小时内使用AMSC-CM治疗对缺血再灌注损伤有一定的益处。这些发现为脑卒中的辅助研究和治疗提供了重要的远景。
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