支持细胞移植后缺血大鼠脑中凋亡蛋白的表达降低。

IF 1.4 4区 医学 Q4 NEUROSCIENCES
Nadia Khoshbaf Khiabanian, M. Bigdeli, S. Khaksar, A. Aliaghaei
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引用次数: 0

摘要

支持细胞(SCs)可能是减少缺血性损伤的新候选细胞,因为它们能够分泌积极保护神经元和抑制不可控制的免疫反应的因子。本研究考虑了用这些细胞进行预处理。利用立体定向技术将SCs注入大鼠右侧纹状体。注射后10天行大脑中动脉闭塞手术。按照这些程序,评估神经功能缺损评分、脑水肿、血脑屏障完整性、梗死体积以及皮层、纹状体和梨状皮质-杏仁核中凋亡因子的表达。分析表明,与对照组相比,同种异体移植物组的行为缺陷、梗死面积、血脑屏障通透性和纹状体区水肿均显著降低。此外,分析纹状体中caspase - 3和Bcl - 2蛋白的表达表明,与对照组相比,同种异体移植物组的caspase - 3和Bcl - 2蛋白的表达分别显著减少和增加。根据所获得的结果,SCs在缺血性脑中诱导神经保护的一种可能机制是减少凋亡因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced expression of apoptotic proteins in the ischemic rat brain following Sertoli cell transplantation.
Sertoli cells (SCs) may be a new candidate to decrease ischemic damage due to their ability to secrete factors that actively protect neurons and inhibit uncontrollable immune responses. Pre‑treatment with these cells was considered in the current study. SCs were injected into the right striatum in rats using the stereotaxic technique. Ten days after injection, middle cerebral artery occlusion surgery was performed. Following these procedures, neurological deficit scores, brain edema, blood‑brain barrier integrity, infarct volume, and the expression of apoptotic factors in the cortex, striatum, and piriform cortex‑amygdala were evaluated. Analysis showed that behavioral deficits, infarct volume, blood‑brain barrier permeability, and edema in the striatal area in the allograft group demonstrated a significant decrease compared to the control group. Additionally, analysis of the expression of caspase‑3 and Bcl‑2 proteins in the striatum indicated a remarkable reduction and increase, respectively, in the allograft group compared to the control group. According to the obtained results, one possible mechanism for the neuroprotection induced by SCs in an ischemic brain is the reduction of apoptotic factors.
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来源期刊
CiteScore
2.20
自引率
7.10%
发文量
40
审稿时长
>12 weeks
期刊介绍: Acta Neurobiologiae Experimentalis (ISSN: 0065-1400 (print), eISSN: 1689-0035) covers all aspects of neuroscience, from molecular and cellular neurobiology of the nervous system, through cellular and systems electrophysiology, brain imaging, functional and comparative neuroanatomy, development and evolution of the nervous system, behavior and neuropsychology to brain aging and pathology, including neuroinformatics and modeling.
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