bFGF对大鼠脑出血病灶周边脑组织细胞凋亡的影响及机制初探
The Influence and Regulatory Mechanism of the Basic Fibroblast Growth Factor (bFGF) on the Apoptosis of Nerve Cells Surrounding Intracerebral Hemorrhage (ICH) in Rat
DOI: 10.12677/JPS.2019.72002, PDF,    科研立项经费支持
作者: 于奎营*, 张 涛*, 徐 迎*, 荀红霞:淄博市第一医院神经内一科,山东 淄博
关键词: 碱性成纤维细胞生长因子脑出血p-AKT (Ser473)细胞凋亡 Basic Fibreglass Growth Factor Hemorrhage p-AKT (Ser473) Apoptosis
摘要: 目的:观察碱性成纤维细胞生长因子(basic fibreglass growth factor, bFGF)对大鼠脑出血周边脑组织神经细胞凋亡的影响,并进行相关机制的初步探讨,为进一步深入了解bFGF对脑出血后神经细胞的保护机制的研究奠定基础。方法:通过脑内定位注射胶原酶,建立大鼠脑出血模型;使用假手术组和出血模型组作为对照,采用Zea Longa 5分制评分法对术后大鼠神经功能进行评价,出血模型建立成功的大鼠又分为对照组和bFGF治疗组,bFGF治疗组按8 ug/kg剂量肌内注射;各组分别于术给药后48小时取血肿旁大脑皮质,TUNEL法检测细胞凋亡数目,免疫组化检测p-AKT表达,并对结果进行统计分析。结果:大鼠脑出血模型构建成功;bFGF治疗组与对照组相比,Zea Longa评分显著降低,血肿旁大脑皮质凋亡细胞数量减少,p-AKT表达增高(P < 0.05)。结论:bFGF对大鼠脑出血后周边脑组织具有保护作用,其可能机制是通过提高大鼠脑出血周边脑组织p-AKT的表达来减少神经细胞凋亡数量,从而对脑出血后脑损伤具有保护作用实现。
Abstract: Objective: To study the influence and regulatory mechanism of the basic fibroblast growth factor (bFGF) on the apoptosis of nerve cells surrounding intracerebral hemorrhage (ICH) in Rat. Methods: The rat model of experimental ICH was established by injection of collagenase VII into internal capsule of cerebrum. Then bFGF treatment group was injected with bFGF 8 vg/kg. After 48 h of treatment, we detected apoptosis of the cerebral cortex near the hematoma by TUNEL, and the phosphorylation level of AKT by immunohistochemistry. Results: Compared with control group, the apoptosis cells surrounding intracerebral hemorrhage of bFGF treatment group were decreased, and the phosphorylation level of AKT was enhanced (P < 0.05). According to Zea Longa method, the neurological score was decreased in the bFGF treatment group. Conclusion: bFGF could enhance the AKT phosphorylation level and reduce apoptosis of the cells surrounding intracerebral hemorrhage.
文章引用:于奎营, 张涛, 徐迎, 荀红霞. bFGF对大鼠脑出血病灶周边脑组织细胞凋亡的影响及机制初探[J]. 生理学研究, 2019, 7(2): 7-12. https://doi.org/10.12677/JPS.2019.72002

参考文献

[1] Tsai, C.F., Thomas, B. and Sudlow, C.L. (2013) Epidemiology of Stroke and Its Subtypes in Chinese vs. White Popu-lations. A Systematic Review. Neurology, 81, 264-272. [Google Scholar] [CrossRef
[2] Fruman, D.A. and Rommel, C. (2014) PI3K and Cancer: Lessons, Challenges and Opportunities. Nature Reviews Drug Discovery, 13, 140-156. [Google Scholar] [CrossRef] [PubMed]
[3] Sarkaki, A., Raieirad, M., Hossini, S.E., et al. (2013) Improvement in Memory and Brain Long-Term Potentiation Deficits Due to Permanent Hypoperfusion/Ischemia by Grape Seed Extract in Rats. Iranian Journal of Basic Medical Sciences, 16, 1004-1010.
[4] 李倩茗, 黄俊杰. bFGF对大鼠脑出血血肿周围组织SOD活力, MDA含量和Bax, Bcl-2基因表达的影响[J]. 中国实用神经病学杂志, 2008, 11(12): 7-9.
[5] Wakai, T., Sakata, H., Narasimhan, P., et al. (2014) Transplantation of Neural Stem Cells That Overexpress SOD1 Enhances Amelioration of Intracerebral Hemorrhage in Mice. Journal of Cerebral Blood Flow & Metabolism, 34, 441-449. [Google Scholar] [CrossRef] [PubMed]
[6] Yang, C.M., Hsieh, H.L., Lin, C.C., et al. (2013) Multiple Factors from Bradykinin Challenged Astrocytes Contribute to the Neuronal Apoptosis: Involvement of Astroglial ROS, MMP-9, and HOl/CO System. Molecular Neurobiology, 47, 1020-1033. [Google Scholar] [CrossRef] [PubMed]
[7] Wang, J., Wang, P., Li, S., et al. (2014) Multiple Factors from Bradykinin-Challenged Astrocytes Contribute to the Neuronal Apoptosis: Involvement of Astroglial ROS, MMP-9, and HO-1/CO System. Journal of Stroke and Cerebrovascular Diseases, 23, 1491-1499. [Google Scholar] [CrossRef] [PubMed]
[8] Chua, C.C., Rahimi, N., Forsten-Wilhams, K., et al. (2004) Heparan Sulfate Proteoglycans Function as Receptors for Fibroblast Growth Factor-2 Activation of Extracellular Signal-Regulated Kinases 1 and 2. Circulation Research, 94, 316-323. [Google Scholar] [CrossRef