Department of Neuroscience, School of Advanced Technologies, Tehran University of Medical Sciences, Tehran, Iran.
Department of Neuroscience, School of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Exp Physiol. 2020 Sep;105(9):1610-1622. doi: 10.1113/EP088697. Epub 2020 Jul 31.
What is the central question of this study? Can the neuroprotective agent curcumin affect restorative action of neural stem/progenitor cells in the injured rat brain? What is the main finding and its importance? In the presence of curcumin, transplantation of neural stem/progenitor cells in the context of PuraMatrix reduced lesion size and reactive inflammatory responses, and boosted survival rate of grafted neurons. In addition it improved the neurological status of injured animals. This could be beneficial in designing new therapeutic approaches for brain injury based on this combination therapy.
Traumatic brain injury (TBI) is catastrophic neurological damage associated with substantial morbidity and mortality. To date, there is no specific treatment for restoring lost brain tissue. In light of the complex pathology of brain injury, the present study evaluated the effects of combination therapy using autologous neural stem/progenitor cells (NS/PCs), PuraMatrix (PM) and curcumin in an animal model of brain injury. After stereotactic biopsy of subventricular zone tissue and culture of NS/PCs, 36 male Wistar rats (150-200 g) were randomly divided into six groups receiving dimethyl sulfoxide (DMSO), curcumin (100 mg kg in DMSO), PM + curcumin (100 mg kg in DMSO), NS/PCs + curcumin (100 mg kg in DMSO), NS/PCs + PM + curcumin (100 mg kg in DMSO) and NS/PCs + PM + curcumin (1 µm) following acute brain injury. The animals were evaluated in term of neurological status for 4 weeks, then decapitated. Nissl and TUNEL staining and immunohistochemistry for bromodeoxyuridine, glial fibrillary acidic protein, doublecortin, Map2, Olig2, Iba1 and CD68 were performed. We found that combination therapy by NS/PCs + PM + curcumin reduced the lesion size, astrogliosis, macrophage and microglial reaction as well as the number of apoptotic cells. Moreover, the transplanted cells were able to survive and differentiate after 4 weeks. Besides these findings, transplantation of NS/PCs in the context of PM and curcumin improved the neurological status of injured animals. In conclusion, our data suggest that this combination therapy can be beneficial in developing future therapeutic approaches for brain injury.
本研究的核心问题是什么?神经保护剂姜黄素是否会影响损伤大鼠大脑中神经干细胞/祖细胞的修复作用?主要发现及其重要性是什么?在姜黄素存在的情况下,神经干细胞/祖细胞在 PuraMatrix 中的移植减少了损伤大小和反应性炎症反应,并提高了移植神经元的存活率。此外,它改善了受伤动物的神经状态。这可能有益于基于这种联合治疗方法设计新的治疗脑损伤的方法。
创伤性脑损伤 (TBI) 是一种与大量发病率和死亡率相关的灾难性神经损伤。迄今为止,尚无恢复丢失的脑组织的特定治疗方法。鉴于脑损伤的复杂病理学,本研究在动物脑损伤模型中评估了使用自体神经干细胞/祖细胞 (NS/PCs)、PuraMatrix (PM) 和姜黄素联合治疗的效果。在立体定向侧脑室组织活检和 NS/PC 培养后,36 只雄性 Wistar 大鼠(150-200g)被随机分为六组,分别接受二甲基亚砜 (DMSO)、姜黄素(DMSO 中的 100mg/kg)、PM+姜黄素(DMSO 中的 100mg/kg)、NS/PCs+姜黄素(DMSO 中的 100mg/kg)、NS/PCs+PM+姜黄素(DMSO 中的 100mg/kg)和 NS/PCs+PM+姜黄素(1μm)。在急性脑损伤后 4 周内,通过神经状态评估动物,然后断头。进行尼氏染色和 TUNEL 染色以及溴脱氧尿苷、胶质纤维酸性蛋白、双皮质素、Map2、Olig2、Iba1 和 CD68 的免疫组织化学染色。我们发现,NS/PCs+PM+姜黄素联合治疗可减少损伤大小、星形胶质细胞增生、小胶质细胞和巨噬细胞反应以及细胞凋亡数量。此外,移植细胞在 4 周后仍能存活和分化。除了这些发现之外,PM 和姜黄素背景下的 NS/PCs 移植还改善了受伤动物的神经状态。总之,我们的数据表明,这种联合治疗方法可能有益于开发治疗脑损伤的新方法。