Department of Radiation Medicine, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA.
J Neurol Sci. 2011 Jul 15;306(1-2):143-53. doi: 10.1016/j.jns.2011.02.034. Epub 2011 Apr 8.
Studies have shown that aging is a significant factor in worsening stroke outcomes. While many mechanisms may aggravate brain injury in the elderly, one such potential system may involve increased glial proliferation in the aged stroke patient that could result in increased scar formation. We hypothesized that in aged rats a single brain-only exposure to a low radiation dose prior to focal brain ischemia would reduce glial proliferation and confer a long-term neuroprotective effect.
Brain-only proton irradiation (8 Gy) was performed ten days prior to middle cerebral artery occlusion (MCAO) in aged male rats. Magnetic resonance imaging (MRI) was undertaken in naive, radiation-only (Rad), MCAO, and MCAO+Rad groups at 2, 14 and 28 days post-stroke followed by immunohistochemistry (day 28).
Ischemic lesion volume in MCAO+Rad group was decreased by 50.7% with an accelerated temporal reduction in peri-lesional brain edema and increased water mobility within the ischemic core (39.8%) compared to MCAO-only rats. In the peri-lesional brain region of MCAO+Rad rats there was a decreased scar formation (49%, glial fibrillary acidic protein), brain tissue sclerosis (30%, aquaporin-4) and necrosis/apoptosis (58%, TUNEL positive cells) compared to those in MCAO animals.
In aged animals a single exposure to brain-only radiation prior to focal cerebral ischemia is neuroprotective as it prevents glial hyperproliferation, progressive brain tissue sclerosis and reduces the apoptosis/necrosis in the peri-lesional region. Decreased lesion volume is in agreement with accelerated reduction of brain edema in these animals.
研究表明,衰老也是导致中风预后恶化的重要因素。虽然许多机制可能导致老年中风患者的脑损伤加重,但其中一个潜在的系统可能涉及衰老中风患者中神经胶质细胞的过度增殖,从而导致疤痕形成增加。我们假设,在老年大鼠中,在局灶性脑缺血前单次接受低剂量脑部照射,可减少神经胶质细胞的增殖,并产生长期的神经保护作用。
在老年雄性大鼠大脑中动脉闭塞(MCAO)前 10 天进行脑部质子照射(8Gy)。在中风后 2、14 和 28 天,对未照射、单纯照射(Rad)、MCAO 和 MCAO+Rad 组的大鼠进行磁共振成像(MRI)检查,然后进行免疫组织化学检查(第 28 天)。
与单纯 MCAO 组大鼠相比,MCAO+Rad 组的缺血性病灶体积减少了 50.7%,并加速了缺血周边脑水肿的消退和缺血核心内的水流动性增加(39.8%)。在 MCAO+Rad 大鼠的缺血周边脑区,与 MCAO 大鼠相比,疤痕形成减少(49%,胶质纤维酸性蛋白)、脑组织硬化减少(30%,水通道蛋白-4)和坏死/凋亡减少(58%,TUNEL 阳性细胞)。
在老年动物中,在局灶性脑缺血前单次接受脑部照射具有神经保护作用,因为它可防止神经胶质细胞过度增殖、进行性脑组织硬化,并减少缺血周边区的细胞凋亡/坏死。病灶体积的减少与这些动物脑水肿的加速消退一致。