Beom Jaewon, Kim Won, Han Tai Ryoon, Seo Kwan-Sik, Oh Byung-Mo
Department of Rehabilitation Medicine, Chungnam National University Hospital, Daejeon, 301-721, Republic of Korea.
Neurol Sci. 2015 May;36(5):771-7. doi: 10.1007/s10072-014-2046-4. Epub 2014 Dec 21.
We investigated the additive effect of repetitive transcranial magnetic stimulation (rTMS) combined with granulocyte-colony stimulating factor (G-CSF) on functional outcome in the early subacute phase of stroke. Seven-week-old male rats were subjected to permanent middle cerebral artery occlusion (MCAo) and were divided into four groups: normal saline administration with sham rTMS (group 1, n = 15), G-CSF administration with sham rTMS (group 2, n = 15), G-CSF with 1 Hz rTMS (group 3, n = 14), and G-CSF with 20 Hz rTMS (group 4, n = 15). Animals received G-CSF or saline for 5 days from the day of MCAo and were concurrently treated with 20-min rTMS on their lesioned hemisphere for 2 weeks. Neurological functional score was worse in group 4 compared to that in group 2 on day 15. In Western blots conducted on day 25, phosphorylation of endothelial nitric oxide synthase was markedly lower in groups 2, 3, and 4 than that in group 1 in the ischemic border zone. PECAM-1 expression at ischemic core was lower in groups 4 than in group 2. Caspase-3 expression was markedly higher in groups 4 than in group 1, 2, 3 at ischemic core. Iba1 expression was higher in groups 4 than in group 1, 2 at ischemic core. G-CSF combined with rTMS administered in the early subacute phase of ischemic stroke may exert a hazardous effect on functional recovery, possibly due to impaired angiogenic mechanism, decreased cell survival, and increased inflammation.
我们研究了重复经颅磁刺激(rTMS)联合粒细胞集落刺激因子(G-CSF)对卒中亚急性期早期功能结局的附加作用。将7周龄雄性大鼠永久性大脑中动脉闭塞(MCAo),并分为四组:假rTMS联合生理盐水给药(第1组,n = 15)、假rTMS联合G-CSF给药(第2组,n = 15)、1Hz rTMS联合G-CSF(第3组,n = 14)以及20Hz rTMS联合G-CSF(第4组,n = 15)。自MCAo当天起,动物接受G-CSF或生理盐水治疗5天,并同时对其损伤半球进行20分钟的rTMS治疗,持续2周。在第15天,第4组的神经功能评分比第2组差。在第25天进行的蛋白质免疫印迹分析中,缺血边界区第2、3、4组内皮型一氧化氮合酶的磷酸化水平明显低于第1组。缺血核心区第4组的血小板内皮细胞黏附分子-1(PECAM-1)表达低于第2组。缺血核心区第4组的半胱天冬酶-3(Caspase-3)表达明显高于第1、2、3组。缺血核心区第4组的离子钙结合衔接分子1(Iba1)表达高于第1、2组。在缺血性卒中的亚急性期早期给予G-CSF联合rTMS可能会对功能恢复产生有害影响,这可能是由于血管生成机制受损、细胞存活率降低以及炎症增加所致。