Department of Neurology, University of Kentucky, 741 S. Limestone, Lexington, KY 40536, United States.
Department of Radiology, University of Kentucky, 800 Rose St., Lexington, KY 40536, United States.
Brain Res. 2019 Mar 15;1707:62-73. doi: 10.1016/j.brainres.2018.11.017. Epub 2018 Nov 13.
Preclinical studies using rodent models of stroke have had difficulty in translating their results to human patients. One possible factor behind this inability is the lack of studies utilizing aged rodents of both sexes. Previously, this lab showed that leukemia inhibitory factor (LIF) promoted recovery after stroke through antioxidant enzyme upregulation. This study examined whether LIF promotes neuroprotection in aged rats of both sexes. LIF did not reduce tissue damage in aged animals, but LIF-treated female rats showed partial motor skill recovery. The LIF receptor (LIFR) showed membrane localization in young male and aged rats of both sexes after stroke. Although LIF increased neuronal LIFR expression in vitro, it did not increase LIFR in the aged brain. Levels of LIFR protein in brain tissue were significantly downregulated between young males and aged males/females at 72 h after stroke. These results demonstrated that low LIFR expression reduces the neuroprotective efficacy of LIF in aged rodents of both sexes. Furthermore, the ability of LIF to promote motor improvement is dependent upon sex in aged rodents.
啮齿动物卒中模型的临床前研究在将其结果转化为人类患者方面一直存在困难。这种无能的一个可能因素是缺乏利用两性老年啮齿动物的研究。此前,本实验室表明白血病抑制因子 (LIF) 通过上调抗氧化酶来促进卒中后的恢复。本研究探讨了 LIF 是否促进两性老年大鼠的神经保护。LIF 并未减少老年动物的组织损伤,但 LIF 治疗的雌性大鼠显示出部分运动技能恢复。LIF 受体 (LIFR) 在卒中后年轻雄性和两性老年大鼠中显示出膜定位。尽管 LIF 在体外增加了神经元 LIFR 的表达,但它并没有增加老年大脑中的 LIFR。卒中后 72 小时,脑组织中的 LIFR 蛋白水平在年轻雄性和老年雄性/雌性之间显著下调。这些结果表明,LIFR 表达水平降低降低了 LIF 在两性老年啮齿动物中的神经保护作用。此外,LIF 促进运动改善的能力取决于老年啮齿动物的性别。