Departments of Physiology & Biophysics, Case Western Reserve University, Cleveland, OH, USA.
Department of Neurobiology, Duke University School of Medicine, Durham, NC, USA.
Adv Exp Med Biol. 2021;1269:317-322. doi: 10.1007/978-3-030-48238-1_50.
We have previously reported that in a rat model of chronic hypoxia, HIF-1α and its target genes have significantly accumulated by 3 days of exposure, whereas no significant increase in capillary density has occurred; there is a significant increase in capillary density at 21 days of chronic hypoxic exposure. In this study we hypothesize that by utilizing 3 days and 21 days of hypoxic preconditioning, we would distinguish between the relative neuroprotective contributions of the accumulation of HIF-1α and its target genes and angiogenic adaptation in a rat middle cerebral artery occlusion (MCAO) model. Rats were randomly assigned to either hypoxic precondition groups (3-day and 21-day hypoxia) or normoxic control group. Hypoxic animals were kept in a hypobaric chamber at a constant pressure of 0.5 atmosphere (380 mmHg, equivalent to 10% normobaric oxygen at sea level) for either 3 or 21 days. Normoxic controls were housed in the same room next to the hypobaric chamber. Erythropoietin (EPO) was measured at 3 and 21 days of hypoxia using Western blotting analysis. Infarct volumes were measured following 24 hours of permanent MCAO. We found that EPO is upregulated at 3 days of hypoxia and returns to baseline by 21 days of hypoxia. The infarct volumes following 24-hour MCAO were significantly reduced with 3-day hypoxic preconditioning when compared to normoxic controls (%, 31.8 ± 5, n = 9 vs. 50.1 ± 10.9, n = 7). No significant differences in infarct volume were seen between the normoxic controls and 21-day hypoxic preconditioned rats. We have shown that a 3-day hypoxic preconditioning, but not 21-day hypoxic preconditioning, provides significant neuroprotection against focal ischemia in rats, supporting a larger role for the accumulations of HIF-1α and upregulation of its target genes in the neuroprotection against focal ischemia.
我们之前的研究表明,在慢性缺氧的大鼠模型中,HIF-1α及其靶基因在暴露 3 天后显著积累,而毛细血管密度没有显著增加;在慢性缺氧暴露 21 天后,毛细血管密度显著增加。在这项研究中,我们假设通过利用 3 天和 21 天的缺氧预处理,我们可以区分 HIF-1α及其靶基因的积累和血管生成适应在大鼠大脑中动脉闭塞(MCAO)模型中的相对神经保护作用。大鼠被随机分配到缺氧预处理组(3 天和 21 天缺氧)或常氧对照组。缺氧动物被放置在一个恒压的低压舱中,压力为 0.5 个大气压(380mmHg,相当于海平面 10%的常压氧气),持续 3 天或 21 天。常氧对照组被安置在低压舱旁边的同一个房间里。在 3 天和 21 天缺氧后,使用 Western blot 分析测量促红细胞生成素(EPO)的水平。在永久性 MCAO 24 小时后测量梗死体积。我们发现,EPO 在缺氧 3 天后上调,并在缺氧 21 天后恢复到基线。与常氧对照组相比,3 天的缺氧预处理可显著减少 24 小时 MCAO 后的梗死体积(%,31.8±5,n=9 与 50.1±10.9,n=7)。常氧对照组与 21 天缺氧预处理大鼠之间的梗死体积无显著差异。我们已经证明,3 天的缺氧预处理,而不是 21 天的缺氧预处理,可显著提供对大鼠局灶性缺血的神经保护作用,这支持 HIF-1α的积累及其靶基因的上调在局灶性缺血的神经保护中起更大的作用。