Jochmans-Lemoine Alexandra, Revollo Susana, Villalpando Gabriella, Valverde Ibana, Gonzales Marcelino, Laouafa Sofien, Soliz Jorge, Joseph Vincent
Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Québec, Université Laval, Quebec City, QC, Canada.
Instituto Boliviano de Biologia de Altura, Universidad Mayor de San Andrés, La Paz, Bolivia.
Front Physiol. 2018 Apr 4;9:311. doi: 10.3389/fphys.2018.00311. eCollection 2018.
Compared with mice, adult rats living at 3,600 m above sea level (SL-La Paz, Bolivia) have high hematocrit, signs of pulmonary hypertension, and low lung volume with reduced alveolar surface area. This phenotype is associated with chronic mountain sickness in humans living at high altitude (HA). We tested the hypothesis that this phenotype is associated with impaired gas exchange and oxidative stress in the lungs. We used rats and mice (3 months old) living at HA (La Paz) and SL (Quebec City, Canada) to measure arterial oxygen saturation under graded levels of hypoxia (by pulse oximetry), the alveolar surface area in lung slices and the activity of pro- (NADPH and xanthine oxidases-NOX and XO) and anti- (superoxide dismutase, and glutathione peroxidase-SOD and GPx) oxidant enzymes in cytosolic and mitochondrial lung protein extracts. HA rats have a lower arterial oxygen saturation and reduced alveolar surface area compared to HA mice and SL rats. Enzymatic activities (NOX, XO, SOD, and GPx) in the cytosol were similar between HA and SL animals, but SOD and GPx activities in the mitochondria were 2-3 times higher in HA vs. SL rats, and only marginally higher in HA mice vs. SL mice. Furthermore, the maximum activity of cytochrome oxidase-c (COX) measured in mitochondrial lung extracts was also 2 times higher in HA rats compared with SL rats, while there was only a small increase in HA mice vs. SL mice. Interestingly, compared with SL controls, alterations in lung morphology are not observed for young rats at HA (15 days after birth), and enzymatic activities are only slightly altered. These results suggest that rats living at HA have a gradual reduction of their alveolar surface area beyond the postnatal period. We can speculate that the elevation of SOD, GPx, and COX activities in the lung mitochondria are not sufficient to compensate for oxidative stress, leading to damage of the lung tissue in rats.
与小鼠相比,生活在海拔3600米(玻利维亚拉巴斯市)的成年大鼠具有高血细胞比容、肺动脉高压迹象、肺容积低以及肺泡表面积减小的情况。这种表型与生活在高海拔地区(HA)的人类慢性高山病有关。我们检验了这样一个假设,即这种表型与肺部气体交换受损和氧化应激有关。我们使用生活在高海拔地区(拉巴斯)和海平面(加拿大魁北克市)的大鼠和小鼠(3个月大)来测量在分级低氧水平下(通过脉搏血氧测定法)的动脉血氧饱和度、肺切片中的肺泡表面积以及肺细胞质和线粒体蛋白提取物中促氧化剂(烟酰胺腺嘌呤二核苷酸磷酸氧化酶和黄嘌呤氧化酶——NOX和XO)和抗氧化剂(超氧化物歧化酶和谷胱甘肽过氧化物酶——SOD和GPx)酶的活性。与高海拔小鼠和海平面大鼠相比,高海拔大鼠的动脉血氧饱和度较低,肺泡表面积减小。高海拔和海平面动物的细胞质中酶活性(NOX、XO、SOD和GPx)相似,但高海拔大鼠线粒体中的SOD和GPx活性比海平面大鼠高2至3倍,而高海拔小鼠与海平面小鼠相比仅略高。此外,在肺线粒体提取物中测得的细胞色素氧化酶-c(COX)的最大活性在高海拔大鼠中也比海平面大鼠高2倍,而高海拔小鼠与海平面小鼠相比仅略有增加。有趣的是,与海平面对照组相比,高海拔地区的幼鼠(出生后15天)未观察到肺部形态改变,酶活性也仅略有改变。这些结果表明,生活在高海拔地区的大鼠在出生后肺泡表面积逐渐减小。我们可以推测,肺线粒体中SOD、GPx和COX活性的升高不足以补偿氧化应激,从而导致大鼠肺组织受损。