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[不同海拔大鼠肺组织中EGLN1基因、蛋白表达与肺动脉压力的相关性]

[Correlation between EGLN1 gene, protein express in lung tissue of rats and pulmonary artery pressure at different altitude].

作者信息

Li S H, Li S, Sun L, Bai Z Z, Yang Q Y, Ga Q, Jin G E

机构信息

Faculty of Basic Medical Science, Qinghai University Medical College, Xining 810001, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2016 Aug 23;96(32):2592-7. doi: 10.3760/cma.j.issn.0376-2491.2016.32.016.

Abstract

OBJECTIVE

To investigate the correlation between pulmonary artery pressure (PAP) and the expression level of Egl nine homologue 1 (EGLN1) gene or its protein in lung tissue of rats at different altitudes.

METHODS

Totally 121 male Wistar rats were randomly divided into low altitude group (n=11), moderate altitude group and high altitude group, the rats in moderate altitude and high altitude group were further divided into 1(st) day, 3(rd) days, 7(th) days, 15(th) day and 30(th) day group according to the exposure time to hypoxic environment, each group 11 rats. The low altitude group, the PAP of rats were determined by physiological signal acquisition system, and tissue samples were collected in liquid nitrogen container for storage at an altitude of 498 m area. Moderate altitude group rats were placed in altitude of 2 260 meters of natural environment, 5 high altitude groups rats were placed in the hypobaric hypoxic chamber, simulating altitude of 4 500 meters. The PAP of rats in moderate altitude group and high altitude group were also determined by physiological signal acquisition system, and tissue samples were collected when rats were exposed to hypoxia at 1(st), 3(rd), 7(th), 15(th) and 30(th) day; Western blot was used to determine expression levels of EGLN1 protein, and person correlation analysis was used to analyze whether the protein was related to the formation of pulmonary arterial hypertension (PH) under hypoxia. Real-time quantitive PCR method determined expression levels of EGLN1 mRNA in lung tissues, and the relative expression method was used to analyze PCR data, and finally assess whether the EGLN1 gene was the initial cause of the formation of PH during hypoxia.

RESULTS

The mean PAP of rats was (20.0±3.2) mmHg (1 mmHg=0.133 kPa) in low altitude group; in moderate altitude group, mean PAP began to increase slightly when rats were exposed to hypoxia on the 15(th) day and reached at (22.7±4.1) mmHg on hypoxic 30(th) day, but compared with the low altitude group, there was no statistical difference (P> 0.05); the mean PAP of rats in high altitude group began to rise on the 7(th) day (28.7±7.7) mmHg, which was higher than that in low altitude group (P<0.05), and significantly increased to (42.3±9.1) mmHg (P<0.001) on hypoxic 30(th) day; it was significantly proportional with exposure to hypoxic time, and compared to low altitude group and moderate altitude group, there was significant difference (P<0.05). EGLN1 protein expression in the lung tissue of rats had no significant difference between the low altitude group and moderate altitude group, and its expression level in the high altitude group were significantly decreased, furthermore, the expression level decreased with the increase of hypoxia exposure time (P<0.05); PAP and EGLN1 protein expression levels showed a negative correlation (r=-0.662). The transcription level of mRNA EGLN1 in high altitude group was significantly increased under hypobaric hypoxia, it was 72 times more than that of the moderate altitude group, and nearly 300 times than that of the low altitude group, respectively (both P<0.001=.

CONCLUSION

EGLN1 gene expression in lung tissue of rat is affected by hypoxia, the expression level increases with the increase of the altitude; but the protein expression level, in contrast with gene expression level, is decreased with the increase of altitude and is significantly negatively correlated with mean PAP.

摘要

目的

探讨不同海拔地区大鼠肺动脉压(PAP)与肺组织中Egl九同源物1(EGLN1)基因及其蛋白表达水平的相关性。

方法

将121只雄性Wistar大鼠随机分为低海拔组(n = 11)、中海拔组和高海拔组,中海拔组和高海拔组大鼠根据缺氧环境暴露时间进一步分为第1天、第3天、第7天、第15天和第30天组,每组11只大鼠。低海拔组大鼠在海拔498 m地区,用生理信号采集系统测定大鼠PAP,并采集组织样本于液氮容器中保存。中海拔组大鼠置于海拔2 260米的自然环境中,5个高海拔组大鼠置于低压缺氧舱中,模拟海拔4 500米。中海拔组和高海拔组大鼠也用生理信号采集系统测定PAP,并在大鼠缺氧暴露第1、3、7、15和30天采集组织样本;采用蛋白质印迹法测定EGLN1蛋白表达水平,用人相关性分析分析该蛋白与缺氧状态下肺动脉高压(PH)形成是否相关。采用实时定量PCR法测定肺组织中EGLN1 mRNA表达水平,用相对表达法分析PCR数据,最终评估EGLN1基因是否为缺氧时PH形成的初始原因。

结果

低海拔组大鼠平均PAP为(20.0±3.2)mmHg(1 mmHg = 0.133 kPa);中海拔组大鼠在缺氧第15天平均PAP开始略有升高,缺氧第30天达到(22.7±4.1)mmHg,但与低海拔组相比,差异无统计学意义(P>0.05);高海拔组大鼠平均PAP在第7天开始升高(28.7±7.7)mmHg,高于低海拔组(P<0.05),缺氧第30天显著升高至(42.3±9.1)mmHg(P<0.001);与缺氧暴露时间呈显著正相关,与低海拔组和中海拔组相比,差异有统计学意义(P<0.05)。低海拔组与中海拔组大鼠肺组织中EGLN1蛋白表达差异无统计学意义,高海拔组其表达水平显著降低,且随着缺氧暴露时间延长表达水平降低(P<0.05);PAP与EGLN1蛋白表达水平呈负相关(r = -0.662)。高海拔组在低压缺氧条件下mRNA EGLN1转录水平显著升高,分别是中海拔组的72倍和低海拔组的近300倍(均P<0.001)。

结论

大鼠肺组织中EGLN1基因表达受缺氧影响,表达水平随海拔升高而增加;但其蛋白表达水平与基因表达水平相反,随海拔升高而降低,且与平均PAP呈显著负相关。

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