Tekin Demet, Dursun Ali Doğan, Baştuğ Metin, Karaorman Gökhan, Fıçıcılar Hakan
Department of Physiology, Faculty of Medicine, Ankara University, Ankara-Turkey.
Anadolu Kardiyol Derg. 2011 Aug;11(5):379-85. doi: 10.5152/akd.2011.104. Epub 2011 Jun 7.
Hypoxia-inducible factor-1 alpha (HIF-1α) and vascular endothelial growth factor (VEGF) are involved in signaling mechanisms of cellular responses to hypoxia. These factors have been investigated in tissue samples by simulating different altitudes by changing the percentage of oxygen. We aimed first to evaluate the effect of normobaric, systemic hypoxia (11% O2) on HIF-1α and VEGF mRNA levels in the heart muscle; secondly, to compare the levels of HIF-1α and VEGF mRNA in the left and right ventricle muscles.
In this experimental study, 33 New Zealand male rabbits were assigned to control, acute hypoxia (4 hours) and intermittent hypoxia (4 hours/day for 14 days) groups (n=11/group). Total RNA was isolated from right and left ventricles of the heart. The expressions of HIF-1α and VEGF mRNAs were investigated by using Reverse Transcription Polymerase Chain Reaction (RT-PCR) method. The obtained data were compared by using ANOVA and paired t-test.
The results indicated that left ventricle VEGF mRNA expressions in both acute and intermittent hypoxia groups (1.08 ± 0.15 and 1.03 ± 0.19, respectively) were higher than that in the control group (0.88 ± 0.15) (p=0.03). Hypoxia treatments did not significantly alter HIF-1α mRNA in both ventricles (p=0.60 and p=0.51 for left and right ventricles, respectively).
Since systemic hypoxia results in induction of VEGF mRNA up-regulation only in left ventricle, it could be related to its higher metabolic activity and oxygen utilization. Hypoxia induced changes in the expression of HIF-1α mRNA may not be the only determining factor for HIF-1/VEGF pathway induction or the observed VEGF induction could be through other hypoxia sensitive pathways.
缺氧诱导因子-1α(HIF-1α)和血管内皮生长因子(VEGF)参与细胞对缺氧反应的信号传导机制。通过改变氧气百分比模拟不同海拔高度,已在组织样本中对这些因子进行了研究。我们的目的首先是评估常压系统性缺氧(11%氧气)对心肌中HIF-1α和VEGF mRNA水平的影响;其次,比较左心室和右心室肌肉中HIF-1α和VEGF mRNA的水平。
在本实验研究中,将33只新西兰雄性兔子分为对照组、急性缺氧组(4小时)和间歇性缺氧组(每天4小时,共14天)(每组n = 11)。从心脏的右心室和左心室分离总RNA。采用逆转录聚合酶链反应(RT-PCR)方法研究HIF-1α和VEGF mRNA的表达。使用方差分析和配对t检验对所得数据进行比较。
结果表明,急性和间歇性缺氧组左心室VEGF mRNA表达(分别为1.08±0.15和1.03±0.19)高于对照组(0.88±0.15)(p = 0.03)。缺氧处理并未显著改变两个心室中的HIF-1α mRNA(左心室和右心室分别为p = 0.60和p = 0.51)。
由于系统性缺氧仅导致左心室中VEGF mRNA上调,这可能与其较高的代谢活性和氧利用有关。缺氧诱导的HIF-1α mRNA表达变化可能不是HIF-1/VEGF途径诱导的唯一决定因素,或者观察到的VEGF诱导可能通过其他缺氧敏感途径。