High Altitude Hypoxia

Title:High Altitude Hypoxia

Volume: 18 Issue: 4

Author(s): Asma Babar*, Kifayatullah Mengal, Abdul Hanan Babar, Shixin Wu, Mujahid Ali Shah, Chuanfei Xu, Xuegang Luo and Xin Cai*

Affiliation:

• School of Life Science and Engineering, Southwest University of Science and Technology, Mianyang, Sichuan 621010,China

• School of Life Science and Engineering, Southwest University of Science and Technology, Mianyang, Sichuan 621010,China

Keywords: Hypoxia, mammals, adaptation, HIFs, ER stress, unfolded proteins response.

Abstract: The world's highest and largest altitude area is called the Qinghai-Tibetan plateau QTP, which harbors unique animal and plant species. Mammals that inhabit the higher altitude regions have adapted well to the hypoxic conditions. One of the main stressor at high altitudes is hypoxia. Metabolic responses to hypoxia play important roles in cell survival strategies and some diseases. However, the homeostatic alterations that equilibrate variations in the demand and supply of energy to maintain organismal function in a prolonged low O₂ environment persist partly in understood, making it problematic to differentiate adaptive from maladaptive responses in hypoxia. Tibetans and yaks are two perfect examples innate to the plateau for high altitude adaptation. By the scan of the whole-genome, EPAS1 and EGLN1 were identified as key genes associated with sustained hemoglobin concentration in high altitude mammals for adaptation. The yak is a much more ancient mammal that has existed on QTP longer than humans. It is, therefore, possible that natural selection represented a diverse group of genes/pathways in yaks. Physiological characteristics are extremely informative in revealing molecular networks associated with inherited adaptation, in addition to the whole-genome adaptive changes at the DNA sequence level. Gene-expression can be changed by a variety of signals originating from the environment, and hypoxia is the main factor amongst them. The hypoxia-inducible factors (HIF-1α and EPAS1/HIF-2α) are the main regulators of oxygen in homeostasis, which play a role as maestro regulators of adaptation in the hypoxic reaction of molecular mechanisms. The basis of this review is to present recent information regarding the molecular mechanism involved in hypoxia that regulates candidate genes and proteins. Many transcriptional responses toward hypoxia are facilitated by HIFs that change the number of gene expressions and help in angiogenesis, erythropoiesis, metabolic reprogramming, and metastasis. HIFs also activate several signals highlighting a strong association between hypoxia, the misfolded proteins’ accumulation in the endoplasmic reticulum in stress, and activation of Unfolded Protein Response (UPR). It was observed that at high-altitudes, pregnancies yield a low birth weight 100 g per1000 m of the climb. It may involve variation in the events of energy-demand, like protein synthesis. Prolonged hypobaric hypoxia causes placental ER stress, which, in turn, moderates protein synthesis and reduces proliferation. Further, Cardiac hypertrophy by cytosolic Ca²⁺ raises and Ca²⁺/calmodulin, calcineurin stimulation, NF-AT3 pathway might be caused by an imbalance in Sarcoplasmic reticulum ER Ca²⁺, which might be adaptive in the beginning but severe later on.

Cite this article as:

Babar Asma *, Mengal Kifayatullah , Babar Hanan Abdul , Wu Shixin , Shah Ali Mujahid , Xu Chuanfei , Luo Xuegang and Cai Xin *, High Altitude Hypoxia, Current Proteomics 2021; 18 (4) . https://dx.doi.org/10.2174/1570164617999201002144747