AI Article Synopsis

  • Oxygen is vital for life, and a lack of it (hypoxia) can lead to severe health issues, but some species, like Qinghai and Brandt's voles, have adapted to thrive in low-oxygen environments.
  • The study compared the physiological and molecular responses of these voles under hypoxic and normoxic conditions, finding they tolerate low oxygen much better than Kunming mice, which suffered significant cardiac damage.
  • The voles employ different strategies to cope with hypoxia, with Qinghai voles enhancing heart function and oxygen transport, while Brandt's voles focus on increasing red blood cell production, illustrating their unique adaptations to oxygen scarcity.

Article Abstract

Oxygen is essential for most life forms. Insufficient oxygen supply can disrupt homeostasis and compromise survival, and hypoxia-induced cardiovascular failure is fatal in many animals, including humans. However, certain species have adapted and evolved to cope with hypoxic environments and are therefore good models for studying the regulatory mechanisms underlying responses to hypoxia. Here, we explored the physiological and molecular responses of the cardiovascular system in two closely related hypoxia-adapted species with different life histories, namely, Qinghai voles ( ) and Brandt's voles ( ), under hypoxic (10% O for 48 h) and normoxic (20.9% O for 48 h) exposure. Kunming mice ( ) were used for comparison. Qinghai voles live in plateau areas under hypoxic conditions, whereas Brandt's voles only experience periodic hypoxia. Histological and hematological analyses indicated a strong tolerance to hypoxia in both species, but significant cardiac tissue damage and increased blood circulation resistance in mice exposed to hypoxia. Comparative transcriptome analysis revealed enhanced oxygen transport efficiency as a coping mechanism against hypoxia in both and , but with some differences. Specifically, showed up-regulated expression of genes related to accelerated cardiac contraction and angiogenesis, whereas showed significant up-regulation of erythropoiesis-related genes. Synchronized up-regulation of hemoglobin synthesis-related genes was observed in both species. In addition, differences in cardiometabolic strategies against hypoxia were observed in the rodents. Notably, relied on adenosine triphosphate (ATP) generation via fatty acid oxidation, whereas shifted energy production to glucose oxidation under hypoxic conditions and employed a conservative strategy involving down-regulation of fatty acid and glucose oxidation and a bradycardia phenotype. In conclusion, the cardiovascular systems of and have evolved different adaptation strategies to enhance oxygen transport capacity and conserve energy under hypoxia. Our findings suggest that the coping mechanisms underlying hypoxia tolerance in these closely related species are context dependent.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336456PMC
http://dx.doi.org/10.24272/j.issn.2095-8137.2022.011DOI Listing

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