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Genetic mechanism prevents kidney injury after severe dehydration

Date:
August 14, 2017
Source:
University of New Hampshire
Summary:
In humans, even the most minor dehydration can compromise the kidneys causing lifelong, irreparable issues or even death. However, some animals living in desert environments are able to survive both acute and chronic dehydration. While these animals, like cactus mice, have evolved over time to deal with environmental stressors like dehydration, researchers have found it's not the physical makeup that is helping them survive, but rather their genetic makeup.
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Millions of people die every year from dehydration as a result of exposure and illness. In humans, even the most minor dehydration can compromise the kidneys causing lifelong, irreparable issues or even death. However, some animals living in desert environments are able to survive both acute and chronic dehydration. While these animals, like cactus mice, have evolved over time to deal with environmental stressors like dehydration, researchers at the University of New Hampshire have found it's not the physical makeup that is helping them survive, but rather their genetic makeup.

"Initially, we thought that maybe their kidneys are structurally different from people, but they're not," said Matt MacManes, assistant professor of genome enabled biology at UNH and lead author of the study. "However, when exposed to acute dehydration, no kidney injury was apparent, which would definitely be the case for humans exposed to similar levels of dehydration, suggesting their genes may be what's preventing widespread kidney damage."

"The kidney is the canary in the coal mine when it comes to dehydration," continues MacManes. "The exciting outcome of this research is that the molecular toolkit of the cactus mouse has orthologues, or related genes, in humans. These provide the potential for development of drugs or other therapies that could help protect the human body from the damages of dehydration." Such a response could be extremely valuable in a wide variety of situations -- for people with renal failure, where water is severally limited due to geography or possibly global climate change, for troops deployed in the desert, and perhaps even in space travel.

To understand how desert-adapted cactus mice (Peromyscus eremicus) survive, the study recently published in the American Journal of Renal Physiology outlines how the researchers modeled a desert-like condition. The mice that went without water for 72 hours lost on average 23 percent of their body weight, which would be fatal for humans. Even though dehydrated, the mice continued to be active, eat, and interact normally. Researchers analyzed several other factors including serum electrolytes (sodium, calcium, bicarbonate ion) as well as blood urea nitrogen (BUN) and creatinine. While both were slightly elevated, gene-based biomarkers for kidney injury, were not, which suggests kidney injury is not occurring.

Further analysis found genes that are important in modulating electrolytes were very active, as were genes responsible for maintaining kidney blood pressure.


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Materials provided by University of New Hampshire. Note: Content may be edited for style and length.


Journal Reference:

  1. Matthew David MacManes. Severe acute dehydration in a desert rodent elicits a transcriptional response that effectively prevents kidney injury. American Journal of Physiology - Renal Physiology, 2017; 313 (2): F262 DOI: 10.1152/ajprenal.00067.2017

Cite This Page:

University of New Hampshire. "Genetic mechanism prevents kidney injury after severe dehydration." ScienceDaily. ScienceDaily, 14 August 2017. <www.sciencedaily.com/releases/2017/08/170814120855.htm>.
University of New Hampshire. (2017, August 14). Genetic mechanism prevents kidney injury after severe dehydration. ScienceDaily. Retrieved December 21, 2024 from www.sciencedaily.com/releases/2017/08/170814120855.htm
University of New Hampshire. "Genetic mechanism prevents kidney injury after severe dehydration." ScienceDaily. www.sciencedaily.com/releases/2017/08/170814120855.htm (accessed December 21, 2024).

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