But turning up the temperature can have a down side: in about one in 25 infants or small children, high fever can trigger fever-induced (febrile) seizures. While the seizures themselves are generally harmless, a prolonged fever resulting from infection or heatstroke of over 108°F (42°C) can eventually lead to respiratory distress, cognitive dysfunction, brain damage or death.
New research by scientists at the University of Toronto Mississauga and Queen’s University has shown that genetic variation in the foraging gene results in different tolerance for heat stress, and demonstrates how the use of specific drugs can replicate this effect in fruit flies and locusts. While the findings are at an early stage, the researchers suggest that since this genetic pathway is found in other organisms, it could lead to ways to rapidly protect the brain from extremely high fevers in mammals, including humans. The new study appears in the August 22 issue of the journal PLoS ONE, the online, open-access journal from the Public Library of Science.
“Our research suggests that manipulation of a single gene or genetic pathway will be sufficient to rapidly protect the nervous system from damage due to extreme heat stress,” says senior researcher, Professor Marla B. Sokolowski, who holds a Canada Research Chair in Genetics.
In their research, post-doctoral fellow Ken Dawson-Scully and Sokolowski demonstrate that the foraging gene, responsible for a protein called PKG, protects against heat-induced neural failure in fruit flies and locusts. When they increased the temperature by 5°C per minute (starting from 22°C and rising to 42°C), they found that fruit flies with a lower level of PKG experienced neural failure at much higher temperatures than those with higher levels of PKG.
Using drugs that interact with the PKG molecule, the researchers showed it is possible to induce an extremely rapid protection of neural function during heat stress. Queen's biologists Gary Armstrong and Mel Robertson exposed locusts to increasing heat while monitoring the neural circuit that controls breathing. At approximately 30°C (about three minutes before expected neural failure), the researchers injected the locusts with a PKG inhibitor. Compared to locusts who received a placebo injection, the treated locusts showed a rapid and significant protection of their neural circuitry.
“During heat trauma to the brain, there exists a window of opportunity between the time of occurrence of neural dysfunction and eventual brain damage or death,” says Dawson-Scully. “Manipulation of the PKG pathway during this period should increase an individual’s chance of survival.”
Andrew Hyde | alfa
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