New drug protects against the deadly effects of nuclear radiation 24 hours after exposure
Exposure to high doses of radiation triggers a number of potentially lethal effects. Among the most severe of these effects is the gastrointestinal, or GI, toxicity syndrome that is caused by radiation-induced destruction of the intestinal lining. This type of GI damage decreases the ability of the body to absorb water and causes electrolyte imbalances, bacterial infection, intestinal leakage, sepsis and death.
The GI toxicity syndrome is triggered by radiation-induced damage to crypt cells in the small intestines and colon that must continuously replenish in order for the GI tract to work properly. Crypt cells are especially susceptible to radiation damage and serve as an indicator of whether someone will survive after total body radiation exposure.
The peptide drug TP508 was developed for use in stimulating repair of skin, bone and muscle tissues. It has previously been shown to begin tissue repair by stimulating proper blood flow, reducing inflammation and reducing cell death. In human clinical trials, the drug has been reported to increase healing of diabetic foot ulcers and wrist fractures with no drug-related adverse events.
"The current results suggest that the peptide may be an effective emergency nuclear countermeasure that could be delivered within 24 hours after exposure to increase survival and delay mortality, giving victims time to reach facilities for advanced medical treatment," Kantara said.
Original publication
Original publication
Carla Kantara, Stephanie M Moya, Courtney W Houchen, Shahid Umar, Robert L Ullrich, Pomila Singh and Darrell H Carney; "Novel regenerative peptide TP508 mitigates radiation-induced gastrointestinal damage by activating stem cells and preserving crypt integrity"; Laboratory Investigation; 2015
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