Posted on 09/21/2022 12:38:25 PM PDT by ConservativeMind
Researchers in China have discovered that inhibiting a protein called the GABAA receptor can protect intestinal stem cells from the toxic effects of chemotherapy and radiotherapy.
The study suggests that the FDA-approved anti-sedative flumazenil, which targets GABAA receptors, could alleviate some of the common gastrointestinal side effects, such as diarrhea and vomiting, induced by many cancer treatments.
Because they have to continually proliferate and replace the cells lining the wall of the gut, intestinal stem cells are highly sensitive to chemotherapy and radiotherapy. These treatments damage the DNA of intestinal stem cells and cause them to die, leading to intestinal injury and a variety of painful gastrointestinal symptoms. These toxic side effects, which can persist long after treatment is finished, limit the drug or radiation dose that can be given to cancer patients and worsen their quality of life.
Chen and colleagues found that inhibiting the GABAA receptor protects intestinal stem cells from DNA damage by limiting the formation of free radicals in response to chemoradiotherapy. Crucially, however, the researchers determined that inhibiting the GABAA receptor does not prevent radiation or chemotherapy drugs from killing cancer cells.
Flumazenil is a cheap, GABAA receptor inhibitor approved by the U.S. Food and Drug Administration to treat benzodiazepine overdoses and reverse anesthesia. Chen and colleagues found that flumazenil was also able to protect the intestines of mice from the toxic effects of chemoradiotherapy. Moreover, flumazenil also protected human colonic organoids—miniature organs grown in the lab from human colonic stem cells—from chemotherapy drugs and irradiation.
"Taken together, our data suggest that inhibiting the GABAA receptor is a promising strategy to specifically protect the intestine from chemoradiotherapy," Chen says. "Future studies are required to investigate the pharmacodynamics and tolerability of flumazenil in cancer patients undergoing treatment in the clinic."
(Excerpt) Read more at medicalxpress.com ...
Don’t they give rats that stuff when they’re studying seizures?
“This has been available in the US for decades and is primarily used for benzodiazepine overdoses.”
Makes sense.
I find it interesting that they say the mechanism for villi protection is decrease in free radicals.
I don’t think Gabaergic transmission has been associated with free radical levels in the past.
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