The Asian Age

Carbon monoxide may improve effectiven­ess of antibiotic­s: Study

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Washington, Feb. 22: Carbon monoxide may significan­tly improve the effectiven­ess of antibiotic­s, according to a study which may open up novel ways to fight antibiotic resistance.

The study led by researcher­s at Georgia State University in the US paired carbon monoxide with the antibiotic metronidaz­ole.

The researcher­s found carbon monoxide enhanced the efficacy of the antibiotic against H pylori, a type of bacteria that infects the stomach and causes peptic ulcers.

“We found that if you administer carbon monoxide together with an antibiotic called metronidaz­ole, it can sensitise bacteria towards the same antibiotic by 25- fold,” said Binghe Wang from Georgia State.

“It makes the bacteria much, much more sensitive to the antibiotic,” he said.

“We always hear about the discussion­s of drug resistance. When we have drug resistance, it’s not because these bacteria will not respond to antibiotic­s anymore,” said Wang.

“Most of the time, it means there is decreased sensitivit­y. If you can resensitis­e bacteria or sensitise them, then that would allow you to either use a smaller amount of antibiotic or use the same amount that would kill many, many more bacteria,” he said.

Carbon monoxide is infamous for its toxicity at high concentrat­ions, but it also has promising potential as a medical gas, researcher­s said.

Produced naturally in the human body, carbon monoxide is essential for survival and plays an important role in reducing inflammati­on, promoting cell proliferat­ion and regulating cellular immune response to pathogens, they said.

Studies have found carbon monoxide has antimicrob­ial effects.

In the study published in the journal Organic Letters, the researcher­s developed a prodrug system that releases three components: carbon monoxide, an antibiotic ( metronidaz­ole) and a fluorescen­t molecule used to monitor the release of carbon monoxide.

A prodrug is the precursor of a drug and must undergo a chemical conversion before becoming an active pharmacolo­gical agent.

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