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Harvard and University of Pittsburgh Researchers Explain Carbon Monoxide’s Anti-inflammatory Effects - In April’s The FASEB Journal, scientists from Harvard and U. Pittsburgh describe for the first time that anti-inflammatory effects of CO originate within cells’ mitochondria, raising possibilities for development of new anti-inflammatory therapies
Harvard and University of Pittsburgh Researchers Explain Carbon Monoxide’s Anti-inflammatory Effects

 

NewswireToday - /newswire/ - Bethesda, MD, United States, 2007/03/30 - In April’s The FASEB Journal, scientists from Harvard and U. Pittsburgh describe for the first time that anti-inflammatory effects of CO originate within cells’ mitochondria, raising possibilities for development of new anti-inflammatory therapies.

   
 
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In a study appearing in the April 2007 issue of The FASEB Journal, scientists from Harvard University and the University of Pittsburgh have shown for the first time that the anti-inflammatory effects of carbon monoxide originate within cells’ own molecular engines, mitochondria. Specifically, mitochondria react to low levels of carbon monoxide by releasing chemical signals that reduce or shut down the body’s inflammatory response, raising the possibility for the development of new anti-inflammatory therapies, one of which may be low levels of inhaled carbon monoxide.

According to the study’s first author, Brian S. Zuckerbraun, M.D. of the University of Pittsburgh, “this study may contribute to our understanding and development of controlled carbon monoxide as a therapeutic agent.”

Inflammation is a normal defense mechanism used by the body to ward off infection, but over time, severe or chronic inflammation can damage tissues. In some cases, such as in organ transplantation, the body’s inflammatory response over the short-term also can cause more harm than good. Current approaches to controlling inflammation are not always successful, making the need for new approaches urgent. In particular, inhaled medical grade carbon monoxide has been shown to be useful in animal models for organ transplantation, vascular injury, inflammatory bowel disease, organ injury resulting from severe blood loss, as well as experimental hepatitis and experimental pulmonary hypertension.

“The findings described in this study are particularly relevant, given that April is National Donate Life Month,” said Gerald Weissmann, M.D., Editor-in-Chief of The FASEB Journal. “Transplants are rejected because of inflammation gone awry. If we block inflammation, as with carbon monoxide or agents that release it in a controlled fashion, we can not only make transplantation safer, but extend its benefits to many more who need it.”

The FASEB Journal (fasebj.org) is published by the Federation of American Societies for Experimental Biology (FASEB) and is consistently ranked among the top three biology journals worldwide by the Institute for Scientific Information. FASEB comprises 21 nonprofit societies with more than 80,000 members, making it the largest coalition of biomedical research associations in the United States. FASEB advances biological science through collaborative advocacy for research policies that promote scientific progress and education and lead to improvements in human health.

Since 2003, April has been proclaimed by the U.S. President as National Donate Life Month to recognize those who have saved lives by becoming organ, tissue, marrow, and blood donors and to encourage more Americans to follow their examples. During National Donate Life Month, Americans are urged to become donors and to learn more about becoming an organ and tissue donor.

 
 
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Harvard and University of Pittsburgh Researchers Explain Carbon Monoxide’s Anti-inflammatory Effects

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Publisher Contact: Cody Mooneyhan - FASEB.Org 
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