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New light shed on traumatic brain injuries

Date:
April 15, 2013
Source:
University of Kentucky
Summary:
A new article offers the latest information concerning a "switch" that turns "on" and "off" inflammation in the brain after trauma.
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Even a mild injury to the brain can have long lasting consequences, including increased risk of cognitive impairment later in life. While it is not yet known how brain injury increases risk for dementia, there are indications that chronic, long-lasting, inflammation in the brain may be important. A new paper by researchers at the University of Kentucky Sanders-Brown Center on Aging (SBCoA), appearing in the Journal of Neuroscience, offers the latest information concerning a "switch" that turns "on" and "off" inflammation in the brain after trauma.

A team of researchers led by Linda Van Eldik, director of SBCoA, used a mouse model to study the role of p38a MAPK in trauma-induced injury responses in the microglia resident immune cell of the brain.

"The p38α MAPK protein is an important switch that drives abnormal inflammatory responses in peripheral tissue inflammatory disorders, including chronic debilitating diseases like rheumatoid arthritis," said Van Eldik.

"However, less is known about the potential importance of p38α MAPK in controlling inflammatory responses in the brain. Our work supports p38α MAPK as a promising clinical target for the treatment of CNS disorders associated with uncontrolled brain inflammation, including trauma, and potentially others like Alzheimer's disease. We are excited by our findings, and are actively working to develop drugs targeting p38a MAPK designed specifically for diseases of the brain."

Lead author of the paper Adam D. Bachstetter said, "I was surprised when I looked under the microscope at the brain tissue of mice that had a diffuse brain injury. Microglia normally look like a small spider, but after suffering a brain injury the microglia become like angry spiders from a horror movie. In brain-injured mice that lack p38a MAPK there were no angry-looking microglia, only the normal small spider-like cells. When I started the study I never expected the results to be so clear and striking. I believe that the p38a MAPK is a promising clinical target for the treatment of CNS disorders with dysregulated inflammatory responses, but we are still a long way from development of CNS-active p38 inhibitor drugs. "


Story Source:

The above post is reprinted from materials provided by University of Kentucky. Note: Materials may be edited for content and length.


Journal Reference:

  1. A. D. Bachstetter, R. K. Rowe, M. Kaneko, D. Goulding, J. Lifshitz, L. J. Van Eldik. The p38  MAPK Regulates Microglial Responsiveness to Diffuse Traumatic Brain Injury. Journal of Neuroscience, 2013; 33 (14): 6143 DOI: 10.1523/JNEUROSCI.5399-12.2013

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University of Kentucky. "New light shed on traumatic brain injuries." ScienceDaily. ScienceDaily, 15 April 2013. <www.sciencedaily.com/releases/2013/04/130415151444.htm>.
University of Kentucky. (2013, April 15). New light shed on traumatic brain injuries. ScienceDaily. Retrieved July 4, 2015 from www.sciencedaily.com/releases/2013/04/130415151444.htm
University of Kentucky. "New light shed on traumatic brain injuries." ScienceDaily. www.sciencedaily.com/releases/2013/04/130415151444.htm (accessed July 4, 2015).

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