4.5 Article

Administration of riboflavin improves behavioral outcome and reduces edema formation and glial fibrillary acidic protein expression after traumatic brain injury

Journal

JOURNAL OF NEUROTRAUMA
Volume 22, Issue 10, Pages 1112-1122

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2005.22.1112

Keywords

vitamin B-2; Recovery of Function; GFAP; Rat; sensorimotor behavior; antioxidant

Funding

  1. NINDS NIH HHS [1R15NS045647-01] Funding Source: Medline

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Previous studies have shown that administration of riboflavin, vitamin B-2, significantly reduced edema formation following experimental stroke. The present study evaluated the ability of B-2 to improve behavioral function, reduce edema formation, and limit glial fibrillary acidic protein (GFAP) expression following frontal cortex contusion injury. Groups of rats were assigned to B-2 (7.5 mg/kg) or saline (1.0 ml/kg) treatment conditions and received contusion injuries or sham procedures. Drug treatment was administered 15 min and 24 h following injury. Rats were examined on a variety of tests to measure sensorimotor performance (bilateral tactile removal test), and cognitive ability (acquisition of reference and working memory) in the Morris water maze. Administration of B-2 following injury significantly reduced the behavioral impairments observed on the bilateral tactile removal test and improved the acquisition of both reference and working memory tests compared to saline-treated rats. The lesion analysis showed that B-2 reduced the size of the lesion. Examination of GFAP expression around the lesion revealed that B-2 significantly reduced the number of GFAP(+) astrocytes. Edema formation following injury was also significantly reduced by B-2 administration. These findings are the first to show that B-2 administration significantly improved behavioral outcome and reduced lesion volume, edema formation, and the expression of GFAP following traumatic brain injury. These findings suggest that B-2 may have therapeutic potential for the treatment of TBI.

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