Anti-Stroke Drug Effective Treatment for Middle-Ear Infections, Researchers Say
(PRWEB) May 21, 2015 -- An existing anti-stroke drug is an effective treatment for middle-ear infections, showing the ability to suppress mucus overproduction, improve bacterial clearance and reduce hearing loss, according to researchers at Georgia State University and the University of Rochester.
The findings, published May 13 in the Journal of Immunology, could result in a novel, non-antibiotic treatment for otitis media, or middle-ear infection, possibly through topical drug delivery. Vinpocetine, the drug involved in the study, has long been used to treat neurological disorders such as stroke.
The study found topical administration of Vinpocetine suppressed inflammation and the overproduction of mucus induced by Streptococcus pneumonia bacteria, improved hearing loss in the middle ear and significantly improved bacterial clearance in animal studies.
“Our encouraging preliminary data suggest that the repurposed drug Vinpocetine may play a critical role in inhibiting inflammation and enhancing antimicrobial defenses in otitis media,” said Dr. Jian-Dong Li, director of the Institute for Biomedical Sciences at Georgia State and a Georgia Research Alliance Eminent Scholar in Inflammation and Immunity. “Our proposed studies may lead to developing novel, non-antibiotic therapeutic strategies to control immunopathology, reduce mucus overproduction, improve hearing loss and enhance host defense for otitis media.”
Otitis media is the most common childhood bacterial infection and the leading cause of conductive hearing loss. Streptococcus pneumonia is one of the most common bacterial pathogens causing middle-ear infection.
In the United States, there are 24.5 million visits to physicians’ offices each year because of otitis media and more than $5 billion is spent annually for the care of this disease, according to studies in Pediatric Annals and Otolaryngology - Head and Neck Surgery.
Children with frequent middle-ear infections may suffer from speech and language disabilities because otitis media causes hearing loss during a crucial period for speech and language development.
There is an urgent need for novel, non-antibiotic agents to suppress overactive inflammation without significant side effects. There are no effective non-antibiotic agents for otitis media because of poor understanding of the Streptococcus pneumonia pathogenesis. Inappropriate antibiotic use has led to increased antibiotic resistance. Vaccines against Streptococcus pneumonia have a limited impact on otitis media, Li said.
Mucin, the major component of mucus, plays an important role in the clearance of bacterial pathogens, but uncontrolled, excessive mucus production can lead to conductive hearing loss and decreased bacterial clearance. There is also a lack of effective therapeutic agents for controlling mucus overproduction in otitis media.
This study’s findings could also have a significant impact as a new treatment option in countries where surgery is not readily available, Li said.
Drug repositioning has several advantages over traditional drug discovery, such as reduced safety risk, side effects, time and costs. There have been no reports of significant adverse effects and toxicity at therapeutic doses of Vinpocetine in adults and children. As a result, Vinpocetine is attractive to scientists and clinicians seeking novel therapeutic applications.
Vinpocetine, an alkaloid extracted from the periwinkle plant, was originally discovered and marketed in 1978 under the trade name Cavinton. It is used as an anti-stoke drug in most countries and a dietary supplement worldwide.
The research discovery was accomplished through collaboration with Dr. Chen Yan of the University of Rochester Medical Center. The research team also includes Ji-Yun Lee, Kensei Komatsu, Byung-Cheol Lee, Masanori Miyata, Ashley O’Neill Bohn and Haidong Xu of Georgia State.
The study is mainly supported by the National Institute on Deafness and Other Communication Disorders.
LaTina Emerson, Georgia State University, +1 (404) 413-1353, [email protected]
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