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New drugs target delay of Huntington’s symptoms

Date:
June 1, 2011
Source:
McMaster University
Summary:
The drug restores a critical chemical change that should occur in the huntingtin protein, but does not occur in people with Huntington's disease.
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McMaster University researchers have discovered a new drug target that may be effective at preventing the onset of Huntington's disease, working much the same way heart medications slow the progression of heart disease and reduce heart attacks.

Their landmark research discovered a family of kinase inhibitor drugs -- that all target one enzyme called IKK beta kinase -- as effective for Huntington's.

Basically, the drug restores a critical chemical change that should occur in the huntingtin protein, but does not occur in people with Huntington's disease.

The research appears in the May 29 online edition of Nature Chemical Biology.

"It is the first time anyone has identified drugs that affect how the huntington protein gets modified at one critical site, and through what pathway," said Ray Truant, professor in the Department of Biochemistry and Biomedical Sciences of the Michael G. DeGroote School of Medicine at McMaster.

Huntington's disease, which impacts one in 4,000 Canadians, is an inherited disease that causes certain nerve cells in the brain to waste away. People are born with a defective gene, but symptoms usually don't appear until middle age. Early symptoms include depression and cognitive changes, with later symptoms including uncontrolled movements, clumsiness and balance problems. At some point patients may have difficulty walking, talking or swallowing. There is no specific treatment for the disease.

Currently kinase inhibitor drugs form a family of successful, new generation drugs that are coming on the market or have been approved for a wide range of diseases including stroke, arthritis and cancer.

The McMaster researchers are currently looking at inhibitors that can cross the blood to brain barrier, before starting preliminary trials. If successful, human clinical trials are five or more years away.

Truant and Randy Singh Atwal, a PhD graduate, discovered the huntintin protein has an essential role in chemical stresses relating to human aging and the protein is not properly modified in response to these stresses during Huntington's Disease.

"This is one explanation as to why it takes until middle age for Huntington's to develop in most patients, because the role of the huntingtin protein is more critical as a person ages," said Truant.

The research is supported by the Canadian Institutes of Health Research; the not-for-profit Cure for Huntington's Disease Initiative Inc.; and the Toronto-based Krembil Family Foundation. Truant is chair of the Huntington Society of Canada's scientific advisory board.

"These new results are extremely important because they may help to delay the progression of Huntington's disease," said Dr. Anthony Phillips, scientific director of the Canadian Institutes of Health Research (CIHR) Institute of Neurosciences, Mental Health and Addiction. "CIHR is proud to support researchers who devote their time to look into this genetic brain disorder that has such challenging effects on individuals and their families in Canada."


Story Source:

Materials provided by McMaster University. Note: Content may be edited for style and length.


Journal Reference:

  1. Randy Singh Atwal, Carly R Desmond, Nicholas Caron, Tamara Maiuri, Jianrun Xia, Simonetta Sipione, Ray Truant. Kinase inhibitors modulate huntingtin cell localization and toxicity. Nature Chemical Biology, 2011; DOI: 10.1038/nchembio.582

Cite This Page:

McMaster University. "New drugs target delay of Huntington’s symptoms." ScienceDaily. ScienceDaily, 1 June 2011. <www.sciencedaily.com/releases/2011/05/110531092345.htm>.
McMaster University. (2011, June 1). New drugs target delay of Huntington’s symptoms. ScienceDaily. Retrieved March 29, 2024 from www.sciencedaily.com/releases/2011/05/110531092345.htm
McMaster University. "New drugs target delay of Huntington’s symptoms." ScienceDaily. www.sciencedaily.com/releases/2011/05/110531092345.htm (accessed March 29, 2024).

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