Biologists identify promising drug for ALS treatment

Biologists identify promising drug for ALS treatment
Ted Allison (left) and Michele DuVal found that telbivudine, a drug already approved to treat hepatitis, may slow the progression of ALS. Credit: John Ulan

A drug typically used to treat hepatitis could slow the progression of ALS, also known as Lou Gehrig's disease, according to new research by University of Alberta scientists.

The drug, called telbivudine, targets a protein called SOD1 that misfolds in most cases of patients with ALS.

"We showed that telbivudine can greatly reduce the toxic properties of SOD1, including improving the health of the subject's and improving movement," said U of A biologist and study co-author Ted Allison.

Current treatments slow the progression of the degenerative disease by only a few months, and these findings could improve the treatment of patients suffering from ALS by extending and improving their quality of life.

The used to identify drugs with the potential for targeting the SOD1 protein. From this shortlist, the scientists identified and tested the most likely candidates—including telbivudine—using animal models.

"ALS is not well understood," said lead author Michele DuVal, who recently completed the Ph.D. portion of the Faculty of Medicine & Dentistry's MD/Ph.D. program under Allison's supervision.

"We don't yet know exactly what goes wrong first in the motor neurons or how the misbehaving SOD1 causes toxicity. Because there is still much to learn about the disease, the ALS research community focuses both on understanding ALS and on developing promising therapies."

The next step for the researchers is further testing to see how effective telbivudine is in reducing the progression of ALS in other animal models.

The discovery is particularly exciting because since the drug is already in use for treating patients with hepatitis, and has therefore been approved by health regulators, in human patients could happen more quickly.

"It is already proven safe to use in patients, and it has very good potential for repurposing to use in a new clinical setting against ALS," said Allison.

The study, "Tryptophan 32 Mediates SOD1 Toxicity in a In Vivo Motor Neuron Model of ALS and Is a Promising Target for Small Molecule Therapeutics," was published in Neurobiology of Disease.

More information: Michèle G. DuVal et al. Tryptophan 32 mediates SOD1 toxicity in a in vivo motor neuron model of ALS and is a promising target for small molecule therapeutics, Neurobiology of Disease (2018). DOI: 10.1016/j.nbd.2018.11.025

Journal information: Neurobiology of Disease

Citation: Biologists identify promising drug for ALS treatment (2018, December 18) retrieved 23 March 2023 from
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