Promising ALS Drug Candidate Extends Lifespan
A research team at the University of Helsinki, in collaboration with partners, has identified a hopeful drug candidate, the CDNF protein, for addressing amyotrophic lateral sclerosis (ALS). In animal studies involving rats and mice, the cerebral dopamine neurotrophic factor (CDNF) has demonstrated the ability to extend lifespan and alleviate disease symptoms ().
What is Amyotrophic Lateral Sclerosis?
Amyotrophic lateral sclerosis (ALS) is a rapidly progressing fatal neurodegenerative disease that affects the nerve cells in the brain and spinal cord. Specifically, a selective degeneration of motoneurons occurs in the spinal cord, leading to muscle atrophy and paralysis. Most patients with ALS die from respiratory failure, usually within 1 to 3 years from symptom onset. There is no cure for ALS, and the only drug available in Europe, riluzole, only prolongs ALS patient survival by a couple of months.
Assistant professor Merja Voutilainen and researchers from the Regenerative Neuroscience Group, Faculty of Pharmacy and Institute of Biotechnology, University of Helsinki, together with their national and international collaborators, investigated the therapeutic effect of a protein called cerebral dopamine neurotrophic factor (CDNF) in several cellular and animal models of ALS.
‘Administering CDNF protein to mice and rats afflicted with amyotrophic lateral sclerosis leads to enhancement in their motor function and effectively arrests the advancement of paralysis symptoms. #als #nervousdisorder’
The CDNF protein, discovered by Professor Mart Saarma laboratory in 2007, is mostly found in the endoplasmic reticulum (ER) within cells. ER is an important cell organelle mainly involved in the synthesis and maturation of circa one-third of all proteins in the cell. CDNF has previously shown therapeutic potential in Parkinsons disease.
In this study, the Regenerative Neuroscience Group used three animal models that were genetically modified to express human mutations (TDP43-M337V and SOD1-G93A) affecting ALS patients. They were particularly interested in studying ER stress, which is a cellular response to protecting cells and its proteins. If ER stress becomes chronic, as is the case in many neurological diseases, it can cause cell death.
"Symptom amelioration is reflected in an increased number of surviving motoneurons in the spinal cord of the animals compared to rodents that did not receive CDNF. Our experiments suggest that CDNF may rescue motoneurons by reducing the ER stress response and, therefore, cell death. Importantly, ER stress was present in all our animal models, independently of the specific genetic mutations" says Dr. Francesca De Lorenzo, lead author of the study, from the University of Helsinki.
Professor Michael Sendtner from the University of W�rzburg, Germany, one of the world's leading researchers in the field of ALS research and co-author of the study, comments: "This study opens the way to a rational therapy to counteract one of the most severe cellular pathologies in ALS: ER stress".
Reference:
- CDNF rescues motor neurons in models of amyotrophic lateral sclerosis by targeting endoplasmic reticulum stress - (https:academic.oup.com/brain/article/146/9/3783/7078992)
Source: Eurekalert