Visualizing muscle disease
Researchers at ETH Zurich have developed a new marker substance for positron emission tomography (PET) that will allow them to monitor the progression of the degenerative muscle disease amyotrophic lateral sclerosis (ALS) in a patient’s brain. Many people will remember the Ice Bucket Challenge back in the summer of 2014. This social media campaign helped patient support groups to promote public awareness of the rare, but debilitating and incurable muscle disease, amyotrophic lateral sclerosis (ALS). The challenge involved one person nominating three others through social media, creating a snowball effect, to make a financial donation to an ALS support group, or – as a forfeit – to pour a bucket of ice-cold water over their heads. This action was supposed to give participants a brief insight into one of the symptoms experienced by someone suffering from degenerative muscle disease.
ALS induces progressive degeneration of the motor neurons that control the muscles. The patient suffers from muscular atrophy and paralysis, accompanied by symptoms such as difficulty walking, speaking and swallowing. At best, drugs can delay the progression of the disease, but oft en life expectancy is only a few years after the initial diagnosis. Very little is known about the causes of the disease.
A new marker substance developed by ETH researchers in collaboration with specialists at St. Gallen Cantonal Hospital and University Hospital Zurich could potentially make a vital contribution to ALS research. The new substance could perhaps make it possible to monitor the progression of ALS in patients using positron emission tomography (PET). The PET imaging technique renders specific molecules on the cell surface visible within the body tissue. The scan uses marker substances, known as PET ligands, that adhere to these molecules via the lock-and-key principle. The radiation emitted by the radioactive markers is very short lived, with a half-life between several minutes and a few hours. This radiation is measured during the PET scan.
The newly developed PET ligand binds to a receptor molecule in the body’s neurotransmitter system for cannabis-based substances, known as the cannabinoid receptor 2 (CNR2). This is very common in inflamed nerve tissue, and is also found in the central nervous system of patients suffering from ALS.
‘The big challenge we faced was to develop a PET ligand that only binds to CNR2, but not to the related cannabinoid receptor 1 (CNR1),’ explains Simon Ametamey, a professor at the Institute of Pharmaceutical Sciences at ETH Zurich. CNR1 occurs naturally in the human brain, where it elicits the pain-relieving and intoxicating effect of cannabis.
The researchers in Professor Ametamey’s group synthesized a series of molecules and performed an in vitro study to measure their ability to bind to the receptors CNR2 and CNR1. The team went on to successfully test the molecule with the most obvious preference for CNR2 in rats and mice with inflamed nerve tissue. Th e scientists have filed a patent for this molecule. The next step will be to perform clinical trials in humans.
‘The new PET ligand could help us to research ALS more effectively and to understand how the disease progresses,’ says Professor Ametamey. It could also improve the early diagnosis of the disease. It might also be potentially interesting for research and diagnosis of other neurological disorders such as Alzheimer’s, Parkinson’s or multiple sclerosis.