The pioneering research supports the fast-tracking of the drug ursodeoxycholic acid (UDCA) for a clinical trial in Parkinson's patients, researchers said.
"We demonstrated the beneficial effects of UDCA in the tissue of LRRK2 carriers with Parkinson's disease as well as currently asymptomatic LRRK2 carriers," Dr Heather Mortiboys, Parkinson's UK Senior Research Fellow from the University of Sheffield, said.
"In both cases, UDCA improved mitochondrial function as demonstrated by the increase in oxygen consumption and cellular energy levels," said Mortiboys.
"Our hope is therefore, that UDCA might be beneficial for other types of Parkinson's disease and might also show benefits in other neurodegenerative diseases," said Bandmann.
The research is also the first to demonstrate beneficial effects of UDCA on dopaminergic neurons, the nerve cells affected in Parkinson's disease, in a fly model of Parkinson's disease which carries the same genetic change as some patients with the condition.
Defects in mitochondria, and as a consequence reduced energy levels, are a factor in a number of diseases that affect the nervous system including Parkinson's and Motor Neuron Disease.
Nerve cells have a particularly high energy demands, therefore defects in the cell's energy generators will crucially affect their survival.
"Following on from the promising results of our in vitro drug screen, we were keen to further investigate and confirm the potential of UDCA in vivo - in a living organism," Bandmann added.
Researchers from the University of York's Department of Biology demonstrated the beneficial effects of UDCA in vivo using the fruit fly (Drosophila melanogaster).
The study was published in the journal Neurology.
