As the second most common cause of parkinsonism after Parkinson’s disease, drug-induced parkinsonism is affecting more and more people’s lives and health particularly in an aging society. Chronic use of flunarizine (FNZ), a drug often used for treating dizziness, migraine, epilepsy, and peripheral vascular diseases, may induce parkinsonism. Previous investigations point out that the disruption of mitochondrial quality control, essential for mitochondrial homeostasis and function, degrades brain functions, and is causally related to parkinsonism disease. Still, there is limited knowledge about the exact mechanism of drug-induced parkinsonism, which hinders the development of prevention and treatment.

Recently, researchers from the Guangzhou Institutes of Biomedicine and Health (GIBH) of the Chinese Academy of Sciences (CAS) and the Second Affiliated Hospital of Zhejiang University School of Medicine have revealed the mechanisms of FNZ-induced parkinsonism by integrating mitochondria and lysosomes into mitolysosome, and using it to cause mitochondrial reduction in the brains of mice.

Mitolysosome exocytosis in drug-induced parkinsonism [IMAGE: GIBH]

This study was published in Science Advances on April 13.

The researchers noticed that mice treated with FNZ showed parkinsonism-like symptoms in the rotarod test, the open-field test and Morris water maze test, including decreased coordination and balance and weakened abilities to learn and to memorize.

The researchers took a step further. They detected an increase in glucose uptake in the brains of FNZ-treated mice by [18F]-fluoro-2-deoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) scanning, and significant reductions of mitochondrial proteins specifically in brains, but not in other tissues.

Looking into the mechanism of mitochondrial elimination, the researchers uncovered that FNZ induced mitochondrial direct entry into lysosomes, formatting mitolysosome, a new organelle structure, which then mediated a VAMP2/STX4-dependent exocytosis, leading to the reduction of the amount of mitochondria. Such process was canonical or noncanonical mitophagy independent. Furthermore, a genome-wide CRISPR/Cas9 knockout screening was employed to identify genes which were necessary for mitochondrial elimination. Results indicated that lysosome associated mitochondrial exocytosis may contribute to parkinsonism.

More importantly, this study has shown an FNZ-based method for total depletion of mitochondria can be used to explore the novel function of mitochondria, or to replace the mitochondrial DNA mutations of patients with functional mitochondria.

For more information, please contact:

Liu Xinguo, Ph.D Principal Investigator

E-mail: liu_xingguo@gibh.ac.cn

Guangzhou Institutes of Biomedicine and Health (GIBH),

Chinese Academy of Sciences

Source: Guangzhou Institutes of Biomedicine and Health (GIBH),

Chinese Academy of Sciences