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Scientists find potential treatment for Parkinson’s disease.

(Photo ⁤by FRED TANNEAU/AFP via Getty Images)

OAN’s Abril Elfi
6:31 PM – Wednesday, August⁣ 2, 2023

An​ assistant professor‌ at⁢ the University⁣ of Connecticut has made an ⁤exciting discovery in the field of Parkinson’s disease treatment.

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On Tuesday, UConn Health, a branch of the university, announced that Yulan Xiong and her team have uncovered a key mechanism​ in Parkinson’s disease research.

Parkinson’s disease is typically caused by a gene mutation called LRRK2. This gene plays a role in regulating cell function ⁣and transmitting signals.

The mutation in LRRK2 leads​ to an ​overproduction of a protein called ‌dardarin, rather ​than causing it to ‌become deformed. Until now, scientists were unsure of how to control this protein expression due to a lack of understanding of the underlying mechanisms.

In a recent publication in The ⁢Embo Journal, Xiong ‍revealed that her lab team has solved this mystery by identifying an enzyme called ATIC, which acts ‍as a regulator for LRRK2, and a potential pharmaceutical ⁣treatment.

To find potential candidates for genes that⁣ control LRRK2, the researchers conducted a genome-wide search in yeast cells.

Xiong and PhD‍ candidate ‍Qinfang Liu discovered that the enzyme ATIC controls the gene at the messenger-RNA ‍level, which instructs the body on how to build proteins. This was ⁣a surprising discovery ‍for the team.

“This was a surprising discovery,” Xiong says. “At the beginning we did a⁢ screening, we identified a candidate, ⁣and we ‍found that it ⁤was targeted at the mRNA level.‌ This is a new ⁢discovery for us ​too.”

The researchers then ⁢examined ATIC in human neural cells, as well as fruit⁣ fly ‌and mouse models, to understand its impact on Parkinson’s disease. They ⁢found that AICAr, a ⁤medication that mimics ATIC activity, significantly reduced LRRK2 levels.

“We used a primary neuronal culture to ‍see ​how those candidates can regulate LRRK2,” Xiong says. “And we found that it can significantly regulate the ⁤LRRK2 expression.”

AICAr has ⁢shown promise as a therapy for metabolic disorders and cardiovascular illnesses in preclinical studies. However,‍ its usage ⁣in treating Parkinson’s disease has been limited ⁤due to the blood-brain‌ barrier.

To overcome this hurdle, Xiong and her colleagues are⁤ currently modifying AICAr. They are also collaborating with UConn’s⁢ Technology Commercialization Services (TCS)⁣ to further advance this technology and prepare for clinical human trials.

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