. Scientific Frontline: Oregon State researchers uncover mechanism for treating dangerous liver condition

Wednesday, October 25, 2023

Oregon State researchers uncover mechanism for treating dangerous liver condition

Illustration Credit: Julien Tromeur

A study spearheaded by Oregon State University has shown why certain polyunsaturated fatty acids work to combat a dangerous liver condition, opening a new avenue of drug research for a disease that currently has no FDA-approved medications.

Scientists led by Oregon State’s Natalia Shulzhenko, Andrey Morgun and Donald Jump used a technique known as multi-omic network analysis to identify the mechanism through which dietary omega 3 supplements alleviated nonalcoholic steatohepatitis, usually abbreviated to NASH.

The mechanism involves betacellulin, a protein growth factor that plays multiple positive roles in the body but also contributes to liver fibrosis, or scarring, and the progression to cirrhosis and liver cancer.

“We only succeeded in finding these surprising results because we implemented an entirely unbiased approach that incorporated a diverse type of big data analysis ranging from lipids and metabolites to whole tissue and single-cell RNA sequences,” said Morgun, a researcher in the OSU College of Pharmacy.

Findings were published in EMBO Molecular Medicine.

NASH is associated with a disorder known as metabolic syndrome. It develops when fat in the liver becomes toxic, killing liver cells, inflaming the organ and promoting fibrosis. The disease can lead to permanent scarring (cirrhosis), liver failure and possibly death.

People are considered to have metabolic syndrome if they have at least two of the following conditions: abdominal obesity, high blood pressure, high blood sugar, low blood levels of “good” cholesterol and high levels of bad cholesterol and triglycerides.

A diet high in saturated fat and refined sugars causes chronic low-grade inflammation that contributes to the development of metabolic syndrome. Metabolic syndrome is also associated with cognitive dysfunction and dementia as well as being a major risk factor for cardiovascular disease, Type 2 diabetes and NASH.

An estimated 35% of U.S. adults have metabolic syndrome, the researchers note.

In this study, scientists used both a mouse model and human liver transcriptome data – the total of all the messenger RNA molecules expressed from the genes – to uncover betacellulin as the target of omega-3 polyunsaturated fatty acids, often abbreviated as omega 3 PUFA. 

“Via large meta-analysis, we found betacellulin is consistently up-regulated in livers of cancer patients – there’s more of it than there should be,” Morgun said. “And omega 3 PUFA lower, or down-regulate, betacellulin in both mice and humans with NASH. Targeting betacellulin expression is one of the mechanisms for omega 3 PUFA reduction of western-diet-induced NASH.”

Beyond greatly advancing the understanding of how NASH starts and progresses, the findings open a new door for pharmaceutical research, he added.

“We found a novel drug target, and our results may aid in the quest for a precision-medicine approach to NASH treatment and liver cancer prevention by using specific omega 3 PUFA,” Morgun said. “One thought is that patients’ betacellulin could be monitored during treatment to determine optimal dosages for each patient.”

In addition to dietary supplements, omega 3 PUFA, such as docosahexaenoic acid, are found in cold-water fatty fish such as salmon and mackerel and in some nuts, seeds and plant oils. 

Omega 3 PUFAs are not manufactured by the body but are essential fatty acids that must be acquired from the diet. These fatty acids are involved in a wide range of bodily processes including cognitive function, vision, cell growth, regulation of multiple metabolic processes and cardiovascular function.

Funding: The research was supported by grants from the National Institute of Diabetes and Digestive Kidney Diseases, part of the National Institutes of Health.

Published in journalEMBO Molecular Medicine

Authors: Jyothi Padiadpu, a postdoctoral researcher in the OSU College of Pharmacy, was the lead first author on the study. Other Oregon State researchers contributing to the paper were Nolan Newman, Richard Rodrigues, Sehhajvir Singh, Manuel Garcia-Jaramillo, Jacob Pederson, Zhipeng Li, Philip Monnier and Kevin Brown.

Additional information: The collaboration included scientists from the National Institutes of Health’s National Cancer Institute.

Source/CreditOregon State University | Steve Lundeberg

Reference Number: med102523_01

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