HCV Antiviral Properties Found in South American Plant Compounds

DECEMBER 08, 2017
Gail Connor Roche
Ana Carolina Gomes Jardim, PhDAna Carolina Gomes Jardim, PhD
Compounds derived from a South American plant showed antiviral properties in a study investigating the substances’ effects on the hepatitis C virus (HCV).

The findings support that the natural flavonoid isolates from Brazilian plants possess anti-HCV potential, corresponding author Ana Carolina Gomes Jardim, PhD, told MD Magazine.

“They could represent different approaches or be used as template to the development of drugs for future HCV therapy,” Jardim said.
        
Jardim, along with biologists, chemists and pharmacists from Brazil and the UK, investigated 2 flavonoids found in Pterogyne nitens, a member of the legume family. P. nitens is commonly known as cocal, bálsamo, and tipa colorado in its native Brazil, Paraguay, Bolivia and Argentina.

Previous studies investigating these flavonoids — called sorbifolin and pedalitin — have shown that they possess antiproliferative effects against melanoma cells. The compounds also have demonstrated antioxidant and antifungal activity, the authors said.
        
“We showed that these 2 compounds already previously described in the literature posses anti-HCV activity,’’ Jardim, Professor in Virology, Federal University of Uberlândia, in Minas Gerais, Brazil, said. “This was the first description of antiviral activity for these flavonoids.”
        
Flavonoids represent an important class of compounds in medical research. The substances are produced by plants as a response to microbial infections. Epigallocatechin derived from green tea and naringenin from grapefruit have been reported to possess antiviral activities, including against HCV.
        
Citing promising past research and the cost and drawbacks of current HCV therapies, the team set out to investigate the potential impact of the 2 P. nitens compounds on the HCV replication cycle. 
        
Researchers from the Federal University of Uberlandia and São Paulo State University in Brazil, and the University of Leeds in the UK contributed to the work.
        
The team used dried P. nitens leaves to extract the compounds for study. After testing for potential toxicity, the researchers found that sorbifolin inhibited hepatitis C virus entry up to 45% and pedalitin inhibited entry by 78.7%.
        
Pedalitin blocked entry by both direct action on the virus particles and interference with the host cells. The activity of sorbifolin was restricted to its viruscidal effect, the team found.
        
“The results showed that flavonoids from P. nitens inhibited HCV entry in vitro,’’ researchers wrote. “Further analyses are necessary to clarify the mechanisms of how these flavonoids act against HCV infection.’’
        
Neither flavonoid had an effect HCV replication or release, the team found.
        
“We came to this conclusion after biochemical studies and several antiviral assays, which allowed us to understand and evaluate the potential of these compounds,’’ Jardim said. “Our findings support that the natural flavonoids isolates from Brazilian plants possess anti-HCV potential.’’

While the results are promising, more tests are needed to ensure that these compounds can be used to help patients with HCV infections, Jardim said.
        
“These findings strengthen the theory that natural compounds may be an alternative pathway in the treatment of hepatitis C,’’ she said. “The benefits are not immediate but can help to improve future therapy against HCV.’’

The study, "Flavonoids from Pterogyne nitens Inhibit Hepatitis C Virus Entry," was published online in Nature last month.

Related Coverage

HCV Patients SVR with Mavyret After Previous DAA Failure
Liver MRI Device Provides Non-invasive Diagnostics
New Guidelines Target HBV as Public Health Priority

Related Coverage >>>
Copyright© MD Magazine 2006-2018 Intellisphere, LLC. All Rights Reserved.
$loginModal$