Literature DB >> 27664407

Anti-adipogenic and antiviral effects of l-carnitine on hepatitis C virus infection.

Yoko Tsukuda1, Goki Suda1, Seiji Tsunematsu, Jun Ito1, Fumiyuki Sato1, Katsumi Terashita1, Masato Nakai1, Takuya Sho1, Osamu Maehara1, Tomoe Shimazaki1, Megumi Kimura1, Kenichi Morikawa1, Mitsuteru Natsuizaka1, Koji Ogawa1, Shunsuke Ohnishi1, Makoto Chuma1, Naoya Sakamoto1.   

Abstract

Hepatitis C virus (HCV) has been reported to hijack fatty acid metabolism in infected hepatocytes, taking advantage of lipid droplets for virus assembly. In this study, we analyzed the anti-HCV activity of l-carnitine, a substance involved in the transport of fatty acids into mitochondria. JFH-1 or HCV replicon-transfected Huh7.5.1 cells were treated with or without l-carnitine to examine its anti-HCV effects. The effects of l-carnitine on HCV entry, HCV-induced adipogenesis and lipid droplet formation, and HCV-induced oxidative stress were examined. Treatment of JFH-1-infected cells with l-carnitine inhibited HCV propagation in a concentration-dependent manner. In contrast, l-carnitine had no anti-HCV activity in the HCV replicon system, which is lacking viral assembly. In addition, l-carnitine did not affect HCV entry. However, l-carnitine treatment decreased intracellular lipid droplets, which are crucial for HCV assembly in JFH-1-infected cells. The expression level of CPT-1 was decreased in JFH-1-infected cells, and l-carnitine treatment restored this expression. HCV-infected cells exhibited increased production of reactive oxygen species and glutathione oxidation. l-carnitine decreased oxidative stress induced by JFH-1-infection, as shown by glutathione/glutathione disulfide assays and MitoSOX staining. l-carnitine exhibited anti-HCV activity, possibly by inhibiting HCV assembly and through its anti-adipogenic activity in HCV-infected cells. Moreover, l-carnitine has antioxidant properties in HCV-infected hepatocytes. Overall, these results indicated that l-carnitine may be an effective adjunctive agent in antiviral therapies to treat chronic hepatitis C. J. Med. Virol. 89:857-866, 2017.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  CPT-1; HCV; anti-viral effect; l-carnitine

Mesh:

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Year:  2016        PMID: 27664407     DOI: 10.1002/jmv.24692

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  8 in total

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Journal:  Hepatol Commun       Date:  2018-08-06

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Journal:  Clin Mol Hepatol       Date:  2019-02-25

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Journal:  PLoS One       Date:  2018-12-21       Impact factor: 3.240

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Journal:  Nutrients       Date:  2021-04-14       Impact factor: 5.717

Review 5.  Metabolic and cardiovascular complications after virological cure in hepatitis C: What awaits beyond.

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Journal:  Front Nutr       Date:  2021-11-25

7.  Tenofovir-disoproxil-fumarate modulates lipid metabolism via hepatic CD36/PPAR-alpha activation in hepatitis B virus infection.

Authors:  Kazuharu Suzuki; Goki Suda; Yoshiya Yamamoto; Ken Furuya; Masaru Baba; Akinobu Nakamura; Hideaki Miyoshi; Megumi Kimura; Osamu Maehara; Ren Yamada; Takashi Kitagataya; Koji Yamamoto; Taku Shigesawa; Akihisa Nakamura; Masatsugu Ohara; Naoki Kawagishi; Masato Nakai; Takuya Sho; Mitsuteru Natsuizaka; Kenichi Morikawa; Koji Ogawa; Shunsuke Ohnishi; Naoya Sakamoto
Journal:  J Gastroenterol       Date:  2020-11-19       Impact factor: 7.527

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Authors:  Atchara Paemanee; Atitaya Hitakarun; Sittiruk Roytrakul; Duncan R Smith
Journal:  BMC Res Notes       Date:  2018-05-16
  8 in total

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