1. Academic Validation
  2. Combination of α-glucosidase inhibitor and ribavirin for the treatment of dengue virus infection in vitro and in vivo

Combination of α-glucosidase inhibitor and ribavirin for the treatment of dengue virus infection in vitro and in vivo

  • Antiviral Res. 2011 Jan;89(1):26-34. doi: 10.1016/j.antiviral.2010.11.002.
Jinhong Chang 1 Wouter Schul Terry D Butters Andy Yip Boping Liu Anne Goh Suresh B Lakshminarayana Dominic Alonzi Gabriele Reinkensmeier Xiaoben Pan Xiaowang Qu Jessica M Weidner Lijuan Wang Wenquan Yu Nigel Borune Mark A Kinch Jamie E Rayahin Robert Moriarty Xiaodong Xu Pei-Yong Shi Ju-Tao Guo Timothy M Block
Affiliations

Affiliation

  • 1 Drexel Institute for Biotechnology and Virology Research, Department of Microbiology and Immunology, Drexel University College of Medicine, 3805 Old Easton Road, Doylestown, PA 18902, United States. jinhong.chang@drexelmed.edu
Abstract

Cellular α-glucosidases I and II are Enzymes that sequentially trim the three terminal glucoses in the N-linked oligosaccharides of viral envelope glycoproteins. This process is essential for the proper folding of viral glycoproteins and subsequent assembly of many enveloped viruses, including Dengue virus (DENV). Imino sugars are substrate mimics of α-glucosidases I and II. In this report, we show that two oxygenated alkyl imino sugar derivatives, CM-9-78 and CM-10-18, are potent inhibitors of both α-glucosidases I and II in vitro and in treated Animals, and efficiently inhibit DENV Infection of cultured human cells. Pharmacokinetic studies reveal that both compounds are well tolerated at doses up to 100mg/kg in rats and have favorable pharmacokinetic properties and bioavailability in mice. Moreover, we showed that oral administration of either CM-9-78 or CM-10-18 reduces the peak viremia of DENV in mice. Interestingly, while treatment of DENV infected mice with ribavirin alone did not reduce the viremia, combination therapy of ribavirin with sub-effective dose of CM-10-18 demonstrated a significantly enhanced Antiviral activity, as indicated by a profound reduction of the viremia. Our findings thus suggest that combination therapy of two broad-spectrum Antiviral agents may provide a practically useful approach for the treatment of DENV Infection.

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