Dogfish Squalamine as a broad-spectrum systemic antiviral agent

Published online before print on September 19, 2011

Squalamine as a broad-spectrum systemic antiviral agent with therapeutic potential

Michael Zasloff et al.


Antiviral compounds that increase the resistance of host tissues represent an attractive class of therapeutic.
Here, we show that squalamine, a compound previously isolated from the tissues of the dogfish shark (Squalus acanthias) and the sea lamprey (Petromyzon marinus), exhibits broad-spectrum antiviral activity against human pathogens, which were studied in vitro as well as in vivo.
Both RNA- and DNA-enveloped viruses are shown to be susceptible. The proposed mechanism involves the capacity of squalamine, a cationic amphipathic sterol, to neutralize the negative electrostatic surface charge of intracellular membranes in a way that renders the cell less effective in supporting viral replication.
Because squalamine can be readily synthesized and has a known safety profile in man, we believe its potential as a broad-spectrum human antiviral agent should be explored.

Proceedings of the National Academy of Sciences (PNAS), doi:10.1073/pnas.1108558108




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