Caulerpin as a potential antiviral drug against herpes simplex virus type 1

• Autor(a) principal: Macedo,Nathália Regina Porto Vieira
• Data de Publicação: 2012
• Outros Autores: Ribeiro,Michele S., Villaça,Roberto C., Ferreira,Wilton, Pinto,Ana Maria, Teixeira,Valéria L., Cirne-Santos,Claudio, Paixão,Izabel C. N. P., Giongo,Viveca
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Revista Brasileira de Farmacognosia (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2012000400022
• topic: Caulerpa; caulerpin; Herpes simplex type 1; cytotoxicity; antiviral

About 80% of the human adult population is infected with HSV-1. Although there are many anti-HSV-1 drugs available (acyclovir, ganciclovir, valaciclovir, foscarnet), their continuous use promotes the selection of resistant strains, mainly in ACV patients. In addition to resistance, the drugs also have toxicity, particularly when administration is prolonged. The study of new molecules isolated from green algae with potential antiviral activity represents a good opportunity for the development of antiviral drugs. Caulerpin, the major product from the marine algae Caulerpa Lamouroux (Caulerpales), is known for its biological activities such as antioxidant, antifungal, acetylcholinesterase inhibitor (AChE) and antibacterial activity. In this work, we show that caulerpin could be an alternative to acyclovir as an anti-HSV-1 drug that inhibits the alpha and beta phases of the replication cycle.