Inhibition of HIV-1 replication in human primary cells by a dolabellane diterpene isolated from the marine algae Dictyota pfaffii.

Abstract

We describe in this paper that the dolabellane diterpene 8,10,18-trihydroxy-2,6-dolabelladiene (3), isolated from the marine algae Dictyota pfaffii, inhibits the HIV-1 infection in human primary cells and tumor cell lines. We initially observed that compound 3 inhibited the activity of a purified HIV-1 enzyme reverse transcriptase (RT) in a dose-dependent manner, with an IC (50) value of 16.5 +/- 4.3 microM. Next, we found that compound 3 inhibited HIV-1 infection by an R5-tropic isolate in peripheral blood mononuclear cells (PBMCs) in a dose-dependent manner with an EC (50) value of 8.4 +/- 2.8 microM. The replication of HIV-1 isolates presenting distinct tropism for chemokine receptors was also inhibited, as analyzed in PBMCs or U87 cells infected with R5-, X4- or R5X4-tropic isolates. Likewise, compound 3 blocked HIV-1 infection in macrophages by R5 and R5X4 viruses in a dose-dependent manner with EC (50) values of 1.7 +/- 0.6 microM and 1.85 +/- 0.75 microM, respectively. Compound 3 sustained antiretroviral activity even when added to HIV-1-infected Sup-T1 cells at 12 h after infection, suggesting that, as well as inhibiting HIV-1 RT, it also blocks HIV-1 replication at a post transcriptional step. Our results support further investigations on compound 3 pharmacokinetics and we propose that this diterpene could be considered as a potential compound for HIV-1 therapy.

• Authors: Claudio Cesar Cirne-Santos, Valéria L Teixeira, Luiz Roberto Castello-Branco, Izabel C P P Frugulhetti, Dumith Chequer Bou-Habib
• Journal: Planta medica (Planta Med) Vol. 72 Issue 4 Pg. 295-9 (Mar 2006) ISSN: 0032-0943 [Print] Germany
• PMID: 16557468 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-HIV Agents
• Diterpenes
• Plant Extracts
• dolabellane

Topics

• Anti-HIV Agents (administration & dosage, pharmacology, therapeutic use)
• Diterpenes (administration & dosage, pharmacology, therapeutic use)
• Dose-Response Relationship, Drug
• Eukaryota
• HIV-1 (drug effects)
• Humans
• Leukocytes, Mononuclear (virology)
• Phytotherapy
• Plant Extracts (administration & dosage, pharmacology, therapeutic use)
• Virus Replication (drug effects)