Interactions between integrase inhibitors and human arginase 1

J Neurochem. 2017 Jul;142(1):153-159. doi: 10.1111/jnc.14039. Epub 2017 May 9.

Abstract

The neuro-pathogenic mechanism(s) underlying HIV-associated neurocognitive disorders are mostly unknown. HIV-infected macrophages and microglial cells play a crucial role and the metabolic fate of l-arginine may be highly relevant to microglia activation. In this context, arginase (ARG), which uses l-arginine as substrate, can be on the same time a target and source of oxidative stress and inflammation. In this study, we investigated whether integrase strand transfer inhibitors share with the other antiretroviral drugs the ability to inhibit ARG activity. We used the previously validated cell model, namely the human microglia cell line, as well as the computational chemistry approach. Furthermore, here we characterized the activity of purified human ARG in a cell-free in vitro system, and investigated the effects of integrase strand transfer inhibitors in this newly validated model. Overall evidence shows that Dolutegravir, Raltegravir and Elvitegravir inhibit ARG activity.

Keywords: arginase 1; integrase strand transfer inhibitors; microglia.

MeSH terms

  • AIDS Dementia Complex / enzymology
  • AIDS Dementia Complex / metabolism
  • Arginase / antagonists & inhibitors*
  • Arginase / metabolism
  • Cell-Free System
  • Cells, Cultured
  • HIV Integrase Inhibitors / metabolism
  • HIV Integrase Inhibitors / pharmacology*
  • Heterocyclic Compounds, 3-Ring / pharmacology
  • Humans
  • Microglia / drug effects
  • Microglia / enzymology
  • Molecular Docking Simulation
  • Oxazines
  • Piperazines
  • Pyridones
  • Quinolones / pharmacology
  • Raltegravir Potassium / pharmacology

Substances

  • HIV Integrase Inhibitors
  • Heterocyclic Compounds, 3-Ring
  • Oxazines
  • Piperazines
  • Pyridones
  • Quinolones
  • Raltegravir Potassium
  • elvitegravir
  • dolutegravir
  • ARG1 protein, human
  • Arginase