Expression of inflammatory cytokines and inducible nitric oxide synthase in brains of SIV-infected rhesus monkeys: Applications to HIV-induced central nervous system disease

Background: Human immunodeficiency virus type 1 (HIV-1) infection of the central nervous system (CNS) can lead to severe impairments in cognition, behavior, and motor skills. The mechanism(s) by which HIV-1 induces CNS disease are not well understood. Recent evidence suggests that expression of inducible nitric oxide synthase (iNOS) and nitric oxide (NO) may contribute to HIV-1-induced neurologic disease. We sought to determine if these factors were present in the CNS of rhesus monkeys with simian immunodeficiency virus (SIV)-induced CNS disease. Materials and Methods: Total NO production in cerebral spinal fluid (CSF) from infected monkeys was determined by measuring nitrite (NO2-) and nitrate (NO3-) (stable NO degradation products) utilizing Greiss reagents. in situ hybridization revealed iNOS, interferon-gamma(IFN gamma), and interleukin 1 beta (IL-1 beta) mRNA in the brains of SN-infected monkeys. Microglia were isolated from animals infected with SIV. Following stimulation with LPS, induction of iNOS mRNA in isolated microglia was analyzed by reverse transcriptase-polymerase chain reaction. Results: Serial CSF samples from an SIV-infected monkey reveal increased levels of NO2-/NO3-. In situ hybridization demonstrated iNOS, IFN gamma, and IL-1 beta mRNAs in post-mortem brain tissue of SN-infected monkeys. Furthermore, stimulated microglia from an SIV-infected monkey could produce iNOS mRNA. Conclusions: The presence of iNOS in the brain and NO2-/NO3- in the CSF indicates that NO is produced in the CN of SIV-infected monkeys. The data suggest that iNOS and NO may be contributing to SIV-induced CNS disease.