학술논문

Attenuation of oxidative stress, inflammation and apoptosis by minocycline prevents retrovirus-induced neurodegeneration in mice
Document Type
Report
Source
Brain Research. August 25, 2009, Vol. 1286, p174, 11 p.
Subject
Antioxidants -- Analysis
Inflammation -- Prevention
Inflammation -- Analysis
Apoptosis -- Prevention
Apoptosis -- Analysis
Oxidative stress -- Prevention
Oxidative stress -- Analysis
Minocycline -- Analysis
Leukemia -- Prevention
Leukemia -- Analysis
Neurons -- Analysis
Dementia -- Prevention
Dementia -- Analysis
Language
English
ISSN
0006-8993
Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.brainres.2009.06.007 Byline: Xianghong Kuang (a), Virginia L. Scofield (a), Mingshan Yan (a), George Stoica (b), Na Liu (a), Paul K.Y. Wong (a) Keywords: Moloney murine leukemia virus-ts1; Minocycline; Oxidative stress; Inflammation; Apoptosis; Nrf2 Abstract: The ts1 mutant of the Moloney murine leukemia virus (MoMuLV) causes neurodegeneration in infected mice that resembles HIV-associated dementia. We have shown previously that ts1 infects glial cells in the brain, but not neurons. The most likely mechanism for ts1-mediated neurodegeneration is loss of glial redox support and glial cell toxicity to neurons. Minocycline has been shown to have neuroprotective effects in various models of neurodegeneration. This study was designed to determine whether and how minocycline prevents paralysis and death in ts1-infected mice. We show here that minocycline delays neurodegeneration in ts1-infected mice, and that it prevents death of cultured astrocytes infected by ts1 through attenuating oxidative stress, inflammation and apoptosis. Although minocycline reduces virus titers in the CNS of infected mice, it does not affect virus titers in infected mice thymi, spleens or infected C1 astrocytes. In addition, minocycline prevents death of primary neurons when they are cocultured with ts1-infected astrocytes, through mechanisms involving both inhibition of oxidative stress and upregulation of the transcription factor NF-E2-related factor 2 (Nrf2), which controls cellular antioxidant defenses. We conclude that minocycline delays retrovirus ts1-induced neurodegeneration involving antioxidant, anti-inflammation and anti-apoptotic mechanisms. Author Affiliation: (a) Department of Carcinogenesis, University of Texas, M.D. Anderson Cancer Center, Science Park-Research Division, 1808 Park Road 1-C, PO Box 389, Smithville, TX 78957, USA (b) Department of Pathobiology, Texas A & M University College of Veterinary Medicine, College Station, TX 77843, USA Article History: Accepted 4 June 2009