Literature DB >> 10534142

Frontal lobe neuronal injury correlates to altered function in FIV-infected cats.

M Podell1, K Maruyama, M Smith, K A Hayes, W R Buck, D S Ruehlmann, L E Mathes.   

Abstract

Six cats infected intravenously at 8 weeks of age with feline immunodeficiency virus Maryland isolate (FIV-MD), were evaluated at 8 and 14 months of age (6 months and 12 months postinfection, respectively) with high spatial resolution proton magnetic resonance spectroscopy (MRS) of the frontal cortex. Two separate control cat groups were evaluated at 8 months and 16 months of age. Single voxel two-dimensional high-resolution proton magnetic resonance imaging was performed using the PRESS sequence by selecting a 0.125 ml volume of interest in the medial frontal cortex. A significant reduction in both N-acetylaspartate (NAA) and NAA: choline ratio was found in the FIV 14-month-old group compared with FIV 8-month-old cats, and to the respective age-matched control 16-month-old cats. A negative correlation between NAA and CD4 lymphocyte count was seen in the FIV-14 group only. This group of FIV cats also exhibited a higher proportion of quantitative electroencephalographic relative slow wave activity (RSWA) that correlated to lower NAA content in the frontal cortical voxel. Although peripheral blood proviral load increased over time of infection, no correlation was found between proviral blood or lymph node load and NAA values, CD4 lymphocyte counts, or frontal cortical RSWA. Thus, this study demonstrated that neurologic functional disruption of the frontal cortex correlated strongly with neuronal injury and/or loss in FIV-MD-infected cats independent of peripheral proviral load. The ability to define in vivo neurodegeneration further in this animal model helps in understanding the neuropathogenesis of lentivirus infection, and possibly, a means to follow progression and reversibility during the initial stages of brain infection as therapeutic agents are identified.

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Year:  1999        PMID: 10534142     DOI: 10.1097/00042560-199909010-00002

Source DB:  PubMed          Journal:  J Acquir Immune Defic Syndr        ISSN: 1525-4135            Impact factor:   3.731


  17 in total

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Authors:  Chadd E Nesbit; Stanley A Schwartz
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4.  Early detection of neuropathophysiology using diffusion-weighted magnetic resonance imaging in asymptomatic cats with feline immunodeficiency viral infection.

Authors:  Daniel S Bucy; Mark S Brown; Helle Bielefeldt-Ohmann; Jesse Thompson; Annette M Bachand; Michelle Morges; John H Elder; Sue Vandewoude; Susan L Kraft
Journal:  J Neurovirol       Date:  2011-07-23       Impact factor: 2.643

5.  Choroid plexus macrophages proliferate and release toxic factors in response to feline immunodeficiency virus.

Authors:  D C Bragg; L C Hudson; Y H Liang; M B Tompkins; A Fernandes; R B Meeker
Journal:  J Neurovirol       Date:  2002-06       Impact factor: 2.643

6.  Methamphetamine enhances cell-associated feline immunodeficiency virus replication in astrocytes.

Authors:  Mikhail A Gavrilin; Lawrence E Mathes; Michael Podell
Journal:  J Neurovirol       Date:  2002-06       Impact factor: 2.643

7.  Infection of the choroid plexus by feline immunodeficiency virus.

Authors:  D C Bragg; T A Childers; M B Tompkins; W A Tompkins; R B Meeker
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Review 8.  Neurologic disease in feline immunodeficiency virus infection: disease mechanisms and therapeutic interventions for NeuroAIDS.

Authors:  Christopher Power
Journal:  J Neurovirol       Date:  2017-12-15       Impact factor: 2.643

Review 9.  Feline immunodeficiency virus neuropathogenesis: from cats to calcium.

Authors:  Rick B Meeker
Journal:  J Neuroimmune Pharmacol       Date:  2006-11-28       Impact factor: 4.147

10.  New insights into the neuroimmunity of SIV infection by magnetic resonance spectroscopy.

Authors:  R Gilberto González; Jane B Greco; Julian He; Margaret R Lentz; Shawn O'Neil; Sarah J Pilkenton; Eva M Ratai; Susan Westmoreland
Journal:  J Neuroimmune Pharmacol       Date:  2006-03-21       Impact factor: 4.147

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