Stressful life events have been associated with the onset and/or exacerbation of
multiple sclerosis (MS). To investigate the effects of stress on the pathogenesis of MS,
we employed restraint stress (RST) in the TheilerâÂÂs virus-induced demyelination
(TVID) model, an animal model for human MS. Intracerebral inoculation of
susceptible strain of mice with TheilerâÂÂs murine encephalomyelitis virus (TMEV)
results in a biphasic disease â an acute encephalomyelitis and chronic demyelination.
The establishment of persistent viral infection is critical in inducing immune-mediated
demyelination during the chronic disease. The exposure of mice to RST prior to viral
infection produced a stress response as evidenced by elevated circulating corticosterone
(CORT). To further study the effect of stress on the immune response to TMEV
infection and demyelination, we first examined the cytokine and chemokine response
during the acute TMEV infection. We demonstrated that RST down-regulated the
virus-induced expression of chemokines, Ltn, IP-10, RANTES, and pro-inflammatory
cytokines, TNF, IFN and LT in both the brain and spleen during early infection.
Histologically, a decreased pattern of inflammation was observed in the brain of
restrained mice as compared to non-restrained mice. The increased viral titer was noted in the CNS of restrained mice and was correlated with the decreased production
of pro-inflammatory cytokine, suggesting an impaired immune response by RST.
Secondly, the duration of stress on the late demyelination was investigated. Repeated
and chronically stressed SJL/J mice developed an early onset of clinical signs and a
delayed onset was observed in acutely stressed mice. Both acute and chronic RST
suppressed the antibody response to TMEV and stressed displayed a higher incidence
of demyelination than non-restrained mice. Axonal loss was also noted in chronic
stressed mice. Additionally, RST caused an increased systemic viral infection in
extraneural organs during the acute infection and cardiotropic TMEV was isolated
from the heart of stressed mice. Taken together, stress resulted in profound
immunsuppression during acute infection, which may consequently increase the
incidence of demyelination. The present study may be generalized in human MS
which is potentially triggered by viral infection.
| Identifer | oai:union.ndltd.org:tamu.edu/oai:repository.tamu.edu:1969.1/4255 |
| Date | 30 October 2006 |
| Creators | Mi, Wentao |
| Contributors | Welsh, C. Jane R. |
| Publisher | Texas A&M University |
| Source Sets | Texas A and M University |
| Language | en_US |
| Detected Language | English |
| Type | Book, Thesis, Electronic Dissertation, text |
| Format | 9376531 bytes, electronic, application/pdf, born digital |
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