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A mouse model linking viral hepatitis and salivary gland dysfunction
Author(s) -
Kasman LM,
London LL,
London SD,
Pilgrim MJ
Publication year - 2009
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/j.1601-0825.2009.01600.x
Subject(s) - saliva , cytomegalovirus , salivary gland , immunology , viral hepatitis , spleen , hepatitis , medicine , betaherpesvirinae , herpesviridae , viral disease , pathology , virology , virus
Objective: Viral hepatitis is known to cause xerostomia in humans, but this has not been reported in an animal model. We report a severe, acute, highly reproducible saliva deficiency occurring in BALB/c mice as a result of experimental viral hepatitis. Materials and Methods: BALB/c mice, splenectomized or carrying genetic mutations to detect immunological contributions to the saliva deficiency syndrome, were infected intraperitoneally with a non‐lethal dose of murine cytomegalovirus. Pilocarpine‐stimulated saliva volumes were determined between 0 and 15 days after infection. Salivary gland, liver, spleen, and sera were analyzed for the presence of virus, cytokines, inflammatory infiltrates, and tissue damage. Results: Saliva deficiency was detectable 2 days after cytomegalovirus infection, peaked at 88% below normal by day 7, and resolved partially in all mice by 15 days postinfection as sialoadenitis increased. Neither salivary gland viral titers, sialoadenitis, splenectomy, nor systemic inflammatory markers correlated with hyposalivation severity. Elevated liver enzymes did correlate with hyposalivation, and mice genetically resistant to murine cytomegalovirus‐induced hepatitis were significantly protected. Conclusions: Murine cytomegalovirus‐induced salivary gland dysfunction is biphasic, with an acute hepatitis‐associated phase and a later sialoadenitis‐associated phase. Acute murine cytomegalovirus infection of BALB/c mice may provide a model for investigation of hepatitis‐associated xerostomia.