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Division of Cardiology, The University of Texas Health Science Center at San Antonio, and Audie L. Murphy Memorial Veterans Hospital, San Antonio, Texas 78284
We assessed two strains of mice [CD-1 and
C3H.HeJ (C3H)] with different responses to coxsackievirus B3
(CVB3) infection at 7, 14, and 21 days after inoculation with
105 pfu of CVB3. CD-1 mice
developed inflammatory lesions at 7 days that nearly recovered by 21 days; C3H mice demonstrated persistence of infiltrates. Although there
were differences in the baseline fractional shortening, it was further
reduced at 7 and 14 days in both strains. It recovered in CD-1 mice but
remained depressed at 21 days in C3H mice. Interleukin-6 and tumor
necrosis factor-
transcripts were increased in both strains at 7 days. Levels dropped to near control in CD-1 mice at 21 days but
remained elevated in C3H mice. Interleukin-1
was minimally elevated
in CD-1 mice but increased progressively in C3H mice. mRNA for the
inducible form of NO synthase (iNOS) was increased at 7 days in the
CD-1 mice, returning to baseline by 14 days; it rose progressively in
C3H mice, with a fivefold increase at 21 days. We conclude that mice
infected with CVB3 show increased expression of proinflammatory cytokines as well as iNOS associated with reduced contractile performance. In more susceptible mice, contractile depression and
cytokine and iNOS expression are more pronounced.
myocardial contraction; coxsackievirus; inducible nitric oxide synthase; mice
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