Key result
Metoprolol increases 30-day mortality to ~ with saline in acute viral myocarditis.
Why the study?
Beta-adrenergic blocking agents had shown promise in managing cardiomyopathies, but their role in acute myocarditis was unknown.
Does intraperitoneal metoprolol affect mortality, viral replication, and myocardial pathology in mice with acute coxsackievirus B3 myocarditis?
Does intraperitoneal metoprolol affect mortality, viral replication, and myocardial pathology in mice with acute coxsackievirus B3 myocarditis?
In a murine model of acute coxsackievirus B3 myocarditis, early administration of metoprolol was deleterious, significantly increasing mortality, viral replication, and late myocardial damage.
Answers are grounded in this paper and cite their sources.
Metoprolol increased mortality in murine viral myocarditis; challenges beta-blocker assumptions and leaves open human relevance.
Recent studies suggest that beta-adrenergic blocking agents show promise in the management of cardiomyopathies; however, their role in acute myocarditis is unknown. One hundred 3 week old mice were infected with coxsackievirus B3 and were given either metoprolol (n = 50) or normal saline solution (n = 50) intraperitoneally for 10 days. Twenty mice from each group were observed for mortality for 30 days. Of the remaining 60 mice, 10 from each group were killed on day 3, 6 or 10 and examined for heart viral titers and pathologic changes. Mortality rate in the metoprolol group was 60% compared with 0% in the saline group (p less than 0.005). Viral titers on day 10 of infection were 10(2.6 +/- 0.2) median tissue culture infective dose for the metoprolol group versus 10(2.1 +/- 0.1) for the saline group (p less than 0.05). Whereas pathologic changes at days 3, 6 and 10 of infection were similar in both groups, on day 30 of infection, inflammation, necrosis and mineralization scores (mean +/- SEM) were 1.1 +/- 0.3, 2.1 +/- 0.4, 2.2 +/- 0.5 for the metoprolol group versus 0.3 +/- 0.1, 0.4 +/- 0.3, 0.4 +/- 0.3 for the saline group, respectively (p less than 0.01). Six noninfected mice received metoprolol intraperitoneally for 10 days; there was no mortality during 30 days of observation. In conclusion, metoprolol administration exerts deleterious effects in acute coxsackievirus B3 murine myocarditis.
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Rezkalla et al. (1988) studied Acute coxsackievirus B3 murine myocarditis (n=100). Metoprolol vs. Normal saline solution intraperitoneally for 10 days was evaluated on 30-day mortality rate (p=<0.005). Metoprolol increased 30-day mortality compared with normal saline in mice with acute coxsackievirus B3 myocarditis.
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