Biomol Ther.  2017 May;25(3):279-287. 10.4062/biomolther.2016.070.

Cinnamaldehyde Derivatives Inhibit Coxsackievirus B3-Induced Viral Myocarditis

• Li XQ
• Liu XX
• Wang XY
• Xie YH
• Yang Q
• Liu XX
• Ding YY
• Cao W
• Wang SW

• KMID: 2378806
• DOI: http://doi.org/10.4062/biomolther.2016.070

Abstract

The chemical property of cinnamaldehyde is unstable in vivo, although early experiments have shown its obvious therapeutic effects on viral myocarditis (VMC). To overcome this problem, we used cinnamaldehyde as a leading compound to synthesize derivatives. Five derivatives of cinnamaldehyde were synthesized: 4-methylcinnamaldehyde (1), 4-chlorocinnamaldehyde (2), 4-methoxycinnamaldehyde (3), α-bromo-4-methylcinnamaldehyde (4), and α-bromo-4-chlorocinnamaldehyde (5). Neonatal rat cardiomyocytes and HeLa cells infected by coxsackievirus B3 (CVB3) were used to evaluate their antiviral and cytotoxic effects. In vivo BALB/c mice were infected with CVB3 for establishing VMC models. Among the derivatives, compound 4 and 5 inhibited the CVB3 in HeLa cells with the half-maximal inhibitory concentrations values of 11.38 ± 2.22 μM and 2.12 ± 0.37 μM, respectively. The 50% toxic concentrations of compound 4 and 5-treated cells were 39-fold and 87-fold higher than in the cinnamaldehyde group. Compound 4 and 5 effectively reduced the viral titers and cardiac pathological changes in a dose-dependent manner. In addition, compound 4 and 5 significantly inhibited the secretion, mRNA and protein expressions of inflammatory cytokines TNF-α, IL-1β and IL-6 in CVB3-infected cardiomyocytes, indicating that brominated cinnamaldehyde not only improved the anti-vital activities for VMC, but also had potent anti-inflammatory effects in cardiomyocytes induced by CVB3.

Keyword

Anti-inflammatory; Cinnamaldehyde; Coxsackievirus B3; Myocarditis

MeSH Terms

Animals
Cytokines
HeLa Cells
Humans
Interleukin-6
Mice
Myocarditis*
Myocytes, Cardiac
Rats
RNA, Messenger
Therapeutic Uses
Cytokines
Interleukin-6
RNA, Messenger
Therapeutic Uses