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1.
Chinese Journal of Experimental and Clinical Virology ; (6): 238-240, 2007.
Article in Chinese | WPRIM | ID: wpr-248792

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the CVB3 RNA concentration in myocardial tissues and inhibitory effect of Chinese herbal medicine Xin-Kang oral liquid on viral RNA replication in Coxsackievirus B3 infected myocardium.</p><p><b>METHODS</b>The total RNA was extracted from the infected murine myocardium, the reverse transcription-polymerase chain reaction (RT-PCR) was performed to detect enterovirus RNA concentration in infected mice with Coxsackievirus B3 gene band. We used "Gel works system" to scan the electrophoresis image to detect CVB3 gene band.</p><p><b>RESULTS</b>The mean concentration of myocardial CVB3 RNA of Xin-Kang oral liquid treated groups was markedly lower than that of virus control group (P>0.01), but the CVB3 RNA in myocardial tissues has not been destroyed by Xin-Kang oral liquid feed in different phase.</p><p><b>CONCLUSION</b>Chinese herbal medicine Xin-Kang oral liquid could inhibit CVB3 RNA replication in myocardial tissue, but it did not destruct the virus.</p>


Subject(s)
Animals , Mice , Coxsackievirus Infections , Drug Therapy , Drugs, Chinese Herbal , Pharmacology , Enterovirus B, Human , Genetics , Myocarditis , Drug Therapy , Virology , Phytotherapy , RNA, Viral , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Treatment Outcome , Virus Replication , Genetics
2.
Chinese Journal of Experimental and Clinical Virology ; (6): 77-79, 2005.
Article in Chinese | WPRIM | ID: wpr-333043

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of Chinese herbal medicine Xin-kang oral liquid on interferon (IFN)-induction and its antiviral activity in Coxsackievirus B3 virus strain (CVB3) infected mice.</p><p><b>METHODS</b>The Xin-kang oral liquid was given orally to mice two days prior to the challenge of CVB3 virus to induce myocarditis. Two dosages of Xin-kang oral liquid crude herbal medicine 30 g x kg(-1) x d(-1) and 12 g x kg(-1) x d(-1) were given to the mice of different treatment groups respectively, sterilized water was given to the mice of virus control group. IFN-alpha 10(6) U x kg(-1) x d(-1) S.C was given to the infected mice as positive drug control group. The mice were sacrificed on 5th, 10th and 20th day of infection for evaluation, the levels of serum interferon (IFN) were titrated with vesicular stomatitis virus (VSV) and cardiac tissue was fixed and sectioned. The quantitative histological changes at various stages of myocarditis were observed.</p><p><b>RESULTS</b>In the infected mice fed with 30 g x kg(-1) x d(-1) or 12 g x kg(-1) x d(-1) of Xin-kang oral liquid orally for 5, 10 and 20 days, the mean titer of serum IFN of Xin-Kang oral liquid treated group was markedly higher (29.3 U/0.1 ml) than that of virus control group (12.6 U/0.1 ml). The level of serum IFN in IFN treated positive control mice was lower than that of Xin-kang treatment groups. The histological examination showed extensive myocardial necrosis and cellular infiltration in virus control group, but necrosis and cellular infiltration were less severe in Xin-kang treatment goups of mice. It is demonstrated that there were close correlation between the degree of myocardial lesions and the level of IFN-induction in treated mice.</p><p><b>CONCLUSION</b>Xin-kang oral liquid could facilitate the induction of endogenous interferon that exerted its antiviral activity in CVB3 infected mice. This can help us to understand better the mechanism of anti-CVB3 effect of Xin-Kang oral liquid.</p>


Subject(s)
Animals , Mice , Animals, Newborn , Cell Line , Coxsackievirus Infections , Blood , Drug Therapy , Virology , Dose-Response Relationship, Drug , Drugs, Chinese Herbal , Therapeutic Uses , Enterovirus B, Human , Interferons , Blood , Myocarditis , Blood , Drug Therapy , Virology , Myocardium , Pathology , Phytotherapy
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