Wan, Sj., Zhao, H., Li, Jn. et al. Effect of prevention and treatment of murine acute viral myocarditis and protection of lymphoid organ atrophy with xinkang oral liquid, ., CJIM 8, 48–50 (2002). https://doi.org/10.1007/BF02934619
Su-jun Wan, Hong Zhao, Jian-nong Li, et al. Effect of prevention and treatment of murine acute viral myocarditis and protection of lymphoid organ atrophy with xinkang oral liquid. [J]. Chinese Journal of Integrative Medicine 8(1):48-50(2002)
Wan, Sj., Zhao, H., Li, Jn. et al. Effect of prevention and treatment of murine acute viral myocarditis and protection of lymphoid organ atrophy with xinkang oral liquid, ., CJIM 8, 48–50 (2002). https://doi.org/10.1007/BF02934619DOI:
Su-jun Wan, Hong Zhao, Jian-nong Li, et al. Effect of prevention and treatment of murine acute viral myocarditis and protection of lymphoid organ atrophy with xinkang oral liquid. [J]. Chinese Journal of Integrative Medicine 8(1):48-50(2002) DOI: 10.1007/BF02934619.
Effect of prevention and treatment of murine acute viral myocarditis and protection of lymphoid organ atrophy with xinkang oral liquid
摘要
The effect of prevention and treatment of Xinkang oral liquid
(
XKOL) on experimental coxsackievirus B3 (CVB3) myocarditis mice model were investigated. The mice were inoculated intraperitoneally with 0.3 ml of 105 TCID50 of CVB3 to induce acute viral myocarditis model. These mice were divided into model control group (Group A)
prevention high dosage group (Group B) and prevention low dosage group (Group C)
treatment high dosage group (Group D) and treatment low dosage group (Group E)
respectively. In addition
XKOL control group (Group F) and normal control group (Group G) were not infected with CVB3 intraperitoneally. The administration of XKOL in Group B and C began 2 days before virus infection. All animals were sacrificed on day 20 for evaluation. Histological examination showed extensive myocardial necrosis and cell infiltration in most of Group A mice
but necrosis and cell infiltration were less severe in Group B
C
D and E mice. Thymus weight in Group B
C
D and E mice were heavier and less cell depletion occurred than those in Group A. The XKOL could effectively inhibit myocardial CVB3 replication
reduce the myocardial inflammatory response
lower incidence rate of myocarditis and prevent the disease associated lymphoid organ atrophy in this animal models.
Abstract
The effect of prevention and treatment of Xinkang oral liquid
(
XKOL) on experimental coxsackievirus B3 (CVB3) myocarditis mice model were investigated. The mice were inoculated intraperitoneally with 0.3 ml of 105 TCID50 of CVB3 to induce acute viral myocarditis model. These mice were divided into model control group (Group A)
prevention high dosage group (Group B) and prevention low dosage group (Group C)
treatment high dosage group (Group D) and treatment low dosage group (Group E)
respectively. In addition
XKOL control group (Group F) and normal control group (Group G) were not infected with CVB3 intraperitoneally. The administration of XKOL in Group B and C began 2 days before virus infection. All animals were sacrificed on day 20 for evaluation. Histological examination showed extensive myocardial necrosis and cell infiltration in most of Group A mice
but necrosis and cell infiltration were less severe in Group B
C
D and E mice. Thymus weight in Group B
C
D and E mice were heavier and less cell depletion occurred than those in Group A. The XKOL could effectively inhibit myocardial CVB3 replication
reduce the myocardial inflammatory response
lower incidence rate of myocarditis and prevent the disease associated lymphoid organ atrophy in this animal models.
关键词
Xinkang oral liquidCoxsackievirus B3Myocarditis
Keywords
Xinkang oral liquidCoxsackievirus B3Myocarditis
references
GS Sainani, MP Dekate and CP Rao. Heart disease caused by coxsackievirus B infection. British Heart J 1975, 37: 819.
M Herzum, SA Huber, R Weller, et al. Treatment of experimental murine coxsackie B3 myocarditis. Eur Heart J 1991; 12(suppl D): 220.
C Kishimoto, CS Crumpacker, WH Abelmann. Prevention of murine coxsackie B3 viral myocarditis and associated lymphoid organ atrophy with recombinant human leukocyte interferona A/D. Cardiovascular Res 1988; 22: 732.
NV Houten and SA Huber. Genetics of coxsackie B3 myocarditis. Eur Heart J 1991; 12(Suppl D): 108–112.
D Matteucci, A Toniolo, PG Conaldi, et al. Systemic lymphoid atrophy in coxsackie virus B3 infected mice. J Infect Dis 1985; 151: 110.
Antiviral effects of aqueous extract from Spatholobus suberectus Dunn. against coxsackievirus B3 in mice
A comparative study on the therapeutic effect of Astragaloside ( ) and Perindopril in treating CVB3-infected cardiomyocytes in rats) and Perindopril in treating CVB3-infected cardiomyocytes in rats
Effect of Tripterygium wilfordii on Th1, Th2 cytokines production in asthma patients
Experimental study on effect of Qishejingkang recipe on activity of alkaline phosphatases in osteophyte formation of degenerated cerebral vertebrae of rabbitson activity of alkaline phosphatases in osteophyte formation of degenerated cerebral vertebrae of rabbits
Effects of astragaloside in treating myocardial injury and myocardial sarco/endoplasmic ca2+ -atpase of viral myocarditis mice
Related Author
No data
Related Institution
Institution of Healthy and Toxicology, Beijing Centers for Disease Prevention and Control
Disease Prevention and Control Institute of the Chinese People’s Liberation Army
Department of Environment and Health, Institute of Environmental and Health
Research Institute of Cardiovascular Diseases, The First Affiliated Hospital of Nanjing Medical University
Institute of Internal medicine of Respiratory Diseases, Xinqiao Hospital, The Third Medical University of PLA