Guo, Q., Peng, TQ., Yang, YZ. et al. Effect of Astragalus Membranaceus on Ca2+ influx and CVB3 RNA replication in cultured neonatal rat heart cells infected with CVB3., CJIM 2, 64–67 (1996). https://doi.org/10.1007/BF02934230
Qi Guo, Tian-Qing Peng, Ying-Zhen Yang, et al. Effect of Astragalus Membranaceus on Ca2+ influx and CVB3 RNA replication in cultured neonatal rat heart cells infected with CVB3. [J]. Chinese Journal of Integrative Medicine 2(1):64-67(1996)
Guo, Q., Peng, TQ., Yang, YZ. et al. Effect of Astragalus Membranaceus on Ca2+ influx and CVB3 RNA replication in cultured neonatal rat heart cells infected with CVB3., CJIM 2, 64–67 (1996). https://doi.org/10.1007/BF02934230DOI:
Qi Guo, Tian-Qing Peng, Ying-Zhen Yang, et al. Effect of Astragalus Membranaceus on Ca2+ influx and CVB3 RNA replication in cultured neonatal rat heart cells infected with CVB3. [J]. Chinese Journal of Integrative Medicine 2(1):64-67(1996) DOI: 10.1007/BF02934230.
Effect of Astragalus Membranaceus on Ca2+ influx and CVB3 RNA replication in cultured neonatal rat heart cells infected with CVB3
摘要
Here was investigated the effect of Radix Astragalus Membranaceus (AM) on Ca2+ influx across the myocardial plasma membrane and coxsackie virus B3(CVB3)-RNA replication in cultured neonatal rat heart cells infected with CVB3. It was found that the Ca2+ influx could be inhibited significantly by AM both in heart cells infected with CVB3 for 48 hours and in normal control heart cells. In addition
the Ca2+ influx and the amounts of CVB3-RNA in myocytes simultaneously infected with CVB3 and treated with AM for 48 hours were statistically decreased compared with that in CVB3-infected control cells. These phenomena suggested that AM could exert the effects of decreasing the secondary Ca2+ damages
improving the abnormal myocardial electric activity and inhibiting replication of CVB3-RNA in myocardium. Thus
it is a rational choice to treat patients with AM in viral myocarditis.
Abstract
Here was investigated the effect of Radix Astragalus Membranaceus (AM) on Ca2+ influx across the myocardial plasma membrane and coxsackie virus B3(CVB3)-RNA replication in cultured neonatal rat heart cells infected with CVB3. It was found that the Ca2+ influx could be inhibited significantly by AM both in heart cells infected with CVB3 for 48 hours and in normal control heart cells. In addition
the Ca2+ influx and the amounts of CVB3-RNA in myocytes simultaneously infected with CVB3 and treated with AM for 48 hours were statistically decreased compared with that in CVB3-infected control cells. These phenomena suggested that AM could exert the effects of decreasing the secondary Ca2+ damages
improving the abnormal myocardial electric activity and inhibiting replication of CVB3-RNA in myocardium. Thus
it is a rational choice to treat patients with AM in viral myocarditis.
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