* Food Animal Health Research Program, Ohio Agricultural Research and Development Center, The Ohio State University, Columbus, Ohio, USA.
‡ Mom-Pyon Han Pharmacy, Nambusoonhwan-ro 770, Seosan City, Chungnam, Republic of Korea.
Am J Chin Med. 2018;46(8):1663-1700. doi: 10.1142/S0192415X18500854.
The rapidly changing influenza virus has remained a consistent threat to the well-being of a variety of species on the planet. Influenza virus' high mutation rate has allowed the virus to rapidly and continuously evolve, as well as generate new strains that are resistant to the current commercially available antivirals. Thus, the increased resistance has compelled the scientific community to explore alternative compounds that have antiviral effects against influenza virus. In this paper, the authors systematically review numerous herbal extracts that were shown to have antiviral effects against the virus. Specifically, the herbal antiviral targets mainly include hemagglutinin, neuraminidase and matrix 2 proteins. In some instances, herbal extracts inhibited the replication of oseltamivir-resistant strains and certain pentacyclic triterpenes exhibited higher antiviral activity than oseltamivir. This paper also explores the possibility of targeting various host-cell signaling pathways that are utilized by the virus during its replication process. Infected cell pathways are hijacked by intracellular signaling cascades such as NF-kB signaling, PI3K/Akt pathway, MAPK pathway and PKC/PKR signaling cascades. Herbal antivirals have been shown to target these pathways by suppressing nuclear export of influenza vRNP and thus inhibiting the phosphorylation signaling cascade. In conclusion, copious amounts of herbal antivirals have been shown to inhibit influenza virus, however further studies are needed for these new compounds to be up to modern pharmacological standards.
不断变化的流感病毒仍然是地球上各种物种健康的持续威胁。流感病毒的高突变率使其能够快速持续地进化,并产生新的、对现有市售抗病毒药物具有耐药性的菌株。因此,耐药性的增加迫使科学界探索具有抗流感病毒作用的替代化合物。在本文中,作者系统地综述了大量具有抗流感病毒作用的草药提取物。具体来说,草药抗病毒的靶标主要包括血凝素、神经氨酸酶和基质 2 蛋白。在某些情况下,草药提取物抑制了奥司他韦耐药株的复制,某些五环三萜的抗病毒活性高于奥司他韦。本文还探讨了靶向病毒在复制过程中利用的各种宿主细胞信号通路的可能性。感染细胞途径被细胞内信号级联反应劫持,如 NF-κB 信号、PI3K/Akt 途径、MAPK 途径和 PKC/PKR 信号级联反应。草药抗病毒药物已被证明通过抑制流感病毒 vRNP 的核输出从而抑制磷酸化信号级联反应来靶向这些途径。总之,大量的草药抗病毒药物已被证明可以抑制流感病毒,但这些新化合物需要进一步研究才能达到现代药理学标准。