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小檗碱的抗病毒活性。

Antiviral activity of berberine.

机构信息

Department of Animal Physiology and Developmental Biology, Institute of Experimental Biology, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.

NanoBioMedical Centre, Adam Mickiewicz University, Poznań, Poland.

出版信息

Arch Virol. 2020 Sep;165(9):1935-1945. doi: 10.1007/s00705-020-04706-3. Epub 2020 Jun 28.

Abstract

Plants are a rich source of new antiviral, pharmacologically active agents. The naturally occurring plant alkaloid berberine (BBR) is one of the phytochemicals with a broad range of biological activity, including anticancer, anti-inflammatory and antiviral activity. BBR targets different steps in the viral life cycle and is thus a good candidate for use in novel antiviral drugs and therapies. It has been shown that BBR reduces virus replication and targets specific interactions between the virus and its host. BBR intercalates into DNA and inhibits DNA synthesis and reverse transcriptase activity. It inhibits replication of herpes simplex virus (HSV), human cytomegalovirus (HCMV), human papillomavirus (HPV), and human immunodeficiency virus (HIV). This isoquinoline alkaloid has the ability to regulate the MEK-ERK, AMPK/mTOR, and NF-κB signaling pathways, which are necessary for viral replication. Furthermore, it has been reported that BBR supports the host immune response, thus leading to viral clearance. In this short review, we focus on the most recent studies on the antiviral properties of berberine and its derivatives, which might be promising agents to be considered in future studies in the fight against the current pandemic SARS-CoV-2, the virus that causes COVID-19.

摘要

植物是新的抗病毒、具有药理活性的药物的丰富来源。天然存在的植物生物碱小檗碱(BBR)是具有广泛生物活性的植物化学物质之一,包括抗癌、抗炎和抗病毒活性。BBR 针对病毒生命周期的不同步骤,因此是新型抗病毒药物和疗法的理想候选药物。已经表明,BBR 可减少病毒复制,并针对病毒与其宿主之间的特定相互作用。BBR 嵌入 DNA 并抑制 DNA 合成和逆转录酶活性。它抑制单纯疱疹病毒(HSV)、人巨细胞病毒(HCMV)、人乳头瘤病毒(HPV)和人类免疫缺陷病毒(HIV)的复制。这种异喹啉生物碱具有调节 MEK-ERK、AMPK/mTOR 和 NF-κB 信号通路的能力,这些通路对于病毒复制是必需的。此外,据报道,BBR 支持宿主免疫反应,从而导致病毒清除。在这篇简短的综述中,我们重点介绍了小檗碱及其衍生物的抗病毒特性的最新研究,这些特性可能是未来对抗当前 SARS-CoV-2 大流行的有前途的候选药物,SARS-CoV-2 是导致 COVID-19 的病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8641/7406480/2bb59d6fb502/705_2020_4706_Fig1_HTML.jpg

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