Department of Central Laboratory, Chongqing University Three Gorges Hospital, Chongqing, China.
College of Life Sciences, Chongqing Medical University, Yuzhong, China.
Pharm Biol. 2021 Dec;59(1):1517-1527. doi: 10.1080/13880209.2021.1995005.
Chinese herbs such as Cortex Mori [ L. (Moraceae)] may inhibit human immunodeficiency virus (HIV), but active compounds are unknown.
Screening of Cortex Mori and other herbs for anti-HIV active compounds.
HIV-1 virus (multiplicity of infection: 20), and herbs (dissolved in dimethyl sulfoxide, working concentrations: 10, 1, and 0.1 mg/mL) such as Cortex Mori, etc., were added to 786-O cells (10 cell/well). Zidovudine was used as a positive control. Cell survival and viral inhibition rates were measured. The herb that was the closest inactivity to zidovudine was screened. Mass spectrometry identified the active compounds in herbs (mobile phase: 0.05% formic acid aqueous solution and acetonitrile, gradient elution, detection wavelength: 210 nm). The effect of the compounds on reverse transcriptase (RT) products were evaluated by real-time PCR. Gene enrichment was used to analyse underlying mechanisms.
With a dose of 1 mg/mL of Cortex Mori, the cell survival rate (57.94%) and viral inhibition rate (74.95%) were closest to the effect of zidovudine (87.87%, 79.81%, respectively). Neochlorogenic acid, one of the active ingredients, was identified by mass spectrometry in Cortex Mori. PCR discovery total RT products of neochlorogenic acid group (mean relative gene expression: 6.01) significantly inhibited (control: 35.42, < 0.0001). Enrichment analysis showed that neochlorogenic acid may act on haemopoietic cell kinase, epidermal growth factor receptor, sarcoma, etc., thus inhibiting HIV-1 infection.
For people of low socioeconomic status affected by HIV, Chinese medicine (such as Cortex Mori) has many advantages: it is inexpensive and does not easily produce resistance. Drugs based on active ingredients may be developed and could have important value.
中药如桑白皮(桑科)可能抑制人类免疫缺陷病毒(HIV),但活性化合物尚不清楚。
筛选桑白皮和其他草药中的抗 HIV 活性化合物。
HIV-1 病毒(感染倍数:20)和草药(溶于二甲基亚砜,工作浓度:10、1 和 0.1mg/mL),如桑白皮等,加入 786-O 细胞(10 个细胞/孔)。齐多夫定作为阳性对照。测定细胞存活率和病毒抑制率。筛选与齐多夫定最接近无活性的草药。质谱法鉴定草药中的活性化合物(流动相:0.05%甲酸水溶液和乙腈,梯度洗脱,检测波长:210nm)。通过实时 PCR 评估化合物对逆转录酶(RT)产物的影响。基因富集用于分析潜在机制。
桑白皮剂量为 1mg/mL 时,细胞存活率(57.94%)和病毒抑制率(74.95%)最接近齐多夫定的作用(分别为 87.87%、79.81%)。质谱法鉴定出桑白皮中的一种活性成分——新绿原酸。PCR 发现新绿原酸组的总 RT 产物(平均相对基因表达:6.01)显著抑制(对照组:35.42,<0.0001)。富集分析表明,新绿原酸可能作用于造血细胞激酶、表皮生长因子受体、肉瘤等,从而抑制 HIV-1 感染。
对于受 HIV 影响的社会经济地位较低的人群,中药(如桑白皮)有许多优势:价格低廉,不易产生耐药性。基于活性成分的药物可能会被开发出来,具有重要价值。