Natural 7,8-secolignans from Schisandra sphenanthera fruit potently inhibit SARS-CoV-2 3CLpro and inflammation

IF 3.3 3区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Journal of Traditional and Complementary Medicine Pub Date : 2024-01-16 DOI:10.1016/j.jtcme.2024.01.005
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Abstract

The coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), turned into a global pandemic, and there remains an urgent demand for specific/targeted drugs for the disease. The 3C-like protease (3CLpro) is a promising target for developing anti-coronavirus drugs. Schisandra sphenanthera fruit is a well-known traditional Chinese medicine (TCM) with good antiviral activity. This study found that the ethanolic extract displayed a significant inhibitory effect against SARS-CoV-2 3CLpro. Forty-four compounds were identified in this extract using ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS). Combining molecular docking and in vitro experiments, we found that two epimeric 7,8-secolignans, rel-(1S,2R)-1-(3,4-dimethoxyphenyl)-2-methyl-3-oxobutyl-3,4-dimethoxybenzoate (2) and rel-(1S,2S)-1-(3,4-dimethoxyphenyl)-2-methyl-3-oxobutyl-3,4-dimethoxybenzoate (4), potently inhibited 3CLpro with IC50 values of 4.88 ± 0.60 μM and 4.75 ± 0.34 μM, respectively. Moreover, in vivo and in vitro experiments indicated that compounds 2 and 4 were potent in regulating the inflammatory response and preventing lung injury. Our findings indicate that compounds 2 and 4 may emerge as promising SARS-CoV-2 inhibitors via 3CLpro inhibition and anti-inflammatory mechanisms.

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五味子果实中的天然 7,8-secolignans 可有效抑制 SARS-CoV-2 3CLpro 和炎症反应
由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)已演变成全球大流行病,对该疾病的特异性/靶向药物仍有迫切需求。3C 样蛋白酶(3CLpro)是开发抗冠状病毒药物的一个很有前景的靶点。五味子是一种著名的传统中药,具有良好的抗病毒活性。本研究发现,五味子乙醇提取物对 SARS-CoV-2 3CLpro 有明显的抑制作用。利用超高效液相色谱-四极杆飞行时间质谱法(UPLC-Q-TOF/MS)鉴定了该提取物中的 44 种化合物。结合分子对接和体外实验,我们发现了两种7,8-仲木质素的外嵌体,即rel-(1S,2R)-1-(3,4-二甲氧基苯基)-2-甲基-3-氧代丁基-3、(2)和 rel-(1S,2S)-1-(3,4-二甲氧基苯基)-2-甲基-3-氧代丁基-3,4-二甲氧基苯甲酸酯(4)能有效抑制 3CLpro 的 IC50 值为 4.88 ± 0.60 μM 和 4.75 ± 0.34 μM。此外,体内和体外实验表明,化合物 2 和 4 能有效调节炎症反应并防止肺损伤。我们的研究结果表明,化合物 2 和 4 可通过抑制 3CLpro 和抗炎机制成为有前途的 SARS-CoV-2 抑制剂。
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来源期刊
Journal of Traditional and Complementary Medicine
Journal of Traditional and Complementary Medicine Medicine-Complementary and Alternative Medicine
CiteScore
9.30
自引率
6.70%
发文量
78
审稿时长
66 days
期刊介绍: eJTCM is committed to publish research providing the biological and clinical grounds for using Traditional and Complementary Medical treatments as well as studies that demonstrate the pathophysiological and molecular/biochemical bases supporting the effectiveness of such treatments. Review articles are by invitation only. eJTCM is receiving an increasing amount of submission, and we need to adopt more stringent criteria to select the articles that can be considered for peer review. Note that eJTCM is striving to increase the quality and medical relevance of the publications.
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