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
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