Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Faculty of Nursing, Chiang Mai University, Chiang Mai 50200, Thailand.
Molecules. 2021 Dec 9;26(24):7459. doi: 10.3390/molecules26247459.
COVID-19 is the name of the disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that occurred in 2019. The virus-host-specific interactions, molecular targets on host cell deaths, and the involved signaling are crucial issues, which become potential targets for treatment. Spike protein, angiotensin-converting enzyme 2 (ACE2), cathepsin L-cysteine peptidase, transmembrane protease serine 2 (TMPRSS2), nonstructural protein 1 (Nsp1), open reading frame 7a (ORF7a), viral main protease (3C-like protease (3CLpro) or Mpro), RNA dependent RNA polymerase (RdRp) (Nsp12), non-structural protein 13 (Nsp13) helicase, and papain-like proteinase (PLpro) are molecules associated with SARS-CoV infection and propagation. SARS-CoV-2 can induce host cell death via five kinds of regulated cell death, i.e., apoptosis, necroptosis, pyroptosis, autophagy, and PANoptosis. The mechanisms of these cell deaths are well established and can be disrupted by synthetic small molecules or natural products. There are a variety of compounds proven to play roles in the cell death inhibition, such as pan-caspase inhibitor (z-VAD-fmk) for apoptosis, necrostatin-1 for necroptosis, MCC950, a potent and specific inhibitor of the NLRP3 inflammasome in pyroptosis, and chloroquine/hydroxychloroquine, which can mitigate the corresponding cell death pathways. However, NF-κB signaling is another critical anti-apoptotic or survival route mediated by SARS-CoV-2. Such signaling promotes viral survival, proliferation, and inflammation by inducing the expression of apoptosis inhibitors such as Bcl-2 and XIAP, as well as cytokines, e.g., TNF. As a result, tiny natural compounds functioning as proteasome inhibitors such as celastrol and curcumin can be used to modify NF-κB signaling, providing a responsible method for treating SARS-CoV-2-infected patients. The natural constituents that aid in inhibiting viral infection, progression, and amplification of coronaviruses are also emphasized, which are in the groups of alkaloids, flavonoids, terpenoids, diarylheptanoids, and anthraquinones. Natural constituents derived from medicinal herbs have anti-inflammatory and antiviral properties, as well as inhibitory effects, on the viral life cycle, including viral entry, replication, assembly, and release of COVID-19 virions. The phytochemicals contain a high potential for COVID-19 treatment. As a result, SARS-CoV-2-infected cell death processes and signaling might be of high efficacy for therapeutic targeting effects and yielding encouraging outcomes.
新型冠状病毒病(COVID-19)是由 2019 年发生的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)感染引起的疾病。病毒-宿主特异性相互作用、宿主细胞死亡的分子靶标和涉及的信号转导是至关重要的问题,这些问题成为治疗的潜在靶点。刺突蛋白、血管紧张素转化酶 2(ACE2)、组织蛋白酶 L-半胱氨酸蛋白酶、跨膜蛋白酶丝氨酸 2(TMPRSS2)、非结构蛋白 1(Nsp1)、开放阅读框 7a(ORF7a)、病毒主要蛋白酶(3C 样蛋白酶(3CLpro)或 Mpro)、RNA 依赖性 RNA 聚合酶(RdRp)(Nsp12)、非结构蛋白 13(Nsp13)解旋酶和木瓜蛋白酶样蛋白酶(PLpro)是与 SARS-CoV 感染和传播相关的分子。SARS-CoV-2 可以通过五种调控的细胞死亡方式诱导宿主细胞死亡,即凋亡、坏死性凋亡、细胞焦亡、自噬和 PANoptosis。这些细胞死亡的机制已经得到很好的证实,可以被合成的小分子或天然产物破坏。有多种已被证明在细胞死亡抑制中发挥作用的化合物,例如凋亡的泛半胱天冬酶抑制剂(z-VAD-fmk)、坏死性凋亡的 Necrostatin-1、细胞焦亡的强效且特异性的 NLRP3 炎性体抑制剂 MCC950 以及氯喹/羟氯喹,它们可以减轻相应的细胞死亡途径。然而,NF-κB 信号转导是另一种由 SARS-CoV-2 介导的关键抗凋亡或存活途径。该信号转导通过诱导凋亡抑制剂如 Bcl-2 和 XIAP 以及细胞因子(如 TNF)的表达,促进病毒的存活、增殖和炎症。因此,作为蛋白酶体抑制剂的天然小分子化合物,如雷公藤红素和姜黄素,可以用于修饰 NF-κB 信号转导,为治疗 SARS-CoV-2 感染患者提供一种负责任的方法。还强调了有助于抑制冠状病毒感染、进展和扩增的天然成分,它们属于生物碱、类黄酮、萜类、二芳基庚烷和蒽醌类。草药中的天然成分具有抗炎和抗病毒特性,以及对病毒生命周期的抑制作用,包括病毒进入、复制、组装和 COVID-19 病毒粒子的释放。植物化学物质具有治疗 COVID-19 的高潜力。因此,SARS-CoV-2 感染的细胞死亡过程和信号转导可能对治疗靶向作用具有很高的疗效,并产生令人鼓舞的结果。