摘要
新型冠状病毒 SARS-CoV-2 正以惊人的速度发展,以破坏医疗保健系统并引发对公共卫生的担忧。与过去的疫情相比,冠状病毒并不是一种严格的呼吸道病毒。相反,它成为一种多方面的病毒,它通过中断许多导致发病率和死亡率显着的代谢途径来影响多个器官。感染后,它们严格重新编程葡萄糖、脂质、蛋白质、核酸及其代谢物的多种代谢途径,以提取它们存在所需的足够能量和碳骨架,并在宿主细胞内进一步构建分子。尽管这些改变的机制尚不清楚,但这些重编程的影响反映在过度炎症反应中,即所谓的细胞因子风暴和宿主免疫防御系统的障碍。在设计抗击疾病及其进一步并发症的治疗策略时,需要考虑 SARSCoV-2 感染期间的代谢重编程。宿主细胞的胆固醇和磷脂合成抑制剂和细胞膜脂筏可以在很大程度上控制病毒载量和进一步感染。通过抑制糖酵解和己糖胺生物合成途径的激活来消耗能源也可以增强抗病毒治疗。这些途径之间的串扰也需要抑制氨基酸分解代谢和色氨酸代谢。解决代谢途径之间交叉对话的组合策略可能比单一方法更有效,并且感染阶段和治疗时机也会影响抗病毒方法的有效性。我们在此关注于病毒感染过程中的不同代谢改变,这些改变有助于利用细胞机制并设计一种治疗策略,以促进对病毒感染的抵抗力并增强身体的抗病毒机制。这篇综述可能会以新的视角揭示靶向改变的代谢途径以抵御病毒感染的可能性。
关键词: SARS-CoV-2, COVID-19,代谢重编程,治疗靶点,细胞因子风暴,冠状病毒后疾病。
图形摘要
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