Poloznikov Andrey A, Nersisyan Stepan A, Hushpulian Dmitry M, Kazakov Eliot H, Tonevitsky Alexander G, Kazakov Sergey V, Vechorko Valery I, Nikulin Sergey V, Makarova Julia A, Gazaryan Irina G
Faculty of Biology and Biotechnology, HSE University, Moscow, Russia.
P. A. Hertsen Moscow Oncology Research Center, Branch of the National Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Front Pharmacol. 2021 Jan 29;11:621054. doi: 10.3389/fphar.2020.621054. eCollection 2020.
The review analyzes the potential advantages and problems associated with using HIF prolyl hydroxylase inhibitors as a treatment for COVID-19. HIF prolyl hydroxylase inhibitors are known to boost endogenous erythropoietin (Epo) and activate erythropoiesis by stabilizing and activating the hypoxia inducible factor (HIF). Recombinant Epo treatment has anti-inflammatory and healing properties, and thus, very likely, will be beneficial for moderate to severe cases of COVID-19. However, HIF PHD inhibition may have a significantly broader effect, in addition to stimulating the endogenous Epo production. The analysis of HIF target genes reveals that some HIF-targets, such as furin, could play a negative role with respect to viral entry. On the other hand, HIF prolyl hydroxylase inhibitors counteract ferroptosis, the process recently implicated in vessel damage during the later stages of COVID-19. Therefore, HIF prolyl hydroxylase inhibitors may serve as a promising treatment of COVID-19 complications, but they are unlikely to aid in the prevention of the initial stages of infection.
该综述分析了使用缺氧诱导因子脯氨酰羟化酶抑制剂治疗新型冠状病毒肺炎(COVID-19)的潜在优势和问题。已知缺氧诱导因子脯氨酰羟化酶抑制剂可通过稳定和激活缺氧诱导因子(HIF)来提高内源性促红细胞生成素(Epo)并激活红细胞生成。重组促红细胞生成素治疗具有抗炎和愈合特性,因此很可能对COVID-19的中重度病例有益。然而,除了刺激内源性促红细胞生成素的产生外,抑制缺氧诱导因子脯氨酰羟化酶可能具有更广泛的作用。对缺氧诱导因子靶基因的分析表明,一些缺氧诱导因子靶点,如弗林蛋白酶,可能在病毒进入方面起负面作用。另一方面,缺氧诱导因子脯氨酰羟化酶抑制剂可对抗铁死亡,这一过程最近被认为与COVID-19后期的血管损伤有关。因此,缺氧诱导因子脯氨酰羟化酶抑制剂可能是治疗COVID-19并发症的一种有前景的方法,但它们不太可能有助于预防感染的初始阶段。