Galabov Angel S, Mileva Milka, Simeonova Lora, Gegova Galina
The Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, Sofia, Bulgaria
The Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Antivir Chem Chemother. 2015 Aug;24(3-4):83-91. doi: 10.1177/2040206616656263. Epub 2016 Jun 24.
Influenza is a highly contagious viral infection of the respiratory system. To attack two processes involved in flu pathogenesis-viral replication in the infected body and oxidative damages, we studied the combination effect of neuraminidase inhibitor oseltamivir and antioxidant α-tocopherol in experimental model of influenza.
After inoculation of albino mice with 10 MLD50 (50% mouse lethal dose) of influenza virus A/Aichi/2/68 (H3N2), oseltamivir was applied orally at three doses, 2.5 mg/kg, 1.25 mg/kg, and 0.625 mg/kg, for five days post infection. α-Tocopherol (120 mg/kg, in sunflower oil) was administered intraperitoneally. Three schemes of α-tocopherol five-day course were tested: onset five or two days before infection, or on the virus inoculation day.
Strongly dose-dependent augmented antiviral effect of the combination α-tocopherol and 0.625 mg/kg oseltamivir was demonstrated when α-tocopherol was administered simultaneously with oseltamivir: a pronounced decrease in mortality rate (a 78% protection), and a lengthening of mean survival time by 3.2-4 days. Lung parameters showed a substantial decrease in infectious virus content (Δ logs = 3.8/4.1) and a marked diminishment of lung index and pathology. Combination α-tocopherol with 1.25 mg/kg oseltamivir manifested a marked protective effect, but the effect on lung parameters was less. The combination effect of α-tocopherol with 2.5 mg/kg oseltamivir did not surpass the monotherapeutic effect of oseltamivir. When α-tocopherol was applied in courses starting five or two days before infection, its combination with oseltamivir was ineffective.
Evidently, α-tocopherol could be considered as prospective component of influenza therapy in combination with oseltamivir.
流感是一种极具传染性的呼吸系统病毒感染。为了针对流感发病机制中涉及的两个过程——被感染机体中的病毒复制和氧化损伤,我们在流感实验模型中研究了神经氨酸酶抑制剂奥司他韦和抗氧化剂α-生育酚的联合作用。
用10个半数致死剂量(50%小鼠致死剂量)的甲型流感病毒A/爱知/2/68(H3N2)接种白化小鼠后,在感染后5天内,以2.5毫克/千克、1.25毫克/千克和0.625毫克/千克三种剂量口服奥司他韦。α-生育酚(120毫克/千克,溶于葵花籽油)腹腔注射。测试了α-生育酚为期5天疗程的三种方案:在感染前5天或2天开始,或在病毒接种当天开始。
当α-生育酚与奥司他韦同时给药时,α-生育酚与0.625毫克/千克奥司他韦联合显示出强烈的剂量依赖性增强抗病毒作用:死亡率显著降低(保护率达78%),平均存活时间延长3.2 - 4天。肺部参数显示感染性病毒含量大幅降低(对数变化=3.8/4.1),肺指数和病理学明显减轻。α-生育酚与1.25毫克/千克奥司他韦联合表现出显著的保护作用,但对肺部参数的影响较小。α-生育酚与2.5毫克/千克奥司他韦的联合作用未超过奥司他韦的单药治疗效果。当α-生育酚在感染前5天或2天开始的疗程中应用时,其与奥司他韦联合无效。
显然,α-生育酚可被视为与奥司他韦联合用于流感治疗的潜在成分。