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Oseltamivir and S-Adenosyl-L-Methionine Combination as Effective Therapeutic Strategy for Suppression of Oxidative Damage in Lung Caused by Influenza

tetano

Editor, Senior Moderator
Drug Res (Stuttg). 2020 Apr 21. doi: 10.1055/a-1147-8824. [Epub ahead of print]
Oseltamivir and S-Adenosyl-L-Methionine Combination as Effective Therapeutic Strategy for Suppression of Oxidative Damage in Lung Caused by Influenza Virus Infection in Mice.


Mileva M[SUP]1[/SUP], Dimitrova A[SUP]1[/SUP], Krastev D[SUP]2[/SUP], Alexandrova A[SUP]3[/SUP], Tsvetanova E[SUP]3[/SUP], Georgieva A[SUP]3[/SUP], Galabov A[SUP]1[/SUP].

Author information




Abstract

BACKGROUND AND OBJECTIVES:

The pathogenesis of influenza infection is associated with two general processes in the body: (a) lung damage based on virus replication; (b) overproduction of free radicals, antioxidant deficiency, and development of oxidative stress. To attack these aspects of flu pathogenesis, we explored the combined effect of the antiviral agent oseltamivir, and s-adenosyl-l-methionine (SAM) as a precursor of the endogenous antioxidant glutathione, in mice infected with influenza virus.
METHODS:

After inoculation of albino mice with 10 MLD[SUB]50[/SUB] of influenza virus A/Aichi/2/68 (H3N2), oseltamivir was applied twice a day, for five days post-infection in doses of 1.25 and 2.5 mg/kg. SAM was administered once a day for 10 days, starting 5 days before infection in doses of 50, 100 and 150 mg/kg.
RESULTS:

Monotherapy with SAM did not influence the markers of oxidative stress in the lung. Combination of SAM 50 mg/kg and oseltamivir 2.5 mg/kg affected best the virological parameters - viral titer, protection index, and mean survival time, as well as the biochemical markers of oxidative stress.
INTERPRETATION AND CONCLUSIONS:

Combining of SAM and oseltamivir in a dose of 1/4 of optimal therapeutic could be considered as a perspective therapy of influenza viral infection.
? Georg Thieme Verlag KG Stuttgart ? New York.



PMID:32316058DOI:10.1055/a-1147-8824
 
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