Prophylactic/therapeutic agent for influenza virus infection
Provided is a prophylactic/therapeutic agent for influenza viral infection that is effective not only before and at an early stage of infection with influenza virus but also at an intermediate or late stage of the infection and is highly safe for human bodies. A prophylactic/therapeutic drug for influenza viral infection comprising, as active ingredients, 5-aminolevulinic acid (5-ALA), a derivative thereof or a salt of the 5-ALA or the derivative, and an iron compound is prepared. This prophylactic/therapeutic agent can be used for ameliorating (preventing) depression in food consumption, water consumption and body weight, for ameliorating (decreasing) increase in ketone body levels in blood that may otherwise cause ketosis, for ameliorating (preventing) depression in ATP levels in blood, or for ameliorating (increasing) a survival rate and depression in a body surface temperature.
1. A method for ameliorating: depression in food consumption, water consumption and/or body weight; increase in ketone body levels in blood; depression in ATP levels in blood; survival rate; and/or abnormality in a body surface temperature in a subject having an influenza viral infection, comprising administering to the subject a therapeutic agent for influenza viral infection comprising a compound represented by formula (I) or a salt thereof:
(wherein R 1 represents a hydrogen atom or an acyl group, and R 2 represents a hydrogen atom, a linear or branched alkyl group, a cycloalkyl group, an aryl group or an aralkyl group).
2. The method according to claim 1 , wherein R 1 and R 2 represent a hydrogen atom.
3. The method according to claim 1 , wherein the therapeutic agent for influenza viral infection further comprises an iron compound.
4. The method according to claim 3 , wherein the iron compound is one or more compounds selected from ferric chloride, iron sesquioxide, iron sulfate, ferrous pyrophosphate, ferrous citrate, iron sodium citrate, sodium ferrous citrate, iron ammonium citrate, ferric pyrophosphate, iron lactate, ferrous gluconate, iron sodium diethylenetriaminepentaacetate, iron ammonium diethylenetriaminepentaacetate, iron sodium ethylenediamine tetraacetate, iron ammonium ethylenediamine tetraacetate, iron sodium dicarboxymethylglutamate, iron ammonium dicarboxymethylglutamate, ferrous fumarate, iron acetate, iron oxalate, ferrous succinate, sodium iron succinate citrate, heme iron, iron dextran, iron triethylenetetramine, lactoferrin iron, transferrin iron, sodium iron chlorophyllin, ferritin iron, saccharated iron oxide and iron glycine sulfide.
5. The method according to claim 4 , wherein the iron compound is sodium ferrous citrate.
6. The method according to claim 2 , wherein the therapeutic agent for influenza viral infection further comprises an iron compound.
7. The method according to claim 6 , wherein the iron compound is one or more compounds selected from ferric chloride, iron sesquioxide, iron sulfate, ferrous pyrophosphate, ferrous citrate, iron sodium citrate, sodium ferrous citrate, iron ammonium citrate, ferric pyrophosphate, iron lactate, ferrous gluconate, iron sodium diethylenetriaminepentaacetate, iron ammonium diethylenetriaminepentaacetate, iron sodium ethylenediamine tetraacetate, iron ammonium ethylenediamine tetraacetate, iron sodium dicarboxymethylglutamate, iron ammonium dicarboxymethylglutamate, ferrous fumarate, iron acetate, iron oxalate, ferrous succinate, sodium iron succinate citrate, heme iron, iron dextran, iron triethylenetetramine, lactoferrin iron, transferrin iron, sodium iron chlorophyllin, ferritin iron, saccharated iron oxide and iron glycine sulfide.
8. The method according to claim 7 , wherein the iron compound is sodium ferrous citrate.