[Objectives]To study the acute toxicity of total flavonoids in Penthorum chinense Pursh. and the therapeutic effect on AFL( Alcoholic Fatty Liver). [Methods] The liquid of total flavonoids in P. chinense Pursh. was in...[Objectives]To study the acute toxicity of total flavonoids in Penthorum chinense Pursh. and the therapeutic effect on AFL( Alcoholic Fatty Liver). [Methods] The liquid of total flavonoids in P. chinense Pursh. was intragastrically administered to the test group rats in the maximum concentration and the maximum administration volume,an equal volume of solvent was given to the control group,and it was observed continuously for 14 d; 1. 5% ferrous sulfate feed was used for feeding,the alcohol intragastric administration method was used to copy the AFL rats model,and the therapeutic effect of total flavonoids in P. chinense Pursh. on the fatty liver rats was observed. [Results]No rat died in the medication administration group and the control group,there was no acute toxicity reaction,and the maximum tolerance dose of total flavonoids in P. chinense Pursh. for the rats by intragastric administration was 33. 6 g/kg; rats suffered AFL 6 weeks after the alcohol intragastric administration. For the 800 mg/kg P. chinense Pursh. total flavonoids and 2 000 mg/kg P. chinense Pursh. extract with the same dose as that of the P. chinense Pursh. crude drug,P. chinense Pursh. total flavonoids played a more significant role than P. chinense Pursh. extract in lowering oil red O staining area in AFL rats' liver tissue and reducing the ALT,AST,TC,TG content in AFL rats' serum. [Conclusions]The P. chinense Pursh. total flavonoids had low acute toxicity,and had a greater therapeutic effect on the AFL rats than the P. chinense Pursh.extract.展开更多
Aim:Protective effects of aqueous extract of Amaranthus hybridus against afl atoxin B1(AFB_(1))and/or fumonisin B1(FB_(1))on the H4IIE-luc cell line were determined by use of the methyl thiazol tetrazolium viability a...Aim:Protective effects of aqueous extract of Amaranthus hybridus against afl atoxin B1(AFB_(1))and/or fumonisin B1(FB_(1))on the H4IIE-luc cell line were determined by use of the methyl thiazol tetrazolium viability assay and disruption of DNA integrity.Methods:H4IIE-luc cells were incubated with different concentrations of AFB_(1) and/or FB_(1) for 24 and 48 h with or without aqueous extract of A.hybridus.Results:AFB_(1) decreased the viability of cells after 24 and 48 h of exposure.EC_(50)values for AFB_(1) were 10.5 and 1.8μmol/L for the two periods,respectively.When the 48 h exposure to mycotoxin repeated with a pre-treatment of 20 and 40μg/mL extract of A.hybridus,the EC_(50)changed to 3.88 and 7.67μmol/L,respectively.H4IIE-luc cells exposed to FB_(1) for 24 h responded more than those incubated for 48 h.Cells treated with a combination of AFB_(1) and FB_(1) were less viable with a signifi cant decrease in the greater concentration.The mixture of AFB_(1) and FB_(1) resulted in a signifi cant threat to H4IIE-luc as indicated by the absence or appearance of new bands in random amplifi ed polymorphic DNA analysis,which demonstrated damage to DNA.The protective effects were probably due to greater content of total phenolics,carotenoids,β-carotene,folic-,linolenic-,linoleic and palmitic acids,as well as calcium,magnesium,iron,zinc,and selenium observed in the extract.Conclusion:Exposure to 40μg/mL of extract of A.hybridus protected cells from damage to DNA by stabilizing DNA.展开更多
基金Supported by Luzhou Municipal Government-Luzhou Medical College Joint Project(2013LZLY-K78)Project of Sichuan Provincial Department of Education in 2015[2015-Chuan Jiao Han(2014)794)]Key Project of Southwest Medical University in 2015(2015-9)
文摘[Objectives]To study the acute toxicity of total flavonoids in Penthorum chinense Pursh. and the therapeutic effect on AFL( Alcoholic Fatty Liver). [Methods] The liquid of total flavonoids in P. chinense Pursh. was intragastrically administered to the test group rats in the maximum concentration and the maximum administration volume,an equal volume of solvent was given to the control group,and it was observed continuously for 14 d; 1. 5% ferrous sulfate feed was used for feeding,the alcohol intragastric administration method was used to copy the AFL rats model,and the therapeutic effect of total flavonoids in P. chinense Pursh. on the fatty liver rats was observed. [Results]No rat died in the medication administration group and the control group,there was no acute toxicity reaction,and the maximum tolerance dose of total flavonoids in P. chinense Pursh. for the rats by intragastric administration was 33. 6 g/kg; rats suffered AFL 6 weeks after the alcohol intragastric administration. For the 800 mg/kg P. chinense Pursh. total flavonoids and 2 000 mg/kg P. chinense Pursh. extract with the same dose as that of the P. chinense Pursh. crude drug,P. chinense Pursh. total flavonoids played a more significant role than P. chinense Pursh. extract in lowering oil red O staining area in AFL rats' liver tissue and reducing the ALT,AST,TC,TG content in AFL rats' serum. [Conclusions]The P. chinense Pursh. total flavonoids had low acute toxicity,and had a greater therapeutic effect on the AFL rats than the P. chinense Pursh.extract.
基金The Morogo Research Program gratefully acknowledges the National Research Foundation of South Africa(Focus Area Grant FA2004050600064)National Research Center,Cairo,Egypt Project No.10070112 for financial support of this study.Prof.Giesy was supported by the Canada Research Chair program,a Visiting Distinguished Professorship in the Department of Biology and Chemistry and State Key Laboratory in Marine Pollution,City University of Hong Kong,the 2012“High Level Foreign Experts”(No.GDT20143200016)program,funded by the State Administration of Foreign Experts Affairs,the P.R.China to Nanjing University and the Einstein Professor Program of the Chinese Academy of Sciences.
文摘Aim:Protective effects of aqueous extract of Amaranthus hybridus against afl atoxin B1(AFB_(1))and/or fumonisin B1(FB_(1))on the H4IIE-luc cell line were determined by use of the methyl thiazol tetrazolium viability assay and disruption of DNA integrity.Methods:H4IIE-luc cells were incubated with different concentrations of AFB_(1) and/or FB_(1) for 24 and 48 h with or without aqueous extract of A.hybridus.Results:AFB_(1) decreased the viability of cells after 24 and 48 h of exposure.EC_(50)values for AFB_(1) were 10.5 and 1.8μmol/L for the two periods,respectively.When the 48 h exposure to mycotoxin repeated with a pre-treatment of 20 and 40μg/mL extract of A.hybridus,the EC_(50)changed to 3.88 and 7.67μmol/L,respectively.H4IIE-luc cells exposed to FB_(1) for 24 h responded more than those incubated for 48 h.Cells treated with a combination of AFB_(1) and FB_(1) were less viable with a signifi cant decrease in the greater concentration.The mixture of AFB_(1) and FB_(1) resulted in a signifi cant threat to H4IIE-luc as indicated by the absence or appearance of new bands in random amplifi ed polymorphic DNA analysis,which demonstrated damage to DNA.The protective effects were probably due to greater content of total phenolics,carotenoids,β-carotene,folic-,linolenic-,linoleic and palmitic acids,as well as calcium,magnesium,iron,zinc,and selenium observed in the extract.Conclusion:Exposure to 40μg/mL of extract of A.hybridus protected cells from damage to DNA by stabilizing DNA.
