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Effects of resveratrol on the sequential expression of SIRT1 in cardiomyocytes

Chen Chun-jua

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Abstract

Objective To observe the effect of resveratrol(RES),an activator of silent information regulator 2,on the sequential expression of SIRT1 in cardiomyocytes.Methods After 48 h culture under normal condition,the embryonal rat heart-derived H9c2 cells were treated with 0(control group),10(low dose group),20(medium dose group)50 and 100 μmol/L(high dose groups)of RES for 0,12,24,36 and 48 h.Cell viability was analyzed by MTT assay,expression of SIRT1 mRNA by RT-RCR and SIRT1 products by Western blot.Results The optical densities(A)of MTT was increased in the low and medium dose groups,appeared markedly higher with 20 μmol/L RES treat-ment(P0.05),and was lower than normal in the high dose groups,particularly in the 100 μmol/L group(P0.05).The expressions of SIRT1 mRNA and protein were increased after treated with different concentrations of RES(P0.05),most notability with 20 μmol/L.At different time spots of incubation with 20 μmol/L RES(0,12,24,36,and 48 h),the A values of SIRT1 mRNA and proteins were higher than those in controls(P0.05),with a peak at 24 h.Conclu-sion The maximum expression of SIRT1 was achieved with treatment of 20 μmol/L RES for 24 h in cadiacmyocytes.

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Objective To observe the effect of resveratrol(RES),an activator of silent information regulator 2,on the sequential expression of SIRT1 in cardiomyocytes.Methods After 48 h culture under normal condition,the embryonal rat heart-derived H9c2 cells were treated with 0(control group),10(low dose group),20(medium dose group)50 and 100 μmol/L(high dose groups)of RES for 0,12,24,36 and 48 h.Cell viability was analyzed by MTT assay,expression of SIRT1 mRNA by RT-RCR and SIRT1 products by Western blot.Results The optical densities(A)of MTT was increased in the low and medium dose groups,appeared markedly higher with 20 μmol/L RES treat-ment(P0.05),and was lower than normal in the high dose groups,particularly in the 100 μmol/L group(P0.05).The expressions of SIRT1 mRNA and protein were increased after treated with different concentrations of RES(P0.05),most notability with 20 μmol/L.At different time spots of incubation with 20 μmol/L RES(0,12,24,36,and 48 h),the A values of SIRT1 mRNA and proteins were higher than those in controls(P0.05),with a peak at 24 h.Conclu-sion The maximum expression of SIRT1 was achieved with treatment of 20 μmol/L RES for 24 h in cadiacmyocytes.

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Available abstract

Objective To observe the effect of resveratrol(RES),an activator of silent information regulator 2,on the sequential expression of SIRT1 in cardiomyocytes.Methods After 48 h culture under normal condition,the embryonal rat heart-derived H9c2 cells were treated with 0(control group),10(low dose group),20(medium dose group)50 and 100 μmol/L(high dose groups)of RES for 0,12,24,36 and 48 h.Cell viability was analyzed by MTT assay,expression of SIRT1 mRNA by RT-RCR and SIRT1 products by Western blot.Results The optical densities(A)of MTT was increased in the low and medium dose groups,appeared markedly higher with 20 μmol/L RES treat-ment(P0.05),and was lower than normal in the high dose groups,particularly in the 100 μmol/L group(P0.05).The expressions of SIRT1 mRNA and protein were increased after treated with different concentrations of RES(P0.05),most notability with 20 μmol/L.At different time spots of incubation with 20 μmol/L RES(0,12,24,36,and 48 h),the A values of SIRT1 mRNA and proteins were higher than those in controls(P0.05),with a peak at 24 h.Conclu-sion The maximum expression of SIRT1 was achieved with treatment of 20 μmol/L RES for 24 h in cadiacmyocytes.

Key concepts: Resveratrol, Western blot, Messenger RNA, Incubation, Activator (genetics), MTT assay, Molecular biology, Chemistry

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