2013Zhongguo shiyan fangjixue zazhiRequires access

Effect of TSG and PDTC on Apoptosis of HUVECs Induced by H_2O_2

Ying Tian

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Abstract

Objective:To study the anti-apoptotic effect and mechanism of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) combined with pyrrolidine dithiocar-bamate(PDTC) on the apoptosis of human umbilical vein endothelial cells(HUVECs) induced by H2O2.Method:HUVECs were divided into five groups:control group,H2O2 group(300 μmol·L-1),TSG group(10 μmol·L-1 TSG + 300 μmol·L-1 H2O2),TSG and PDTC combination group(75 μmol·L-1 PDTC + 10 μmol·L-1 TSG + 300 μmol·L-1 H2O2 group),PDTC group(75 μmol·L-1 PDTC +300 μmol·L-1 H2O2).The viability of HUVECs was detected by MTT assay.The morphology of apoptosis was observed by Hoechst 33258 staining and the rate of apoptosis was determined by flow cytometry.The protein expressions of NF-κB,Caspase-3 were detected by Western-blot.Result:Compared with control group,H2O2 significantly increased the apoptosis,reduced the cell viability,and enhanced the expressions of NF-κB and Caspase-3(P0.01).The proliferation rate increased significantly(P0.01) while the apoptosis rate decreased obviously in TSG or PDTC pretreatment group,and the expression of NF-κB and Caspase-3 down regulated(P0.05) compared with H2O2 group(P0.01).Combination of PDTC and TSG raised the cell viability and attenuated the cell apoptosis rates than pretreatment of TSG or PDTC alone,and the expression of NF-κB and Caspase-3 decreased significantly(P0.01).Conclusion:Both PDTC and TSG pretreatment could inhibit HUVECs apoptosis induced by H2O2,and the combination of PDTC and TSG can lead to the synergistic effect.The mechanism was associated with the expressions of NF-κB and Caspase-3.

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What this paper is about

Objective:To study the anti-apoptotic effect and mechanism of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) combined with pyrrolidine dithiocar-bamate(PDTC) on the apoptosis of human umbilical vein endothelial cells(HUVECs) induced by H2O2.Method:HUVECs were divided into five groups:control group,H2O2 group(300 μmol·L-1),TSG group(10 μmol·L-1 TSG + 300 μmol·L-1 H2O2),TSG and PDTC combination group(75 μmol·L-1 PDTC + 10 μmol·L-1 TSG + 300 μmol·L-1 H2O2 group),PDTC group(75 μmol·L-1 PDTC +300 μmol·L-1 H2O2).The viability of HUVECs was detected by MTT assay.The morphology of apoptosis was observed by Hoechst 33258 staining and the rate of apoptosis was determined by flow cytometry.The protein expressions of NF-κB,Caspase-3 were detected by Western-blot.Result:Compared with control group,H2O2 significantly increased the apoptosis,reduced the cell viability,and enhanced the expressions of NF-κB and Caspase-3(P0.01).The proliferation rate increased significantly(P0.01) while the apoptosis rate decreased obviously in TSG or PDTC pretreatment group,and the expression of NF-κB and Caspase-3 down regulated(P0.05) compared with H2O2 group(P0.01).Combination of PDTC and TSG raised the cell viability and attenuated the cell apoptosis rates than pretreatment of TSG or PDTC alone,and the expression of NF-κB and Caspase-3 decreased significantly(P0.01).Conclusion:Both PDTC and TSG pretreatment could inhibit HUVECs apoptosis induced by H2O2,and the combination of PDTC and TSG can lead to the synergistic effect.The mechanism was associated with the expressions of NF-κB and Caspase-3.

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Available abstract

Objective:To study the anti-apoptotic effect and mechanism of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside(TSG) combined with pyrrolidine dithiocar-bamate(PDTC) on the apoptosis of human umbilical vein endothelial cells(HUVECs) induced by H2O2.Method:HUVECs were divided into five groups:control group,H2O2 group(300 μmol·L-1),TSG group(10 μmol·L-1 TSG + 300 μmol·L-1 H2O2),TSG and PDTC combination group(75 μmol·L-1 PDTC + 10 μmol·L-1 TSG + 300 μmol·L-1 H2O2 group),PDTC group(75 μmol·L-1 PDTC +300 μmol·L-1 H2O2).The viability of HUVECs was detected by MTT assay.The morphology of apoptosis was observed by Hoechst 33258 staining and the rate of apoptosis was determined by flow cytometry.The protein expressions of NF-κB,Caspase-3 were detected by Western-blot.Result:Compared with control group,H2O2 significantly increased the apoptosis,reduced the cell viability,and enhanced the expressions of NF-κB and Caspase-3(P0.01).The proliferation rate increased significantly(P0.01) while the apoptosis rate decreased obviously in TSG or PDTC pretreatment group,and the expression of NF-κB and Caspase-3 down regulated(P0.05) compared with H2O2 group(P0.01).Combination of PDTC and TSG raised the cell viability and attenuated the cell apoptosis rates than pretreatment of TSG or PDTC alone,and the expression of NF-κB and Caspase-3 decreased significantly(P0.01).Conclusion:Both PDTC and TSG pretreatment could inhibit HUVECs apoptosis induced by H2O2,and the combination of PDTC and TSG can lead to the synergistic effect.The mechanism was associated with the expressions of NF-κB and Caspase-3.

Key concepts: Apoptosis, Viability assay, Molecular biology, Western blot, Flow cytometry, Chemistry, MTT assay, Human umbilical vein endothelial cell

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Effect of TSG and PDTC on Apoptosis of HUVECs Induced by H_2O_2 — Research Paper | ScholarLens