Glass fibres/epoxy resins composites have been performed as ideal materials to make support instruments for high-energy and nuclear physics experiments. The effects of the 3,-ray irradiation on the fatigue strength, t...Glass fibres/epoxy resins composites have been performed as ideal materials to make support instruments for high-energy and nuclear physics experiments. The effects of the 3,-ray irradiation on the fatigue strength, thermal conductivities and thermal stabilities of the glass fibres/epoxy resins composites were investigated. And a two-parameter fatigue life model was established to predict the fatigue life of the composites. Results revealed that the y-ray irradiation could probably result in the degradation of epoxy resins, but hardly damage to the glass fibres. And the γ-ray irradiation treatment could significantly affect the fatigue strength of the composites at a low-cycle fatigue stage, but seldom influence at a high-cycle fatigue stage. Furthermore, the fabricated glass fibres/epoxy resins composites after the γ-ray irradiation still presented excellent fatigue strength, ideal thermal conductivities, remarkable dimensional and thermal stabilities, which can meet the actual requirements of normal operation for supporting instruments under high-energy and nuclear physics experiments.展开更多
Objective:Chrysophanol(Chry) displays potent anticancer activity in human cancer cells and animal models,but the cellular targets of Chry have not been fully defined.Herein,we speculated whether mitochondria were a ta...Objective:Chrysophanol(Chry) displays potent anticancer activity in human cancer cells and animal models,but the cellular targets of Chry have not been fully defined.Herein,we speculated whether mitochondria were a target involved in Chry-induced cytotoxicity.Methods:Human liver cancer cell line HepG2 was incubated.The cytotoxicity was evaluated by MTT assay.Mitochondria localization was evaluated by a confocal microscopy.Mitochondrial membrane potential ΔΨm was detected by TMRE staining and determined by the flow cytometer.The levels of ATP,mitochondrial superoxide anions,and GSH/GSSG were determined according to the assay kits.The apoptosis were evaluated through Hoechst33342/PI and Annexin V/PI staining,respectively.The expression of cyclophilin D(CyPD) was determined by immunoblot method,and the interaction between CyPD and Chry was analyzed by molecule docking procedure.Results:Chry itself mainly localized in mitocho ndria to cause mitochondrial dysfunction and cell death in HepG2 cells.As regard to the mechanism,cyclosporin A as the inhibitor for the formation of mitochondrial permeability transition pore(mPTP) moderately suppressed cell death,indicating mPTP involved in the process of cell death.Further,Chry enhanced the protein expression of Cyclophilin D(CyPD) which is a molecular componentry and a modulator of mPTP,while antioxidant N-acetyl-L-cysteine inhibited the expression of CyPD.Molecule docking procedure disclosed two hydrogen-bonds existed in CyPD-Chry complex with-11.94 kal/mol of the binding affinity value.Besides,the mtDNA-deficient HepG_2-ρ0 cells were much resistant to Chry-induced cell death,indicating mtDNA at least partly participated in cell death.A combination of Chry and VP-16 produced the synergism effect toward cell viability andΔΨm,while Chry combined with Cis-Pt elicited the antagonism effect.Conclusion:Taken together,enrichment in mitochondria and actions on mPTP,CyPD and mtDNA provides an insight into the anticancer mechanism of Chry.The combination therapy for Chry with clinical drugs may deserve to further explore.展开更多
基金financially supported by the National Natural Science Foundation of China (No. 51605025)the Major Program of National Key Research and Development Program of China (2016YFC0802905)+2 种基金the Fundamental Research Funds for the Central Universities (FRF-GF-17-B19)the BEPC great reconstruction projectthe Knowledge Innovation Fund of the Chinese Academy of Sciences, U-603 and U-34 (IHEP)
文摘Glass fibres/epoxy resins composites have been performed as ideal materials to make support instruments for high-energy and nuclear physics experiments. The effects of the 3,-ray irradiation on the fatigue strength, thermal conductivities and thermal stabilities of the glass fibres/epoxy resins composites were investigated. And a two-parameter fatigue life model was established to predict the fatigue life of the composites. Results revealed that the y-ray irradiation could probably result in the degradation of epoxy resins, but hardly damage to the glass fibres. And the γ-ray irradiation treatment could significantly affect the fatigue strength of the composites at a low-cycle fatigue stage, but seldom influence at a high-cycle fatigue stage. Furthermore, the fabricated glass fibres/epoxy resins composites after the γ-ray irradiation still presented excellent fatigue strength, ideal thermal conductivities, remarkable dimensional and thermal stabilities, which can meet the actual requirements of normal operation for supporting instruments under high-energy and nuclear physics experiments.
基金supported by the Fundamental Research Funds for the Central Universities (Grant No.lzujbky-2018-131)the National Natural Sciences Foundation of China (Grant No.21302079)。
文摘Objective:Chrysophanol(Chry) displays potent anticancer activity in human cancer cells and animal models,but the cellular targets of Chry have not been fully defined.Herein,we speculated whether mitochondria were a target involved in Chry-induced cytotoxicity.Methods:Human liver cancer cell line HepG2 was incubated.The cytotoxicity was evaluated by MTT assay.Mitochondria localization was evaluated by a confocal microscopy.Mitochondrial membrane potential ΔΨm was detected by TMRE staining and determined by the flow cytometer.The levels of ATP,mitochondrial superoxide anions,and GSH/GSSG were determined according to the assay kits.The apoptosis were evaluated through Hoechst33342/PI and Annexin V/PI staining,respectively.The expression of cyclophilin D(CyPD) was determined by immunoblot method,and the interaction between CyPD and Chry was analyzed by molecule docking procedure.Results:Chry itself mainly localized in mitocho ndria to cause mitochondrial dysfunction and cell death in HepG2 cells.As regard to the mechanism,cyclosporin A as the inhibitor for the formation of mitochondrial permeability transition pore(mPTP) moderately suppressed cell death,indicating mPTP involved in the process of cell death.Further,Chry enhanced the protein expression of Cyclophilin D(CyPD) which is a molecular componentry and a modulator of mPTP,while antioxidant N-acetyl-L-cysteine inhibited the expression of CyPD.Molecule docking procedure disclosed two hydrogen-bonds existed in CyPD-Chry complex with-11.94 kal/mol of the binding affinity value.Besides,the mtDNA-deficient HepG_2-ρ0 cells were much resistant to Chry-induced cell death,indicating mtDNA at least partly participated in cell death.A combination of Chry and VP-16 produced the synergism effect toward cell viability andΔΨm,while Chry combined with Cis-Pt elicited the antagonism effect.Conclusion:Taken together,enrichment in mitochondria and actions on mPTP,CyPD and mtDNA provides an insight into the anticancer mechanism of Chry.The combination therapy for Chry with clinical drugs may deserve to further explore.
