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Zhiwu Zhang,Youping Yi,Wen You,Shiquan Huang,Yonglin Guo,Hailin He 대한금속·재료학회 2022 METALS AND MATERIALS International Vol.28 No.6
To investigate the quenching sensitivity of the 2195 Al–Li alloy rolled sheet and guide the design of the quenching process,the time–temperature-property (TTP) curves of this material were researched through interrupted quenching experiments. The differential scanning calorimetry (DSC) and transmission electron microscope (TEM) were used to characterize theevolution of precipitates during isothermal treatment. The results of this essay demonstrated that the nose temperature of 2195Al–Li alloy is around 370 °C and the temperature range of quenching sensitivity is 340 °C to 400 °C. The microstructureobservation revealed that the T1particles precipitate and grow rapidly at the temperature from 340 to 400 °C, which is dueto the high nucleation rate of phase and fast solute diffusion kinetics, especially at the nose temperature. The needle-shapedθ′/θ″ and T1particles grow up quickly as the isothermal preservation time prolonged, leading to the decrease of the supersaturatedsolid solution of the matrix. This will reduce the number of the age-induced precipitate and weaken the subsequentage hardening effect. Therefore, the rate of cooling should be increased in the quenching sensitivity range (340–400 °C) toinhibit the precipitation of the second phase and obtain excellent mechanical properties. While in other temperature ranges,the cooling rate should be decreased appropriately to reduce residual stress. The appropriate average cooling rate is recommendedto be around 13 °C s−1 at the temperature from 340 to 400 °C.
Tanshinone IIA Protects Endothelial Cells from H2O2-Induced Injuries via PXR Activation
Haiyan Zhu,Zhiwu Chen,Zengchun Ma,Hongling Tan,Chengrong Xiao,Xianglin Tang,Boli Zhang,Yuguang Wang,Yue Gao 한국응용약물학회 2017 Biomolecules & Therapeutics(구 응용약물학회지) Vol.25 No.6
Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic and endobiotic detoxification. Tan IIA is an efficacious PXR agonist that has a potential protective effect on endothelial injuries induced by xenobiotics and endobiotics via PXR activation. Previously numerous studies have demonstrated the possible effects of Tan IIA on human umbilical vein endothelial cells, but the further mechanism for its exerts the protective effect is not well established. To study the protective effects of Tan IIA against hydrogen peroxide (H2O2) in human umbilical vein endothelial cells (HUVECs), we pretreated cells with or without different concentrations of Tan IIA for 24 h, then exposed the cells to 400 μM H2O2 for another 3 h. Therefore, our data strongly suggests that Tan IIA may lead to increased regeneration of glutathione (GSH) from the glutathione disulfide (GSSG) produced during the GSH peroxidase-catalyzed decomposition of H2O2 in HUVECs, and the PXR plays a significant role in this process. Tan IIA may also exert protective effects against H2O2-induced apoptosis through the mitochondrial apoptosis pathway associated with the participation of PXR. Tan IIA protected HUVECs from inflammatory mediators triggered by H2O2 via PXR activation. In conclusion, Tan IIA protected HUVECs against H2O2-induced cell injury through PXR-dependent mechanisms.
( Haiyan Zhu ),( Zhiwu Chen ),( Zengchun Ma ),( Hongling Tan ),( Chengrong Xiao ),( Xianglin Tang ),( Boli Zhang ),( Yuguang Wang ),( Yue Gao ) 한국응용약물학회 2017 Biomolecules & Therapeutics(구 응용약물학회지) Vol.25 No.6
Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic and endobiotic detoxification. Tan IIA is an efficacious PXR agonist that has a potential protective effect on endothelial injuries induced by xenobiotics and endobiotics via PXR activation. Previously numerous studies have demonstrated the possible effects of Tan IIA on human umbilical vein endothelial cells, but the further mechanism for its exerts the protective effect is not well established. To study the protective effects of Tan IIA against hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) in human umbilical vein endothelial cells (HUVECs), we pretreated cells with or without different concentrations of Tan IIA for 24 h, then exposed the cells to 400 μM H<sub>2</sub>O<sub>2</sub> for another 3 h. Therefore, our data strongly suggests that Tan IIA may lead to increased regeneration of glutathione (GSH) from the glutathione disulfide (GSSG) produced during the GSH peroxidase-catalyzed decomposition of H<sub>2</sub>O<sub>2</sub> in HUVECs, and the PXR plays a significant role in this process. Tan IIA may also exert protective effects against H<sub>2</sub>O<sub>2</sub>-induced apoptosis through the mitochondrial apoptosis pathway associated with the participation of PXR. Tan IIA protected HUVECs from inflammatory mediators triggered by H<sub>2</sub>O<sub>2</sub> via PXR activation. In conclusion, Tan IIA protected HUVECs against H<sub>2</sub>O<sub>2</sub>-induced cell injury through PXR-dependent mechanisms.
Optimistic Fault Diagnosis in Discrete Event Systems by Labeled Petri Nets and Basis Markings
Guanghui Zhu,Jiafeng Zhang,Zhong Zheng,Shan Luan,Te Chen,Qiang Ma,Zhiwu Li 제어·로봇·시스템학회 2022 International Journal of Control, Automation, and Vol.20 No.6
This paper deals with the fault diagnosis problem of discrete event systems modeled with labeled Petri nets. Its main contributions are threefold. First, depending on whether a diagnosis function examines the fault transitions that possibly occur after the last observed event, we formally divide the diagnosis functions into two types: optimistic and pessimistic, which aims to facilitate the exploration of different diagnosis approaches. Second, a framework is proposed, which extends a given diagnosis approach for Petri nets to the case of labeled Petri nets. The main idea of the framework is to compute and combine the diagnosis results of observable transition sequences corresponding to an observed word. Third, we convert a basis-marking-based approach that is originally pessimistic to the optimistic case and prove the correctness of this conversion.
Zhu, Haiyan,Chen, Zhiwu,Ma, Zengchun,Tan, Hongling,Xiao, Chengrong,Tang, Xianglin,Zhang, Boli,Wang, Yuguang,Gao, Yue The Korean Society of Applied Pharmacology 2017 Biomolecules & Therapeutics(구 응용약물학회지) Vol.25 No.6
Tanshinone IIA (Tan IIA) is a pharmacologically active substance extracted from the rhizome of Salvia miltiorrhiza Bunge (also known as the Chinese herb Danshen), and is widely used to treat atherosclerosis. The pregnane X receptor (PXR) is a nuclear receptor that is a key regulator of xenobiotic and endobiotic detoxification. Tan IIA is an efficacious PXR agonist that has a potential protective effect on endothelial injuries induced by xenobiotics and endobiotics via PXR activation. Previously numerous studies have demonstrated the possible effects of Tan IIA on human umbilical vein endothelial cells, but the further mechanism for its exerts the protective effect is not well established. To study the protective effects of Tan IIA against hydrogen peroxide ($H_2O_2$) in human umbilical vein endothelial cells (HUVECs), we pretreated cells with or without different concentrations of Tan IIA for 24 h, then exposed the cells to $400{\mu}M$ $H_2O_2$ for another 3 h. Therefore, our data strongly suggests that Tan IIA may lead to increased regeneration of glutathione (GSH) from the glutathione disulfide (GSSG) produced during the GSH peroxidase-catalyzed decomposition of $H_2O_2$ in HUVECs, and the PXR plays a significant role in this process. Tan IIA may also exert protective effects against $H_2O_2$-induced apoptosis through the mitochondrial apoptosis pathway associated with the participation of PXR. Tan IIA protected HUVECs from inflammatory mediators triggered by $H_2O_2$ via PXR activation. In conclusion, Tan IIA protected HUVECs against $H_2O_2$-induced cell injury through PXR-dependent mechanisms.