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Ginsenoside Rb1 Inhibits Doxorubicin-Triggered H9C2 Cell Apoptosis via Aryl Hydrocarbon Receptor
Zhang, Yaxin,Wang, Yuguang,Ma, Zengchun,Liang, Qiande,Tang, Xianglin,Tan, Hongling,Xiao, Chengrong,Gao, Yue The Korean Society of Applied Pharmacology 2017 Biomolecules & Therapeutics(구 응용약물학회지) Vol.25 No.2
Doxorubicin (DOX) is a highly effective chemotherapeutic agent; however, the dose-dependent cardiotoxicity associated with DOX significantly limits its clinical application. In the present study, we investigated whether Rb1 could prevent DOX-induced apoptosis in H9C2 cells via aryl hydrocarbon receptor (AhR). H9C2 cells were treated with various concentrations ($-{\mu}M$) of Rb1. AhR, CYP1A protein and mRNA expression were quantified with Western blot and real-time PCR analyses. We also evaluated the expression levels of caspase-3 to assess the anti-apoptotic effects of Rb1. Our results showed that Rb1 attenuated DOX-induced cardiomyocytes injury and apoptosis and reduced caspase-3 and caspase-8, but not caspase-9 activity in DOX-treated H9C2 cells. Meanwhile, pre-treatment with Rb1 decreased the expression of caspase-3 and PARP in the protein levels, with no effects on cytochrome c, Bax, and Bcl-2 in DOX-stimulated cells. Rb1 markedly decreased the CYP1A1 and CYP1A2 expression induced by DOX. Furthermore, transfection with AhR siRNA or pre-treatment with AhR antagonist CH-223191 significantly inhibited the ability of Rb1 to decrease the induction of CYP1A, as well as caspase-3 protein levels following stimulation with DOX. In conclusion, these findings indicate that AhR plays an important role in the protection of Ginsenoside Rb1 against DOX-triggered apoptosis of H9C2 cells.
Zhang Di,Shin Heesung,Wang Tingting,Zhao Yaxin,Lee Suwon,Lim Chongyoon,Zhang Shiqi 한국미생물·생명공학회 2023 Journal of microbiology and biotechnology Vol.33 No.8
Lactiplantibacillus plantarum, previously named Lactobacillus plantarum, is a facultative, homofermentative lactic acid bacterium widely distributed in nature. Several Lpb. plantarum strains have been demonstrated to possess good probiotic properties, and Lpb. plantarum HOM3204 is a potential probiotic strain isolated from homemade pickled cabbage plants. In this study, wholegenome sequencing was performed to acquire genetic information and predict the function of HOM3204, which has a circular chromosome of 3,232,697 bp and two plasmids of 48,573 and 17,060 bp, respectively. Moreover, various oxidative stress-related genes were identified in the strain, and its antioxidant activity was evaluated in vitro and in vivo. Compared to reference strains, the intracellular cell-free extracts of Lpb. plantarum HOM3204 at a dose of 1010 colony-forming units (CFU)/ml in vitro exhibited stronger antioxidant properties, such as total antioxidant activity, 2,2- diphenyl-1-picrylhydrazyl radical scavenging rate, superoxide dismutase activity, and glutathione (GSH) content. Daily administration of 109 CFU Lpb. plantarum HOM3204 for 45 days significantly improved the antioxidant function by increasing the glutathione peroxidase activity in the whole blood and GSH concentration in the livers of D-galactose-induced aging mice. These results suggest that Lpb. plantarum HOM3204 can potentially be used as a food ingredient with good antioxidant properties.
Ginsenoside Rb1 Inhibits Doxorubicin-Triggered H9C2 Cell Apoptosis via Aryl Hydrocarbon Receptor
( Yaxin Zhang ),( Yuguang Wang ),( Zengchun Ma ),( Qiande Liang ),( Xianglin Tang ),( Hongling Tan ),( Chengrong Xiao ),( Yue Gao ) 한국응용약물학회 2017 Biomolecules & Therapeutics(구 응용약물학회지) Vol.25 No.2
Doxorubicin (DOX) is a highly effective chemotherapeutic agent; however, the dose-dependent cardiotoxicity associated with DOX significantly limits its clinical application. In the present study, we investigated whether Rb1 could prevent DOX-induced apoptosis in H9C2 cells via aryl hydrocarbon receptor (AhR). H9C2 cells were treated with various concentrations (- μM) of Rb1. AhR, CYP1A protein and mRNA expression were quantified with Western blot and real-time PCR analyses. We also evaluated the expression levels of caspase-3 to assess the anti-apoptotic effects of Rb1. Our results showed that Rb1 attenuated DOX-induced cardiomyocytes injury and apoptosis and reduced caspase-3 and caspase-8, but not caspase-9 activity in DOX-treated H9C2 cells. Meanwhile, pre-treatment with Rb1 decreased the expression of caspase-3 and PARP in the protein levels, with no effects on cytochrome c, Bax, and Bcl-2 in DOX-stimulated cells. Rb1 markedly decreased the CYP1A1 and CYP1A2 expression induced by DOX. Furthermore, transfection with AhR siRNA or pre-treatment with AhR antagonist CH-223191 significantly inhibited the ability of Rb1 to decrease the induction of CYP1A, as well as caspase-3 protein levels following stimulation with DOX. In conclusion, these findings indicate that AhR plays an important role in the protection of Ginsenoside Rb1 against DOX-triggered apoptosis of H9C2 cells.
Ruilian Xiu,Jie Jia,Qing Zhang,Fengjiao Liu,Yaxin Jia,Yuanyuan Zhang,Beibei Song,Xiaodan Liu,Jingwei Chen,Dongyang Huang,Fan Zhang,Juanjuan Ma,Honglin Li,Xuan Zhang,Yunyun Geng 대한약리학회 2023 The Korean Journal of Physiology & Pharmacology Vol.27 No.6
Transmembrane protein TMEM16A, which encodes calcium-activated chloride channel has been implicated in tumorigenesis. Overexpression of TMEM16A is associated with poor prognosis and low overall survival in multiple cancers including lung adenocarcinoma, making it a promising biomarker and therapeutic target. In this study, three structure-related sesquiterpene lactones (mecheliolide, costunolide and dehydrocostus lactone) were extracted from the traditional Chinese medicine Aucklandiae Radix and identified as novel TMEM16A inhibitors with comparable inhibitory effects. Their effects on the proliferation and migration of lung adenocarcinoma cells were examined. Whole-cell patch clamp experiments showed that these sesquiterpene lactones potently inhibited recombinant TMEM16A currents in a concentration- dependent manner. The half-maximal concentration (IC50) values for three tested sesquiterpene lactones were 29.9 ± 1.1 μM, 19.7 ± 0.4 μM, and 24.5 ± 2.1 μM, while the maximal effect (Emax) values were 100.0% ± 2.8%, 85.8% ± 0.9%, and 88.3% ± 4.6%, respectively. These sesquiterpene lactones also significantly inhibited the endogenous TMEM16A currents and proliferation, and migration of LA795 lung cancer cells. These results demonstrate that mecheliolide, costunolide and dehydrocostus lactone are novel TMEM16A inhibitors and potential candidates for lung adenocarcinoma therapy.
Zhang, Weiping,Li, Guiying,Wang, Wanjun,Qin, Yaxin,An, Taicheng,Xiao, Xinyan,Choi, Wonyong Elsevier 2018 Applied Catalysis B Vol.232 No.-
<P><B>Abstract</B></P> <P>A chemically modified Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>(M = Mo, W)/rGO composite was firstly synthesized via a liquid-exfoliation solvothermal method. The structure, morphology, optical properties and composition were characterized by X-ray diffraction, FT-IR spectroscopy, scanning electron microscopy, UV–vis diffuse reflectance spectra and X-ray photoelectron spectroscopy, respectively. The characterization results indicated that compact structure could be obtained by using this typical method due to in-situ chemical modification, which could also control the sizes of Ag<SUB>3</SUB>PO<SUB>4</SUB> nano-sheets by adding MS<SUB>2</SUB>/rGO hybrids. More importantly, the resultant Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>/rGO composite exhibited higher photocatalytic activity and stability toward the degradation of 4-nitrophenol than pure Ag<SUB>3</SUB>PO<SUB>4</SUB> under sunlight irradiation. The stable structure of Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>/rGO was closely related with Z-scheme electronic structure and electrical conductivity of MS<SUB>2</SUB>/rGO hybrids, leading to a higher consumption and transfer of photogenerated electrons. However, by controlling the amounts of MS<SUB>2</SUB>/rGO hybrids, more stable but lower photocatalytic activity composites could be obtained. Further analysis found that the holes and O<SUB>2</SUB> <SUP>−</SUP> were the main reactive species involved in the photocatalytic degradation of 4-nitrophenol. In addition, possible photocatalytic degradation pathways of 4-nitrophenol were also proposed based on the identified intermediates. The findings of this work may provide a new method to design efficient composites for photocatalytic degradation of organic pollutants.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>/rGO catalyst was fabricated via a liquid-exfoliation solvothermal method. </LI> <LI> Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>/rGO has high photocatalytic activity and stability under sunlight. </LI> <LI> The stability of Ag<SUB>3</SUB>PO<SUB>4</SUB>@MS<SUB>2</SUB>/rGO was due to its rapid transfer of photogenerated e<SUP>−</SUP>. </LI> <LI> h<SUP>+</SUP> and O<SUB>2</SUB> <SUP>−</SUP> were the main RSs in photocatalytic degradation of 4-nitrophenol. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Qin, Yaxin,Li, Guiying,Gao, Yanpeng,Zhang, Lizhi,Ok, Yong Sik,An, Taicheng Elsevier 2018 Water research Vol.137 No.-
<P><B>Abstract</B></P> <P>With the increased concentrations and kinds of refractory organic contaminants (ROCs) in aquatic environments, many previous reviews systematically summarized the applications of carbon-based materials in the adsorption and catalytic degradation of ROCs for their economically viable and environmentally friendly behavior. Interestingly, recent studies indicated that carbon-based materials in natural environment can also mediate the transformation of ROCs directly or indirectly due to their abundant persistent free radicals (PFRs). Understanding the formation mechanisms of PFRs in carbo-based materials and their interactions with ROCs is essential to develop their further applications in environment remediation. However, there is no comprehensive review so far about the direct and indirect removal of ROCs mediated by PFRs in amorphous, porous and crystalline carbon-based materials. The review aims to evaluate the formation mechanisms of PFRs in carbon-based materials synthesized through pyrolysis and hydrothermal carbonization processes. The influence of synthesis conditions (temperature and time) and carbon sources on the types as well as the concentrations of PFRs in carbon-based materials are also discussed. In particular, the effects of metals on the concentrations and types of PFRs in carbon-based materials are highlighted because they are considered as the catalysts for the formation of PFRs. The formation mechanisms of reactive species and the further transformation mechanisms of ROCs are briefly summarized, and the surface properties of carbon-based materials including surface area, types and number of functional groups, etc. are found to be the key parameters controlling their activities. However, due to diversity and complexity of carbon-based materials, the exact relationships between the activities of carbon-based materials and PFRs are still uncertain. Finally, the existing problems and current challenges for the ROCs transformation with carbon-based materials are also pointed out.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Abundant of PFRs formed in carbon-based materials during the synthesis process. </LI> <LI> The PFRs types and concentrations affected by synthesis conditions. </LI> <LI> The PFRs can activate oxidants and reductants to degrade organic contaminants. </LI> <LI> The PFRs can directly react with organic contaminants. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Wei Zhang,Chao Hu,Jie Tan,Zhujun Fan,Fangli Chi,Yaxin Sun,Songlin Ran,Xianguo Liu,Yaohui Lv 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2016 NANO Vol.11 No.6
The composite α-FeOOH nanorods/Ag3PO4 photocatalyst has been successfully fabricated through a facile hydrothermal process combined with a successive in situ precipitation technique. The SEM and TEM images show that Ag3PO4 particles have been successfully loaded on the surface of FeOOH nanorods. The photocatalytic activities of the α-FeOOH/Ag3PO4 composite were investigated for their efficiency on the degradation of Rhodamine B (RhB) under ultra-violet light and visible light irradiation, and the results showed that the α-FeOOH/Ag3PO4 composite possessed remarkable photocatalytic activities. The enhanced photocatalytic activity can be attributed to the strong absorption in visible light and the effective separation of photogenerated hole–electron pairs between Ag3PO4 and α-FeOOH.
Graphene Enhanced Electrical Properties of Polyethylene Blends for High-Voltage Insulation
Zuojun Wei,Yaxin Hou,Chen Jiang,Haiyan Liu,Xiangrong Chen,Anyun Zhang,Yingxin Liu 대한금속·재료학회 2019 ELECTRONIC MATERIALS LETTERS Vol.15 No.5
Graphene as a novel additive in low density polyethylene (LDPE), high density polyethylene–low density polyethylene blend(10%HDPE–LDPE) and polypropylene–low density polyethylene blend (10%PP–LDPE), is investigated for promising ecofriendlyinsulating materials in high voltage cables. The composites with graphene amounts of 0, 0.002 wt%, 0.02 wt%,and 0.2 wt% are prepared by the solution mixing method. With attempt to disclose the structure–property relationships, thecomposites are extensively characterized by physical techniques including Fourier transform infrared spectroscopy, X-raydiffraction, atomic force microscopy, transmission electron microscopy, scanning electron microscopy, thermogravimetricanalysis and differential scanning calorimetry, and electrical measurements including electrical treeing, direct current conductivityand space charge distributions. Results show that graphene can significantly enhances the thermal stability of LDPEand 10%PP–LDPE, slightly decrease the degree of crystallinity, change the size of the crystal diameters, and improve thephase distribution of the polymer blends. Consequently, graphene can prolong the electrical tree initiation time and blockthe extension of electrical tree. Besides, it can modulate the trap distributions, which will further change the conductivityand ability to suppress space charge accumulations. This excellent performance of graphene could be attributed to its goodexfoliation, uniform dispersion and outstretched morphology in the polymer matrix, as well as its strong ability to captureelectrons.
Chen, Lei,Zhang, Fan,Deng, Xin-Yu,Xue, Xiangxin,Wang, Li,Sun, Yantao,Feng, Jing-Dong,Zhang, Yongjun,Wang, Yaxin,Jung, Young Mee Elsevier 2018 Spectrochimica acta. Part A, Molecular and biomole Vol.189 No.-
<P><B>Abstract</B></P> <P>A plasmon induced carrier movement enhanced mechanism of surface-enhanced Raman scattering (SERS) was investigated using a charge-transfer (CT) enhancement mechanism. Here, we designed a strategy to study SERS in Au@Cu<SUB>2</SUB>O nanoshell nanoparticles with different shell thicknesses. Among the plasmonically coupled nanostructures, Au spheres with Cu<SUB>2</SUB>O shells have been of special interest due to their ultrastrong electromagnetic fields and controllable carrier transfer properties, which are useful for SERS. Au@Cu<SUB>2</SUB>O nanoshell nanoparticles (NPs) with shell thicknesses of 48–56nm are synthesized that exhibit high SERS activity. This high activity originates from plasmonic-induced carrier transfer from Au@Cu<SUB>2</SUB>O to 4-mercaptobenzoic acid (MBA). The CT transition from the valence band (VB) of Cu<SUB>2</SUB>O to the second excited π-π* transition of MBA, and is of b<SUB>2</SUB> electronic symmetry, which was enhanced significantly. The Herzberg-Teller selection rules were employed to predict the observed enhanced b<SUB>2</SUB> symmetry modes. The system constructed in this study combines the long-range electromagnetic effect of Au NPs, localized surface plasmon resonance (LSPR) of the Au@Cu<SUB>2</SUB>O nanoshell, and the CT contribution to assist in understanding the SERS mechanism based on LSPR-induced carrier movement in metal/semiconductor nanocomposites.</P> <P><B>Highlights</B></P> <P> <UL> <LI> We designed a shell-dependent Au@Cu<SUB>2</SUB>O nanoshell for SERS study. </LI> <LI> SERS contribution enables us to understand the possible enhancement of hybrid nanostructures. </LI> <LI> LSPR-induced carrier movement in Au@Cu<SUB>2</SUB>O nanocomposites. </LI> </UL> </P> <P><B>Graphical Abstract</B></P> <P>We designed the shell-dependent Au@Cu<SUB>2</SUB>O core-shell nanoparticles (NPs) for SERS study. For the electron-hole pairs in the Cu<SUB>2</SUB>O, the plasmon induced resonant energy transfer from Au to the Cu<SUB>2</SUB>O and the direct electron transfer simultaneously which can be observed from the SERS intensity.</P> <P>[DISPLAY OMISSION]</P>
Dapeng Li,Peng Zhang,Jiangtao Duan,Yaxin Wu,Na Ding,Zhenyu Wan,Longqi Chen,Jingli Xu,Suxiang Ge,Juntao Ma 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.114 No.-
Utilization of fly ash (FA) wastes as the carriers of catalysts for the environmental application is an economicand practical strategy for their low cost, easy accessibility and thermal stability. However, mostcatalysts immobilized on fly ash were metal or metal oxides, some potential catalysts such as metalphthalocyanine complexes have not been reported upon their heterogeneous catalysis with FA as the carriers. In this paper, highly active iron octacarboxyphthalocyanine were immobilized onto the bird nestlikesurfaces of fly ash microspheres after NaOH activation. It is noted that the FeOCPc@FA compositeswith only 2 wt.% exhibited the high catalytic efficiency in the organic dye degradation. The high concentrationof 30 mg/L rhodamine B and methylene blue could be fast decolorized in the presence ofFeOCPc@FA–2 % and KHSO5. Moreover, the ultrafast decolorization of these dyes could be observed inthe catalytic system composed of FeOCPc@FA–2 %, KHSO5 and BuOOH (tert-butyl hydroperoxide). Simultaneous activation of KHSO5 and BuOOH could be realized in our designed catalytic system. Based on the structural characterizations of composites and active species generated during the catalyticprocesses, the probable generation pathway of metal–oxygen active species and various radicals wereanalyzed to explicate the catalytic mechanism. Our investigation provides a high efficiency, low costand environmentally friendly strategy for advanced oxidation treatment of organic pollutants.