Seismic wavefields propagate through three-dimensional(3D)space,and their precise characterization is crucial for understanding subsurface structures.Traditional 2D algorithms,due to their limitations,are insufficient...Seismic wavefields propagate through three-dimensional(3D)space,and their precise characterization is crucial for understanding subsurface structures.Traditional 2D algorithms,due to their limitations,are insufficient to fully represent three-dimensional wavefields.The classic 3D Radon transform algorithm assumes that the wavefield's propagation characteristics are consistent in all directions,which often does not hold true in complex underground media.To address this issue,we present an improved 3D three-parameter Radon algorithm that considers the wavefield variation with azimuth and provides a more accurate wavefield description.However,introducing new parameters to describe the azimuthal varia-tion also poses computational challenges.The new Radon transform operator involves five variables and cannot be simply decomposed into small matrices for efficient computation;instead,it requires large matrix multiplication and inversion operations,significantly increasing the computational load.To overcome this challenge,we have integrated the curvature and frequency parameters,simplifying all frequency operators to the same,thereby significantly improving computation efficiency.Furthermore,existing transform algorithms neglect the lateral variation of seismic amplitudes,leading to discrepancies between the estimated multiples and those in the data.To enhance the amplitude preservation of the algorithm,we employ orthogonal polynomial fitting to capture the amplitude spatial variation in 3D seismic data.Combining these improvements,we propose a fast,amplitude-preserving,3D three-parameter Radon transform algorithm.This algorithm not only enhances computational efficiency while maintaining the original wavefield characteristics,but also improves the representation of seismic data by increasing amplitude fidelity.We validated the algorithm in multiple attenuation using both synthetic and real seismic data.The results demonstrate that the new algorithm significantly improves both accuracy and computational efficiency,providing an effective tool for analyzing seismic wavefields in complex subsurface structures.展开更多
BACKGROUND Hepatic stellate cell(HSC)activation is key to liver fibrosis.Targeting DNA methylation shows promise.Zebularine,a methylation inhibitor,may suppress HSC activation via the calcineurin(CaN)/NFAT3 pathway.Ma...BACKGROUND Hepatic stellate cell(HSC)activation is key to liver fibrosis.Targeting DNA methylation shows promise.Zebularine,a methylation inhibitor,may suppress HSC activation via the calcineurin(CaN)/NFAT3 pathway.Magnetic resonance imaging(MRI)is a noninvasive tool for evaluating liver fibrosis evaluation tool,but multiparametric MRI for zebularine’s effects in liver fibrosis mouse models has not been studied.AIM To clarify the anti-fibrosis mechanism and MRI-evaluated efficacy of zebularine.METHODS In vitro,transforming growth factor(TGF)-β1-stimulated human HSCs(LX-2)were treated with zebularine.α-smooth muscle actin,fibrotic and anti-fibrotic gene levels,and regulator of calcineurin1(RCAN1)regulation were measured.In vivo,carbon tetrachloride(CCl_(4))-induced liver fibrosis in mice was treated with zebularine,and fibrosis was evaluated using various biochemical,histopathological,and MRI methods.RESULTS Zebularine upregulated RCAN1.4 protein(P<0.01)and inhibited the CaN/NFAT3 pathway(P<0.05).In HSCs,TGF-β1 reduced anti-fibrotic gene massage RNA(mRNA)and increased fibrotic mRNA(P<0.05),whereas zebularine had the opposite effects(P<0.01,P<0.05).CCl4-treated mice exhibited increases in various fibrosis-related indices,all of which were reversed by zebularine treatment(P<0.05).CONCLUSION Zebularine may reduce LX-2 activation and extracellular matrix deposition via RCAN1.4 and CaN/NFAT3 path-ways.Multiparametric MRI can assess its efficacy,suggesting zebularine’s potential as a liver fibrosis treatment.展开更多
背景:骨代谢紊乱会引起骨相关疾病的发生,而叉头框转录因子O3可以通过调节氧化应激、自噬水平等来影响骨组织细胞增殖、分化与凋亡,调控骨代谢过程。目的:系统性分析叉头框转录因子O3调控骨代谢及其在骨科疾病中作用机制的相关研究文献...背景:骨代谢紊乱会引起骨相关疾病的发生,而叉头框转录因子O3可以通过调节氧化应激、自噬水平等来影响骨组织细胞增殖、分化与凋亡,调控骨代谢过程。目的:系统性分析叉头框转录因子O3调控骨代谢及其在骨科疾病中作用机制的相关研究文献,为后续以叉头框转录因子O3为靶点治疗骨疾病的研究提供参考。方法:以“(SU=FoxO3a OR SU=Foxo3 OR SU=Forkhead box O3 OR SU=叉头框转录因子O3)AND SU=骨”为检索句在中国知网进行检索,以“主题:(“FoxO3a”)OR主题:(“Foxo3”)OR主题:(“Forkhead box O3”)OR主题:(“叉头框转录因子O3”)AND主题:(“骨”)”为检索句在万方医学数据库进行检索;以“((FoxO3a)OR(Foxo3)OR(Forkhead box O3))AND((bone)OR(Skeleton))”为检索句在PubMed数据库进行检索,排除陈旧、重复、质量较差以及不相关的文献,最终纳入56篇文献进行综述分析。结果与结论:①叉头框转录因子O3与骨髓间充质干细胞:叉头框转录因子O3能够促进成骨谱系的形成,还可通过激活自噬促进早期成骨分化。同时,叉头框转录因子O3在骨髓间充质干细胞中体现抗氧化特性,保护细胞免受氧化应激诱导的衰老。②叉头框转录因子O3与成骨细胞:叉头框转录因子O3在成骨细胞中能通过干扰Wnt/β-连环蛋白通路抑制成骨,同时能激活抗氧化酶保护成熟成骨细胞。叉头框转录因子O3能促进成骨祖细胞的增殖,并通过激活自噬促进成骨分化。③叉头框转录因子O3与破骨细胞:叉头框转录因子O3表达可抵抗氧化应激和激活自噬抑制破骨细胞生成。④叉头框转录因子O3与骨细胞:叉头框转录因子O3可通过抗氧化作用保护骨细胞,还可通过抑制p16和p53信号通路和抑制衰老相关分泌表型来减少骨流失。⑤叉头框转录因子O3与软骨细胞:叉头框转录因子O3在骨关节炎中对软骨细胞起到保护作用,抑制软骨细胞分解或凋亡,促进软骨细胞外基质合成,可抑制软骨细胞肥大;然而,叉头框转录因子O3与Runt相关转录因子1在软骨细胞中高度共表达却会促进软骨祖细胞的早期软骨形成和终末肥大。⑥叉头框转录因子O3通过参与氧化应激抵抗与调控自噬等过程影响骨代谢,参与多类骨相关疾病的病理进程。展开更多
基金supported in part by National Natural Science Foundation of China(NSFC)under grant 42274139in part by the R&D Department of China National Petroleum Corporation(Investigations on fundamental experiments and advanced theoretical methods in geophysical prospecting applications,2022DQ0604-03).
文摘Seismic wavefields propagate through three-dimensional(3D)space,and their precise characterization is crucial for understanding subsurface structures.Traditional 2D algorithms,due to their limitations,are insufficient to fully represent three-dimensional wavefields.The classic 3D Radon transform algorithm assumes that the wavefield's propagation characteristics are consistent in all directions,which often does not hold true in complex underground media.To address this issue,we present an improved 3D three-parameter Radon algorithm that considers the wavefield variation with azimuth and provides a more accurate wavefield description.However,introducing new parameters to describe the azimuthal varia-tion also poses computational challenges.The new Radon transform operator involves five variables and cannot be simply decomposed into small matrices for efficient computation;instead,it requires large matrix multiplication and inversion operations,significantly increasing the computational load.To overcome this challenge,we have integrated the curvature and frequency parameters,simplifying all frequency operators to the same,thereby significantly improving computation efficiency.Furthermore,existing transform algorithms neglect the lateral variation of seismic amplitudes,leading to discrepancies between the estimated multiples and those in the data.To enhance the amplitude preservation of the algorithm,we employ orthogonal polynomial fitting to capture the amplitude spatial variation in 3D seismic data.Combining these improvements,we propose a fast,amplitude-preserving,3D three-parameter Radon transform algorithm.This algorithm not only enhances computational efficiency while maintaining the original wavefield characteristics,but also improves the representation of seismic data by increasing amplitude fidelity.We validated the algorithm in multiple attenuation using both synthetic and real seismic data.The results demonstrate that the new algorithm significantly improves both accuracy and computational efficiency,providing an effective tool for analyzing seismic wavefields in complex subsurface structures.
基金Supported by the Health Research Foundation of Hunan Provincial Health Commission,No.W20243192Natural Science Foundation of Changsha,No.kq2403086+1 种基金National Natural Science Foundation of China,No.81571784Hunan Provincial Health Commission Hunan Provincial High-level Health Talent Major Scientific Research Project,No.R2023022.
文摘BACKGROUND Hepatic stellate cell(HSC)activation is key to liver fibrosis.Targeting DNA methylation shows promise.Zebularine,a methylation inhibitor,may suppress HSC activation via the calcineurin(CaN)/NFAT3 pathway.Magnetic resonance imaging(MRI)is a noninvasive tool for evaluating liver fibrosis evaluation tool,but multiparametric MRI for zebularine’s effects in liver fibrosis mouse models has not been studied.AIM To clarify the anti-fibrosis mechanism and MRI-evaluated efficacy of zebularine.METHODS In vitro,transforming growth factor(TGF)-β1-stimulated human HSCs(LX-2)were treated with zebularine.α-smooth muscle actin,fibrotic and anti-fibrotic gene levels,and regulator of calcineurin1(RCAN1)regulation were measured.In vivo,carbon tetrachloride(CCl_(4))-induced liver fibrosis in mice was treated with zebularine,and fibrosis was evaluated using various biochemical,histopathological,and MRI methods.RESULTS Zebularine upregulated RCAN1.4 protein(P<0.01)and inhibited the CaN/NFAT3 pathway(P<0.05).In HSCs,TGF-β1 reduced anti-fibrotic gene massage RNA(mRNA)and increased fibrotic mRNA(P<0.05),whereas zebularine had the opposite effects(P<0.01,P<0.05).CCl4-treated mice exhibited increases in various fibrosis-related indices,all of which were reversed by zebularine treatment(P<0.05).CONCLUSION Zebularine may reduce LX-2 activation and extracellular matrix deposition via RCAN1.4 and CaN/NFAT3 path-ways.Multiparametric MRI can assess its efficacy,suggesting zebularine’s potential as a liver fibrosis treatment.
文摘背景:骨代谢紊乱会引起骨相关疾病的发生,而叉头框转录因子O3可以通过调节氧化应激、自噬水平等来影响骨组织细胞增殖、分化与凋亡,调控骨代谢过程。目的:系统性分析叉头框转录因子O3调控骨代谢及其在骨科疾病中作用机制的相关研究文献,为后续以叉头框转录因子O3为靶点治疗骨疾病的研究提供参考。方法:以“(SU=FoxO3a OR SU=Foxo3 OR SU=Forkhead box O3 OR SU=叉头框转录因子O3)AND SU=骨”为检索句在中国知网进行检索,以“主题:(“FoxO3a”)OR主题:(“Foxo3”)OR主题:(“Forkhead box O3”)OR主题:(“叉头框转录因子O3”)AND主题:(“骨”)”为检索句在万方医学数据库进行检索;以“((FoxO3a)OR(Foxo3)OR(Forkhead box O3))AND((bone)OR(Skeleton))”为检索句在PubMed数据库进行检索,排除陈旧、重复、质量较差以及不相关的文献,最终纳入56篇文献进行综述分析。结果与结论:①叉头框转录因子O3与骨髓间充质干细胞:叉头框转录因子O3能够促进成骨谱系的形成,还可通过激活自噬促进早期成骨分化。同时,叉头框转录因子O3在骨髓间充质干细胞中体现抗氧化特性,保护细胞免受氧化应激诱导的衰老。②叉头框转录因子O3与成骨细胞:叉头框转录因子O3在成骨细胞中能通过干扰Wnt/β-连环蛋白通路抑制成骨,同时能激活抗氧化酶保护成熟成骨细胞。叉头框转录因子O3能促进成骨祖细胞的增殖,并通过激活自噬促进成骨分化。③叉头框转录因子O3与破骨细胞:叉头框转录因子O3表达可抵抗氧化应激和激活自噬抑制破骨细胞生成。④叉头框转录因子O3与骨细胞:叉头框转录因子O3可通过抗氧化作用保护骨细胞,还可通过抑制p16和p53信号通路和抑制衰老相关分泌表型来减少骨流失。⑤叉头框转录因子O3与软骨细胞:叉头框转录因子O3在骨关节炎中对软骨细胞起到保护作用,抑制软骨细胞分解或凋亡,促进软骨细胞外基质合成,可抑制软骨细胞肥大;然而,叉头框转录因子O3与Runt相关转录因子1在软骨细胞中高度共表达却会促进软骨祖细胞的早期软骨形成和终末肥大。⑥叉头框转录因子O3通过参与氧化应激抵抗与调控自噬等过程影响骨代谢,参与多类骨相关疾病的病理进程。
