利用第六次国际耦合模式比较计划(CMIP6)中的18个模式,基于欧洲中期天气预报中心第五代再分析资料(ERA5)再分析数据对青藏高原夏季降水数据进行了偏差校正,并从平均降水和极端降水两方面评估了校正前后的CMIP6数据以及单个模式在1979-2...利用第六次国际耦合模式比较计划(CMIP6)中的18个模式,基于欧洲中期天气预报中心第五代再分析资料(ERA5)再分析数据对青藏高原夏季降水数据进行了偏差校正,并从平均降水和极端降水两方面评估了校正前后的CMIP6数据以及单个模式在1979-2014年的表现。研究结果表明,该校正方法高度依赖于用于偏差校正的ERA5再分析数据在研究区域的质量,尽管偏差校正后的青藏高原夏季平均降水的误差和误差率上有所改善,但在年际时间变化特征方面却不如偏差校正前的数据。大多数CMIP6模式能够较好地模拟1979-2014年青藏高原上由西北至东南逐渐递增的平均降水空间变化特征。偏差校正前的降水数据在高原上会出现显著的高估,误差率为60.4%,经过偏差校正后的数据相对观测数据误差降低,误差率为-13.9%,并且偏差校正后的数据与ERA5的平均误差仅为0.003 mm·d^(-1),与ERA5的空间相关性高达0.999。空间趋势方面,观测数据表明青藏高原大部分地区夏季降水在1979-2014年呈现轻微增加的趋势,只有东缘出现明显降低的趋势。偏差校正前后的数据都能够大致刻画出这一空间分布特征,然而,未经偏差校正的大多数单个CMIP6模式与ERA5的空间相关系数未超过0.5。与由独立观测降水数据的年际变化特征相比,偏差校正前的数据高估了高原上的降水量,而偏差校正后的数据相比观测结果则偏低。通过确定95%分位阈值选取了极端降水个例,其集合平均极端降水空间分布与年平均降水类似,也呈西北向东南递增的趋势。部分CMIP6模式较好地模拟了这一特征,如MRI-ESM2-0(The Meteorological Research Institute Earth System Model version 2.0)和ACCESSCM2(Australian Community Climate and Earth System Simulator Climate Model Version 2),与观测结果的空间相关系数分别为0.851和0.821。但偏差校正后的数据在空间相关性方面下降,由偏差校正前的0.861降为0.730,未能准确刻画高原极端降水阶梯式递增的特点。偏差校正后的极端降水数据误差分布与偏差校正前相似,偏低区域主要集中在高原南部腹地和东部。进一步的极端降水贡献率分析结果表明,观测结果与CMIP6降水数据均显示1979-2014年期间极端降水贡献率变化趋势不明显。单个CMIP6模式中,EC-Earth3-Veg(European Community Earth-Vegetation model version 3)和EC-Earth3(European Community Earth Model version 3)及CanESM5(The Canadian Earth System Model version 5)在多个统计评估指标上排名靠前,展示出较好的模拟能力;IPSL-CM6A-LR(Institut Pierre-Simon Laplace Climate Model 6A Low Resolution)在平均降水误差和极端降水的误差指标上表现出色。展开更多
Salsolinol(1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline,Sal)is a catechol isoquinoline that causes neurotoxicity and shares structural similarity with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine,an environme...Salsolinol(1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline,Sal)is a catechol isoquinoline that causes neurotoxicity and shares structural similarity with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine,an environmental toxin that causes Parkinson's disease.However,the mechanism by which Sal mediates dopaminergic neuronal death remains unclear.In this study,we found that Sal significantly enhanced the global level of N~6-methyladenosine(m~6A)RNA methylation in PC12 cells,mainly by inducing the downregulation of the expression of m~6A demethylases fat mass and obesity-associated protein(FTO)and alk B homolog 5(ALKBH5).RNA sequencing analysis showed that Sal downregulated the Hippo signaling pathway.The m~6A reader YTH domain-containing family protein 2(YTHDF2)promoted the degradation of m~6A-containing Yes-associated protein 1(YAP1)mRNA,which is a downstream key effector in the Hippo signaling pathway.Additionally,downregulation of YAP1 promoted autophagy,indicating that the mutual regulation between YAP1 and autophagy can lead to neurotoxicity.These findings reveal the role of Sal on m~6A RNA methylation and suggest that Sal may act as an RNA methylation inducer mediating dopaminergic neuronal death through YAP1 and autophagy.Our results provide greater insights into the neurotoxic effects of catechol isoquinolines compared with other studies and may be a reference for assessing the involvement of RNA methylation in the pathogenesis of Parkinson's disease.展开更多
There is growing evidence that interleukin(IL)-6 plays an important role in neurological and psychiatric disorders.This editorial comments on the study published in the recent issue of the World Journal of Psychiatry,...There is growing evidence that interleukin(IL)-6 plays an important role in neurological and psychiatric disorders.This editorial comments on the study published in the recent issue of the World Journal of Psychiatry,which employed Mendelian randomization to identify a causal relationship between IL-6 receptor blockade and decreased epilepsy incidence.The purpose of this editorial is to highlight the dual effects of IL-6 in epilepsy and its related neuropsychiatric comorbidities.IL-6 plays a critical role in the facilitation of epileptogenesis and maintenance of epileptic seizures and is implicated in neuroinflammatory proce-sses associated with epilepsy.Furthermore,IL-6 significantly influences mood regulation and cognitive dysfunction in patients with epilepsy,highlighting its involvement in neuropsychiatric comorbidities.In summary,IL-6 is not only a pivotal factor in the pathogenesis of epilepsy but also significantly contributes to the emergence of epilepsy-related neuropsychiatric complications.Future resear-ch should prioritize elucidating the specific mechanisms by which IL-6 operates across different subtypes,stages and neuropsychiatric comorbidities of epilepsy,with the aim of developing more precise and effective interventions.Furthermore,the potential of IL-6 as a biomarker for the early diagnosis and prognosis of epile-psy warrants further investigation.展开更多
Geometry optimization of p-C_(6)H_(4)-connected cyclo[20]carbon(p-C_(6)H_(4)-C_(20))was carried out at M062X/6-311G(d,p)level,three kinds of bond orders(Mayer,Laplacian,and Wiberg),electron-hole distributions,localize...Geometry optimization of p-C_(6)H_(4)-connected cyclo[20]carbon(p-C_(6)H_(4)-C_(20))was carried out at M062X/6-311G(d,p)level,three kinds of bond orders(Mayer,Laplacian,and Wiberg),electron-hole distributions,localized orbital locators(LOL),and infrared(IR)spectrum were also performed at the same level.Based on TD-DFT M062X/6-311G(d,p)method,the first 20 excited states and ultraviolet(UV)spectra of p-C_(6)H_(4)-C_(20) were calculated.Calculation results of π-electron delocalization analyses prove thatπ-electron delocalization of p-C_(6)H_(4)-C_(20) is more likely to occur on shorter C-C bonds rather than longer C-C bonds,and inside/outside of the ring plane rather than above/below the ring plane.Two absorption peaks of p-C_(6)H_(4)-C_(20) locate at about 319 nm and 236 nm,respectively.展开更多
Hippocampal neuronal loss causes cognitive dysfunction in Alzheimer’s disease.Adult hippocampal neurogenesis is reduced in patients with Alzheimer’s disease.Exercise stimulates adult hippocampal neurogenesis in rode...Hippocampal neuronal loss causes cognitive dysfunction in Alzheimer’s disease.Adult hippocampal neurogenesis is reduced in patients with Alzheimer’s disease.Exercise stimulates adult hippocampal neurogenesis in rodents and improves memory and slows cognitive decline in patients with Alzheimer’s disease.However,the molecular pathways for exercise-induced adult hippocampal neurogenesis and improved cognition in Alzheimer’s disease are poorly understood.Recently,regulator of G protein signaling 6(RGS6)was identified as the mediator of voluntary running-induced adult hippocampal neurogenesis in mice.Here,we generated novel RGS6fl/fl;APP_(SWE) mice and used retroviral approaches to examine the impact of RGS6 deletion from dentate gyrus neuronal progenitor cells on voluntary running-induced adult hippocampal neurogenesis and cognition in an amyloid-based Alzheimer’s disease mouse model.We found that voluntary running in APP_(SWE) mice restored their hippocampal cognitive impairments to that of control mice.This cognitive rescue was abolished by RGS6 deletion in dentate gyrus neuronal progenitor cells,which also abolished running-mediated increases in adult hippocampal neurogenesis.Adult hippocampal neurogenesis was reduced in sedentary APP_(SWE) mice versus control mice,with basal adult hippocampal neurogenesis reduced by RGS6 deletion in dentate gyrus neural precursor cells.RGS6 was expressed in neurons within the dentate gyrus of patients with Alzheimer’s disease with significant loss of these RGS6-expressing neurons.Thus,RGS6 mediated voluntary running-induced rescue of impaired cognition and adult hippocampal neurogenesis in APP_(SWE) mice,identifying RGS6 in dentate gyrus neural precursor cells as a possible therapeutic target in Alzheimer’s disease.展开更多
文摘利用第六次国际耦合模式比较计划(CMIP6)中的18个模式,基于欧洲中期天气预报中心第五代再分析资料(ERA5)再分析数据对青藏高原夏季降水数据进行了偏差校正,并从平均降水和极端降水两方面评估了校正前后的CMIP6数据以及单个模式在1979-2014年的表现。研究结果表明,该校正方法高度依赖于用于偏差校正的ERA5再分析数据在研究区域的质量,尽管偏差校正后的青藏高原夏季平均降水的误差和误差率上有所改善,但在年际时间变化特征方面却不如偏差校正前的数据。大多数CMIP6模式能够较好地模拟1979-2014年青藏高原上由西北至东南逐渐递增的平均降水空间变化特征。偏差校正前的降水数据在高原上会出现显著的高估,误差率为60.4%,经过偏差校正后的数据相对观测数据误差降低,误差率为-13.9%,并且偏差校正后的数据与ERA5的平均误差仅为0.003 mm·d^(-1),与ERA5的空间相关性高达0.999。空间趋势方面,观测数据表明青藏高原大部分地区夏季降水在1979-2014年呈现轻微增加的趋势,只有东缘出现明显降低的趋势。偏差校正前后的数据都能够大致刻画出这一空间分布特征,然而,未经偏差校正的大多数单个CMIP6模式与ERA5的空间相关系数未超过0.5。与由独立观测降水数据的年际变化特征相比,偏差校正前的数据高估了高原上的降水量,而偏差校正后的数据相比观测结果则偏低。通过确定95%分位阈值选取了极端降水个例,其集合平均极端降水空间分布与年平均降水类似,也呈西北向东南递增的趋势。部分CMIP6模式较好地模拟了这一特征,如MRI-ESM2-0(The Meteorological Research Institute Earth System Model version 2.0)和ACCESSCM2(Australian Community Climate and Earth System Simulator Climate Model Version 2),与观测结果的空间相关系数分别为0.851和0.821。但偏差校正后的数据在空间相关性方面下降,由偏差校正前的0.861降为0.730,未能准确刻画高原极端降水阶梯式递增的特点。偏差校正后的极端降水数据误差分布与偏差校正前相似,偏低区域主要集中在高原南部腹地和东部。进一步的极端降水贡献率分析结果表明,观测结果与CMIP6降水数据均显示1979-2014年期间极端降水贡献率变化趋势不明显。单个CMIP6模式中,EC-Earth3-Veg(European Community Earth-Vegetation model version 3)和EC-Earth3(European Community Earth Model version 3)及CanESM5(The Canadian Earth System Model version 5)在多个统计评估指标上排名靠前,展示出较好的模拟能力;IPSL-CM6A-LR(Institut Pierre-Simon Laplace Climate Model 6A Low Resolution)在平均降水误差和极端降水的误差指标上表现出色。
基金supported by the National Natural Science Foundation of China,Nos.82271283(to XC),91854115(to JW),31970044(to JW)the Natural Science Foundation of Beijing,No.7202001(to XC)the Scientific Research Project of Beijing Educational Committee,No.KM202010005022(to XC)。
文摘Salsolinol(1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline,Sal)is a catechol isoquinoline that causes neurotoxicity and shares structural similarity with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine,an environmental toxin that causes Parkinson's disease.However,the mechanism by which Sal mediates dopaminergic neuronal death remains unclear.In this study,we found that Sal significantly enhanced the global level of N~6-methyladenosine(m~6A)RNA methylation in PC12 cells,mainly by inducing the downregulation of the expression of m~6A demethylases fat mass and obesity-associated protein(FTO)and alk B homolog 5(ALKBH5).RNA sequencing analysis showed that Sal downregulated the Hippo signaling pathway.The m~6A reader YTH domain-containing family protein 2(YTHDF2)promoted the degradation of m~6A-containing Yes-associated protein 1(YAP1)mRNA,which is a downstream key effector in the Hippo signaling pathway.Additionally,downregulation of YAP1 promoted autophagy,indicating that the mutual regulation between YAP1 and autophagy can lead to neurotoxicity.These findings reveal the role of Sal on m~6A RNA methylation and suggest that Sal may act as an RNA methylation inducer mediating dopaminergic neuronal death through YAP1 and autophagy.Our results provide greater insights into the neurotoxic effects of catechol isoquinolines compared with other studies and may be a reference for assessing the involvement of RNA methylation in the pathogenesis of Parkinson's disease.
文摘There is growing evidence that interleukin(IL)-6 plays an important role in neurological and psychiatric disorders.This editorial comments on the study published in the recent issue of the World Journal of Psychiatry,which employed Mendelian randomization to identify a causal relationship between IL-6 receptor blockade and decreased epilepsy incidence.The purpose of this editorial is to highlight the dual effects of IL-6 in epilepsy and its related neuropsychiatric comorbidities.IL-6 plays a critical role in the facilitation of epileptogenesis and maintenance of epileptic seizures and is implicated in neuroinflammatory proce-sses associated with epilepsy.Furthermore,IL-6 significantly influences mood regulation and cognitive dysfunction in patients with epilepsy,highlighting its involvement in neuropsychiatric comorbidities.In summary,IL-6 is not only a pivotal factor in the pathogenesis of epilepsy but also significantly contributes to the emergence of epilepsy-related neuropsychiatric complications.Future resear-ch should prioritize elucidating the specific mechanisms by which IL-6 operates across different subtypes,stages and neuropsychiatric comorbidities of epilepsy,with the aim of developing more precise and effective interventions.Furthermore,the potential of IL-6 as a biomarker for the early diagnosis and prognosis of epile-psy warrants further investigation.
文摘Geometry optimization of p-C_(6)H_(4)-connected cyclo[20]carbon(p-C_(6)H_(4)-C_(20))was carried out at M062X/6-311G(d,p)level,three kinds of bond orders(Mayer,Laplacian,and Wiberg),electron-hole distributions,localized orbital locators(LOL),and infrared(IR)spectrum were also performed at the same level.Based on TD-DFT M062X/6-311G(d,p)method,the first 20 excited states and ultraviolet(UV)spectra of p-C_(6)H_(4)-C_(20) were calculated.Calculation results of π-electron delocalization analyses prove thatπ-electron delocalization of p-C_(6)H_(4)-C_(20) is more likely to occur on shorter C-C bonds rather than longer C-C bonds,and inside/outside of the ring plane rather than above/below the ring plane.Two absorption peaks of p-C_(6)H_(4)-C_(20) locate at about 319 nm and 236 nm,respectively.
基金supported by the National Institutes of Health,Nos.AA025919,AA025919-03S1,and AA025919-05S1(all to RAF).
文摘Hippocampal neuronal loss causes cognitive dysfunction in Alzheimer’s disease.Adult hippocampal neurogenesis is reduced in patients with Alzheimer’s disease.Exercise stimulates adult hippocampal neurogenesis in rodents and improves memory and slows cognitive decline in patients with Alzheimer’s disease.However,the molecular pathways for exercise-induced adult hippocampal neurogenesis and improved cognition in Alzheimer’s disease are poorly understood.Recently,regulator of G protein signaling 6(RGS6)was identified as the mediator of voluntary running-induced adult hippocampal neurogenesis in mice.Here,we generated novel RGS6fl/fl;APP_(SWE) mice and used retroviral approaches to examine the impact of RGS6 deletion from dentate gyrus neuronal progenitor cells on voluntary running-induced adult hippocampal neurogenesis and cognition in an amyloid-based Alzheimer’s disease mouse model.We found that voluntary running in APP_(SWE) mice restored their hippocampal cognitive impairments to that of control mice.This cognitive rescue was abolished by RGS6 deletion in dentate gyrus neuronal progenitor cells,which also abolished running-mediated increases in adult hippocampal neurogenesis.Adult hippocampal neurogenesis was reduced in sedentary APP_(SWE) mice versus control mice,with basal adult hippocampal neurogenesis reduced by RGS6 deletion in dentate gyrus neural precursor cells.RGS6 was expressed in neurons within the dentate gyrus of patients with Alzheimer’s disease with significant loss of these RGS6-expressing neurons.Thus,RGS6 mediated voluntary running-induced rescue of impaired cognition and adult hippocampal neurogenesis in APP_(SWE) mice,identifying RGS6 in dentate gyrus neural precursor cells as a possible therapeutic target in Alzheimer’s disease.
