首页 > 最新文献

中华行为医学与脑科学杂志最新文献

英文 中文
Cognitive function characteristics in patients with myasthenia gravis 重症肌无力患者的认知功能特征
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20191015-00755
Jing Wang, Xin Li, Li-min Li, Lin-Jie Zhang, Li Yang
Objective To evaluate the cognitive function characteristics in patients with myasthenia gravis(MG). Methods The cognitive function of 83 MG patients and 39 healthy controls (HC) were evaluated by MMSE, California verbal learning test( CVLT), brief visuospatial memory test revised(BVMT-R), symbol digit modalities test(SDMT), benton judgment of line orientation test(BJLOT), paced auditory serial addition Test(PASAT) and verbal fluency test(VFT). The depression state was assessed by beck depression inventory (BDI). The results were compared between MG and HC groups.The effect of clinical characteristics such as disease type, comorbidities, course of disease, disease severity, and drug treatment on cognitive impairment in MG group was further analysed. Results The scale scores of MMSE(28(26, 29), 29(28, 30)), CVLT, BVMT-R, SDMT((37.06±12.18), (47.54±14.91)) and PASAT((32.86±10.23), (37.00±8.82)) in MG were significantly lower than those in control group (P 0.05). Spearman correlation analysis showed that QMG scores were negatively correlated with SDMT scores(r=-0.234, P<0.05). MG-ADL scores were inversely correlated with total BVMT-R scores of three trials(r=-0.283, P<0.05). Conclusion Patients with MG suffered from cognitive impairment, mainly in memory, attention, processing speed and visual memory, which supported the hypothesis of CNS involvement in MG.Dysfunction in some cognitive domains may be related to the disease severity.Clinicians need take morce attention to early assessment, developing long-term follow-ups and appropriate intervention. Key words: Myasthenia gravis; Neuropsychology; Cognitive function; Depression
目的探讨重症肌无力(MG)患者的认知功能特点。方法采用MMSE、California言语学习测试(CVLT)、短时视觉空间记忆修正测试(BVMT-R)、符号数字模态测试(SDMT)、benton判断线定向测试(BJLOT)、起搏听觉序列加法测试(PASAT)和语言流利度测试(VFT)对83例MG患者和39例健康对照(HC)的认知功能进行评价。抑郁状态采用贝克抑郁量表(BDI)进行评估。比较MG组和HC组的结果。进一步分析了MG组的疾病类型、合并症、病程、疾病严重程度和药物治疗等临床特征对认知障碍的影响。结果MMSE(28(26,29),29(28,30))、CVLT、BVMT-R、SDMT((37.06±12.18),(47.54±14.91))和PASAT((32.86±10.23)的量表得分,Spearman相关分析显示,QMG评分与SDMT评分呈负相关(r=-0.234,P<0.05),MG-ADL评分与三项试验的BVMT-r总分呈负相关,r=-0.283,P<0.05,处理速度和视觉记忆,这支持了中枢神经系统参与MG的假设。某些认知领域的功能障碍可能与疾病的严重程度有关。临床医生需要注意早期评估,制定长期随访和适当的干预措施。关键词:重症肌无力;神经心理学;认知功能;抑郁症
{"title":"Cognitive function characteristics in patients with myasthenia gravis","authors":"Jing Wang, Xin Li, Li-min Li, Lin-Jie Zhang, Li Yang","doi":"10.3760/CMA.J.CN371468-20191015-00755","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20191015-00755","url":null,"abstract":"Objective \u0000To evaluate the cognitive function characteristics in patients with myasthenia gravis(MG). \u0000 \u0000 \u0000Methods \u0000The cognitive function of 83 MG patients and 39 healthy controls (HC) were evaluated by MMSE, California verbal learning test( CVLT), brief visuospatial memory test revised(BVMT-R), symbol digit modalities test(SDMT), benton judgment of line orientation test(BJLOT), paced auditory serial addition Test(PASAT) and verbal fluency test(VFT). The depression state was assessed by beck depression inventory (BDI). The results were compared between MG and HC groups.The effect of clinical characteristics such as disease type, comorbidities, course of disease, disease severity, and drug treatment on cognitive impairment in MG group was further analysed. \u0000 \u0000 \u0000Results \u0000The scale scores of MMSE(28(26, 29), 29(28, 30)), CVLT, BVMT-R, SDMT((37.06±12.18), (47.54±14.91)) and PASAT((32.86±10.23), (37.00±8.82)) in MG were significantly lower than those in control group (P 0.05). Spearman correlation analysis showed that QMG scores were negatively correlated with SDMT scores(r=-0.234, P<0.05). MG-ADL scores were inversely correlated with total BVMT-R scores of three trials(r=-0.283, P<0.05). \u0000 \u0000 \u0000Conclusion \u0000Patients with MG suffered from cognitive impairment, mainly in memory, attention, processing speed and visual memory, which supported the hypothesis of CNS involvement in MG.Dysfunction in some cognitive domains may be related to the disease severity.Clinicians need take morce attention to early assessment, developing long-term follow-ups and appropriate intervention. \u0000 \u0000 \u0000Key words: \u0000Myasthenia gravis; Neuropsychology; Cognitive function; Depression","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"32 2","pages":"256-261"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41296265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Effect of DL-3-n-butylphthalide on cognitive function and the regulating role of Nrf2/SIRT3 signaling pathway in vascular dementia mice DL-3-正丁基邻苯二甲酸对血管性痴呆小鼠认知功能的影响及Nrf2/SIRT3信号通路的调节作用
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20190806-00527
Liwei Gao, Qiang Zhang, M. Li, Yanhong Dong
Objective To investigate the effects of butylphthalide(NBP) on cognitive function and Nrf2 / SIRT3 signal pathway in vascular dementia (VD) mice. Methods Wild-type mice (Nrf2+ /+ ) were divided into sham group, model group (VD group), butylphthalide treatment group (Nrf2+ /+ NBP group), and Nrf2 gene knockout mice (Nrf2-/-) were divided into Nrf2-/-model group (Nrf2-/-VD group) and Nrf2-/-treatment group (Nrf2-/-NBP group). Both the model group and the treatment group were repeated.The bilateral common carotid arteries were ligated three times to establish a mouse model of cognitive dysfunction caused by cerebral ischemia-reperfusion.The sham group only isolated the bilateral common carotid arteries and threaded the wires, but did not block blood flow.Morris water maze experiment was used to analyze the cognitive function of mice.HE staining was used to observe the changes of neuron morphology and structure in CA1 region of hippocampus, and immunohistochemical analysis was used to analyze the positive expression of caspase 3 and caspase 9 in mouse CA1 region of hippocampus.Western blot was used to detect mouse hippocampus Nrf2, p62, LC3, SIRT3 protein expression. Results (1) In Morris water maze experiment: compared with VD group, the escape latency of Sham group and Nrf2+ /+ NBP group was significantly shorter on the 5th day ((20.69±8.91) s, (7.58±9.47)s, (8.41±12.20)s; q=3.58, 5.07, both P 0.05). (2) Pathological results showed that, compared with VD group, the damage of pyramidal neurons in CA1 area of hippocampus in Sham group and Nrf2+ /+ NBP group was lighter, and that in Nrf2-/- VD group was more serious, and the improvement of neuron morphology was not obvious after NBP treatment.(3) The expression of apoptosis: compared with VD group, the expression of caspase-3 and caspase-9 in the CA1 area of hippocampus in Sham group and Nrf2+ /+ NBP group were significantly lower, and those in Nrf2-/-VD group were significantly higher (t=3.48, 2.95, 3.46, 2.93, -2.99, -3.77, all P 0.05). (4) Expression of related proteins: compared with VD group, Nrf2, SIRT3, p62 protein expression increased, LC3II/I ratio decreased in Nrf2+ /+ NBP group(t=-3.24, -4.04, -4.03, 3.62, all P<0.01); Nrf2, LC3II/ I ratio decreased, SIRT3, p62 protein expression increased in Sham group(t=3.44, 4.72, -3.52, -4.19, all P<0.01); Nrf2, SIRT3, p62 protein expression decreased and LC3II/I ratio increased in Nrf2-/-VD group(t=9.14, 4.20, 4.30, -3.78, all P<0.01); Compared with Nrf2-/- NBP, the expression of Nrf2, SIRT3, p62 decreased, and LC3II/I ratio increased in Nrf2-/-VD group(t=2.40, 3.24, 1.21, -1.16, all P<0.01). The expression of Nrf2, SIRT3, p62 protein in Nrf2+ /+ NBP group increased, and the ratio of LC3II/ I decreased (t=-3.29, -5.00, 6.24, all P<0.01). Conclusion Butylphthalide can reduce the apoptotic damage in hippocampus of VD mice and improve cognitive dysfunction caused by repeated ischemia-reperfusion injury.Regulating Nrf2 / SIRT3 pathway to
目的探讨丁基邻苯二甲酸酯(NBP)对血管性痴呆(VD)小鼠认知功能及Nrf2/SIRT3信号通路的影响。方法将野生型小鼠(Nrf2+/+)分为假手术组、模型组(VD组)、丁基邻苯二甲酸酯治疗组(Nrf2+/+NBP组),将Nrf2基因敲除小鼠(Nrf2-/-)分为Nrf2-/-模型组(Nrf2-/-VD组)和Nrf2--/-治疗组(Nrf2-/-NBP组)。模型组和治疗组均重复。结扎双侧颈总动脉三次,建立脑缺血再灌注引起认知功能障碍的小鼠模型。假手术组仅分离双侧颈总血管并穿线,但不阻断血流。采用Morris水迷宫实验对小鼠的认知功能进行分析。HE染色观察海马CA1区神经元形态结构的变化,免疫组化分析小鼠海马CA1区域caspase 3和caspase 9的阳性表达。免疫印迹法检测小鼠海马Nrf2、p62、LC3、SIRT3蛋白的表达。结果(1)Morris水迷宫实验:与VD组相比,Sham组和Nrf2+/+NBP组在第5天的逃生潜伏期显著缩短((20.69±8.91)s、(7.58±9.47)s、和(8.41±12.20)s;q=3.58,5.07,均P<0.05)。(2)病理结果显示,Sham组和Nrf2+/+NBP组海马CA1区锥体神经元损伤较VD组轻,Nrf2-/-VD组更严重,NBP治疗后神经元形态改善不明显。(3) 凋亡的表达:与VD组相比,Sham组和Nrf2+/+NBP组海马CA1区胱天蛋白酶-3和胱天蛋白酶-9的表达显著降低,Nrf2-/-VD组的表达显著升高(t=3.48、2.95、3.46、2.93、-2.99、-3.77,均P 0.05),Nrf2+/+NBP组p62蛋白表达增加,LC3II/I比值降低(t=-3.24,-4.04,-4.03,3.62,均P<0.01);Sham组Nrf2、LC3II/I比值降低,SIRT3、p62蛋白表达增加(t=3.44、4.72、-3.52、-4.19,均P<0.01);Nrf2-/-VD组Nrf2、SIRT3、p62蛋白表达下降,LC3II/I比值升高(t=9.14,4.20,4.30,3.78,均P<0.01);与Nrf2-/-NBP相比,Nrf2-+/-VD组Nrf2、SIRT3、p62蛋白表达下降,LC3II/I比值升高(t=2.40、3.24、1.21、-1.16,均P<0.01),结论丁基邻苯二甲酰胺能减轻VD小鼠海马细胞凋亡损伤,改善反复缺血再灌注损伤引起的认知功能障碍。调节Nrf2/SIRT3通路抑制海马神经元凋亡和自噬可能是其作用机制。关键词:丁基邻苯二甲酸酯;血管性痴呆;Nrf2;SIRT3;细胞凋亡自噬
{"title":"Effect of DL-3-n-butylphthalide on cognitive function and the regulating role of Nrf2/SIRT3 signaling pathway in vascular dementia mice","authors":"Liwei Gao, Qiang Zhang, M. Li, Yanhong Dong","doi":"10.3760/CMA.J.CN371468-20190806-00527","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20190806-00527","url":null,"abstract":"Objective \u0000To investigate the effects of butylphthalide(NBP) on cognitive function and Nrf2 / SIRT3 signal pathway in vascular dementia (VD) mice. \u0000 \u0000 \u0000Methods \u0000Wild-type mice (Nrf2+ /+ ) were divided into sham group, model group (VD group), butylphthalide treatment group (Nrf2+ /+ NBP group), and Nrf2 gene knockout mice (Nrf2-/-) were divided into Nrf2-/-model group (Nrf2-/-VD group) and Nrf2-/-treatment group (Nrf2-/-NBP group). Both the model group and the treatment group were repeated.The bilateral common carotid arteries were ligated three times to establish a mouse model of cognitive dysfunction caused by cerebral ischemia-reperfusion.The sham group only isolated the bilateral common carotid arteries and threaded the wires, but did not block blood flow.Morris water maze experiment was used to analyze the cognitive function of mice.HE staining was used to observe the changes of neuron morphology and structure in CA1 region of hippocampus, and immunohistochemical analysis was used to analyze the positive expression of caspase 3 and caspase 9 in mouse CA1 region of hippocampus.Western blot was used to detect mouse hippocampus Nrf2, p62, LC3, SIRT3 protein expression. \u0000 \u0000 \u0000Results \u0000(1) In Morris water maze experiment: compared with VD group, the escape latency of Sham group and Nrf2+ /+ NBP group was significantly shorter on the 5th day ((20.69±8.91) s, (7.58±9.47)s, (8.41±12.20)s; q=3.58, 5.07, both P 0.05). (2) Pathological results showed that, compared with VD group, the damage of pyramidal neurons in CA1 area of hippocampus in Sham group and Nrf2+ /+ NBP group was lighter, and that in Nrf2-/- VD group was more serious, and the improvement of neuron morphology was not obvious after NBP treatment.(3) The expression of apoptosis: compared with VD group, the expression of caspase-3 and caspase-9 in the CA1 area of hippocampus in Sham group and Nrf2+ /+ NBP group were significantly lower, and those in Nrf2-/-VD group were significantly higher (t=3.48, 2.95, 3.46, 2.93, -2.99, -3.77, all P 0.05). (4) Expression of related proteins: compared with VD group, Nrf2, SIRT3, p62 protein expression increased, LC3II/I ratio decreased in Nrf2+ /+ NBP group(t=-3.24, -4.04, -4.03, 3.62, all P<0.01); Nrf2, LC3II/ I ratio decreased, SIRT3, p62 protein expression increased in Sham group(t=3.44, 4.72, -3.52, -4.19, all P<0.01); Nrf2, SIRT3, p62 protein expression decreased and LC3II/I ratio increased in Nrf2-/-VD group(t=9.14, 4.20, 4.30, -3.78, all P<0.01); Compared with Nrf2-/- NBP, the expression of Nrf2, SIRT3, p62 decreased, and LC3II/I ratio increased in Nrf2-/-VD group(t=2.40, 3.24, 1.21, -1.16, all P<0.01). The expression of Nrf2, SIRT3, p62 protein in Nrf2+ /+ NBP group increased, and the ratio of LC3II/ I decreased (t=-3.29, -5.00, 6.24, all P<0.01). \u0000 \u0000 \u0000Conclusion \u0000Butylphthalide can reduce the apoptotic damage in hippocampus of VD mice and improve cognitive dysfunction caused by repeated ischemia-reperfusion injury.Regulating Nrf2 / SIRT3 pathway to","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"200-206"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45137469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Silencing long non-coding RNA HCP5 increases the radiosensitivity of glioma cells by up-regulating miR-508-3p expression 沉默长非编码RNA HCP5通过上调miR-508-3p表达增加胶质瘤细胞的放射敏感性
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20191023-00765
Xueyuan Li, Qiankun Liu, Shanpeng Yuan, T. Liang, Wenzheng Luo, Y. Zhen, Lixin Wu, Kang Wang, Dongming Yan
Objective To investigate the effect of long non-coding (lnc) RNA HCP5 on the radiation sensitivity of glioma cells and underlying mechanism. Methods The glioma cells U251 and U87 were irradiated with 0, 2, 4, 6, and 8 Gy rays as different doses.si-Con, si-HCP5, pcDNA, and pcDNA-HCP5 were transfected into cells U251 and U87, recorded as si-con group, si-HCP5 group, pcDNA group, and pcDNA-HCP5 group.si-Con and si-HCP5 were transfected into cells U251 and U87, and then irradiated with 4 Gy rays, respectively, recorded as IR+ si-con group and IR+ si-HCP5 group, the cells only irradiated with 4 Gy rays were recorded as IR group.After si-HCP5 with anti-miR-con and anti-miR-508-3p was co-transfected into cell U251 and U87, respectively, irradiated with 4 Gy rays, recorded as IR+ si-HCP5+ anti-miR-con group and IR+ si-HCP5+ anti-miR-508-3p group, respectively, the transfection was performed by liposome method.RT-qPCR was used to detect the expression of miR-508-3p and HCP5.Cell clone formation assay was used to detect the radiosensitivity of glioma cells.Flow cytometry was used to detect apoptosis, dual luciferase Reporter gene detection experiments detects fluorescence activity. Results HCP5 was highly expressed in radiation-treated glioma cells, and miR-508-3p was lowly expressed.After silenced HCP5, U251 and U87 cells had enhanced radiosensitivity and apoptotic rate((16.67±1.68) vs (3.58±0.62), t=21.929, P<0.05; (12.32±1.08) vs (4.48±0.71), t=18.198, P<0.05) was increased, and γ-H2AX( (0.45±0.04) vs (0.23±0.05), t=10.307, P<0.05; (0.38±0.04) vs (0.24±0.03), t=8.400, P<0.05), Cleaved caspase-3((0.37±0.04) vs (0.16±0.03), t=12.600, P<0.05; (0.38±0.04) vs (0.22±0.03), t=9.600, P<0.05) expressions were increased.Compared with silencing HCP5 or radiation treatment alone, silencing HCP5 and radiation treatment of U251 cells simultaneously, the apoptosis rate ((25.34±1.54) vs (16.67±1.68), t=11.413, P<0.05; (25.34±1.54) vs (11.13±1.06), t=22.802, P<0.05) was significantly increased, and γ-H2AX((0.69±0.05) vs (0.45±0.04), t=11.245, P<0.05; (0.69±0.05) vs (0.31±0.04), t=17.804, P<0.05), Cleaved caspase-3 ((0.52±0.06/0.37±0.04, t=6.240, P<0.05) (0.52±0.06/0.34±0.04, t=7.488, P<0.05) expressions were increased.The expressions of p-PI3K ((0.21±0.02) vs (0.52±0.04), t=20.795, P<0.05; (0.26±0.23 ), ( 0.67±0.07), t=5.116, P<0.05), p- AKT ((0.22±0.03) vs (0.66±0.07), t=17.332, P<0.05; (0.23±0.04) vs (0.71±0.03), t=28.800, P<0.05) in U251 and U87 cells were decreased.HCP5 can target the regulation of miR-508-3p expression; interfering with miR-508-3p reversed the effects of silent HCP5 and radiation on the radiation sensitization and apoptosis of U251 and U87 cells.It reduced the expression levels of reducing γ-H2AX and Cleaved caspase-3, while increased the expression levels of p-PI3K and p-AKT. Conclusion Silencing lncRNA HCP5 can enhance the radiation sensitivity of glioma cells and promote apoptosis.The mechanism may be related with the miR-508-
目的探讨长非编码核糖核酸HCP5对胶质瘤细胞辐射敏感性的影响及其机制。方法分别用0、2、4、6、8Gy射线照射胶质瘤细胞U251和U87,将si-Con、si-HCP5、pcDNA和pcDNA-HCP5转染U251和U27细胞,分别记为si-Con组、si-HCP5组、pcDNA组和pcDNA-HCP5组,记录为IR+si-con组和IR+si-HCP5组。将具有抗-miR-con和抗-miR-508-3p的si-HCP5分别共转染到U251和U87细胞中,用4Gy射线照射,分别记录为IR+si-HCP5+抗-miR-con组和IR+si-HCCP5+抗-miR-508-3p组,然后通过脂质体法进行转染。RT-qPCR检测miR-508-3p和HCP5的表达。细胞克隆形成法检测胶质瘤细胞的放射敏感性。流式细胞术检测细胞凋亡,双荧光素酶报告基因检测实验检测荧光活性。结果HCP5在放射治疗的胶质瘤细胞中高表达,miR-508-3p低表达。在HCP5沉默后,U251和U87细胞的放射敏感性和凋亡率分别为(16.67±1.68)和(3.58±0.62),t=21.929,P<0.05;γ-H2AX((0.45±0.04)vs(0.23±0.05),t=10.307,P<0.05;(0.38±0.04)vs(0.24±0.03),t=8.400,P<0.05),裂解胱天蛋白酶-3((0.37±0.04vs(0.16±0.03),t=12.600,P<0.05;(0.38±0.04)vs(0.22±0.03),t=9.600,P<0.05)表达增加。与单独沉默HCP5或放射线处理、同时沉默HCP5和放射线处理U251细胞相比,凋亡率((25.34±1.54)vs(16.67±1.68),t=11.413,P<0.05;γ-H2AX((0.69±0.05)vs(0.45±0.04),t=11.245,P<0.05;(0.69±0.05)vs(0.31±0.04),t=17.804,P<0.05),裂解胱天蛋白酶-3((0.52±0.06/0.37±0.04,t=6.240,P<0.05)(0.52±06/0.34±0.04,t=7.488,P<0.05)表达增加。p-PI3K的表达(0.21±0.02)vs(0.52±0.04),t=20.795,p<0.05;(0.26±0.23),(0.67±0.07),t=5.116,P<0.05),P-AKT((0.22±0.03)vs(0.66±0.07,t=17.332,P<0.05);(0.23±0.04)vs(0.71±0.03),t=28.800,P<0.05)。HCP5可以靶向调节miR-508-3p的表达;干扰miR-508-3p逆转了沉默HCP5和辐射对U251和U87细胞辐射增敏和凋亡的影响。它降低了还原γ-H2AX和裂解胱天蛋白酶-3的表达水平,同时增加了p-PI3K和p-AKT的表达水平。结论沉默lncRNA HCP5可增强胶质瘤细胞的辐射敏感性,促进细胞凋亡。其机制可能与miR-508-3p和PI3K/Akt信号通路有关,这将为神经胶质瘤的治疗提供新的靶点和新的思路。关键词:LncRNA HCP5;MicroRNA-508-3p;胶质瘤;放射敏感性;细胞凋亡
{"title":"Silencing long non-coding RNA HCP5 increases the radiosensitivity of glioma cells by up-regulating miR-508-3p expression","authors":"Xueyuan Li, Qiankun Liu, Shanpeng Yuan, T. Liang, Wenzheng Luo, Y. Zhen, Lixin Wu, Kang Wang, Dongming Yan","doi":"10.3760/CMA.J.CN371468-20191023-00765","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20191023-00765","url":null,"abstract":"Objective \u0000To investigate the effect of long non-coding (lnc) RNA HCP5 on the radiation sensitivity of glioma cells and underlying mechanism. \u0000 \u0000 \u0000Methods \u0000The glioma cells U251 and U87 were irradiated with 0, 2, 4, 6, and 8 Gy rays as different doses.si-Con, si-HCP5, pcDNA, and pcDNA-HCP5 were transfected into cells U251 and U87, recorded as si-con group, si-HCP5 group, pcDNA group, and pcDNA-HCP5 group.si-Con and si-HCP5 were transfected into cells U251 and U87, and then irradiated with 4 Gy rays, respectively, recorded as IR+ si-con group and IR+ si-HCP5 group, the cells only irradiated with 4 Gy rays were recorded as IR group.After si-HCP5 with anti-miR-con and anti-miR-508-3p was co-transfected into cell U251 and U87, respectively, irradiated with 4 Gy rays, recorded as IR+ si-HCP5+ anti-miR-con group and IR+ si-HCP5+ anti-miR-508-3p group, respectively, the transfection was performed by liposome method.RT-qPCR was used to detect the expression of miR-508-3p and HCP5.Cell clone formation assay was used to detect the radiosensitivity of glioma cells.Flow cytometry was used to detect apoptosis, dual luciferase Reporter gene detection experiments detects fluorescence activity. \u0000 \u0000 \u0000Results \u0000HCP5 was highly expressed in radiation-treated glioma cells, and miR-508-3p was lowly expressed.After silenced HCP5, U251 and U87 cells had enhanced radiosensitivity and apoptotic rate((16.67±1.68) vs (3.58±0.62), t=21.929, P<0.05; (12.32±1.08) vs (4.48±0.71), t=18.198, P<0.05) was increased, and γ-H2AX( (0.45±0.04) vs (0.23±0.05), t=10.307, P<0.05; (0.38±0.04) vs (0.24±0.03), t=8.400, P<0.05), Cleaved caspase-3((0.37±0.04) vs (0.16±0.03), t=12.600, P<0.05; (0.38±0.04) vs (0.22±0.03), t=9.600, P<0.05) expressions were increased.Compared with silencing HCP5 or radiation treatment alone, silencing HCP5 and radiation treatment of U251 cells simultaneously, the apoptosis rate ((25.34±1.54) vs (16.67±1.68), t=11.413, P<0.05; (25.34±1.54) vs (11.13±1.06), t=22.802, P<0.05) was significantly increased, and γ-H2AX((0.69±0.05) vs (0.45±0.04), t=11.245, P<0.05; (0.69±0.05) vs (0.31±0.04), t=17.804, P<0.05), Cleaved caspase-3 ((0.52±0.06/0.37±0.04, t=6.240, P<0.05) (0.52±0.06/0.34±0.04, t=7.488, P<0.05) expressions were increased.The expressions of p-PI3K ((0.21±0.02) vs (0.52±0.04), t=20.795, P<0.05; (0.26±0.23 ), ( 0.67±0.07), t=5.116, P<0.05), p- AKT ((0.22±0.03) vs (0.66±0.07), t=17.332, P<0.05; (0.23±0.04) vs (0.71±0.03), t=28.800, P<0.05) in U251 and U87 cells were decreased.HCP5 can target the regulation of miR-508-3p expression; interfering with miR-508-3p reversed the effects of silent HCP5 and radiation on the radiation sensitization and apoptosis of U251 and U87 cells.It reduced the expression levels of reducing γ-H2AX and Cleaved caspase-3, while increased the expression levels of p-PI3K and p-AKT. \u0000 \u0000 \u0000Conclusion \u0000Silencing lncRNA HCP5 can enhance the radiation sensitivity of glioma cells and promote apoptosis.The mechanism may be related with the miR-508-","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"207-214"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45167793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The role of adenosine deaminase acting on RNA in the remission of aggression behavior in socially isolated mice and the mechanism of 5-serotonin-2C receptor 腺苷脱氨酶作用于RNA在社会隔离小鼠攻击行为缓解中的作用及5-羟色胺- 2c受体的作用机制
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20190712-00455
Xiaonan Zhang, Weizhi Yu, Ying Xue, Hong Xu, Wei Yan, Huairui Li, Xiuli Zhai, Jinying Li, Ye Gao, Lin Gui, Deqin Yu, Zhaoyang Xiao, Yi-yuan Tang, Shengming Yin
Objective To investigate the effect of adenosine deaminase acting on RNA 1 (ADAR1) on 5-serotonin-2c receptor in alleviating aggression in socially isolated mice. Methods Sixty healthy male BALB / c mice aged 21 days were randomly divided into six groups: social isolation group, social control group, ADAR1 inducer social isolation group, ADAR1 inhibitor social isolation group, ADAR1 inducer social control group and ADAR1 inhibitor control group.The mice fed in single cage for 4 weeks were used as social isolation model while the mice fed in group were used as control group.ADAR1 inducer (5.0×104 U/kg) and inhibitor (10 mg/kg) were given intraperitoneally to mice in the ADAR1 inducer social isolation group and the ADAR1 inhibitor social isolation group respectively.The aggressive behavior of mice was evaluated by resident-intruder test.The expression of ADAR1 and 5-serotonin-2c receptors in the brain of mice was detected by immunohistochemistry and Western blot. Results The attack latency of social isolation group was significantly lower than that of social control group ((43.15±6.99) s, (542.40±30.50) s; t=15.906, P<0.01), and the latency of attack ((256.70±29.49) s) in the ADAR1 inducer social isolation group was significantly higher than that in the social isolation group (t=7.046, P<0.01). The latency of attack ((15.25±2.18)s) in the ADAR1 inhibitor social isolation group was significantly lower than that in the social isolation group (t=3.809, P<0.01). The optical density of ADAR1 immunoreactive cells in the amygdala of the social isolation group mice was significantly lower than that in the corresponding brain area of the social control group (BLA: (0.038±0.002), (0.074±0.004); LaDL: (0.033±0.002), (0.060±0.002); LaVM: (0.045±0.003), (0.073±0.004); Lavl area: (0.044±0.003), (0.070±0.003); t=8.428, 9.037, 6.462, 5.698, all P<0.01). The optical density of ADAR1 immunoreactive positive cells in the amygdala (BLA: (0.060±0.003), LaDL: (0.042±0.002), LaVM: (0.056±0.004), Lavl: (0.054±0.003) in the ADAR1 inducer social isolation group was significantly higher than those in the corresponding brain area of the social isolation group mice (t=6.055, 2.876, 2.312, 2.492; all P<0.05). The expression of ADAR1 protein and 5-serotonin-2c receptor protein in amygdala of social isolation group were significantly lower than those of social isolation group (t=11.37, 12.65; P<0.01). The expression of ADAR1 protein and 5-serotonin-2c receptor protein in the amygdala of the ADAR1 inducer social isolation group were significantly higher than those of the social isolation group (t=3.02, 4.401; P<0.05). Conclusion ADAR1 inducer alleviates the aggressive behavior of social isolated BALB / c mice by enhancing the protein expression of 5-serotonin-2c receptor in the amygdala of social isolated BALB/c mice. Key words: Social isolation; Aggressive behavior; Adenosine deaminase acting on RNA 1; 5-serotonin-2C receptor; Mice
目的探讨作用于RNA 1的腺苷脱氨酶(ADAR1)对5-羟色胺-2c受体的抑制作用。方法将60只21日龄健康雄性BALB / c小鼠随机分为6组:社会隔离组、社会对照组、ADAR1诱导剂社会隔离组、ADAR1抑制剂社会隔离组、ADAR1诱导剂社会对照组和ADAR1抑制剂对照组。以单笼饲养4周的小鼠为社会隔离模型,以组鼠饲养4周的小鼠为对照组。ADAR1诱导剂社会隔离组和ADAR1抑制剂社会隔离组小鼠分别腹腔注射ADAR1诱导剂(5.0×104 U/kg)和抑制剂(10 mg/kg)。采用进驻-侵入试验评价小鼠的攻击行为。采用免疫组织化学和Western blot检测小鼠脑组织中ADAR1和5- 5-羟色胺-2c受体的表达。结果社会隔离组的攻击潜伏期显著低于社会对照组((43.15±6.99)s,(542.40±30.50)s;t=15.906, P<0.01), ADAR1诱导性社会隔离组的发作潜伏期((256.70±29.49)s)显著高于社会隔离组(t=7.046, P<0.01)。ADAR1抑制剂社会隔离组的发作潜伏期((15.25±2.18)s)显著低于社会隔离组(t=3.809, P<0.01)。社交隔离组小鼠杏仁核ADAR1免疫反应细胞的光密度显著低于社交对照组相应脑区(BLA:(0.038±0.002),(0.074±0.004);LaDL:(0.033±0.002),(0.060±0.002);LaVM:(0.045±0.003),(0.073±0.004);Lavl面积:(0.044±0.003),(0.070±0.003);t=8.428, 9.037, 6.462, 5.698, P均<0.01)。ADAR1诱导物社会隔离组小鼠杏仁核中ADAR1免疫反应阳性细胞的光密度(BLA:(0.060±0.003)、LaDL:(0.042±0.002)、LaVM:(0.056±0.004)、Lavl:(0.054±0.003)显著高于社会隔离组小鼠相应脑区(t=6.055、2.876、2.312、2.492;所有P < 0.05)。社会隔离组杏仁核中ADAR1蛋白和5-羟色胺-2c受体蛋白的表达量显著低于社会隔离组(t=11.37, 12.65;P < 0.01)。ADAR1诱导物社会隔离组杏仁核中ADAR1蛋白和5-羟色胺-2c受体蛋白的表达量显著高于社会隔离组(t=3.02, 4.401;P < 0.05)。结论ADAR1诱变剂通过提高社会孤立BALB/c小鼠杏仁核中5- 5-羟色胺-2c受体的蛋白表达,减轻了BALB/c小鼠的攻击行为。关键词:社会隔离;攻击行为;作用于RNA 1的腺苷脱氨酶;5-serotonin-2C受体;老鼠
{"title":"The role of adenosine deaminase acting on RNA in the remission of aggression behavior in socially isolated mice and the mechanism of 5-serotonin-2C receptor","authors":"Xiaonan Zhang, Weizhi Yu, Ying Xue, Hong Xu, Wei Yan, Huairui Li, Xiuli Zhai, Jinying Li, Ye Gao, Lin Gui, Deqin Yu, Zhaoyang Xiao, Yi-yuan Tang, Shengming Yin","doi":"10.3760/CMA.J.CN371468-20190712-00455","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20190712-00455","url":null,"abstract":"Objective \u0000To investigate the effect of adenosine deaminase acting on RNA 1 (ADAR1) on 5-serotonin-2c receptor in alleviating aggression in socially isolated mice. \u0000 \u0000 \u0000Methods \u0000Sixty healthy male BALB / c mice aged 21 days were randomly divided into six groups: social isolation group, social control group, ADAR1 inducer social isolation group, ADAR1 inhibitor social isolation group, ADAR1 inducer social control group and ADAR1 inhibitor control group.The mice fed in single cage for 4 weeks were used as social isolation model while the mice fed in group were used as control group.ADAR1 inducer (5.0×104 U/kg) and inhibitor (10 mg/kg) were given intraperitoneally to mice in the ADAR1 inducer social isolation group and the ADAR1 inhibitor social isolation group respectively.The aggressive behavior of mice was evaluated by resident-intruder test.The expression of ADAR1 and 5-serotonin-2c receptors in the brain of mice was detected by immunohistochemistry and Western blot. \u0000 \u0000 \u0000Results \u0000The attack latency of social isolation group was significantly lower than that of social control group ((43.15±6.99) s, (542.40±30.50) s; t=15.906, P<0.01), and the latency of attack ((256.70±29.49) s) in the ADAR1 inducer social isolation group was significantly higher than that in the social isolation group (t=7.046, P<0.01). The latency of attack ((15.25±2.18)s) in the ADAR1 inhibitor social isolation group was significantly lower than that in the social isolation group (t=3.809, P<0.01). The optical density of ADAR1 immunoreactive cells in the amygdala of the social isolation group mice was significantly lower than that in the corresponding brain area of the social control group (BLA: (0.038±0.002), (0.074±0.004); LaDL: (0.033±0.002), (0.060±0.002); LaVM: (0.045±0.003), (0.073±0.004); Lavl area: (0.044±0.003), (0.070±0.003); t=8.428, 9.037, 6.462, 5.698, all P<0.01). The optical density of ADAR1 immunoreactive positive cells in the amygdala (BLA: (0.060±0.003), LaDL: (0.042±0.002), LaVM: (0.056±0.004), Lavl: (0.054±0.003) in the ADAR1 inducer social isolation group was significantly higher than those in the corresponding brain area of the social isolation group mice (t=6.055, 2.876, 2.312, 2.492; all P<0.05). The expression of ADAR1 protein and 5-serotonin-2c receptor protein in amygdala of social isolation group were significantly lower than those of social isolation group (t=11.37, 12.65; P<0.01). The expression of ADAR1 protein and 5-serotonin-2c receptor protein in the amygdala of the ADAR1 inducer social isolation group were significantly higher than those of the social isolation group (t=3.02, 4.401; P<0.05). \u0000 \u0000 \u0000Conclusion \u0000ADAR1 inducer alleviates the aggressive behavior of social isolated BALB / c mice by enhancing the protein expression of 5-serotonin-2c receptor in the amygdala of social isolated BALB/c mice. \u0000 \u0000 \u0000Key words: \u0000Social isolation; Aggressive behavior; Adenosine deaminase acting on RNA 1; 5-serotonin-2C receptor; Mice","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"193-199"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42152289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Effect of music training and art training on letters-speech sounds audiovisual integration in college students 音乐训练与艺术训练对大学生信-言-声-视融合的影响
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20190808-00536
Shengnan Li, Weiping Yang
Objective To investigate the effects of music training and art training on the audiovisual integration of letters-speech sounds in college students. Method Visual letters and auditory speech sounds were used to conduct a discrimination task test in music students, art students and ordinary college students (n=30 for each group). SPSS17.0 was used to conduct ANOVA and Race model analysis on reaction time and hit rate. Results (1) Reaction time: the results showed that the interaction between group and stimulus type was significant(F=7.89, P<0.01). The simple effect analysis found that all the participants reacted faster to consistent audiovisual(letters B and speech B) stimuli in comparison to unimodal stimuli, and the redundant signal effect occured.(2) Race model analysis showed that the time window of audiovisual integration were 120-130 ms in the music group, 130-190 ms in the art group, and 120-170 ms in the general group(P<0.01). The positive area (pAUC) under the Race model curve of the music group(18.95) was significantly smaller than that of the art group(159.43) and the general group(125.01)(P<0.01), and there was no significant difference between the art group and the general group(P=0.13). Conclusion Music training has a regulating effect on the integration of letters and speech sounds, while art training has no significant effect on it. Key words: Audiovisual integration; The redundant signal effect; Race model; Music training; Art training
目的探讨音乐训练和艺术训练对大学生字母语音视听整合的影响。方法采用视觉字母和听觉语音分别对音乐系学生、艺术系学生和普通大学生进行辨别任务测试,每组各30人。采用SPSS17.0对反应时间和命中率进行方差分析和Race模型分析。结果(1)反应时间:结果显示,组与刺激类型交互作用显著(F=7.89, P<0.01)。(2)种族模型分析显示,音乐组、艺术组和普通组的视听融合时间窗分别为120 ~ 130 ms、130 ~ 190 ms和120 ~ 170 ms (P<0.01)。音乐组Race模型曲线下的阳性面积(pac)(18.95)显著小于美术组(159.43)和普通组(125.01)(P<0.01),美术组与普通组之间差异无统计学意义(P=0.13)。结论音乐训练对字母语音整合有调节作用,而艺术训练对字母语音整合无显著影响。关键词:视听集成;冗余信号效应;竞争模型;音乐培训;艺术培训
{"title":"Effect of music training and art training on letters-speech sounds audiovisual integration in college students","authors":"Shengnan Li, Weiping Yang","doi":"10.3760/CMA.J.CN371468-20190808-00536","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20190808-00536","url":null,"abstract":"Objective \u0000To investigate the effects of music training and art training on the audiovisual integration of letters-speech sounds in college students. \u0000 \u0000 \u0000Method \u0000Visual letters and auditory speech sounds were used to conduct a discrimination task test in music students, art students and ordinary college students (n=30 for each group). SPSS17.0 was used to conduct ANOVA and Race model analysis on reaction time and hit rate. \u0000 \u0000 \u0000Results \u0000(1) Reaction time: the results showed that the interaction between group and stimulus type was significant(F=7.89, P<0.01). The simple effect analysis found that all the participants reacted faster to consistent audiovisual(letters B and speech B) stimuli in comparison to unimodal stimuli, and the redundant signal effect occured.(2) Race model analysis showed that the time window of audiovisual integration were 120-130 ms in the music group, 130-190 ms in the art group, and 120-170 ms in the general group(P<0.01). The positive area (pAUC) under the Race model curve of the music group(18.95) was significantly smaller than that of the art group(159.43) and the general group(125.01)(P<0.01), and there was no significant difference between the art group and the general group(P=0.13). \u0000 \u0000 \u0000Conclusion \u0000Music training has a regulating effect on the integration of letters and speech sounds, while art training has no significant effect on it. \u0000 \u0000 \u0000Key words: \u0000Audiovisual integration; The redundant signal effect; Race model; Music training; Art training","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"266-270"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44693090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Research progress of immune regulation in antidepressant treatment 免疫调节在抗抑郁治疗中的研究进展
Pub Date : 2020-03-20 DOI: 10.3760/CMA.J.CN371468-20191204-00885
Peilin Wang, Nan Zhang, Simeng Ma, Zhongchun Liu
In recent years, the role of inflammation in depression has received people's attention.Studies have suggested that immune disorder may play an important role in depression, and patients with depression exhibit characteristic immunophenotypes.Inflammation seems to interact with a variety of pathogenesis of depression.Therefore, immunoregulation is becoming an adjuvant therapy for depression.Clinically, not only antidepressants show anti-inflammatory effects, but also anti-inflammatory drugs show antidepressant effects, and they mainly including non-steroidal anti-inflammatory drugs, statins, and cytokine inhibitors.In addition, some non-drug treatment methods are also given immunomodulatory effects, such as electric shock therapy, vagus nerve stimulation, acupuncture and exercise therapy.However, there are still some problems in immunomodulation therapy, such as immunomodulation therapy may be only effective for some subgroups of patients, and its efficacy and safety need to be evaluated.In the future, looking for more effective biomarkers and identifying immune-inflammation-related subtype of depression, will serve to explore new diagnosis and treatment strategies. Key words: Major depression disorder; Immunomodulation; Inflammation; Anti-inflammatory; Therapy
近年来,炎症在抑郁症中的作用受到了人们的关注。研究表明,免疫障碍可能在抑郁症中发挥重要作用,抑郁症患者表现出特征性的免疫表型。炎症似乎与抑郁症的多种发病机制相互作用。因此,免疫调节正成为抑郁症的辅助治疗手段。临床上,不仅抗抑郁药具有抗炎作用,抗炎药也具有抗抑郁作用,它们主要包括非甾体抗炎药、他汀类药物和细胞因子抑制剂。此外,一些非药物治疗方法也具有免疫调节作用,如电击疗法、迷走神经刺激、针灸和运动疗法。然而,免疫调节疗法仍存在一些问题,如免疫调节疗法可能仅对某些亚组患者有效,其疗效和安全性有待评估。未来,寻找更有效的生物标志物并识别免疫炎症相关的抑郁症亚型,将有助于探索新的诊断和治疗策略。关键词:重度抑郁症;免疫调节;炎症;抗炎;治疗
{"title":"Research progress of immune regulation in antidepressant treatment","authors":"Peilin Wang, Nan Zhang, Simeng Ma, Zhongchun Liu","doi":"10.3760/CMA.J.CN371468-20191204-00885","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20191204-00885","url":null,"abstract":"In recent years, the role of inflammation in depression has received people's attention.Studies have suggested that immune disorder may play an important role in depression, and patients with depression exhibit characteristic immunophenotypes.Inflammation seems to interact with a variety of pathogenesis of depression.Therefore, immunoregulation is becoming an adjuvant therapy for depression.Clinically, not only antidepressants show anti-inflammatory effects, but also anti-inflammatory drugs show antidepressant effects, and they mainly including non-steroidal anti-inflammatory drugs, statins, and cytokine inhibitors.In addition, some non-drug treatment methods are also given immunomodulatory effects, such as electric shock therapy, vagus nerve stimulation, acupuncture and exercise therapy.However, there are still some problems in immunomodulation therapy, such as immunomodulation therapy may be only effective for some subgroups of patients, and its efficacy and safety need to be evaluated.In the future, looking for more effective biomarkers and identifying immune-inflammation-related subtype of depression, will serve to explore new diagnosis and treatment strategies. \u0000 \u0000Key words: \u0000Major depression disorder; Immunomodulation; Inflammation; Anti-inflammatory; Therapy","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"284-288"},"PeriodicalIF":0.0,"publicationDate":"2020-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44109482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reconsideration on the multiple value of Behavior determining Health: in the perspective of the situation of COVID-19/ 中华行为医学与脑科学杂志 重新思考行为决定健康的多重价值——基于新冠肺炎疫情的视角
Pub Date : 2020-02-24 DOI: 10.3760/CMA.J.ISSN.1674-6554.2020.0002
Lifang Zhu, Mingke Bie, Guojian Song, Zhiyin Yang
Why has the concept of behavior determining health created more and more extensive and far-reaching influence ever since it was put forward? The reason lies in its multiple values. It is of great practical significance and has important implications for long-term health care to explore and analyze in the perspective of the situation of COVID-19 its philosophical values, cultural values, methodological values, social values and the national strategic value of "healthy China".
为什么行为决定健康的概念自提出以来产生了越来越广泛和深远的影响?原因在于它的多重价值。从新冠疫情形势出发,探讨和分析其哲学价值、文化价值、方法论价值、社会价值和“健康中国”的国家战略价值,对长期医疗保健具有重要的现实意义和重要启示。
{"title":"Reconsideration on the multiple value of Behavior determining Health: in the perspective of the situation of COVID-19/ 中华行为医学与脑科学杂志","authors":"Lifang Zhu, Mingke Bie, Guojian Song, Zhiyin Yang","doi":"10.3760/CMA.J.ISSN.1674-6554.2020.0002","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1674-6554.2020.0002","url":null,"abstract":"Why has the concept of behavior determining health created more and more extensive and far-reaching influence ever since it was put forward? The reason lies in its multiple values. It is of great practical significance and has important implications for long-term health care to explore and analyze in the perspective of the situation of COVID-19 its philosophical values, cultural values, methodological values, social values and the national strategic value of \"healthy China\".","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47855941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Expressions of triggering receptor expressed on myeloid cell 2 in different brain regions in tyrosine kinase binding protein gene knockout mice 酪氨酸激酶结合蛋白基因敲除小鼠不同脑区髓细胞2表达触发受体
Pub Date : 2020-02-20 DOI: 10.3760/CMA.J.CN371468-20191025-00782
Tongxiao Xu, Zhao-xia Wang, Yanxin Li, Kuo H. Yang, Wei Zhang, Wei Li, Yanlei Hao
Objective To compare the expression of myeloid cell trigger receptor expressed on myoid cell 2 (TREM2) in different brain regions of tyrosine kinase binding protein(TYROBP) knockout mice and wild-type mice at different months of age, and to explore the relationship between TREM2, TYROBP and early onset Alzheimer's disease(EOAD). Methods Healthy TYROBP gene knockout mice were divided into three groups according to the results of gene sequencing: the homozygous (TYROBP-/-) group, the heterozygous (TYROBP-/+ ) group, and the wild type (WT) group.Western blot and RT-qPCR were used to detect the expression of TREM2 in prefrontal cortex and hippocampus of 2, 4 and 6 month old mice in the three groups and with 10 in each group at each time point. Results (1) In the prefrontal cortex: Western blot and RT-qPCR results showed that compared with WT mice (2-month-old: (0.993±0.048), (1.654±0.033); 4-month-old: (0.503±0.019), (2.169±0.023); 6-month-old: (0.600±0.036), (1.468±0.057)), the levels of TREM2 protein and mRNA in 2-month-old TYROBP-/+ group ((0.746±0.062), (1.137±0.067)) and TYROBP-/- group ((0.661±0.028), (0.644±0.012)) were decreased.While in 4-month-old and 6-month-old TYROBP-/+ group (4-month-old: (1.140±0.006), (5.483±0.088); 6-month-old: (0.827±0.043), (3.020±0.082)) and TYROBP-/- group (4-month-old: (1.071±0.010), (3.012±0.150); 6-month-old: (0.627±0.026), (1.633±0.027)) were increased, especially in 4-month-old mice and the differences were statistically significant (F=12.946, 134.445; 725.318, 289.202; 12.172, 202.791; all P<0.05). (2) In the hippocampus: Western blot results showed that compared with WT mice (2-month-old: (1.268±0.036); 4-month-old: (0.813±0.010); 6-month-old: (0.312±0.021)), the level of TREM2 protein in 2-month-old TYROBP-/+ group ((0.804±0.034)) and TYROBP-/- group ((0.534±0.020)) were decreased.While in 4-month-old and 6-month-old TYROBP-/+ group ((0.932±0.011); (0.769±0.031)) and TYROBP-/- group ((0.910±0.014); (0.609±0.018)) were increased, especially in 4-month-old mice and the differences were statistically significant (F=142.807; 27.884; 94.067; all P<0.05). Conclusion The expression level of TREM2 decreases in 2-month-old TYROBP gene knockout mice while increases in 4-month-old and 6-month-old TYROBP gene knockout mice.It is presumed that TREM2/TYROBP signal pathway participates in the pathological process of EOAD and plays different roles in different pathological stages of EOAD. Key words: Tyrosine kinase binding protein; Triggering receptor expressed on myeloid cell 2; Alzheimer's disease; Mice
目的比较酪氨酸激酶结合蛋白(TYROBP)敲除小鼠和不同月龄野生型小鼠不同脑区肌样细胞2(TREM2)上表达的髓细胞触发受体的表达,探讨TREM2、TYROBP与早发性阿尔茨海默病(EOAD)的关系。方法根据基因测序结果将健康的TYROBP基因敲除小鼠分为三组:纯合型(TYROBP-/-)组、杂合型(TYROBP-/+)组和野生型(WT)组。采用Western blot和RT-qPCR检测三组2、4和6月龄小鼠前额叶皮层和海马TREM2的表达,每组10只。结果(1)前额叶皮层:Western blot和RT-qPCR结果显示,与WT小鼠(2月龄:(0.993±0.048),(1.654±0.033)相比;4月龄:(0.503±0.019),(2.169±0.023);6个月龄:(0.600±0.036),(1.468±0.057),2个月龄TYROBP-/+组(0.746±0.062),(1.137±0.067)和TYROBP/-组(0.661±0.028),(0.644±0.012)TREM2蛋白和mRNA水平降低。而在4个月大和6个月大的TYROBP-/+组(4个月龄:(1.140±0.006),(5.483±0.088);6个月龄:(0.827±0.043),(3.020±0.082))和TYROBP-/-组(4个月龄,(1.071±0.010),(3.0 12±0.150);6个月大:(0.627±0.026),(1.633±0.027))增加,特别是在4个月大的小鼠中,差异具有统计学意义(F=12.94613.445;725.318289.202;12.17202.791;均P<0.05);4月龄:(0.813±0.010);6月龄:(0.312±0.021)),2月龄TYROBP-/+组(0.804±0.034)和TYROBP/-组(0.534±0.020)TREM2蛋白水平下降。而在4个月大和6个月大的TYROBP-/+组((0.932±0.011);(0.769±0.031))和TYROAP-/-组(0.910±0.014);(0.609±0.018))表达增加,尤其是在4月龄小鼠中,差异有统计学意义(F=142.807;27.884;94.067;均P<0.05)。TREM2/TYROBP信号通路参与EOAD的病理过程,在EOAD的不同病理阶段发挥不同的作用。关键词:酪氨酸激酶结合蛋白;骨髓细胞2上表达的触发受体;阿尔茨海默病;老鼠
{"title":"Expressions of triggering receptor expressed on myeloid cell 2 in different brain regions in tyrosine kinase binding protein gene knockout mice","authors":"Tongxiao Xu, Zhao-xia Wang, Yanxin Li, Kuo H. Yang, Wei Zhang, Wei Li, Yanlei Hao","doi":"10.3760/CMA.J.CN371468-20191025-00782","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20191025-00782","url":null,"abstract":"Objective \u0000To compare the expression of myeloid cell trigger receptor expressed on myoid cell 2 (TREM2) in different brain regions of tyrosine kinase binding protein(TYROBP) knockout mice and wild-type mice at different months of age, and to explore the relationship between TREM2, TYROBP and early onset Alzheimer's disease(EOAD). \u0000 \u0000 \u0000Methods \u0000Healthy TYROBP gene knockout mice were divided into three groups according to the results of gene sequencing: the homozygous (TYROBP-/-) group, the heterozygous (TYROBP-/+ ) group, and the wild type (WT) group.Western blot and RT-qPCR were used to detect the expression of TREM2 in prefrontal cortex and hippocampus of 2, 4 and 6 month old mice in the three groups and with 10 in each group at each time point. \u0000 \u0000 \u0000Results \u0000(1) In the prefrontal cortex: Western blot and RT-qPCR results showed that compared with WT mice (2-month-old: (0.993±0.048), (1.654±0.033); 4-month-old: (0.503±0.019), (2.169±0.023); 6-month-old: (0.600±0.036), (1.468±0.057)), the levels of TREM2 protein and mRNA in 2-month-old TYROBP-/+ group ((0.746±0.062), (1.137±0.067)) and TYROBP-/- group ((0.661±0.028), (0.644±0.012)) were decreased.While in 4-month-old and 6-month-old TYROBP-/+ group (4-month-old: (1.140±0.006), (5.483±0.088); 6-month-old: (0.827±0.043), (3.020±0.082)) and TYROBP-/- group (4-month-old: (1.071±0.010), (3.012±0.150); 6-month-old: (0.627±0.026), (1.633±0.027)) were increased, especially in 4-month-old mice and the differences were statistically significant (F=12.946, 134.445; 725.318, 289.202; 12.172, 202.791; all P<0.05). (2) In the hippocampus: Western blot results showed that compared with WT mice (2-month-old: (1.268±0.036); 4-month-old: (0.813±0.010); 6-month-old: (0.312±0.021)), the level of TREM2 protein in 2-month-old TYROBP-/+ group ((0.804±0.034)) and TYROBP-/- group ((0.534±0.020)) were decreased.While in 4-month-old and 6-month-old TYROBP-/+ group ((0.932±0.011); (0.769±0.031)) and TYROBP-/- group ((0.910±0.014); (0.609±0.018)) were increased, especially in 4-month-old mice and the differences were statistically significant (F=142.807; 27.884; 94.067; all P<0.05). \u0000 \u0000 \u0000Conclusion \u0000The expression level of TREM2 decreases in 2-month-old TYROBP gene knockout mice while increases in 4-month-old and 6-month-old TYROBP gene knockout mice.It is presumed that TREM2/TYROBP signal pathway participates in the pathological process of EOAD and plays different roles in different pathological stages of EOAD. \u0000 \u0000 \u0000Key words: \u0000Tyrosine kinase binding protein; Triggering receptor expressed on myeloid cell 2; Alzheimer's disease; Mice","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"102-108"},"PeriodicalIF":0.0,"publicationDate":"2020-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49333881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of behavioral intervention on scratching behavior in patients with senile pruritus 行为干预对老年瘙痒症患者抓挠行为的影响
Pub Date : 2020-02-20 DOI: 10.3760/CMA.J.CN371468-20190516-00326
Xiaopei Du, Chen Shaoxiu, Z. Xia, Duhong Chen, Wang Chao
Objective To explore the impact of behavioral intervention on scratching behavior of patients with senile pruritus. Methods One hundred cases of senile pruritus were randomly divided into observation group (n=50) and control group (n=50). All subjects received oral antihistamine.The observation group received behavioral intervention based on the trans-theoretical model, and the control group received routine health education.Visual analogue scale (VAS), Pittsburgh sleep quality index (PSQI) and dermatology life quality index (DLQI) were used to compare the itching symptoms, sleep quality and quality of life of senile pruritus patients in the two groups. Results After 6 months intervention, the change of scratching behavior in the observation group((1.96±1.54), (8.83±2.05), (10.46±2.24)) was significantly better than those in the control group((4.68±1.48), (12.89±2.02), (14.62±2.12)), and the differences were statistically significant (all P<0.01). Conclusion Health intervention based on trans-theoretical model can effectively change scratching behavior, relieve itching symptoms, improve sleep quality and the quality of life of senile pruritus patients. Key words: Senile pruritus; Scratching behavior; Trans-theoretical model; Quality of life
目的探讨行为干预对老年性瘙痒患者抓挠行为的影响。方法将100例老年性瘙痒患者随机分为观察组(n=50)和对照组(n=50)。所有受试者口服抗组胺药。观察组采用跨理论模式进行行为干预,对照组采用常规健康教育。采用视觉模拟量表(VAS)、匹兹堡睡眠质量指数(PSQI)和皮肤科生活质量指数(DLQI)比较两组老年瘙痒患者的瘙痒症状、睡眠质量和生活质量。结果干预6个月后,观察组挠痒行为变化((1.96±1.54)、(8.83±2.05)、(10.46±2.24)明显优于对照组((4.68±1.48)、(12.89±2.02)、(14.62±2.12),差异均有统计学意义(P<0.01)。结论基于跨理论模型的健康干预能有效改变老年瘙痒患者的抓痒行为,缓解瘙痒症状,改善睡眠质量和生活质量。关键词:老年性瘙痒;抓挠行为;Trans-theoretical模型;生活质量
{"title":"Effect of behavioral intervention on scratching behavior in patients with senile pruritus","authors":"Xiaopei Du, Chen Shaoxiu, Z. Xia, Duhong Chen, Wang Chao","doi":"10.3760/CMA.J.CN371468-20190516-00326","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20190516-00326","url":null,"abstract":"Objective \u0000To explore the impact of behavioral intervention on scratching behavior of patients with senile pruritus. \u0000 \u0000 \u0000Methods \u0000One hundred cases of senile pruritus were randomly divided into observation group (n=50) and control group (n=50). All subjects received oral antihistamine.The observation group received behavioral intervention based on the trans-theoretical model, and the control group received routine health education.Visual analogue scale (VAS), Pittsburgh sleep quality index (PSQI) and dermatology life quality index (DLQI) were used to compare the itching symptoms, sleep quality and quality of life of senile pruritus patients in the two groups. \u0000 \u0000 \u0000Results \u0000After 6 months intervention, the change of scratching behavior in the observation group((1.96±1.54), (8.83±2.05), (10.46±2.24)) was significantly better than those in the control group((4.68±1.48), (12.89±2.02), (14.62±2.12)), and the differences were statistically significant (all P<0.01). \u0000 \u0000 \u0000Conclusion \u0000Health intervention based on trans-theoretical model can effectively change scratching behavior, relieve itching symptoms, improve sleep quality and the quality of life of senile pruritus patients. \u0000 \u0000 \u0000Key words: \u0000Senile pruritus; Scratching behavior; Trans-theoretical model; Quality of life","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"148-152"},"PeriodicalIF":0.0,"publicationDate":"2020-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46458067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Changes of resting state fMRI brain imaging in patients with depression after antidepressant treatment 抑郁症患者抗抑郁治疗后静息状态fMRI脑成像的变化
Pub Date : 2020-02-20 DOI: 10.3760/CMA.J.CN371468-20190523-00335
Jian Cui, Yun Wang, Yuan Zhou, Gang Wang
Antidepressant therapy is effective for patients with major depressive disorder, however the mechanism is unclear and it is difficult to predict the efficacy objectively. At present, the changes of local spontaneous brain activity in patients with major depressive disorder after antidepressant treatment are mostly located in the dorsolateral prefrontal cortex, ventromedial prefrontal cortex, anterior cingulate gyrus and precuneus. The changes of brain function interaction involved in emotional circuit, default mode network, central executive network and hypothalamus-pituitary-adrenal axis.Future researches should optimize the experimental design, enlarge the sample size, reduce the sample heterogeneity, and compare the effects of different types of antidepressants. This paper reviews the effects of antidepressant therapy on brain function in patients with major depressive disorder from the perspective of resting fMRI, to promote our understanding of the mechanism of antidepressant therapy and to promote the discovery of objective biomarkers which can predict the response of antidepressant therapy. Key words: Major depressive disorder; Antidepressants; Resting state; Functional magnetic resonance imaging
抗抑郁治疗对重度抑郁症患者是有效的,但其作用机制尚不清楚,也难以客观预测其疗效。目前,重度抑郁症患者在抗抑郁治疗后局部自发脑活动的变化主要位于背外侧前额叶皮层、腹内侧前额叶皮质、前扣带回和楔前叶。脑功能相互作用的变化涉及情绪回路、默认模式网络、中枢执行网络和下丘脑-垂体-肾上腺轴。未来的研究应该优化实验设计,扩大样本量,减少样本异质性,并比较不同类型抗抑郁药的效果。本文从静息功能磁共振成像的角度综述了抗抑郁治疗对重度抑郁障碍患者大脑功能的影响,以促进我们对抗抑郁治疗机制的理解,并促进发现可以预测抗抑郁治疗反应的客观生物标志物。关键词:重度抑郁障碍;抗抑郁药;休息状态;功能性磁共振成像
{"title":"Changes of resting state fMRI brain imaging in patients with depression after antidepressant treatment","authors":"Jian Cui, Yun Wang, Yuan Zhou, Gang Wang","doi":"10.3760/CMA.J.CN371468-20190523-00335","DOIUrl":"https://doi.org/10.3760/CMA.J.CN371468-20190523-00335","url":null,"abstract":"Antidepressant therapy is effective for patients with major depressive disorder, however the mechanism is unclear and it is difficult to predict the efficacy objectively. At present, the changes of local spontaneous brain activity in patients with major depressive disorder after antidepressant treatment are mostly located in the dorsolateral prefrontal cortex, ventromedial prefrontal cortex, anterior cingulate gyrus and precuneus. The changes of brain function interaction involved in emotional circuit, default mode network, central executive network and hypothalamus-pituitary-adrenal axis.Future researches should optimize the experimental design, enlarge the sample size, reduce the sample heterogeneity, and compare the effects of different types of antidepressants. This paper reviews the effects of antidepressant therapy on brain function in patients with major depressive disorder from the perspective of resting fMRI, to promote our understanding of the mechanism of antidepressant therapy and to promote the discovery of objective biomarkers which can predict the response of antidepressant therapy. \u0000 \u0000 \u0000Key words: \u0000Major depressive disorder; Antidepressants; Resting state; Functional magnetic resonance imaging","PeriodicalId":9940,"journal":{"name":"Chinese Journal of Behavioral Medicine and Brain Science","volume":"29 1","pages":"177-182"},"PeriodicalIF":0.0,"publicationDate":"2020-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47063603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
中华行为医学与脑科学杂志
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1