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Expression of c-Fos protein and nitricoxide synthase in neurons of cerebral cortex from fetal rats in hypoxia and protective role of Angelica sinensis 被引量:1
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作者 Hong Yu Hongxian Zhao Yuling Wu 《Neural Regeneration Research》 SCIE CAS CSCD 2006年第1期74-77,共4页
BACKGROUND: Both c-Fos protein and nitricoxide synthase (NOS) have been used as general indexes in relative research about neurons, but it is lack of reports that c-Fos protein and NOS are applied synchronously to ... BACKGROUND: Both c-Fos protein and nitricoxide synthase (NOS) have been used as general indexes in relative research about neurons, but it is lack of reports that c-Fos protein and NOS are applied synchronously to study the neurons of hypoxic fetal rats in uterus. OBJECTIVE: To study the effect of hypoxia in uterus on the expression of c-Fos protein and NOS in neurons of cerebral cortex from fetal rats and whether Angelica sinensis has the protective effect on these neurons in hypoxia. DESIGN: Randomized control experiment.SETTING : Department of Histology and Embryology, Luzhou Medical College.MATERIALS : Twelve adult female Wistar rats in oestrum and 1 male Wistar rat with bodymass from 220 to 250 g were chosen. Parenteral solution of Angelica sinensis mainly contained angelica sinensis, 10 mL/ampoule, was provided by Department of Agent of the Second Hospital Affiliated to Hubei Medical University (batch number: 01062310). METHODS : This experiment was completed in the Department of Histology and Embryology of Luzhou Medical College from September 2003 to June 2004. ①Twelve adult female Wistar rats in oestrum and 1 male Wistar rat were housed in one rearing cage. Vaginal embolus was performed on conceive female rat at 8: 00 am next day. On the 15^th conceiving day, all conceiving rats were divided randomly into three groups: control group, hypoxia group and Angelica group with 4 in each group. Rats in hypoxia group and Angelica group were modeled with hypotonic hypoxia in uterus. Angelica group: Rats were injected with 8 mL/kg Angelica sinensis injection through caudal veins before hypoxia. Hypoxia group: Rats were injected with the same volume of saline. Control group: Rats were not modeled and fed with normal way. ② Twenty embryos of rats were chosen randomly from each group and then routinely embedded in paraffin. Paraffin sections were cut from the brain of embryos to anterior fontanelle. Double-label staining was used to detect the expression of nNOS and c-Fos in neurons of cerebral cortex from embryos of rats. OLYMPUS Bx-50 microscope was used to observe sections and DP12 digit camera was also used under 400 times to detect types of cells. Under microscope, the number of c-Fos, NOS, c-Fos/NOS positive neurons in cerebral cortex from embryos of rats were counted in 2 fields with magnification of 400 in one section per animal. ③ The data in experiments were analyzed by one-way analysis of variance (ANOVA) followed by q test. MAIN OUTCOME MEASURES: ① Results of immunohistochemical double-label staining of c-Fos/NOS from cerebral cortex; ② Comparison of amount immunohistochemical double-label staining of c-Fos/NOS positive cells from cerebral cortex. RESULTS:① The positive NOS cells and c-Fos/NOS cells in the three groups were mainly distributed in cerebral cortex, but positive c-Fos neurons were not observed. ② Positive NOS cells and c-Fos/NOS cells in hypoxia group were more than those in control group (76.55±12.02, 50.45±10.39; 33.35±7.42, 26.35±6.67, P 〈 0.05), but those in Angelica group were less than those in hypoxia group (51.70±9.82, 35.65±8.37, P 〈 0.05). CONCLUSION: Hypoxia can stimulate the increase of expression of c-Fos protein and NOS in neurons of cerebral cortex. However, Angelica sinensis can decrease this expression so as to play a protective role in cerebral neurons of hypoxic fetal rats. 展开更多
关键词 FOS Expression of c-fos protein and nitricoxide synthase in neurons of cerebral cortex from fetal rats in hypoxia and protective role of Angelica sinensis
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Effects of acute and chronic administration of MK-801 on c-Fos protein expression in mice brain regions implicated in schizophrenia and antagonistic action of clozapine 被引量:1
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作者 ZUO Dai-ying1,CAO Yue2,ZHANG Lan1,WANG Hai-feng1,WU Ying-liang1(1.Department of Pharmacology,Shenyang Pharmaceutical University,Shenyang 110016,China 2.Liaoning Institute for Drug Control,Shenyang 110023,China) 《沈阳药科大学学报》 CAS CSCD 北大核心 2008年第S1期55-56,共2页
Objective To investigate the effects of acute and chronic administration of the non-competitive NMDA receptor antagonists MK-801 on c-Fos protein expression in different brain regions of mice and an-tagonistic action ... Objective To investigate the effects of acute and chronic administration of the non-competitive NMDA receptor antagonists MK-801 on c-Fos protein expression in different brain regions of mice and an-tagonistic action of clozapine.Methods Immunohistochemistry was used to detect the expression of c-Fos protein.Results MK-801(0.6 mg·kg-1)acute administration produced a significant increase in the expression of c-Fos protein in the layers Ⅲ-Ⅳ of posterior cingulate and retrosplenial(PC/RS)cortex,which was consistent with the previous reports.Moreover,we presented a new finding that MK-801(0.6 mg·kg-1)chronic administration for 8 days produced a significant increase of c-Fos protein expression in the PC/RS cortex,prefrontal cortex(PFC)and hypothalamus of mice.Among that,c-Fos protein expression in the PC/RS cortex of mice was most significant.Compared acute administration with chronic administration,we found that MK-801 chronic administration significantly increased the expression of c-Fos protein in the PC/RS cortex,PFC and hypothalamus.Furthermore,pretreatment of mice with clozapine significantly decreased the expression of c-Fos protein induced by MK-801 acute and chronic administration.Conclusions Marked expression of c-Fos protein induced by MK-801 is associated with neurotransmitters' change noted in our previous studies,and c-Fos protein,the marker of neuronal activation,might play an important role in the chronic pathophysiological process of schizophrenic model induced by NMDA receptor antagonist. 展开更多
关键词 c-fos protein CLOZAPINE MK-801 SCHIZOPHRENIA
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Activation of immediate-early response gene c-Fos protein in the rat paralimbic cortices after myocardial infarction 被引量:2
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作者 Ji Yun Ahn Hyun-Jin Tae +9 位作者 Jeong-Hwi Cho In Hye Kim Ji Hyeon Ahn Joon Ha Park Dong Won Kim Jun Hwi Cho Moo-Ho Won Seongkweon Hong Jae-Chul Lee Jeong Yeol Seo 《Neural Regeneration Research》 SCIE CAS CSCD 2015年第8期1251-1257,共7页
c-Fos is a good biological marker for detecting the pathogenesis of central nervous system disorders. Few studies are reported on the change in myocardial infarction-induced c-Fos expression in the paralimbic regions.... c-Fos is a good biological marker for detecting the pathogenesis of central nervous system disorders. Few studies are reported on the change in myocardial infarction-induced c-Fos expression in the paralimbic regions. Thus, in this study, we investigated the changes in c-Fos expression in the rat cingulate and piriform cortices after myocardial infarction. Neuronal degeneration in cingulate and piriform cortices after myocardial infarction was detected using cresyl violet staining, Neu N immunohistochemistry and Fluoro-Jade B histofluorescence staining. c-Fos-immunoreactive cells were observed in cingulate and piriform cortices at 3 days after myocardial infarction and peaked at 7 and 14 days after myocardial infarction. But they were hardly observed at 56 days after myocardial infarction. The chronological change of c-Fos expression determined by western blot analysis was basically the same as that of c-Fos immunoreactivity. These results indicate that myocardial infarction can cause the chronological change of immediate-early response gene c-Fos protein expression, which might be associated with the neural activity induced by myocardial infarction. 展开更多
关键词 nerve regeneration paralimbic cortices myocardial infarction c-fos cingulate cortex piriform cortex immunohistochemistry western analysis neural regeneration
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四神丸对腹泻型肠易激综合征大鼠结肠MCT、c-fos表达的影响
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作者 蔺晓源 邓娜 +2 位作者 夏旭婷 刘富林 刘杰民 《中成药》 CAS CSCD 北大核心 2024年第5期1658-1661,共4页
目的观察四神丸对腹泻型肠易激综合征(IBS-D)模型大鼠结肠MCT、c-fos表达的影响。方法将40只大鼠随机分为正常组、模型组、匹维溴铵组(15.23 mg/kg)和四神丸组(7.32 mg/kg),每组10只,采用番泻叶灌胃联合避水应激法造模,灌胃给药14 d后,... 目的观察四神丸对腹泻型肠易激综合征(IBS-D)模型大鼠结肠MCT、c-fos表达的影响。方法将40只大鼠随机分为正常组、模型组、匹维溴铵组(15.23 mg/kg)和四神丸组(7.32 mg/kg),每组10只,采用番泻叶灌胃联合避水应激法造模,灌胃给药14 d后,观察一般状态,测定体质量、粪便含水量和AWR评分,ELISA法检测血清MCT、c-fos水平,免疫组织化学法、Western blot法分别检测结肠组织MCT、c-fos蛋白定位及表达,RT-qPCR法检测结肠组织MCT、c-fos mRNA表达。结果与模型组比较,四神丸组和匹维溴铵组大鼠一般状态明显好转,体质量升高(P<0.01),粪便含水量、AWR评分以及血清中MCT、c-fos水平均降低(P<0.05,P<0.01),结肠组织MCT、c-fos蛋白及mRNA表达均降低(P<0.05,P<0.01);四神丸组结肠组织MCT蛋白表达及c-fos蛋白表达均低于匹维溴铵组(P<0.05)。结论四神丸对IBS-D大鼠内脏敏感的保护机制可能与调节结肠肥大细胞活化指标MCT、c-fos的表达有关。 展开更多
关键词 四神丸 腹泻型肠易激综合征 内脏敏感性 MCT c-fos
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艾灸对创伤后应激障碍小鼠行为学及下丘脑外侧区c-fos的影响及c-fos与行为学的相关性分析
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作者 王含笑 张雪涛 +3 位作者 汪雅璐 王震 钟文 吴生兵 《安徽中医药大学学报》 CAS 2024年第3期37-41,共5页
目的观察艾灸“内关”“阳陵泉”对创伤后应激障碍(post traumatic stress disorder,PTSD)小鼠行为及小鼠下丘脑外侧区c-fos表达的影响。方法将C57小鼠随机分为正常组、模型组、艾灸组,每组6只。模型组、艾灸组采用改良的单次长时间应... 目的观察艾灸“内关”“阳陵泉”对创伤后应激障碍(post traumatic stress disorder,PTSD)小鼠行为及小鼠下丘脑外侧区c-fos表达的影响。方法将C57小鼠随机分为正常组、模型组、艾灸组,每组6只。模型组、艾灸组采用改良的单次长时间应激和电刺激(single prolonged stress and electrical stimulation,SPS&S)方法复制PTSD模型。艾灸组予艾灸“内关”“阳陵泉”连续干预7 d。利用旷场实验、高架十字迷宫实验和条件性恐惧测试实验检测小鼠行为,采用免疫荧光检测小鼠下丘脑外侧区c-fos的表达水平。结果与正常组比较,模型组小鼠体质量,旷场实验中央场时间、中央场距离显著减少(P<0.05),高架十字迷宫实验开臂进入次数和时间均显著减少(P<0.05);条件性恐惧测试实验中,背景恐惧和声音恐惧的冻结时间均显著增加(P<0.05);小鼠下丘脑外侧区c-fos表达水平显著升高(P<0.05)。与模型组比较,艾灸组小鼠体质量,旷场实验中央场时间、中央场距离显著增加(P<0.05),高架十字迷宫实验开臂进入次数和时间均显著增加(P<0.05);条件性恐惧测试实验中,背景恐惧和声音恐惧的冻结时间均显著减少(P<0.05);小鼠下丘脑外侧区c-fos表达水平显著降低(P<0.05)。结论艾灸“内关”“阳陵泉”穴能够显著改善PTSD小鼠焦虑抑郁样行为,其机制可能与调节下丘脑外侧区的c-fos表达有关。 展开更多
关键词 创伤后应激障碍 艾灸 c-fos 下丘脑外侧区
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电针心经穴位对急性心肌缺血模型大鼠内侧隔核白细胞介素-2、JunB蛋白及c-fos表达水平的影响
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作者 李锦航 周美启 《安徽中医药大学学报》 CAS 2024年第2期38-42,共5页
目的观察电针心经对急性心肌缺血(acute myocardial ischemia,AMI)大鼠内侧隔核白细胞介素(interleukin,IL)-2水平、JunB蛋白及c-fos表达水平的影响,探究内侧隔核在针刺抗AMI中的作用及机制。方法将大鼠分为伪手术组、模型组和电针组,每... 目的观察电针心经对急性心肌缺血(acute myocardial ischemia,AMI)大鼠内侧隔核白细胞介素(interleukin,IL)-2水平、JunB蛋白及c-fos表达水平的影响,探究内侧隔核在针刺抗AMI中的作用及机制。方法将大鼠分为伪手术组、模型组和电针组,每组6只;结扎冠状动脉左前降支复制AMI大鼠模型;电针组大鼠选取手少阴心经“神门—通里”段进行干预,每次30 min,每日1次,连续电针3 d,刺激电流为1 mA,频率为2 Hz;伪手术组、模型组大鼠不进行电针干预。采用ELISA法检测大鼠大脑内侧隔核IL-2水平,Western blot法检测大鼠大脑内侧隔核区JunB蛋白表达水平,免疫荧光法检测大鼠大脑内侧隔核区c-fos免疫反应阳性神经元表达水平。结果与伪手术组比较,模型组大鼠大脑内侧隔核区IL-2、JunB蛋白水平显著升高(P<0.05),c-fos免疫反应阳性神经元数和平均吸光度(optical density,OD)值显著增加(P<0.05);与模型组比较,电针组大鼠大脑内侧隔核区IL-2、JunB蛋白水平显著降低(P<0.05),c-fos免疫反应阳性神经元数和平均OD值显著减少(P<0.05)。结论内侧隔核参与电针心经抗AMI的作用,其机制可能与电针降低大脑内侧隔核区IL-2、JunB蛋白及c-fos表达水平有关。 展开更多
关键词 急性心肌缺血 内侧隔核 JunB蛋白 c-fos 电针
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骨疏康干预破骨细胞:激活核因子E2相关因子2调控c-Fos/NFATc1通路
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作者 侯成志 韩佳童 +4 位作者 魏光成 卓泽川 李秋月 赵勇 俞张镜泽 《中国组织工程研究》 CAS 北大核心 2025年第2期279-285,共7页
背景:已有研究表明,骨疏康通过调节核苷酸、氨基酸代谢和免疫机制影响骨骼代谢,目前骨疏康治疗骨质疏松症的机制研究主要聚焦于调控成骨细胞,对破骨细胞的关注较少。目的:以RAW 264.7细胞为实验对象,从破骨细胞角度探讨骨疏康治疗骨质... 背景:已有研究表明,骨疏康通过调节核苷酸、氨基酸代谢和免疫机制影响骨骼代谢,目前骨疏康治疗骨质疏松症的机制研究主要聚焦于调控成骨细胞,对破骨细胞的关注较少。目的:以RAW 264.7细胞为实验对象,从破骨细胞角度探讨骨疏康治疗骨质疏松症的机制。方法:取8周龄雌性SD大鼠24只,采用随机数字表法分为4组(n=6),3个实验组分别灌胃给予1,2,4 g/kg的骨疏康药液(2次/d),对照组灌胃给予等量蒸馏水(2次/d),连续灌胃7 d后抽取大鼠主动脉血,离心收集血清,同组血清合并,获得低、中、高浓度的骨疏康含药血清及正常血清,进行后续实验。①将RAW 264.7细胞分6组培养:对照组加入正常血清,低、中、高浓度组分别加入低、中、高浓度的骨疏康含药血清,Nrf2抑制剂组加入核因子E2相关因子2(nuclear factor erythroid 2-related factor 2,Nrf2)抑制剂ML385,Nrf2激活剂组加入Nrf2激活剂t-BHQ,采用CCK8法检测细胞相对活性。②将第3代RAW 264.7细胞分5组培养:空白对照组加入正常血清,破骨组加入核因子κB受体活化因子配体(receptor activator of nuclear factorκB ligand,RANKL),低、中、高浓度组在加入RANKL的基础上分别加入低、中、高浓度的骨疏康含药血清,培养5 d后进行抗酒石酸酸性磷酸染色。③将RAW 264.7细胞分5组培养:空白对照组加入正常血清,破骨组加入正常血清与RANKL,高浓度+破骨组加入RANKL+高浓度骨疏康含药血清,破骨+Nrf2激动剂组加入RANKL+t-BHQ,高浓度+破骨+Nrf2抑制剂组加入RANKL+高浓度骨疏康含药血清+ML385,培养5 d后进行Western Blot与活性氧含量检测。结果与结论:①CCK8检测结果显示,骨疏康含药血清及Nrf2抑制剂、激动剂对RAW 264.7细胞活力无明显影响;②抗酒石酸酸性磷酸染色结果显示,骨疏康含药血清呈浓度依赖性抑制破骨细胞的分化;③Western Blot与活性氧含量检测结果显示,与空白对照组比较,破骨组Nrf2蛋白表达降低(P<0.05),c-Fos、NFATc1蛋白表达与活性氧含量升高(P<0.05);与破骨组比较,高浓度+破骨组、破骨+Nrf2激动剂组、高浓度+破骨+Nrf2抑制剂组Nrf2蛋白表达升高、活性氧含量降低(P<0.05),高浓度+破骨组、破骨+Nrf2激动剂组c-Fos、NFATc1蛋白表达降低(P<0.05);与高浓度+破骨组比较,高浓度+破骨+Nrf2抑制剂组Nrf2蛋白表达降低(P<0.05),活性氧含量升高(P<0.05);④结果表明,骨疏康通过激活Nrf2减少活性氧生成,进而抑制下游c-Fos/NFATc1通路表达和破骨细胞分化。 展开更多
关键词 骨质疏松症 骨疏康 含药血清 破骨细胞 Nrf2 c-fos/NFATc1通路 RAW 264.7细胞
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老年心肌梗死患者外周血单个核细胞中c-fos c-myc表达及临床意义
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作者 李新峰 李满生 +2 位作者 蔡华 陈军军 张领 《临床心身疾病杂志》 CAS 2024年第3期36-40,共5页
目的分析老年心肌梗死(MI)患者外周血单个核细胞中c-fos与c-myc表达,并探讨二者与老年MI的关系。方法将78例老年MI患者设为研究1组,73例稳定型心绞痛患者设为研究2组,同期纳入74名健康体检志愿者作为对照组。采用实时荧光定量聚合酶链... 目的分析老年心肌梗死(MI)患者外周血单个核细胞中c-fos与c-myc表达,并探讨二者与老年MI的关系。方法将78例老年MI患者设为研究1组,73例稳定型心绞痛患者设为研究2组,同期纳入74名健康体检志愿者作为对照组。采用实时荧光定量聚合酶链反应检测三组被试者外周血单个核细胞中c-fos、c-myc水平。采用Pearson法分析c-fos、c-myc与血糖、高密度脂蛋白、三酰甘油的相关性,采用Logistic回归分析探讨MI预后的影响因素。结果研究1组被试者血糖水平高于对照组,三酰甘油水平及c-fos、c-myc水平高于研究2组和对照组,高密度脂蛋白水平低于研究2组和对照组;研究2组被试者高密度脂蛋白水平低于对照组,c-fos、c-myc水平高于对照组(P<0.05)。MI患者外周血单个核细胞中c-fos、c-myc水平与血糖、三酰甘油水平均呈正相关(P<0.01),与高密度脂蛋白呈负相关(P<0.01)。预后不良组患者c-fos、c-myc水平、三酰甘油水平高于预后良好组(P<0.01)。Logistic回归分析结果显示,c-fos、c-myc是影响MI患者预后不良的危险因素(P<0.01)。结论老年MI患者外周血单个核细胞中c-fos、c-myc呈高表达,二者与MI病情发展密切相关,c-fos、c-myc对预测老年MI不良预后具有一定的作用。 展开更多
关键词 老年心肌梗死 外周血 单个核细胞 c-fos C-MYC
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推拿对坐骨神经慢性压迫损伤大鼠脊髓背角小胶质细胞P2Y12/RhoA/ROCK2通路及c-Fos蛋白表达的影响
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作者 蒋晶晶 林志刚 +5 位作者 黄红叶 张幻真 陈乐春 林惠 伍诗烨 陈水金 《中国中医药信息杂志》 CAS CSCD 2024年第7期100-105,共6页
目的观察推拿对坐骨神经慢性压迫损伤大鼠脊髓背角小胶质细胞P2Y12/RhoA/ROCK2通路及c-Fos蛋白表达的影响,探讨推拿治疗腰椎间盘突出症的作用机制。方法采用右侧坐骨神经慢性压迫损伤模拟腰椎间盘突出症神经性疼痛。将24只雄性SD大鼠随... 目的观察推拿对坐骨神经慢性压迫损伤大鼠脊髓背角小胶质细胞P2Y12/RhoA/ROCK2通路及c-Fos蛋白表达的影响,探讨推拿治疗腰椎间盘突出症的作用机制。方法采用右侧坐骨神经慢性压迫损伤模拟腰椎间盘突出症神经性疼痛。将24只雄性SD大鼠随机分为空白组、模型组和推拿组,每组8只。造模后第4日,推拿组以按揉法干预,连续14 d。测量造模前及造模后第4、10、17 d大鼠机械缩足阈值(PWT)、热痛阈值(PWL),免疫荧光染色检测大鼠右侧脊髓背角Iba1、P2Y12蛋白表达,Western blot检测右侧脊髓背角RhoA、ROCK2蛋白表达,免疫组化检染色测右侧脊髓背角c-Fos阳性细胞数量。结果与空白组比较,模型组大鼠造模后第4、10、17日PWT、PWL明显降低(P<0.001),右侧脊髓背角Iba1、P2Y12、RhoA、ROCK2蛋白表达明显升高(P<0.001,P<0.05),c-Fos阳性细胞数明显增加(P<0.001);与模型组比较,推拿组大鼠造模后第10、17日PWT、PWL明显升高(P<0.05,P<0.01,P<0.001),右侧脊髓背角Iba1、P2Y12、RhoA、ROCK2蛋白表达明显降低(P<0.001,P<0.01,P<0.05),c-Fos阳性细胞数明显减少(P<0.001)。结论推拿可能通过调控脊髓背角P2Y12/RhoA/ROCK2通路及c-Fos表达抑制小胶质细胞激活,降低神经元兴奋性,对腰椎间盘突出症发挥镇痛作用。 展开更多
关键词 腰椎间盘突出症 推拿 脊髓背角 小胶质细胞 P2Y12/RhoA/ROCK2通路 c-fos 大鼠
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苏葶平喘汤对激素抵抗型哮喘小鼠模型AP-1、c-Fos表达的影响
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作者 宋桂华 周琼阁 +5 位作者 张岩 于素平 孙萌萌 张贵春 张冰雪 彭明浩 《中华中医药学刊》 CAS 北大核心 2023年第2期5-8,共4页
目的探讨苏葶平喘汤对激素抵抗型难治性哮喘小鼠癌蛋白Fos(c-Fos)及血清核转录因子激活蛋白-1(activator protein 1,AP-1)表达的影响,试分析苏葶平喘汤对难治性哮喘的干预机制。方法将50只雌性SPF级BALB/c小鼠随机分为5组,分别为空白组... 目的探讨苏葶平喘汤对激素抵抗型难治性哮喘小鼠癌蛋白Fos(c-Fos)及血清核转录因子激活蛋白-1(activator protein 1,AP-1)表达的影响,试分析苏葶平喘汤对难治性哮喘的干预机制。方法将50只雌性SPF级BALB/c小鼠随机分为5组,分别为空白组(A)、模型组(B)、苏葶平喘汤组(C)、地塞米松组(D)和苏葶平喘汤+地塞米松组(E),每组10只。除空白组外,剩余4组均将小鼠建立为激素抵抗型哮喘模型。药物干预结束后进行取材,利用酶联免疫吸附测定(ELISA)法、实时荧光定量聚合酶链式反应(Real-time PCR)分别检测小鼠血清AP-1、肺组织c-Fos的表达水平。结果1.ELISA检测结果显示:模型组小鼠较空白组小鼠血清中AP-1的值明显增高(P<0.05),苏葶平喘汤组、地塞米松组及苏葶平喘汤+地塞米松组较空白组的小鼠血清AP-1值均降低(P<0.05),其中以苏葶平喘汤+地塞米松组的降低最为显著(P<0.05)。2.PCR检测结果显示:模型组与其余各组相比小鼠肺组织的c-FosmRNA表达明显升高(P<0.05),苏葶平喘汤组、地塞米松组和苏葶平喘汤+地塞米松组c-FosmRNA表达下降(P<0.05),地塞米松组、苏葶平喘汤组和苏葶平喘汤+地塞米松组小鼠的肺组织c-FosmRNA表达水平则无明显差异。结论苏葶平喘汤治疗激素抵抗型哮喘可通过影响AP-1及c-Fos的表达水平来实现抑制哮喘炎症反应控制激素抵抗型哮喘症状的作用。 展开更多
关键词 苏葶平喘汤 激素抵抗型哮喘 AP-1 c-fos 动物实验
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c-Fos、Cyclin-D1、CDK4在乳腺癌中的表达及相关性分析
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作者 胡文慧 居红格 +5 位作者 李峰 张伟 马俊兵 陈鹏 李园园 孙杨 《包头医学院学报》 CAS 2023年第9期1-7,共7页
目的:探讨癌基因c-Fos、细胞周期蛋白D1(cyclin-D1)、细胞周期蛋白依赖性激酶4(CDK4)在乳腺癌及癌旁组织中的表达情况以及其与临床病理特征相关性,并进行生存分析。方法:随机选取20例乳腺癌及癌旁组织进行蛋白印迹实验(western blot,WB... 目的:探讨癌基因c-Fos、细胞周期蛋白D1(cyclin-D1)、细胞周期蛋白依赖性激酶4(CDK4)在乳腺癌及癌旁组织中的表达情况以及其与临床病理特征相关性,并进行生存分析。方法:随机选取20例乳腺癌及癌旁组织进行蛋白印迹实验(western blot,WB)和实时定量反转录聚合酶链反应(real-time quantitative reverse transcription-polymerase chain reaction,RT-qPCR),分别检测乳腺癌组织中c-Fos的蛋白表达和c-Fos、Cyclin-D1、CDK4的mRNA含量;购买乳腺癌组织芯片进行免疫组织化学(immunohistochemistry,IHC)实验,研究c-Fos、Cyclin-D1、CDK4的表达与乳腺癌临床病理特征及预后的关系。结果:WB实验结果提示c-Fos在乳腺癌组织表达高于癌旁组织,差异有统计学意义(P<0.05);RT-qPCR实验结果提示乳腺癌组织中c-Fos mRNA含量与癌旁组织比较差异无统计学意义(P>0.05),乳腺癌组织中Cyclin-D1 mRNA、CDK4 mRNA含量高于癌旁组织,差异有统计学意义(P<0.05);IHC实验表明c-Fos、Cyclin-D1、CDK4在乳腺癌组织中的表达明显高于癌旁组织,差异有统计学意义(P<0.05);癌组织中三者的表达均呈正相关(r=0.320,r=0.486,r=0.514,P<0.05);在乳腺癌组织中,c-Fos的表达与临床分期有关(P<0.05);Cyclin-D1的表达与脉管侵犯有关(P<0.05);CDK4的表达与淋巴结转移有关(P<0.05);生存分析提示三者的高表达是乳腺癌患者总生存时间的危险因素。结论:乳腺癌组织中c-Fos、Cyclin-D1、CDK4高表达并存在正相关性,且与乳腺癌的临床病理特征相关,提示共同参与乳腺癌的发生及发展过程;三者的高表达影响乳腺癌患者的预后。 展开更多
关键词 c-fos CYCLIN-D1 CDK4 乳腺癌 免疫组化 生存分析
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翘嘴鳜早期基因c-fos的分子特征与表达
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作者 张丽欣 梁旭方 武佳琪 《广东海洋大学学报》 CAS CSCD 北大核心 2023年第3期117-123,共7页
【目的】分析翘嘴鳜(Siniperca chuatsi)早期基因c-fos的两个亚型fosaa和fosab的分子特征,探究二者学习记忆功能。【方法】根据翘嘴鳜c-fos编码区设计引物,克隆翘嘴鳜fosab基因,通过翘嘴鳜全基因组数据库获取fosaa基因,用生物信息学分... 【目的】分析翘嘴鳜(Siniperca chuatsi)早期基因c-fos的两个亚型fosaa和fosab的分子特征,探究二者学习记忆功能。【方法】根据翘嘴鳜c-fos编码区设计引物,克隆翘嘴鳜fosab基因,通过翘嘴鳜全基因组数据库获取fosaa基因,用生物信息学分析翘嘴鳜fosaa、fosab的结构特征,用荧光定量PCR检测fosaa、fosab在翘嘴鳜健康组织以及投喂饲料7、56 d后脑组织中的表达量。【结果】fosab全长2498 bp,开放阅读框(ORF)1152 bp,与fosaa基因相同,有4段外显子;二者基因序列差异较大,DNA序列及氨基酸序列相似性分别为40.4%、46.0%。进化树分析显示,翘嘴鳜FOSAB与其他鱼类以及人(Homo sapiens)、褐家鼠(Rattus norvegic)、小鼠(Mus musculus)和野猪(Sus scrofa)等哺乳动物的C-FOS聚为一支,所有动物FOSAA聚为一支,翘嘴鳜FOSAB蛋白与哺乳类动物C-FOS亲缘关系比与FOSAA的关系更近。同线性分析显示,c-fos基因进化较为保守,处于tmed10和jdp基因之间。荧光定量分析表明,翘嘴鳜fosaa和fosab基因在脑和皮肤中均有较高的表达量,fosaa基因在脑中表达量最高,而fosab基因在皮肤中表达量最高。经饲料驯食后,驯化56 d时fosaa基因表达量显著高于驯化7 d(P<0.05),而驯化7、56 d的fosab基因相对表达量无显著差异(P>0.05)。【结论】翘嘴鳜fosaa和fosab基因分子特征差异较大,发挥的功能不尽相同,学习记忆相关基因fosaa在56 d饲料驯食中有重要作用。 展开更多
关键词 c-fos 克隆 组织表达 进化分析 学习记忆
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Research on Acupuncture Regulation of Visual Cortex c-Fos Protein Expression in Monocular Deprivation Cats 被引量:2
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作者 Zhu Tian-tian Ma Chong-bing +3 位作者 Liu An-guo Dong Li-li Wang Jun-yan Yan Xing-ke 《Journal of Acupuncture and Tuina Science》 2013年第3期133-137,共5页
Objective: To explore the mechanism underlying acupuncture regulation of the visual cortex plasticity. Methods: Eighteen kittens of four weeks were randomly divided into 3 groups, a normal group, a model group and ... Objective: To explore the mechanism underlying acupuncture regulation of the visual cortex plasticity. Methods: Eighteen kittens of four weeks were randomly divided into 3 groups, a normal group, a model group and an acupuncture group, with six in each group. There was no treatment to those in the normal group. Unilateral eyelid suture method was used to establish the deprivation amblyopia cat model in the model group and the acupuncture group. After that, kittens in the model group didn't receive any treatment, but those in the acupuncture group were treated with acupuncture therapy of 12 weeks. Pattern Visual Evoked Potential (P-VEP) and c-Fos protein expression of visual cortex of kittens in each group were tested before and after acupuncture treatment. Results: P-VEP waveform changed significantly in kittens of the model group, the time value of P100was significantly delayed (P〈0.01) and N4s-P100 amplitude was significantly lower (P〈0.01) compared with the normal group. After treatment, the time value of P100in kittens of the acupuncture group was significantly shorter (P〈0.01) and N4s-P100 amplitude was significantly higher (P〈0.01) when compared with the model group. Expression of c-Fos positive neurons can be seen in the visual cortex layers II-IV of kittens in the acupuncture group, and the density and percentage of c-Fos immunoreactive neurons of cortex layers II-IV in kittens of the model group were significantly lower than those in the acupuncture group. Conclusion: Acupuncture has obvious improvement for abnormal changes of P-VEP waveform of monocular visual deprivation kittens; it can also increase the c-Fos protein expression in visual cortex after form- deprived. 展开更多
关键词 Acupuncture Therapy AMBLYOPIA Proto-Oncogene proteins c-fos Evoked Potentials Vision
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产前应激对情绪相关脑区c-Fos神经元激活的影响
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作者 李志恒 于鑫 +1 位作者 袁莹 徐志卿 《首都医科大学学报》 北大核心 2023年第6期1014-1021,共8页
目的探讨产前应激(prenatal stress,PS)对抑郁样行为子代大鼠情绪相关脑区c-Fos神经元激活的影响。方法利用产前束缚应激建立抑郁样行为子代大鼠模型。应用免疫荧光染色方法检测正常对照组和PS组大鼠在内侧前额叶皮质(medial prefrontal... 目的探讨产前应激(prenatal stress,PS)对抑郁样行为子代大鼠情绪相关脑区c-Fos神经元激活的影响。方法利用产前束缚应激建立抑郁样行为子代大鼠模型。应用免疫荧光染色方法检测正常对照组和PS组大鼠在内侧前额叶皮质(medial prefrontal cortex,mPFC)脑区、基底外侧杏仁核(basolateral amygdala,BLA)脑区、腹侧海马(ventral hippocampus,VH)脑区和腹外侧中脑导水管周围黑质(ventrolateral periaqueductal gray,vlPAG)脑区等情绪相关脑区的c-Fos与NeuN蛋白的表达并观察上述脑区应激敏感性神经元密度和比例的改变。结果与对照组相比,PS组大鼠mPFC及BLA脑区c-Fos应激敏感性神经元密度和比例降低,VH脑区c-Fos应激敏感性神经元密度降低;vlPAG脑区c-Fos应激敏感性神经元密度不变。结论PS导致子代大鼠mPFC、BLA及VH脑区c-Fos神经元激活密度下降,这种改变可能与抑郁样行为存在相关性。 展开更多
关键词 产前应激 c-fos 情绪相关脑区 抑郁样行为
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Effect of phosphorylation of MAPK and Stat3 and expression of c-fos and c-jun proteins on hepatocarcinogenesis and their clinical significance 被引量:76
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作者 De Yun Feng Hui Zheng +1 位作者 Yi Tan Rui Xue Cheng Department of Pathology, Hunan Medical University, Changsha 410078, Hunan Province, China New England Biolab, MA, USA 《World Journal of Gastroenterology》 SCIE CAS CSCD 2001年第1期33-36,共4页
AIM To study the effect of phosphorylation ofMAPK and Stat3 and the expression of c-fos andc-jun proteins on hepatocellular carcinogenesisand their clinical significance.METHODS SP immunohistochemistry was usedto dete... AIM To study the effect of phosphorylation ofMAPK and Stat3 and the expression of c-fos andc-jun proteins on hepatocellular carcinogenesisand their clinical significance.METHODS SP immunohistochemistry was usedto detect the expression of p42/44MAPK, p-Stat3,c-fos and c-jun proteins in 55 hepatocellularcarcinomas (HCC) and their surrounding livertissues.RESULTS The positive rates and expressionlevels of p42/44MAPK, p-Stat3, c-fos and c-junproteins in HCCs were significantly higher thanthose in pericarcinomatous liver tissues (PCLT).A positive correlation was observed between theexpression of p42/44MAPK and c-fos proteins, andbetween p-Stat3 and c-jun, but there was nosignificant correlation between p42/44MAPK and p-Stat3 in HCCs and their surrounding livertissues.CONCLUSION The abnormalities of Ras/Rat/MAPK and JAKs/ Stat3 cascade reaction maycontribute to malignant transformation ofhepatocytes. Hepatocytes which are positive forp42/ 44MAPK, c-fos or c-jun proteins may bepotential malignant pre-cancerous cells.Activation of MAPK and Stat3 proteins may be anearly event in hepatocellular carcinogenesis. 展开更多
关键词 liver neoplasms MITOGEN-ACTIVATED protein KINASES signal transduction TRANS-ACTIVATORS ONCOGENES immunohistochemistry PRECANCEROUS conditions
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Inhibition of protein degradation increases the Bt protein concentration in Bt cotton 被引量:1
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作者 Yuting Liu Hanjia Li +6 位作者 Yuan Chen Tambel Leila.I.M Zhenyu Liu Shujuan Wu Siqi Sun Xiang Zhang Dehua Chen 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2024年第6期1897-1909,共13页
Bacillus thuringiensis(Bt)cotton production is challenged by two main problems,i.e.,the low concentration of Bt protein at the boll setting stage and the lowest insect resistance in bolls among all the cotton plant’s... Bacillus thuringiensis(Bt)cotton production is challenged by two main problems,i.e.,the low concentration of Bt protein at the boll setting stage and the lowest insect resistance in bolls among all the cotton plant’s organs.Therefore,increasing the Bt protein concentration at the boll stage,especially in bolls,has become the main goal for increasing insect resistance in cotton.In this study,two protein degradation inhibitors(ethylene diamine tetra acetic acid(EDTA)and leupeptin)were sprayed on the bolls,subtending leaves,and whole cotton plants at the peak flowering stage of two Bt cultivars(medium maturation Sikang 1(SK1))and early maturation Zhongmian 425(ZM425)in 2019 and 2020.The Bt protein content and protein degradation metabolism were assessed.The results showed that the Bt protein concentrations were enhanced by 21.3 to 38.8%and 25.0 to 38.6%in the treated bolls of SK1 and ZM425 respectively,while they were decreased in the subtending leaves of these treated bolls.In the treated leaves,the Bt protein concentrations increased by 7.6 to 23.5%and 11.2 to 14.9%in SK1 and ZM425,respectively.The combined application of EDTA and leupeptin to the whole cotton plant increased the Bt protein concentrations in both bolls and subtending leaves.The Bt protein concentrations in bolls were higher,increasing by 22.5 to 31.0%and 19.6 to 32.5%for SK1 and ZM425,respectively.The organs treated with EDTA or/and leupeptin showed reduced free amino acid contents,protease and peptidase activities and significant enhancements in soluble protein contents.These results indicated that inhibiting protein degradation could improve the protein content,thus increasing the Bt protein concentrations in the bolls or/and leaves of cotton plants.Therefore,the increase in the Bt protein concentration without yield reduction suggested that these two protein degradation inhibitors may be applicable for improving insect resistance in cotton production. 展开更多
关键词 Bt cotton Bt protein inhibition of protein degradation protein degradation metabolism
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Major royal-jelly proteins intake modulates immune functions and gut microbiota in mice 被引量:2
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作者 Hang Wu Shican Zhou +7 位作者 Wenjuan Ning Xiao Wu Xiaoxiao Xu Zejin Liu Wenhua Liu Kun Liu Lirong Shen Junpeng Wang 《Food Science and Human Wellness》 SCIE CSCD 2024年第1期444-453,共10页
In this study,we investigated the effects of major royal jelly proteins(MRJPs)on the estrogen,gut microbiota,and immunological responses in mice.Mice given 250 or 500 mg/kg,not 125 mg/kg of MRJPs,enhanced the prolifer... In this study,we investigated the effects of major royal jelly proteins(MRJPs)on the estrogen,gut microbiota,and immunological responses in mice.Mice given 250 or 500 mg/kg,not 125 mg/kg of MRJPs,enhanced the proliferation of splenocytes in response to mitogens.The splenocytes and mesenteric lymphocytes activated by T-cell mitogens(Con A and anti-CD3/CD28 antibodies)released high levels of IL-2 but low levels of IFN-γand IL-17A.The release of IL-4 was unaffected by MRJPs.Additionally,splenocytes and mesenteric lymphocytes activated by LPS were prevented by MRJPs at the same dose as that required for producing IL-1βand IL-6,two pro-inflammatory cytokines.The production of IL-1β,IL-6,and IFN-γwas negatively associated with estrogen levels,which were higher in the MRJP-treated animals than in the control group.Analysis of the gut microbiota revealed that feeding mice 250 mg/kg of MRJPs maintained the stability of the natural intestinal microflora of mice.Additionally,the LEf Se analysis identified biomarkers in the MRJP-treated mice,including Prevotella,Bacillales,Enterobacteriales,Gammaproteobacteria,Candidatus_Arthromitus,and Shigella.Our results showed that MRJPs are important components of royal jelly that modulate host immunity and hormone levels and help maintain gut microbiota stability. 展开更多
关键词 Major royal-jelly proteins Immunity ESTROGEN Gut microbiota Cytokines
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GmSTF accumulation mediated by DELLA protein GmRGAs contributes to coordinating light and gibberellin signaling to reduce plant height in soybean 被引量:1
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作者 Zhuang Li Qichao Tu +7 位作者 Xiangguang Lyu Qican Cheng Ronghuan Ji Chao Qin Jun Liu Bin Liu Hongyu Li Tao Zhao 《The Crop Journal》 SCIE CSCD 2024年第2期432-442,共11页
Plant height influences plant architecture,lodging resistance,and yield performance.It is modulated by gibberellic acid(GA)metabolism and signaling.DELLA proteins,acting as central repressors of GA signaling,integrate... Plant height influences plant architecture,lodging resistance,and yield performance.It is modulated by gibberellic acid(GA)metabolism and signaling.DELLA proteins,acting as central repressors of GA signaling,integrate various environmental and hormonal signals to regulate plant growth and development in Arabidopsis.We examined the role of two DELLA proteins,GmRGAa and GmRGAb,in soybean plant height control.Knockout of these proteins led to longer internodes and increased plant height,primarily by increasing cell elongation.GmRGAs functioned under different light conditions,including red,blue,and far-red light,to repress plant height.Interaction studies revealed that GmRGAs interacted with the blue light receptor GmCRY1b.Consistent with this,GmCRY1b partially regulated plant height via GmRGAs.Additionally,DELLA proteins were found to stabilize the protein GmSTF1/2,a key positive regulator of photomorphogenesis.This stabilization led to increased transcription of GmGA2ox-7b and subsequent reduction in plant height.This study enhances our understanding of DELLA-mediated plant height control,offering Gmrgaab mutants for soybean structure and yield optimization. 展开更多
关键词 DELLA protein GmRGAs GmSTFs Plant height SOYBEAN
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Impact of apolipoprotein E isoforms on sporadic Alzheimer's disease:beyond the role of amyloid beta 被引量:2
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作者 Madia Lozupone Francesco Panza 《Neural Regeneration Research》 SCIE CAS CSCD 2024年第1期80-83,共4页
The impact of apolipoprotein E(ApoE)isoforms on sporadic Alzheimer's disease has long been studied;however,the influences of apolipoprotein E gene(APOE)on healthy and pathological human brains are not fully unders... The impact of apolipoprotein E(ApoE)isoforms on sporadic Alzheimer's disease has long been studied;however,the influences of apolipoprotein E gene(APOE)on healthy and pathological human brains are not fully understood.ApoE exists as three common isoforms(ApoE2,ApoE3,and ApoE4),which differ in two amino acid residues.Traditionally,ApoE binds cholesterol and phospholipids and ApoE isoforms display diffe rent affinities for their receptors,lipids transport and distribution in the brain and periphery.The role of ApoE in the human depends on ApoE isoforms,brain regions,aging,and neural injury.APOE E4 is the strongest genetic risk factor for sporadic Alzheimer's disease,considering its role in influencing amyloid-beta metabolism.The exact mechanisms by which APOE gene variants may increase or decrease Alzheimer's disease risk are not fully understood,but APOE was also known to affect directly and indirectly tau-mediated neurodegeneration,lipids metabolism,neurovascular unit,and microglial function.Consistent with the biological function of ApoE,ApoE4 isoform significantly alte red signaling pathways associated with cholesterol homeostasis,transport,and myelination.Also,the rare protective APOE variants confirm that ApoE plays an important role in Alzheimer's disease pathogenesis.The objectives of the present mini-review were to describe classical and new roles of various ApoE isoforms in Alzheimer's disease pathophysiology beyond the deposition of amyloid-beta and to establish a functional link between APOE,brain function,and memory,from a molecular to a clinical level.APOE genotype also exerted a heterogeneous effect on clinical Alzheimer's disease phenotype and its outcomes.Not only in learning and memory but also in neuro psychiatric symptoms that occur in a premorbid condition.Cla rifying the relationships between Alzheimer's disease-related pathology with neuropsychiatric symptoms,particularly suicidal ideation in Alzheimer's disease patients,may be useful for elucidating also the underlying pathophysiological process and its prognosis.Also,the effects of anti-amyloid-beta drugs,recently approved for the treatment of Alzheimer's disease,could be influenced by the APOE genotype. 展开更多
关键词 Alzheimer's disease AMYLOID-BETA apolipoprotein E DEMENTIA glymphatic transport LIPIDS neuropsychiatric symptoms neurovascular unit tau protein
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The pathogenic mechanism of TAR DNA-binding protein 43(TDP-43)in amyotrophic lateral sclerosis 被引量:1
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作者 Xinxin Wang Yushu Hu Renshi Xu 《Neural Regeneration Research》 SCIE CAS CSCD 2024年第4期800-806,共7页
The onset of amyotrophic lateral sclerosis is usually characterized by focal death of both upper and/or lower motor neurons occurring in the motor cortex,basal ganglia,brainstem,and spinal cord,and commonly involves t... The onset of amyotrophic lateral sclerosis is usually characterized by focal death of both upper and/or lower motor neurons occurring in the motor cortex,basal ganglia,brainstem,and spinal cord,and commonly involves the muscles of the upper and/or lower extremities,and the muscles of the bulbar and/or respiratory regions.However,as the disease progresses,it affects the adjacent body regions,leading to generalized muscle weakness,occasionally along with memory,cognitive,behavioral,and language impairments;respiratory dysfunction occurs at the final stage of the disease.The disease has a complicated pathophysiology and currently,only riluzole,edaravone,and phenylbutyrate/taurursodiol are licensed to treat amyotrophic lateral sclerosis in many industrialized countries.The TAR DNA-binding protein 43 inclusions are observed in 97%of those diagnosed with amyotrophic lateral sclerosis.This review provides a preliminary overview of the potential effects of TAR DNAbinding protein 43 in the pathogenesis of amyotrophic lateral sclerosis,including the abnormalities in nucleoplasmic transport,RNA function,post-translational modification,liquid-liquid phase separation,stress granules,mitochondrial dysfunction,oxidative stress,axonal transport,protein quality control system,and non-cellular autonomous functions(e.g.,glial cell functions and prion-like propagation). 展开更多
关键词 amyotrophic lateral sclerosis axonal transport liquid-liquid phase separation noncellular autonomous functions oxidative stress PATHOGENESIS post-translational modification protein quality control system stress granules TAR DNA-binding protein 43(TDP-43)
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