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国家自然科学基金(81000107)

作品数:2 被引量:11H指数:2
相关作者:陈文轩刘慧荣祝红闫莉谭晓秋更多>>
相关机构:中国医学科学院北京协和医学院中国人民大学首都医科大学更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划更多>>
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Effect of Active Immunization with Peptides Corresponding to the Second Extracellular Loop of Alpha1-Adrenoceptor on Vascular Structure and Function in Rats
Aims:Autoantibody against the second extracellular loop ofα-adrenoceptor(α-AA) which had been found in hyperte...
Li Yan,Xiu-Li Cheng,Fan Ding,Yun-Hui Du,Hui-Rong Liu,Ji-Min Cao 1 Department of Physiology and Pathophysiology,Institute of Basic Medical Sciences,Chinese Academy of Medical Sciences,School of Basic Medicine,Peking Union Medical College,Beijing 100005,P.R.China
关键词:AUTOANTIBODY
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自发性高血压大鼠血管对α_1肾上腺素受体自身抗体的血管收缩作用敏感性增强被引量:2
2014年
自身免疫学机制在高血压的发生发展中具有不可忽视的作用.本研究组的前期研究表明,高血压患者血清中存在高水平的α1肾上腺素受体自身抗体(α1-AA),并对正常大鼠具有α1-AR激动剂样缩血管效应.本研究利用血管环张力测定技术观察并比较该抗体对自发性高血压大鼠(SHR)和Wistar-Kyoto(WKY)大鼠胸主动脉的收缩作用,分别采用酶联免疫吸附测定、免疫组化和免疫印迹技术观察主动脉中硝基酪氨酸和诱导性一氧化氮合酶(iNOS)的表达情况.结果表明,自发性高血压大鼠胸主动脉对去氧肾上腺素(α1-AR特异性激动剂)与α1-AA(1 nmol/L^10μmol/L)的缩血管作用明显增强(P<0.05);去除内皮或利用非特异性一氧化氮合酶阻断剂(L-NAME)后,α1-AA的缩血管作用明显增强(P<0.05).iNOS特异性阻断剂1400W(10μmol/L)可以削弱上述WKY大鼠胸主动脉收缩的增强作用,而在SHR未观察到.SHR胸主动脉组织中硝基酪氨酸和iNOS的蛋白表达水平明显高于WKY大鼠.本研究结果表明,SHR对α1-AA的缩血管反应明显增强,这一变化与血管内皮功能障碍以及NO生物利用率降低有关,提示α1-AR自身免疫在高血压的发病机制和控制中,尤其是对α1-AA阳性的高血压患者发挥重要作用.
闫莉谭晓秋陈文轩祝红曹济民刘慧荣
关键词:肾上腺素受体血管蛋白质硝基化高血压
促离子型谷氨酸受体介导RAW264.7巨噬细胞释放TNF-α
目的外周谷氨酸信号通路与炎症和动脉粥样硬化的关系尚不明确。该工作探讨促离子型谷氨酸受体与RAW264.7巨噬细胞释放促炎细胞因子TNF-α的关系。方法将RAW264.7细胞分成正常对照组、谷氨酸单钠组(10 ML-glu...
程秀丽丁帆闫莉谷婧丽郝维高雪曹济民
关键词:谷氨酸受体RAW264.7巨噬细胞TNF-Α
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Endothelial modulation of the alpha1 adrenoceptor autoantibody-induced arterial contraction in spontaneously hypertensive rats
Background:Growing evidence indicates that primary or secondary activation of immune mechanisms have been impl...
Zhong-Hua DAI~1,Li YAN~1,Guang-Zhao YANG~2,Su-Li ZHANG~2,Hui-Rong LIU~(2,3),Ji-Min CAO ~1 1 Department of Physiology and Pathophysiology,Institute of Basic Medical Sciences,Chinese Academy of Medical Sciences,School of Basic Medicine,Peking Union Medical College,Beijing 100005,China
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Enhanced vasoconstriction to α_1 adrenoceptor autoantibody in spontaneously hypertensive rats被引量:10
2014年
Autoimmune activities have been implicated in the pathogenesis of hypertension.High levels of autoantibodies against the second extracellular loop of α1-adrenoceptor(α1-AR autoantibody,α1-AA) are found in patients with hypertension,and α1-AA could exert a α1-AR agonist-like vasoconstrictive effect.However,whether the vasoconstrictive effect of α1-AA is enhanced in hypertension is unknown.Using aortic rings of spontaneously hypertensive rats(SHR) and normotensive Wistar-Kyoto(WKY) rats,we observed the vasoconstrictive responses to α1-AA with phenylephrine(α1-AR agonist) as a positive control drug.Aortic nitrotyrosine levels were also measured by ELISA and immunohistochemistry.The results showed that the aortic constrictive responses to α1-AA and phenylephrine(both 1 nmol L-1-10 μmol L-1) were greater in SHR than in WKY rats.Endothelial denudation or L-NAME(a non-selective NOS inhibitor)(100 μmol L-1) increased α1-AA- or phenylephrine-induced vasoconstrictions both in SHR and WKY.However,selective iNOS inhibitor 1400W(10 μmol L-1) enhanced the α1-AA-induced aortic constriction in WKY,but not in SHR.The aortic nitrotyrosine level was significantly higher in SHR than WKY,as shown by both ELISA and immunohistochemistry.These results indicate that the vasoconstrictive response to α1-AA is enhanced in SHR,and this altered responsiveness is due to endothelial dysfunction and decreased NO bioavailability.The study suggests an important role of α1-AR autoimmunity in the pathogenesis and management of hypertension especially in those harboring high α1-AA levels.
YAN LiTAN XiaoQiuCHEN WenXuanZHU HongCAO JiMinLIU HuiRong
关键词:AUTOIMMUNITYENDOTHELIUM
Altered Endothelial Modulation of Vasoconstriction to Alphal Adrenoceptor Autoantibodies in Spontaneously Hypertensive Rats:a Potential Mechanism for Primary Hypertension Development
Objective Primary or secondary activation of immune mechanisms has been implicated in the pathogenesis of hype...
Li YAN~1,Yun-hui DU~2,Zhong-mei HE~3,Hui-rong LIU~(2,3),Ji-min CAO~1 (1.Department of Physiology and Pathophysiology,Institute of Basic Medical Sciences Chinese Academy of Medical Sciences,School of Basic Medical Sciences Peking Union Medical College,Beijing 100005,China
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