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Relationship of Intracellular Free Ca^(2+) Concentration and Calcium-activated Chloride Channels of Pulmonary Artery Smooth Muscle Cells in Rats under Hypoxic Conditions 被引量:3
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作者 杨朝 张珍祥 +2 位作者 徐永健 李亚清 叶涛 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2006年第2期172-174,191,共4页
To investigate the relationship between intracellular free Ca^2+ concentration ([Ca^2+ ]i ) and calcium-activated chloride (Clca) channels of pulmonary artery smooth muscle cells (PASMCs) in rats under acute a... To investigate the relationship between intracellular free Ca^2+ concentration ([Ca^2+ ]i ) and calcium-activated chloride (Clca) channels of pulmonary artery smooth muscle cells (PASMCs) in rats under acute and chronic hypoxic conditions, acute hypoxia-induced contraction was observed in rat pulmonary artery by using routine blood vascular perfusion in vitro. The fluorescence Ca^2+ indicator Fura-2/AM was used to observe [Ca^2+ ]i of rat PASMCs under normal and chronic hypoxic condition. The effect of Clca channels on PASMCs proliferation was assessed by MTT assay. The Clca channel blockers niflumic acid (NFA) and indaryloxyacetic acid (IAA-94) exerted inhibitory effects on acute hypoxia-evoked contractions in the pulmonary artery. Under chronic hypoxic condition, [Ca^2+ ]i was increased. Under normoxic condition, [Ca^2+ If was (123.634-18.98) nmol/ L, and in hypoxic condition, [Ca^2+]i wag (281. 754-16.48) nmol/L (P〈0. 01). Under normoxic condition, [Ca^2+ ]i showed no significant change and no effect on Clca channels was observed (P〉 0. 05). Chronic hypoxia increased [Ca^2+ ]i which opened Clca channels. The NFA and IAA-94 blocked the channels and decreased [Ca^2+ ]i from (281.75± 16.48) nmot/L to (117.66 ±15.36) nmol/L (P〈0.01). MTT assay showed that under chronic hypoxic condition NFA and IAA-94 decreased the value of absorbency (A value) from 0. 459±0. 058 to 0. 224±0. 025 (P〈0. 01). Hypoxia increased [Ca^2+ ]i which opened Cl~ channels and had a positive-feedback in [Ca^2+ ]i. This may play an important role in hypoxic pulmonary hypertension. Under chronic hypoxic condition, Clca channel may play a part in the regulation of proliferation of PASMCs. 展开更多
关键词 Ca^2+-activated Cl^- channels intracellular free Ca^2+ concentration pulmonary artery smooth muscle HYPOXIA
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体外培养小鼠小肠Cajal间质细胞的电生理学特性 被引量:1
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作者 张扬 朴莲花 +3 位作者 黄旭 韩燕飞 赵鹏 许文燮 《上海交通大学学报(医学版)》 CAS CSCD 北大核心 2007年第11期1301-1304,共4页
目的采用膜片钳技术观察体外培养的小鼠Cajal间质细胞(ICC)的电生理学特性,为进一步研究不同种类ICC的功能奠定实验基础。方法用C-Kit染色法对ICC进行形态学鉴定后,分别在全细胞模式、膜内向外和细胞吸附的钳制模式下,观察胞内低钙和钙... 目的采用膜片钳技术观察体外培养的小鼠Cajal间质细胞(ICC)的电生理学特性,为进一步研究不同种类ICC的功能奠定实验基础。方法用C-Kit染色法对ICC进行形态学鉴定后,分别在全细胞模式、膜内向外和细胞吸附的钳制模式下,观察胞内低钙和钙调蛋白抑制剂对ICC起搏电流的影响。结果免疫学鉴定结果表明,培养的大部分细胞均为ICC。在全细胞模式下,高浓度钙鳌合剂使细胞内游离钙浓度降低后,可以激活持续性内向电流;在膜内向外的膜片钳模式下,当灌流液中钙浓度由1μmol/L降低到0.1μmol/L时,激活幅度大和频率快的自发性内向电流;在全细胞模式下,钙调蛋白抑制剂(W-7)可以激活持续性内向电流的同时增加自发性内向电流的幅度;在细胞吸附模式下,W-7激活幅度大和频率快的自发性内向电流。另一种细胞电生理学特性却不受细胞内低钙环境和W-7的影响。结论在培养的ICC中对细胞内低钙和W-7敏感的细胞可能就是具有起搏功能的肌层间ICC,而对细胞内低钙和W-7不敏感细胞可能就是不具有起搏功能的肌间ICC。 展开更多
关键词 CAJAL间质细胞 钙调蛋白抑制剂 胞内游离钙
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Studies on the Effects of Epimedium Extract on Erythrocytes 被引量:3
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作者 Xiao Yu ZHANG Feng Hua CHEN +1 位作者 Ping Hui WEI Jia Zuan NI 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第8期1105-1108,共4页
The effect of Epimedium extract (EE) on erythrocytes was investigated by atomic force microscopy (AFM). The images of the surface structures showed clear concave and progressive increase of surface roughness of er... The effect of Epimedium extract (EE) on erythrocytes was investigated by atomic force microscopy (AFM). The images of the surface structures showed clear concave and progressive increase of surface roughness of erythrocyte after incubation with EE at concentration of 0.2 or 0.05 g/L, far below its critical hemolytic levels. The AFM results also indicated that the granules of the fine surface structure increased, which caused by aggregation of membrane protein. Further study showed that the change in surface topography of erythrocyte membrane might be connected with the increase of intracellular free Ca^2+ induced by EE. 展开更多
关键词 AFM Epimedium extract (EE) ERYTHROCYTE intracellular free Ca^2+.
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