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Two outward potassium current types are expressed during the neural differentiation of neural stem cells 被引量:3
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作者 Ruiying Bai Guowei Gao +1 位作者 Ying Xing Hong Xue 《Neural Regeneration Research》 SCIE CAS CSCD 2013年第28期2656-2665,共10页
The electrophysiological properties of potassium ion channels are regarded as a basic index for determining the functional differentiation of neural stem cells.In this study,neural stem cells from the hippocampus of n... The electrophysiological properties of potassium ion channels are regarded as a basic index for determining the functional differentiation of neural stem cells.In this study,neural stem cells from the hippocampus of newborn rats were induced to differentiate with neurotrophic growth factor,and the electrophysiological properties of the voltage-gated potassium ion channels were observed.Immunofluorescence staining showed that the rapidly proliferating neural stem cells formed spheres in vitro that expressed high levels of nestin.The differentiated neurons were shown to express neuron-specific enolase.Flow cytometric analysis revealed that the neural stem cells were actively dividing and the percentage of cells in the S+G2/M phase was high.However,the ratio of cells in the S+G2/M phase decreased obviously as differentiation proceeded.Whole-cell patch-clamp recordings revealed apparent changes in potassium ion currents as the neurons differentiated.The potassium ion currents consisted of one transient outward potassium ion current and one delayed rectifier potassium ion current,which were blocked by 4-aminopyridine and tetraethylammonium,respectively.The experimental findings indicate that neural stem cells from newborn rat hippocampus could be cultured and induced to differentiate into functional neurons under defined conditions in vitro.The differentiated neurons expressed two types of outward potassium ion currents similar to those of mature neurons in vivo. 展开更多
关键词 神经干细胞 分化过程 钾电流 神经元特异性烯醇化酶 类型 钾离子通道 流式细胞仪分析 免疫荧光染色
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西洛他唑对人心房肌细胞瞬间外向钾电流的影响 被引量:5
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作者 肖国胜 廖玉华 《中国应用生理学杂志》 CAS CSCD 北大核心 2004年第3期238-241,共4页
目的 :观察西洛他唑对人心房肌细胞瞬间外向钾电流 (Ito1)的影响 ,探讨该药抗心律失常作用的机制。方法 :二步酶解法分离人单个右心房肌细胞 ,应用全细胞膜片钳技术记录人心房肌细胞Ito1。结果 :在保持电位 - 5 0mV和去极化脉冲为 +5 0m... 目的 :观察西洛他唑对人心房肌细胞瞬间外向钾电流 (Ito1)的影响 ,探讨该药抗心律失常作用的机制。方法 :二步酶解法分离人单个右心房肌细胞 ,应用全细胞膜片钳技术记录人心房肌细胞Ito1。结果 :在保持电位 - 5 0mV和去极化脉冲为 +5 0mV条件下 ,30 μmol/L西洛他唑显著降低Ito1,使Ito1幅值由加药前 (8.16± 0 .70 ) pA/pF降至 (4 .84±0 .6 0 )pA/ pF(P <0 .0 1)。西洛他唑在 1~ 5 0 μmol/L范围内呈浓度依赖性的抑制Ito1,1μmol/L时即产生作用 ,5 0μmol/L时达最大效应 (降低 5 1.0 9%± 3.0 0 % ) ,IC50 为 (13.18± 2 .6 0 ) μmol/L。此外 ,该药对Ito1的电压依赖性激活和失活曲线以及恢复曲线均无显著影响。结论 展开更多
关键词 西洛他唑 瞬间外向钾电流 人心房肌 离子通道 膜片钳技术
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Crim1过表达抑制肥大乳鼠心室肌细胞瞬时外向钾电流改变 被引量:1
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作者 何炯红 邓娜 +5 位作者 杨龙 唐倩 夏桂玲 杨英 黄勇淇 赵义冬 《国际心血管病杂志》 2019年第6期346-350,共5页
目的:探讨半胱氨酸丰富跨膜成骨蛋白调控因子(Crim1)对肥大乳鼠心室肌细胞瞬时外向钾电流(Ito)的调控作用.方法:将1d龄SD乳鼠心室肌细胞培养48 h后分组干预.重组腺病毒空载体(Ad-null)组给予Ad-null感染细胞32 h.重组腺病毒空载体+苯肾... 目的:探讨半胱氨酸丰富跨膜成骨蛋白调控因子(Crim1)对肥大乳鼠心室肌细胞瞬时外向钾电流(Ito)的调控作用.方法:将1d龄SD乳鼠心室肌细胞培养48 h后分组干预.重组腺病毒空载体(Ad-null)组给予Ad-null感染细胞32 h.重组腺病毒空载体+苯肾上腺素(Ad-null+PE)组予Ad-null感染细胞8h后,再予苯肾上腺素(PE)干预24 h.Crim1过表达重组腺病毒+苯肾上腺素(Ad-Crim1+PE)组给予携带Crim1基因的重组腺病毒感染细胞8h后,再予PE干预24 h.结晶紫染色培养细胞,ImageJ软件计算细胞表面积.全细胞膜片钳技术检测Ito,计算电流密度.结果:PE干预诱导心室肌细胞肥大,减小Ito电流密度;该效应可被过表达Crim1所抑制.结论:过表达Crim1可抑制PE诱导的心室肌细胞肥大及Ito改变. 展开更多
关键词 心室肥大 半胱氨酸丰富跨膜成骨蛋白调控因子 瞬时外向钾电流 离子通道
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