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离子转运

离子转运的相关文献在1986年到2022年内共计164篇,主要集中在内科学、细胞生物学、基础医学 等领域,其中期刊论文103篇、会议论文1篇、专利文献253053篇;相关期刊84种,包括生物化学与生物物理进展、生理科学进展、肾脏病与透析肾移植杂志等; 相关会议1种,包括中华中医药学会脾胃病分会第二十四次全国脾胃病学术交流会等;离子转运的相关文献由396位作者贡献,包括毛裕民、谢毅、M·F·卡罗兰等。

离子转运—发文量

期刊论文>

论文:103 占比:0.04%

会议论文>

论文:1 占比:0.00%

专利文献>

论文:253053 占比:99.96%

总计:253157篇

离子转运—发文趋势图

离子转运

-研究学者

  • 毛裕民
  • 谢毅
  • M·F·卡罗兰
  • 刘晶
  • 张显
  • 徐美娟
  • 杨套伟
  • 饶志明
  • 余玲
  • 卢丽丽
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 邢磊; 王文磊; 徐燕; 纪德华; 许凯; 陈昌生; 谢潮添
    • 摘要: 从离子实时动态转运的角度出发,分析坛紫菜应答低盐胁迫的策略.研究结果表明:1)坛紫菜在正常状态下吸收K+、Na+以维持自身稳态;在低盐胁迫下,坛紫菜藻体的Na+显著外排,以积极应对外界低渗环境,同时,藻体的K+虽然有一定流失,但显著低于高盐胁迫条件下的K+外排幅度,使坛紫菜能够维持较高的K+/Na+,从而保证坛紫菜可以适应盐度5的环境条件.2)加入Na+/H+逆向转运蛋白抑制剂阿米洛利后,并不能显著抑制坛紫菜藻体Na+的外排,表明低盐胁迫下藻体并不是通过质膜质子泵驱动Na+/H+逆向转运蛋白将Na+排出藻体,可能通过非选择性阳离子通道外排Na+至细胞外.3)加入质膜质子泵抑制剂钒酸钠后,藻体K+的流速并没有受钒酸钠影响,初步说明低盐胁迫下坛紫菜K+的流失并不是通过去极化激活的外向通道来完成.这从离子动态的角度证明了低盐胁迫下坛紫菜排钠保钾的方式和应答高盐胁迫时存在明显区别.
    • 韩晓春; 吕佳楗; 顾良臻; 田升; 杨哲; 张璐; 郭良清; 赵海军; 王世军
    • 摘要: 目的 探讨脾虚湿阻证大鼠离子转运功能变化及薏苡仁健脾利湿作用机制.方法 通过游泳致劳联合特制饲料方法构建脾虚湿阻证动物模型,将模型大鼠随机分为6组,除模型组外其余各组分别采用薏苡仁水煎液(6.25 g/kg)及不同组分(薏苡仁油287.5 mg/kg、薏苡仁多糖911.3 mg/kg、薏苡仁蛋白281.3 mg/kg、薏苡仁淀粉1798.1 mg/kg)每日灌胃1次进行干预,另取10只正常大鼠为对照组.干预14 d后,采集小肠标本,以Agilent公司全基因组表达谱芯片检测大鼠肠道全基因表达,筛选模型组和对照组离子转运功能(ion transport)差异基因后,对各组差异基因进行主成分分析和聚类分析,并对主成分分析的载荷和得分进行Bi分析.结果 模型大鼠与对照大鼠离子转运功能差异基因为38条;对差异基因主成分分析的载荷和得分进行Bi分析,其二维投影显示模型组与对照组最远,与样本聚类结果一致,而采用薏苡仁不同组分治疗后,各治疗组均处于模型组和对照组之间;从其差异基因的作用权重来看,各差异基因作用效果不同,位居前10的是Atox1、Slc5a4、Slc40a1、Slc5a1、Slc11a2、Cftr、Fxyd5、Cacna1i、Kcnj13、Atp5d,而这些差异基因在聚类分析中也多处于同一类.结论 模型大鼠肠上皮细胞存在明显离子转运功能家族基因改变,薏苡仁的不同组分、尤其是油组分和蛋白组分在离子转运功能上作用效果较强,溶质载体Slc家族是其发挥健脾利湿作用的主要靶点,Atox1和Cftr也在健脾利湿中发挥了重要作用.
    • Yu Shoushui; Wang Gangping; Leng Jing; Zhao Tao; Wang Shilei; Wang Yong
    • 摘要: Objective To evaluate the role of mitochondrial calcium uniporter ( MCU) in mitoph-agy in SH-SY5Y cells subjected to oxygen-glucose deprivation and restoration (OGD∕R). Methods SH-SY5Y cells were cultured in vitro, seeded in 96-well plates at a density of 2×105cells∕ml, and randomly di-vided into 4 groups (n=6 each) using a random number table method: control group (group C), group OGD∕R, OGD∕R plus MCU inhibitor group ( group OGD∕R + Ru360) and MCU inhibitor group ( group Ru360) . Cells were cultured in normal culture medium in group C. Cells were subjected to O2-glucose dep-rivation for 6 h followed by restoration of O2-glucose supply for 24 h in group OGD∕R. In group OGD∕R+Ru360, Ru360 at a final concentration of 10 μmol∕L was added at 30 min before O2-glucose deprivation, and the other treatments were similar to those previously described in group OGD∕R. Ru360 was added at a final concentration of 10 μmol∕L, and 30 min later cells were cultured under normoxic conditions in group Ru360. At 24 h of restoration of O2-glucose supply, cell counting kit-8 assay was used to detect the cell survival rate, JC-1 assay was used to detect mitochondrial membrane potential ( MMP ) , the ultrastructure of cells was observed with a transmission electron microscope, and the expression of p62, Tom20 and Bec-lin-1 was detected by Western blot. Results Compared with group C, no significant change was found in each parameter in group Ru360 ( P>0. 05) , the cell survival rate and MMP were significantly decreased, the expression of Tom20 and p62 was down-regulated, Beclin-1 expression was up-regulated (P0.05),OGD∕R组细胞存活率和MMP下降,Tom20和p62表达下调,Beclin-1表达上调(P<0.01),线粒体肿胀,线粒体自噬体增多;与OGD∕R组比较,OGD∕R+Ru360组细胞存活率和MMP升高,Tom20和p62表达上调,Beclin-1表达下调(P<0.01),线粒体形态较完整,线粒体自噬体数量减少.结论 MCU参与了氧糖剥夺-复氧复糖SH-SY5Y细胞线粒体自噬的过程.
    • 闫改各; 周建
    • 摘要: 为探索外源水杨酸(SA)对盐碱胁迫下海滨锦葵生长与Na+富集特性的影响,在不同盐碱胁迫下,以0.5 mmol/L和1.5 mmol/L的SA对海滨锦葵幼苗进行叶面喷施处理,测定其植株株高、地径、干质量、组织Na+含量及Na+转移系数.结果表明:SA对海滨锦葵幼苗的生长起抑制作用,并促进了Na+在叶和根部富集,降低其在茎部富集,从而提高了Na+向根、叶部的转移,其中0.5 mmol/L的SA作用效果更显著.
    • 吴元圣; 李雄; 杨永平; 杨永红
    • 摘要: 该研究以芜菁(Brassica rapa var.rapa)为材料,克隆得到重金属ATP酶(HMA)家族1对同源基因BrrHMA2.1(GenBank登录号:MG_283237)和BrrHMA2.2(GenBank登录号:MG_283238),并对其蛋白质序列特征和基因表达模式进行分析.结果表明:(1) BrrHMA2.1和BrrHMA2.2基因的全长开放阅读框分别为2 619和2 724 bp,分别编码872和907个氨基酸;序列结构分析显示,BrrHMA2.1和BrrHMA2.2蛋白含有6个跨膜区和HMA蛋白家族保守结构域;系统进化树结果显示,BrrHMA2.1和BrrHMA2.2蛋白与拟南芥HMA家族成员AtHMA2进化关系最近.(2)亚细胞定位结果表明,BrrHMA2.1和BrrHMA2.2蛋白都定位于细胞膜上.(3)qRT-PCR分析表明,芜菁生长初期BrrHMA2.1和BrrHMA2.2基因在叶中的表达量最高;随着生长时间的延长,叶中的表达量逐渐降低,而根中的表达量逐渐增加.(4)研究发现,BrrHMA2.1受Cd2+、Zn2+、Na+、Mg2+胁迫诱导表达,BrrHMA2.2受Cd2+、Na+、Cu2+胁迫诱导表达,表明2个基因可能参与这些金属离子的转运过程.该研究结果为进一步研究植物HMA基因在重金属吸收和转运过程中的功能奠定了基础.%In the present study,a pair of homologous genes BrrHMA2.1 (GenBank is MG_283237) and BrrHMA2.2 (GenBank is MG_283238) of the heavy metal ATPase (HMA) family in turnip (Brassica rapa var.rapa) was cloned and their protein sequence characteristics and gene expression patterns were analyzed.(1) The full-length open reading frames of these two genes were 2 619 and 2 724 bp and they encoded 872 and 907 amino acids,respectively.Sequence structure analysis showed that both BrrHMA2.1 and BrrHMA2.2 proteins included six transmembrane regions and conserved domains of HMA family.Phylogenetic tree analysis showed that BrrHMA2.1 and BrrHMA2.2 proteins had the closest evolutionary homology with AtHMA2.(2) The results of subcellular localization indicated that both BrrHMA2.1 and BrrHMA2.2 proteins were localized in the plasma membrane.(3) qRT-PCR analysis showed that the expression levels of BrrHMA2.1 and BrrHMA2.2 genes were much higher in leaves at the early stage of turnip.However,the expression levels of these two genes in leaves gradually decreased whereas those in roots gradually increased with the increasing growth time.In addition,the results also found that BrrHMA2.1 gene was induced by Cd2+,Zn2+,Na+ and Mg2+ while BrrHMA2.2 gene was induced by Cd2+,Na+ and Cu2+ stresses,indicating these two genes may play roles in coping with these metal ions.This study provides foundation for further functional studies on plant HMA genes in heavy metal tolerance or transport.
    • 陈红霞
    • 摘要: 为了有效防治动物寄生虫病,要适时对动物进行动物抗寄生虫药的注射和喂食,有效维护畜牧业健康发展,提高公共卫生安全管理水平.而要想维护抗寄生虫药物的药效,就要对其作用机理有一定的认知,从而制订契合实际情况的治疗计划.基于此,本文简要分析动物抗寄生虫药物酶的作用机理,并集中讨论影响物质代谢及离子转运的机理.
    • 刘杰; 耿淑娟
    • 摘要: 以向日葵品种白葵杂6号为试验材料,中性盐NaCl、Na2 SO4按摩尔比9:1混合模拟盐胁迫,通过测定其木质部液的成分来探讨盐胁迫对向日葵木质部液中离子转运的影响.结果表明,向日葵的子叶节区对离子的向上运输具有截流作用,尤其是Na+;同时,盐胁迫下,向日葵保持了较高的K+吸收率及贡献率,从而使向日葵体内保持高K低Na状态,这可能是向日葵抗盐性高于其他作物的主要原因.
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