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在部分抑制钠钾泵后,周期性钠离子进入葡萄糖刺激的胰腺β细胞的现象被揭示。

Unmasking of a periodic Na+ entry into glucose-stimulated pancreatic beta-cells after partial inhibition of the Na/K pump.

作者信息

Grapengiesser E

机构信息

Department of Medical Cell Biology, Uppsala University, Sweden.

出版信息

Endocrinology. 1998 Jul;139(7):3227-31. doi: 10.1210/endo.139.7.6106.

Abstract

The cytoplasmic concentration of Na+ ([Na+]i) was measured in individual mouse beta-cells using dual wavelength microfluorometry and the indicator sodium-binding benzofuran isophtalate. Under conditions known to induce large amplitude oscillations in cytoplasmic Ca2+ (1.3 mM Ca2+; 11 mM glucose), [Na+]i remained low and stable at 10-14 mM. Partial suppression of the Na/K pump with 50 microM ouabain resulted in oscillations of [Na+]i in 65% of the cells (frequency, 0.13+/-O.O1 min(-l); amplitude, 4.4 +/-0.3 mM). The oscillations were unaffected by the presence of 3 microM tetrodotoxin, but disappeared when the medium was depleted of Ca2+ or supplemented with 10 microM methoxyverapamil. The analysis of the ouabain effect was facilitated by replacing extracellular Ca2+ with 5 mM Sr2+. In the Sr2+-containing medium, oscillations of [Na+]i were seen in more than 70% of the beta-cells exposed to 11 mM glucose. Ouabain (50 microM) modified the [Na+]i oscillations by increasing their amplitudes almost 3-fold and reducing the frequency from once every 3 min to once every 10 min. A relationship between oscillations of cytoplasmic Sr2+ and Na+ was apparent both from observations of similar frequencies and for the modifications obtained with ouabain. It is concluded that the glucose-induced oscillations of cytoplasmic Ca2+ result in a rhythmic entry of Na+, usually balanced by the Na/K pump. A resulting periodic consumption of ATP in the Na/K pump might have implications for the release of insulin by affecting ATP-dependent processes associated with the plasma membrane.

摘要

利用双波长显微荧光测定法和指示剂钠结合苯并呋喃异邻苯二甲酸酯,在单个小鼠β细胞中测量了钠离子的胞质浓度([Na⁺]i)。在已知会诱导胞质钙离子大幅振荡的条件下(1.3 mM Ca²⁺;11 mM葡萄糖),[Na⁺]i保持在10 - 14 mM的低水平且稳定。用50 μM哇巴因部分抑制钠钾泵,导致65%的细胞中[Na⁺]i出现振荡(频率,0.13 ± 0.01 min⁻¹;振幅,4.4 ± 0.3 mM)。这些振荡不受3 μM河豚毒素存在的影响,但当培养基中钙离子耗尽或添加10 μM甲氧基维拉帕米时会消失。用5 mM Sr²⁺替代细胞外钙离子有助于分析哇巴因的作用。在含Sr²⁺的培养基中,超过70%暴露于11 mM葡萄糖中的β细胞出现了[Na⁺]i振荡。哇巴因(50 μM)改变了[Na⁺]i振荡,使其振幅几乎增加了3倍,频率从每3分钟一次降低到每10分钟一次。从相似频率的观察以及用哇巴因获得的变化来看,胞质Sr²⁺和Na⁺的振荡之间的关系很明显。得出的结论是,葡萄糖诱导的胞质钙离子振荡导致钠离子有节奏地进入,通常由钠钾泵平衡。钠钾泵中由此产生的ATP周期性消耗可能通过影响与质膜相关的ATP依赖过程对胰岛素释放产生影响。

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