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首页> 外文期刊>Archives of Insect Biochemistry and Physiology >Fractional contribution of major ions to the membrane potential of Drosophila melanogaster oocytes
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Fractional contribution of major ions to the membrane potential of Drosophila melanogaster oocytes

机译:主要离子对果蝇卵母细胞膜电位的部分贡献

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In ovarian follicles of Drosophila melanogaster, ion substitution experiments revealed that K(+) is the greatest contributor (68%) in setting oocyte steady-state potential (E(m)), while Mg(2+) and a metabolic component account for the rest. Because of the intense use made of Drosophila ovarian follicles in many lines of research, it is important to know how changes in the surrounding medium, particularly in major diffusible ions, may affect the physiology of the cells. The contributions made to the Drosophila oocyte membrane potential (E(m)) by [Na(+)](o), [K(+)](o), [Mg(2+)](o), [Ca(2+)](o), [Cl(-)](o), and pH (protons) were determined by substitutions made to the composition of the incubation medium. Only K(+) and Mg(2+) were found to participate in setting the level of E(m). In follicles subjected to changes in external pH from the normal 7.3 to either pH 6 or pH 8, E(m) changed rapidly by about 6 mV, but within 8 min had returned to the original E(m). Approximately half of all follicles exposed to reduced [Cl(-)](o) showed no change in E(m), and these all had input resistances of 330 kOmega or greater. The remaining follicles had smaller input resistances, and these first depolarized by about 5 mV. Over several minutes, their input resistances increased and they repolarized to a value more electronegative than their value prior to reduction in [Cl(-)](o). Together, K(+) and Mg(2+) accounted for up to 87% of measured steady-state potential. Treatment with sodium azide, ammonium vanadate, or chilling revealed a metabolically driven component that could account for the remaining 13%.
机译:在果蝇的卵泡中,离子替代实验表明,K(+)是设定卵母细胞稳态电位(E(m))的最大贡献者(68%),而Mg(2+)和代谢成分占其余的部分。由于果蝇卵巢卵泡在许多研究领域都得到了广泛使用,因此了解周围介质(尤其是主要的可扩散离子)的变化如何影响细胞的生理至关重要。 [Na(+)](o),[K(+)](o),[Mg(2 +)](o),[Ca(对果蝇卵母细胞膜电位(E(m))的贡献) 2 +)](o),[Cl(-)](o)和pH(质子)是通过对孵育培养基的组成进行替换来确定的。发现只有K(+)和Mg(2+)参与设定E(m)的水平。在受到外部pH从正常7.3更改为pH 6或pH 8的卵泡中,E(m)迅速变化约6 mV,但在8分钟内恢复到原始E(m)。暴露于还原的[Cl(-)](o)的所有卵泡中大约有一半的E(m)没有变化,并且所有这些都具有330 kOmega或更大的输入电阻。其余的滤泡输入电阻较小,并且首先将它们去极化约5 mV。在几分钟内,它们的输入电阻增加,并且它们的极化强度比[Cl(-)](o)减小之前的负电性更大。 K(+)和Mg(2+)总计占测量的稳态电势的87%。用叠氮化钠,钒酸铵或冷水处理表明,由代谢驱动的成分可能占剩余的13%。

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