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兔睫状体上皮的电子探针X射线微分析

Electron probe X-ray microanalysis of rabbit ciliary epithelium.

作者信息

Bowler J M, Peart D, Purves R D, Carré D A, Macknight A D, Civan M M

机构信息

Department of Physiology, University of Otago Medical School, Dunedin, New Zealand.

出版信息

Exp Eye Res. 1996 Feb;62(2):131-9. doi: 10.1006/exer.1996.0017.

Abstract

Rabbit iris-ciliary bodies were preincubated in control and experimental Ringer's solutions before quick freezing, cryosectioning, dehydration and electron probe X-ray microanalysis. After preincubation in a baseline bicarbonate-free Cl- Ringer's solution, the ciliary epithelial intracellular Na+, K+ and Cl- concentrations were estimated to be 15 +/- 3, 162 +/- 14 and 46 +/- 5 mmol kg-1 intracellular water, respectively. The water and elemental Na, K, Cl and P contents were similar in the non-pigmented (NPE) and pigmented (PE) ciliary epithelial cells. As expected, inhibition of the Na,K-exchange pump by preincubation with ouabain markedly increased the intracellular Na content, and markedly reduced the intracellular K content, verifying the validity of the experimental analysis. The Cl- channels of the NPE cells likely play a critical role in determining the rate of aqueous humor formation. Therefore, we have examined the effects of altering Cl- transport on the intracellular composition in this initial microprobe study of the ciliary epithelium. As expected, exposure to bicarbonate increased the intracellular Cl and water contents. Replacement of external Cl- by NO3- was twice as effective as replacement by gluconate in leaching Cl- out of the intracellular compartment. An unexpected finding was that NO3- replacement of internal Cl- substantially increased the intracellular Na and decreased the intracellular K content, possibly by stabilizing the Na,K-pump in the E1P form and inhibiting enzyme activity.

摘要

兔虹膜睫状体在快速冷冻、冰冻切片、脱水及电子探针X射线微分析之前,先在对照和实验林格氏液中进行预孵育。在无碳酸氢盐的Cl-林格氏液中预孵育后,睫状体上皮细胞内Na+、K+和Cl-浓度估计分别为15±3、162±14和46±5 mmol/kg细胞内水。非色素(NPE)和色素(PE)睫状体上皮细胞中的水及元素Na、K、Cl和P含量相似。正如预期的那样,用哇巴因预孵育抑制Na,K-交换泵会显著增加细胞内Na含量,并显著降低细胞内K含量,从而验证了实验分析的有效性。NPE细胞的Cl-通道可能在决定房水生成速率方面起关键作用。因此,在这项关于睫状体上皮的初步微探针研究中,我们研究了改变Cl-转运对细胞内成分的影响。正如预期的那样,暴露于碳酸氢盐会增加细胞内Cl和水含量。用NO3-替代外部Cl-从细胞内室浸出Cl-的效果是用葡萄糖酸盐替代的两倍。一个意外发现是,用NO3-替代细胞内Cl-会显著增加细胞内Na含量并降低细胞内K含量,这可能是通过将Na,K-泵稳定在E1P形式并抑制酶活性实现的。

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