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鸭红细胞对去甲肾上腺素和细胞外钾升高的反应。等渗介质中的体积调节。

The response of duck erythrocytes to norepinephrine and an elevated extracellular potassium. Volume regulation in isotonic media.

作者信息

Kregenow F M

出版信息

J Gen Physiol. 1973 Apr;61(4):509-27. doi: 10.1085/jgp.61.4.509.

Abstract

This paper presents evidence that duck erythrocytes regulate their size in isotonic media by utilizing a previously reported "volume-controlling mechanism." Two different experimental situations are examined. In the first, cells enlarge in a solution containing norepinephrine and an elevated K; and in the second, enlarged cells shrink to their original size if the norepinephrine and excess potassium are removed. As the erythrocytes enlarge, K, Cl, and H(2)O accumulate. Shrinkage, in contrast, is accompanied by the controlled loss of K, Cl, and H(2)O. These changes and the associated changes in membrane permeability resemble those reported previously when duck erythrocytes incubate in anisotonic media. There cells, after first shrinking or swelling, utilize a "volume-controlling mechanism" to reestablish their original size. The mechanism regulates cell size by adjusting the total number of osmotically active intracellular particles. The present studies indicate duck red cells use this mechanism to readjust their total monovalent cation content and thus their solute content in isotonic media as well. In addition, evidence is presented which indicates that the "volume-controlling mechanism" and ouabain-inhibitable cation pump differ functionally.

摘要

本文提供证据表明,鸭红细胞通过利用先前报道的“体积控制机制”在等渗介质中调节其大小。研究了两种不同的实验情况。第一种情况是,细胞在含有去甲肾上腺素和升高的K的溶液中会增大;第二种情况是,如果去除去甲肾上腺素和过量的钾,增大的细胞会收缩至其原始大小。随着红细胞增大,K、Cl和H₂O会积累。相反,收缩伴随着K、Cl和H₂O的受控流失。这些变化以及膜通透性的相关变化类似于先前报道的鸭红细胞在非等渗介质中孵育时的情况。在首次收缩或肿胀后,这些细胞利用“体积控制机制”重新建立其原始大小。该机制通过调节细胞内具有渗透活性的颗粒总数来调节细胞大小。目前的研究表明,鸭红细胞也利用这种机制在等渗介质中重新调整其总单价阳离子含量,从而调整其溶质含量。此外,本文还提供了证据,表明“体积控制机制”和哇巴因抑制性阳离子泵在功能上有所不同。

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本文引用的文献

1
Metabolism of intracellular water.
Physiol Rev. 1960 Jan;40:112-49. doi: 10.1152/physrev.1960.40.1.112.
2
A study of the osmotic behavior of the human erythrocyte.
J Clin Invest. 1959 Sep;38(9):1587-98. doi: 10.1172/JCI103937.

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