Movements of Na∗ and K+ in slices of herring-gull salt gland

G.D.V. Van Rossum
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引用次数: 18

Abstract

  • 1.

    1. Fresh slices of salt gland from the herring gull contained approx. 290 mmoles 3+ and 350 mmoles Na+ per kg dry weight.

  • 2.

    2. During incubation at 1° for up to 4 h there was a loss of some 75 mmoles K+ per kg dry weight and an equivalent gain of Na+; the slices did not swell significantly. The loss of K+ was not increased by incubation at 1° in a K+-free medium.

  • 3.

    3. The rate of 24Na+ efflux from the slices and the ability of the slices to maintain their Na+ and K+ contents during incubation at 25°, were both dependent upon aerobic conditions and the presence of K+ (5 mM) in teh medium, and were inhibited by ouabain (0.05 mM).

  • 4.

    4. Methacholine (0.33 mM) induced a temporary stimulation of 24Na+ efflux. This stimulation was smaller in the presence than in the absence of K+ in the medium, but the sum of the effects of K+ adn of methacholine in the presence of K+ was greater than the effect of methacholine alone in the K+-free medium.

  • 5.

    5. Methacholine had no significant effect on the Na+ and K+ contents of the slices, but did cause a decrease in the specific radioactivity of the Na+ of the slices at 25°.

  • 6.

    6. The results suggest that methacholine and K+ both act on salt-gland cells by increasing the permeability to Na+ and that, in addition, K+ stimulates a mechanism for coupled movements of Na+ adn K+

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Na *和K+在鲱鱼盐腺切片中的运动
1.1. 新鲜的银鸥盐腺切片含有大约。每公斤干重290毫摩尔3+和350毫摩尔Na+。在1°温度下孵育长达4小时,每千克干重损失约75毫摩尔K+, Na+增加等量;切片没有明显膨胀。在无K+的培养基中1°孵育不增加K+的损失。24Na+流出的速率以及在25°孵育期间保持Na+和K+含量的能力都取决于有氧条件和培养基中K+ (5 mM)的存在,并被瓦巴因(0.05 mM)抑制。甲基胆碱(0.33 mM)诱导24Na+外排的暂时性刺激。这种刺激在有K+的培养基中比在没有K+的培养基中要小,但在有K+的培养基中,K+和甲基胆碱的作用加起来比在无K+的培养基中单独使用甲基胆碱的作用大。甲基胆碱对Na+和K+含量无显著影响,但在25°0.6.6时,会使Na+的比放射性降低。结果表明,甲胆碱和K+都通过增加盐腺细胞对Na+的渗透性来作用于盐腺细胞,此外,K+刺激Na+和K+的耦合运动机制
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