{"title":"Movements of Na∗ and K+ in slices of herring-gull salt gland","authors":"G.D.V. Van Rossum","doi":"10.1016/0926-6585(66)90071-9","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. Fresh slices of salt gland from the herring gull contained approx. 290 mmoles 3<sup>+</sup> and 350 mmoles Na<sup>+</sup> per kg dry weight.</p></span></li><li><span>2.</span><span><p>2. During incubation at 1° for up to 4 h there was a loss of some 75 mmoles K<sup>+</sup> per kg dry weight and an equivalent gain of Na<sup>+</sup>; the slices did not swell significantly. The loss of K<sup>+</sup> was not increased by incubation at 1° in a K<sup>+</sup>-free medium.</p></span></li><li><span>3.</span><span><p>3. The rate of <sup>24</sup>Na<sup>+</sup> efflux from the slices and the ability of the slices to maintain their Na<sup>+</sup> and K<sup>+</sup> contents during incubation at 25°, were both dependent upon aerobic conditions and the presence of K<sup>+</sup> (5 mM) in teh medium, and were inhibited by ouabain (0.05 mM).</p></span></li><li><span>4.</span><span><p>4. Methacholine (0.33 mM) induced a temporary stimulation of <sup>24</sup>Na<sup>+</sup> efflux. This stimulation was smaller in the presence than in the absence of K<sup>+</sup> in the medium, but the sum of the effects of K<sup>+</sup> adn of methacholine in the presence of K<sup>+</sup> was greater than the effect of methacholine alone in the K<sup>+</sup>-free medium.</p></span></li><li><span>5.</span><span><p>5. Methacholine had no significant effect on the Na<sup>+</sup> and K<sup>+</sup> contents of the slices, but did cause a decrease in the specific radioactivity of the Na<sup>+</sup> of the slices at 25°.</p></span></li><li><span>6.</span><span><p>6. The results suggest that methacholine and K<sup>+</sup> both act on salt-gland cells by increasing the permeability to Na<sup>+</sup> and that, in addition, K<sup>+</sup> stimulates a mechanism for coupled movements of Na<sup>+</sup> adn K<sup>+</sup></p></span></li></ul></div>","PeriodicalId":100158,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis","volume":"126 2","pages":"Pages 338-349"},"PeriodicalIF":0.0000,"publicationDate":"1966-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6585(66)90071-9","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926658566900719","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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+