Abstract
1. The intracellular Cl- concentration, [Cl-]1, of rat renal outer medullary slices has been studied in iso-osmolal media containing 42, 93, 144, 189 or 225 mM chloride, [Cl-]0. Equilibrium values for [Cl-]1 were attained within 25-50 min from the start of incubation such that [Cl-]1/[Cl-]0 = 0-46. This ratio was independent of [Cl-]0 within the range studied. Intracellular Na+ was unaffected, and only minor variations of cell volume were observed (calculated from slice weight changes and [14C]carboxyl inulin spaces. 2. When [Cl-]0 = 189 mM, [Cl-]1 remained constant at 87 mM for up to 50 min, indicating that these figures may represnet the interstitial [Cl-] and mean intracellular [Cl-] respectively in outer medulla. 3. Omission of bicarbonate from medium containing 189 mM-Cl- caused an increase in [Cl-]1/[Cl-]0 to 0-58, which was not significantly affected by anoxia or by the presence of arsenite (5 X 10(-3) M) or 2,4-dinitrophenol (10(-3) M). Significant further increases were observed in the presence of iodoacetic acid (5 X 10(-3) M) (0-70), acetazolamide (10(-3) M or 5 M 10(-3) M) (0-71) and iodacetic acid plus 2,4-dinitrophenol (0-85). The addition of the diuretic agents ouabain, ethacrynic acid-cysteine and frusemide (all 10(-3) M) to 189 mM-Cl- media containing bicarbonate reduced [Cl-]1/[Cl-]0 to 0-36, 0-37 and 0-42 respectively. 4. The mean 36Cl- space of outer medulla after 50 min incubation in 189 mM Cl- medium was 49-7 +/- 2-1 micronl./100 mg wet wt. The volume of distribution was not significantly affected by ouabain, ethacrynic acid-cysteine or frusemide (10(-3) mM). 5. Net efflux of 36Cl- from slices loaded with isotope into 'cold' 189 mM Cl medium showed three components with rate constants of 69 X 10(-3), 18 X 10(-3) and 9-9 X 10(-5) sec-1 respectively. Efflux was not affected by ouabain, ethacrynic acid-cysteine or frusemide (10(-3) mM). 6. The main conclusions drawn from this study are: (i) the interstitial fluid Cl- concentration of normally hydrated rat outer medulla is approx. 189 mM; (ii) the [Cl-]1/[Cl-]0 ratio 0-46 may represent a chiefly passive distribution maintained by the opposing gradient of a second anion, probably bicarbonate; (iii) the energy required to maintain unequal distribution of Cl- in the absence of external bicarbonate is derived chiefly from glycolysis, with a small aerobic component; (iv) there may be two intracellular chloride pools whose net rates of Cl- exchange differ by a factor of approx. 180.
Full text
PDF
















Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BERNANKE D., EPSTEIN F. H. METABOLISM OF THE RENAL MEDULLA. Am J Physiol. 1965 Mar;208:541–545. doi: 10.1152/ajplegacy.1965.208.3.541. [DOI] [PubMed] [Google Scholar]
- Burg M. B., Green N. Function of the thick ascending limb of Henle's loop. Am J Physiol. 1973 Mar;224(3):659–668. doi: 10.1152/ajplegacy.1973.224.3.659. [DOI] [PubMed] [Google Scholar]
- Burg M. B. Tubular chloride transport and the mode of action of some diuretics. Kidney Int. 1976 Feb;9(2):189–197. doi: 10.1038/ki.1976.20. [DOI] [PubMed] [Google Scholar]
- Burg M., Green N. Effect of ethacrynic acid on the thick ascending limb of Henle's loop. Kidney Int. 1973 Nov;4(5):301–308. doi: 10.1038/ki.1973.121. [DOI] [PubMed] [Google Scholar]
- Burg M., Stoner L., Cardinal J., Green N. Furosemide effect on isolated perfused tubules. Am J Physiol. 1973 Jul;225(1):119–124. doi: 10.1152/ajplegacy.1973.225.1.119. [DOI] [PubMed] [Google Scholar]
- Cousin J. L., Motais R., Sola F. Transmembrane exchange of chloride with bicarbonate ion in mammalian red blood cells: evidence for a sulphonamide-sensitive "carrier". J Physiol. 1975 Dec;253(2):385–399. doi: 10.1113/jphysiol.1975.sp011195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cousin J. L., Motais R. The role of carbonic anhydrase inhibitors on anion permeability into ox red blood cells. J Physiol. 1976 Mar;256(1):61–80. doi: 10.1113/jphysiol.1976.sp011311. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dalmark M. Chloride and water distribution in human red cells. J Physiol. 1975 Aug;250(1):65–84. doi: 10.1113/jphysiol.1975.sp011043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dalmark M. Chloride transport in human red cells. J Physiol. 1975 Aug;250(1):39–64. doi: 10.1113/jphysiol.1975.sp011042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dalmark M., Wieth J. O. Temperature dependence of chloride, bromide, iodide, thiocyanate and salicylate transport in human red cells. J Physiol. 1972 Aug;224(3):583–610. doi: 10.1113/jphysiol.1972.sp009914. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gunn R. B., Dalmark M., Tosteson D. C., Wieth J. O. Characteristics of chloride transport in human red blood cells. J Gen Physiol. 1973 Feb;61(2):185–206. doi: 10.1085/jgp.61.2.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harris E. J., Pressman B. C. Obligate cation exchanges in red cells. Nature. 1967 Dec 2;216(5118):918–920. doi: 10.1038/216918a0. [DOI] [PubMed] [Google Scholar]
- KLEINZELLER A., KNOTKOVA A. THE EFFECT OF OUABAIN ON THE ELECTROLYTE AND WATER TRANSPORT IN KIDNEY CORTEX AND LIVER SLICES. J Physiol. 1964 Dec;175:172–192. doi: 10.1113/jphysiol.1964.sp007510. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Law R. O. Proceedings: Intracellular chloride concentrations in rat renal outer medulla. J Physiol. 1976 Mar;256(1):13P–14P. [PubMed] [Google Scholar]
- Law R. O. The effects of ouabain and ethacrynic acid on the intracellular sodium and potassium concentrations in renal medullary slices incubated in cold potassium-free ringer solution and re-incubated at 37 degrees C in the presence of external potassium. J Physiol. 1976 Jan;254(3):743–758. doi: 10.1113/jphysiol.1976.sp011256. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Law R. O. The inulin space, solute concentrations, and weight changes in rat renal medullary slices incubated in iso-osmolal media, and their modification during anoxia and hypothermia. J Physiol. 1975 May;247(1):37–54. doi: 10.1113/jphysiol.1975.sp010919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Law R. O. Volume adjustment by renal medullary cells in hypo- and hyperosmolal solutions containing permeant and impermeant solutes. J Physiol. 1975 May;247(1):55–70. doi: 10.1113/jphysiol.1975.sp010920. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Macknight A. D. Water and electrolyte contents of rat renal cortical slices incubated in potassium-free media and media containing ouabain. Biochim Biophys Acta. 1968 Mar 1;150(2):263–270. doi: 10.1016/0005-2736(68)90169-7. [DOI] [PubMed] [Google Scholar]
- Maren T. H., Wiley C. W. Kinetics of carbonic anhydrase in whole red cells as measured by transfer of carbon dioxide and ammonia. Mol Pharmacol. 1970 Jul;6(4):430–440. [PubMed] [Google Scholar]
- Mikulski P., Angielski S., Rogulski J. Metabolism of tricarboxylic acid cycle in rat kidney medulla in vitro. Am J Physiol. 1972 Sep;223(3):485–491. doi: 10.1152/ajplegacy.1972.223.3.485. [DOI] [PubMed] [Google Scholar]
- Pietrzyk C., Heinz E. The sequestration of Na+, K+ and Cl- in the cellular nucleus and its energetic consequences for the gradient hypothesis of amino acid transport in Ehrlich cells. Biochim Biophys Acta. 1974 Jun 29;352(3):397–411. doi: 10.1016/0005-2736(74)90231-4. [DOI] [PubMed] [Google Scholar]
- Proverbio F., Whittembury G. Cell electrical potentials during enhanced sodium extrusion in guinea-pig kidney cortex slices. J Physiol. 1975 Sep;250(3):559–578. doi: 10.1113/jphysiol.1975.sp011070. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rocha A. S., Kokko J. P. Sodium chloride and water transport in the medullary thick ascending limb of Henle. Evidence for active chloride transport. J Clin Invest. 1973 Mar;52(3):612–623. doi: 10.1172/JCI107223. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WHITTAM R. The permeability of kidney cortex to chloride. J Physiol. 1956 Mar 28;131(3):542–554. doi: 10.1113/jphysiol.1956.sp005481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Whittembury G., Proverbio F. Two modes of Na extrusion in cells from guinea pig kidney cortex slices. Pflugers Arch. 1970;316(1):1–25. doi: 10.1007/BF00587893. [DOI] [PubMed] [Google Scholar]
