|
|
||||||||
WATER AND ELECTROLYTE HOMEOSTASIS
Institut für Physiologie, Charité Campus Mitte, Berlin, Germany
Submitted 19 September 2005 ; accepted in final form 20 December 2005
Alterations in total body sodium (TBSodium) that covered the range from moderate deficit to large surplus were induced by 10 experimental protocols in 66 dogs to study whether large amounts of Na+ are stored in an osmotically inactive form during Na+ retention. Changes in TBSodium, total body potassium (TBPotassium), and total body water (TBWater) were determined by 4-day balance studies. A rather close correlation was found between individual changes in TBSodium and those in TBWater (r2 = 0.83). Changes in TBSodium were often accompanied by changes in TBPotassium. Taking changes of both TBSodium and TBPotassium into account, the correlation with TBWater changes became very close (r2 = 0.93). The sum of changes in TBSodium and TBPotassium was accompanied by osmotically adequate TBWater changes, and plasma osmolality remained unchanged. Calculations reveal that even moderate TBSodium changes often included substantial Na+/K+ exchanges between extracellular and cellular space. The results support the theory that osmocontrol effectively adjusts TBWater to the body's present content of the major cations, Na+ and K+, and do not support the notion that, during Na+ retention, large portions of Na+ are stored in an osmotically inactive form. Furthermore, the finding that TBSodium changes are often accompanied by TBPotassium changes and also include Na+/K+ redistributions between fluid compartments suggests that cells may serve as readily available Na+ store. This Na+ storage, however, is osmotically active, since osmotical equilibration is achieved by opposite redistribution of K+.
water-electrolyte balance; osmocontrol; total body sodium; total body potassium; sodium-potassium-exchange
This article has been cited by other articles:
![]() |
M. Schafflhuber, N. Volpi, A. Dahlmann, K. F. Hilgers, F. Maccari, P. Dietsch, H. Wagner, F. C. Luft, K.-U. Eckardt, and J. Titze Mobilization of osmotically inactive Na+ by growth and by dietary salt restriction in rats Am J Physiol Renal Physiol, May 1, 2007; 292(5): F1490 - F1500. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. D. Noakes and D. Speedy The aetiology of exercise--associated hyponatraemia is established and is not "mythical" Br. J. Sports Med., February 1, 2007; 41(2): 111 - 113. [Full Text] [PDF] |
||||
![]() |
M. K. Nguyen and I. Kurtz Is the osmotically inactive sodium storage pool fixed or variable? J Appl Physiol, January 1, 2007; 102(1): 445 - 447. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. H. Rosner and J. Kirven Exercise-Associated Hyponatremia Clin. J. Am. Soc. Nephrol., January 1, 2007; 2(1): 151 - 161. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. B. Weschler and M. Heer UNDER WHAT CONDITIONS IS INGESTED SODIUM RENDERED OSMOTICALLY INACTIVE? Am J Physiol Regulatory Integrative Comp Physiol, September 1, 2006; 291(3): R856 - R857. [Full Text] [PDF] |
||||
![]() |
M. Ferreria Jr., N. Sahibzada, J. G. Verbalis, R. A. Gillis, G. E. Hermann, E. Seeliger, M. Ladwig, and H. W. Reinhardt Comments on: "Esophageal-gastric relaxation reflex in rat: dual control of peripheral nitrergic and cholinergic transmission" Am J Physiol Regulatory Integrative Comp Physiol, September 1, 2006; 291(3): R854 - R855. [Full Text] [PDF] |
||||
![]() |
T. Ring, M. K. Nguyen, and I. Kurtz Master equation for dysnatremia or intractable abracadabra J Appl Physiol, August 1, 2006; 101(2): 692 - 694. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |