Journal of Comparative Physiology B

, Volume 154, Issue 2, pp 159–166 | Cite as

Effect of cold acclimation on Na+/K+ transport in hamster liver cells

  • B. A. Horwitz
  • S. D. Clark
  • J. Hamilton
  • J. Guttas
Article

Summary

The effects of prolonged cold exposure of Syrian hamsters on liver membrane (Na+/K+-ATPase activity and on liver intracellular K+ levels was examined. Membrane preparations from cold-acclimated hamsters (6°C for 3 weeks) exhibited significantly higherVmax values for (Na+/K+)-ATPase and significantly greater ouabain binding. These data support the view that in the liver of these cold-exposed hamsters, there is an increase in the number of operational pumps. The fact that the intact liver cells (isolated via liver perfusion) from the cold-acclimated hamsters: (a) did not have higher concentrations of intracellular K+ (despite the presence of more operational pumps); and (b) exhibited greater rates of K+ loss when the pumps were inhibited by maximal ouabain suggests that the K+ leak across the liver cell plasma membrane is increased in the cold-acclimated hamsters. Although the physiological significance of these results needs further evaluation, these membrane changes may be of adaptive value for hibernation.

Keywords

Liver Cell ATPase Activity Ouabain Cold Acclimation Cold Exposure 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Abbreviations

CA

cold-acclimated

Pi

inorganic phosphate

KRB

Krebs-Ringer-bicarbonate buffer

BSA

bovine serum albumin

ECF

extracellular fluid

ICF

intracellular fluid

dcs

dry cell solid

N

nitrogen

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References

  1. Asano Y (1978) Increased cell membrane permeability to Na+ and K+ induced by thyroid hormone in rat skeletal muscle. In: Girardier L, Seydoux J (eds) Effectors of Thermogenesis. Birkhäuser, Basel, pp 199–203Google Scholar
  2. Cala PM (1977) Volume regulation by flounder red blood cells in anisotonic media. J Gen Physiol 69:537–552Google Scholar
  3. Foster DO, Frydman ML (1978) Nonshivering thermogenesis in the rat. II. Measurements of blood flow with microspheres point to brown adipose tissue as the dominant site of the calorigenesis induced by noradrenaline. Can J Physiol Pharmacol 56:110–112Google Scholar
  4. Gomori GA (1942) A modification of the colorimetric phosphorous determination for use with the photoelectric colorimeter. J Lab Clin Med 27:955–960Google Scholar
  5. Guernsey DL, Stevens ED (1976) The cell membrane sodium pump as a mechanism for increasing thermogenesis during cold acclimation in rats. Science 196:908–910Google Scholar
  6. Hems R, Ross BD, Berry MN, Krebs HA (1966) Gluconeogenesis in the perfused rat liver. Biochem J 101:284–292Google Scholar
  7. Horwitz BA (1976) The effect of cold exposure on liver mitochondrial and peroxisomal distribution in the rat, hamster and bat. Comp Biochem Physiol [A] 54:45–48Google Scholar
  8. Horwitz BA, Eaton M (1977) Ouabain-sensitive liver and diaphragm respiration in cold-acclimated hamster. J Appl Physiol 42:150–153Google Scholar
  9. Liberman UA, Asano Y, Lo C-S, Edelman IS (1979) Relationship between Na+-dependent respiration and Na++K+-adenosine triphosphatase activity in the action of thyroid hormone on rat jejunal mucosa. Biophys J 27:127–144Google Scholar
  10. Lin ML, Akera T (1978) Increased (Na+, K+)-ATPase concentrations in various tissues of rats caused by thyroid hormone treatment. J Biol Chem 253:723–726Google Scholar
  11. Lo C-S, August TR, Liberman UA, Edelman IS (1976) Dependence of renal (Na++K+)-adenosine triphosphatase activity on thyroid status. J Biol Chem 251:7826–7833Google Scholar
  12. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275Google Scholar
  13. Ma T, Zuazaga S, Zuazaga C (1942) Micro-Kjedahl determination of nitrogen. A new indicator and an improved rapid method. Ind Eng Chem Anal Edn 14:280–282Google Scholar
  14. Neville DM (1960) The isolation of a cell membrane fraction from rat liver. J Biophys Biochem Cyto 8:413–422Google Scholar
  15. Ray TK (1970) A modified method for the isolation of the plasma membrane from rat liver. Biochem Biophys Acta 196:1–9Google Scholar
  16. Ross BD (1972) Perfusion Techniques in Biochemistry. Clarendon Press, Oxford (England), pp 1–479Google Scholar
  17. Skou JC, Hilberg C (1965) The effect of sulphydryl-blocking reagents and of urea on the (Na+−K+)-activated enzyme system. Biochem Biophys Acta 110:359–369Google Scholar
  18. Willis JS (1979) Hibernation: Cellular aspects. Annu Rev Physiol 41:275–286Google Scholar

Copyright information

© Springer-Verlag 1984

Authors and Affiliations

  • B. A. Horwitz
    • 1
  • S. D. Clark
    • 1
  • J. Hamilton
    • 1
  • J. Guttas
    • 1
  1. 1.Department of Animal PhysiologyUniversity of CaliforniaDavisUSA

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