Skip to main content
Log in

Studies on oxygen and volume restriction in cultured cardiac cell: possible rearrangement of sarcolemmal lipid moieties during anoxia and ischemia-like states

  • Original Article
  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Summary

Cultured heart cells have been shown useful for investigating states of oxygen and volume restrictions, simulating anoxia and ischemia-like states at cellular levels. The sarcolemma has been implicated as one of the early sites of ischemic damage; therefore, lactoperoxidase catalyzed radioiodination was used to study accessibility of the sarcolemmal lipid moieties to this enzymatic probe, reflecting their exposure to the extracellular environment, hence the biophysical state of the sarcolemma. These studies have shown that within one hour of ‘ischemic’ injuries: (1) The degree of labelling in the total phospholipid fraction is consideraly increased; and (2) Profound changes in the relative extent of labelling of different phospholipid classes were observed. The PE/PC labelling ratio increases dramatically with the progress of ischemia-like state. We suggest that early during ischemic injury, reorganization of the cell surface phospholipids occurs and discuss possible relations to the energy charge of the cell.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hillis LD, Braunwald E: N Engl J Med 296:971–978 (Part I), 1034–1042 (Part II). 1093–1096, (Part II), 1977

    Google Scholar 

  2. Neely JR, Feuvray D: Am J Pathol 102:282–291, 1981

    Google Scholar 

  3. Parmelt WW, Chatterjee K: J Cardiovasc Pharmacol 6:(Suppl. 6), 888–894, 1984

    Google Scholar 

  4. Pantely GA, Bristow JD: Prog Cardiovasc Dis 27:95–114, 1984

    Google Scholar 

  5. Acosta D, Puckett M, McMillan R: In Vitro 14:728–732, 1978

    Google Scholar 

  6. Acosta D, Puckett M, McMillin R: Experientia 34:1338–1339, 1978

    Google Scholar 

  7. Higgins TJC, Allsopp D, Bailey PJ: J Mol Cell Cardiol 12:909–927, 1980

    Google Scholar 

  8. Van der Laarse A, Hollaar L, Van den Valk LJM, Witteveen SAGJ: J Mol Med 3:123–131, 1978

    Google Scholar 

  9. Wenzel DG, Acosta D: Res Common Chem Pathol Pharmacol 12:173–176, 1975

    Google Scholar 

  10. Higgins TC, Allsopp D, Bailey PJ, D'Souza EDA: J Mol Cell Cardiol 13:599–611, 1981

    Google Scholar 

  11. Vemuri R, Yagev S, Heller M, Pinson A: In Vitro 21:521–525, 1985

    Google Scholar 

  12. Vemuri R, Heller M, Pinson A: Basic Res Cardiol 80 (Suppl. 2):140–144, 1985

    Google Scholar 

  13. Zimmerman ARE, Dames W, Hülsmann WD, Snidjeder J, Wisse E, Durrer D: Cardiovasc Res 1:210–209, 1967

    Google Scholar 

  14. Jennings RJ, Reimer KA: Am J Pathol 102:241–245, 1981

    Google Scholar 

  15. Hess ML, Krausse S, Kontos HA: Adv Exptl Med Biol. 161:3777–3779, 1983

    Google Scholar 

  16. Benenson A, Mersel M, Heller M, Pinson A. In: Dhalla NM (ed) Methods in Studying Cardiac Membranes CRC Press Inc., Boca Raton, Vol. II, 1984, pp 59–61

    Google Scholar 

  17. Benenson, A, Mersel M, Pinson A, Heller M: Anal Biochem, 101:507–512, 1980

    Google Scholar 

  18. Mersel M, Benenson A, Pinson A, Heller M: FEBS Lett, 110:69–72, 1980

    Google Scholar 

  19. Benenson A, Heller M, Pinson A, Mersel M: In: Calderera CM, and Harris P (eds) advances in Studies on Heart Metabolism CLUEB, Bologna, Italy, 1982, pp 49–56

    Google Scholar 

  20. Gross Z, Rottem S: Biochim Biophys Acta 555:547–542, 1979

    Google Scholar 

  21. Schlager SI: Methods in Enzymol 70:252–265, 1980

    Google Scholar 

  22. Morisson M, Schonbaum GR: Annu Rev Biochem 45: 861–888, 1976

    Google Scholar 

  23. Monteralo RC, Rueckert RR: Archiv Biochem Phys 178:555–564, 1970

    Google Scholar 

  24. Yagev S, Heller M, Pinson A: In Vitro, 20:893–898, 1984

    Google Scholar 

  25. Heller M, Harary I: Biochim Biophys Acta 467:29–43, 1977

    Google Scholar 

  26. Mersel M, Malvina AN, Hindelang C, Mandel P: Biochim Biophys Acta, 778:144–154, 1984

    Google Scholar 

  27. Dhalla NS, Pierce GN. In: Dhalla NS (ed) Methods in Studying Cardiac Membranes CRC Press, Boca Raton, Fl. Vol I, 1984, pp 3–18

    Google Scholar 

  28. Rouser D, Kritschevski G, Yamamoto A. In: Marinetti GV (ed) Lipid Chromatography Analysis M. Dekker, New York 1967, pp 99

    Google Scholar 

  29. Burton LM, Hagler HK, Templeton GH, Willerson J, Buja LMJ: J Clin Investig 60:1289–1302, 1977

    Google Scholar 

  30. Burton LM, Hagler HK, Willerson JT, Buja LM: Am J Physiol 241:H714-H723, 1981

    Google Scholar 

  31. Burton LM, Templeton GHJ, Hagler HK, Willerson JT, Buja LM: J Mol Cell Cardiol 12: 109–133, 1980

    Google Scholar 

  32. Chien KR, Reeves JP, Buja LM, Bonte F, Parkey RW Willerson JT Cir Res 48:711–719, 1981

    Google Scholar 

  33. Langer GA, Frank JA, Brady AJ: Int Rev Physio 9:191–237, 1976

    Google Scholar 

  34. Gould BJ, Ginsberg BH. In: Allan R (ed) Membrane, Detergents and Receptor Solubilization Liss Inc. New York, 1984, pp 65–83

    Google Scholar 

  35. Dessort D, Mersel M, Lepage P, Van Doersaller A: Anal Biochem 142:43–52, 1984

    Google Scholar 

  36. Dominski J, Binaglia L, Dreyfus H, Massarelli R, Mersel M, Freysz L: Biochim Biophys Acta 734:257–266, 1983

    Google Scholar 

  37. Mersel M, Benenson A, Mandel P, Freysz L. In: Phospholipids in the Nervous System Vol 1: Metabolism (Horroks GB, Ansell GB and Porcellati G, eds) Raven Press, New York, 1982, p 329

  38. Vemuri R, Huizer T, De Jong JW, Hegge JAJ, Heller M, Pinson A: (submitted)

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Vemuril, R., Mersel, M., Heller, M. et al. Studies on oxygen and volume restriction in cultured cardiac cell: possible rearrangement of sarcolemmal lipid moieties during anoxia and ischemia-like states. Mol Cell Biochem 79, 39–46 (1988). https://doi.org/10.1007/BF00229396

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00229396

Key words

Navigation