The Journal of Membrane Biology

, Volume 89, Issue 1, pp 65–73 | Cite as

Demarcation of Ca2+ transport processes in guinea pig stomach smooth muscle

  • Yasushi Sakai
  • Akiyo Isobe
  • Santa Ichikawa
Articles

Summary

Microsomal fractions were isolated from gastric antrum and fundus smooth muscle of guinea pigs. Ca2+ uptake into and Ca2+ release from the membrane vesicles were studied by a rapid filtration method, and Ca2+ transport properties of the different regions of the stomach were compared. ATP-dependent Ca2+ uptake was similar in microsomes isolated from both regions. This uptake was increased by oxalate and was not affected by NaN3. Oxalate affected Ca2+ permeability of both antrum and fundus microsome vesicles similarly. Fundus microsome vesicles preincubated in 100mm NaCl and then diluted to 1/20 concentration with Na+-free medium had significantly higher ATP-independent Ca2+ uptake than vesicles preincubated in 100mm KCl and treated the same way. This was not true for antrum vesicles. Monensin abolished Na+-dependent Ca2+ uptake, and NaCl enhanced Ca2+ efflux from fundus microsome vesicles. The halflife values of Ca2+ loss from fundus vesicles in the presence of NaCl were significantly smaller than those in the presence of KCl. The release of Ca2+ from the vesicles within the first 3 min was accelerated by NaCl to three times that by KCl. However, NaCl had ro effect on Ca2+ release from antrum microsome vesicles.

Results suggest two distinct mechanisms of stomach membrane Ca2+ transport: (1) ATP-dependent Ca2+ uptake and (2) Na+−Ca2+ exchange; the latter in the fundus only.

Key Words

concentration-relaxation Ca2+ transport Na+−Ca2+ exchange microsome smooth muscle 

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References

  1. Brading, A.F. 1978. Calcium-induced increase in membrane permeability in the guinea-pig taenia coli: Evidence for involvement of a sodium-calcium exchange mechanism.J. Physiol. (London) 275:65–84Google Scholar
  2. Bray, G.A. 1960. A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counter.Anal. Biochem. 1:279–285Google Scholar
  3. Casteels, R., Droogmans, G., Hendricks, H. 1973. Effect of sodium and sodium-substitutes on the active ion transport and on the membrane potential of smooth muscle cells.J. Physiol. (London) 228:733–748Google Scholar
  4. Devine, C.E., Somlyo, A.V., Somlyo, A.P. 1972. Sarcoplasmic reticulum and excitation-contraction coupling in mammalian smooth muscles.J. Cell Biol. 52:690–718Google Scholar
  5. Fiske, C.H., Subbarow, Y. 1925. The colorimetric determination of phosphorus.J. Biol. Chem. 66:375–400Google Scholar
  6. Grover, A.K., Kwan, C.Y., Daniel, E.E. 1981. Na−Ca exchange in rat myometrium membrane vesicles highly enriched in plasma membranes.Am. J. Physiol. 240:c175-c182Google Scholar
  7. Grover, A.K., Kwan, C.Y., Daniel, E.E. 1982. Ca2+ dependence of calcium uptake by rat myometrium plasma membrane-enriched fraction.Am. J. Physiol. 242:c278-c282Google Scholar
  8. Grover, A.K., Kwan, C.Y., Rangachari, P.K., Daniel, E.E. 1983. Na−Ca exchange in a smooth muscle plasma membrane-enriched fraction.Am. J. Physiol. 244:c158-c165Google Scholar
  9. Hasselbach, W. 1978. The reversibility of the sarcoplasmic calcium pump.Biochim. Biophys. Acta 515:23–53Google Scholar
  10. Janis, R.A., Crankshaw, D.J., Daniel, E.E. 1977. Control of intracellular calcium activity in rat myometrium.Am. J. Physiol. 232:c50-c58Google Scholar
  11. Kuriyama, H., Osa, T., Ito, Y., Suzuki, H., Mishima, K. 1976. Topical differences in excitation and contraction between guinea pig stomach smooth muscles.In: Physiology of Smooth Muscle. E. Bülbring and M.F. Shuba, editors. pp. 185–196. Raven, New YorkGoogle Scholar
  12. Kwan, C.Y. 1982. Mg2+- or Ca2+-activated ATPase activities of plasma membrane isolated from vascular smooth muscle.Enzyme 28:317–327Google Scholar
  13. Kwan, C.Y., Sakai, Y., Grover, A.K., Lee, R.M.K.W. 1982. Isolation and characterization of plasma membrane fraction from gastric fundus smooth muscle of the rat.Mol. Physiol. 2:107–120Google Scholar
  14. Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randall, R.J. 1951. Protein measurement with the Folin phenol reagent.J. Biol. Chem. 193:265–275Google Scholar
  15. Matlib, M.A., Crankshaw, J., Garfield, R.E., Chrankshaw, D.J., Kwan, C.Y., Branda, L.A., Daniel, E.E. 1979. Characterization of membrane fractions and isolation of purified plasma membrane from rat myometrium.J. Biol. Chem. 254:1834–1840Google Scholar
  16. Miyagawa, M., Sakai, Y. 1985. Characterization of Ca2+ transport and enzyme activity in microsomes isolated from guineapig stomach smooth muscle.Comp. Biochem. Physiol. 80A:565–570Google Scholar
  17. Ozaki, H., Urakawa, N. 1979. Na−Ca exchange and tension development in guinea-pig aorta.Naunyn-Schmiedeberg's Arch. Pharmacol. 309:171–178Google Scholar
  18. Pitts, B.J.R. 1979. Stoichiometry of Na−Ca exchange in cardiac sarcolemmal vesicles.J. Biol. Chem. 254:6232–6235Google Scholar
  19. Raeymaekers, L., Wuytack, F., Batra, S., Casteels, R. 1977. A comparative study of the Ca accumulation by mitochondria and microsomes isolated from the smooth muscle of the guinea-pig taenia coli.Pfluegers Arch. 368:217–223Google Scholar
  20. Reuter, H., Blaustein, M.P., Haeusler, G. 1973. Na−Ca exchange and tension development in arterial smooth muscle.Phil. Trans. R. Soc. London B 265:87–94Google Scholar
  21. Sakai, Y., Grover, A.K., Fox, J.E.T., Daniel, E.E. 1983. Uptake and release of calcium by canine gastric corpus smooth muscle plasma membrane enriched fractionCan. J. Physiol. Pharmacol. 61:669–774Google Scholar
  22. Sakai, Y., Ichikawa, S., Yoshida, M., Oouchi, M., Miyagawa, M. 1982. ATPase activity and calcium uptake of microsomes isolated from stomach smooth muscle after exposure to phospholipase C.Jpn. J. Smooth Muscle Res. 18:339–345Google Scholar
  23. Sakai, Y., McLean, J., Grover, A.K., Garfield, R.E., Fox, J.E.T., Daniel, E.E. 1981. Isolation and characterization of subcellular membranes from canine stomach smooth muscle.Can. J. Physiol. Pharmacol. 59:1260–1267Google Scholar
  24. Szurszewski, J.H. 1981. Electrical basis for gastrointestinal motility.In: Physiology of the Gastrointestinal Tract. L.R. Johnson, editor. Chap. 58, pp. 1435–1466. Raven, New YorkGoogle Scholar
  25. Taylor, G.S., Paton, D.M., Daniel, E.E. 1970. Characterization of electrogenic sodium pumping in rat myometrium.J. Gen. Physiol. 56:360–375Google Scholar
  26. Van Breemen, C., Aaronson, P., Loutzenliser, R. 1979. Sodiumcalcium interactions in mammalian smooth muscle.Pharmacol. Rev. 30:167–208Google Scholar
  27. Wibo, M., Morel, N., Godfraind, 1981. Differentiation of Ca2+ pumps linked to plasma membrane and endoplasmic reticulum in the microsomal fraction from intestinal smooth muscle.Biochim. Biophys. Acta 649:651–660Google Scholar
  28. Wuytack, F., Landon, E., Fleisher, S., Hardman, J.G. 1978. The calcium accumulation in a microsomal fraction from porcine coronary artery smooth muscle: A study of the heterogeneity of the fraction.Biochim. Biophys. Acta 540:253–269Google Scholar
  29. Yasuda, N., Sakai, Y. 1984. A possible explanation for effects of Sr2+ on contraction-relaxation cycle in canine stomach.Comp. Biochem. Physiol. 78A:35–41Google Scholar

Copyright information

© Springer-Verlag 1986

Authors and Affiliations

  • Yasushi Sakai
    • 1
  • Akiyo Isobe
    • 1
  • Santa Ichikawa
    • 1
  1. 1.2nd Department of PhysiologyShowa University School of MedicineTokyoJapan

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