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Na+–K+ transport, motility and tegumental membrane potential in adult male Schistosoma mansoni

Published online by Cambridge University Press:  06 April 2009

R. H. Fetterer
Affiliation:
Department of Zoology, Michigan State University, East Lansing, Michigan 48824
R. A. Pax
Affiliation:
Department of Zoology, Michigan State University, East Lansing, Michigan 48824
J. L. Bennett
Affiliation:
Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan 48824

Summary

Ouabain applied to adult male Schistosoma mansoni causes a large, non-reversible tension increase of the parasite's musculature and elimination of spontaneous contractions. The tension increase and the time-course of tension development caused by ouabain are dose dependent with significant effects obtained at 3 × 10−6m. Digoxin and digoxigenin act in a similar manner with a relative potency of ouabain ≃ digoxin > digoxigenin. Lowered temperature as well as substitution of Li+ for Na+ increases muscle tension. The membrane potential recorded from the ventral tegument is also affected by treatments which interact with Na+–K+ transport systems. Ouabain (0·1 mm) causes a rapid depolarization without a significant effect on membrane resistance. The tegument is depolarized by temperatures below 30 °C. The effect of temperature is readily reversible and the temperature sensitivity is eliminated by pretreatment with ouabain. Substitution of Li+ for Na+ also causes a depolarization of the tegument. Tracer experiments show both an increase in Na+ and a decrease in K+ in the parasite within 10 min after treatment with ouabain (1 × 10−5m). Decreasing temperature of the bathing medium also causes an accumulation of Na+ as well as a decrease in the animals. The above results indicate a significant role for active Na+–K+ transport in muscle contraction and in maintenance of the tegumental membrane potential. The data also suggest that the Na+–K+ transport in S. mansoni may be electrogenic.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1981

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References

REFERENCES

Beauge, L. (1978). Activiation by lithium ions of the inside sodium sites in (Na–K)-ATPases. Biochimica et biophysica acta 527, 472–84.CrossRefGoogle Scholar
Bennett, J. L. & Seed, J. L. (1977). Characterization and isolation of conconavalin A binding sites from the epidermis of S. mansoni. Journal of Parasitology 63, 250–8.CrossRefGoogle Scholar
Fetterer, R. H., Pax, R. A., Strand, S. & Bennett, J. L. (1978). Schistosoma mansoni. Physical and chemical factors affecting adult male musculature. Experimental Parasitology 46, 5971.CrossRefGoogle ScholarPubMed
Fetterer, R. H., Pax, R. A. & Bennett, J. L. (1980). Schistosoma mansoni: characterization of electrical potential from tegument of adult males. Experimental Parasitology 49, 353–65.CrossRefGoogle ScholarPubMed
Glynn, I. M. & Karlish, S. J. D. (1975). The sodium pump. Physiological Reviews 26, 1355.CrossRefGoogle Scholar
Pax, R. A., Bennett, J. L. & Fetterer, R. H. (1978). A benzodiazepine derivative and praziquantel: effects on musculature of Schistosoma mansoni and Schistosoma japonicum. Naunyn-Schmiedeberg's Archiv für Pharmakologie 34, 309–15.CrossRefGoogle Scholar
Smith, J. H., Reynolds, E. S. & von Lichtenberg, F. (1969). The integument of Schistosoma mansoni. American Journal of Tropical Medicine and Hygiene 18, 2849.CrossRefGoogle ScholarPubMed
Thomas, R. C. (1972). Electrogenic sodium pump in nerve and muscle cells. Physiological Reviews 52, 563–94.CrossRefGoogle ScholarPubMed
Willis, J. S. & Fang, L. S. T. (1970). Li+ stimulation of ouabain sensitive respiration and (Na+-K+)-ATPase of kidney cortex of ground squirrels. Biochimica et biophysica acta 219, 486–9.CrossRefGoogle Scholar