Abstract
MUSCULAR dystrophy has been regarded as a “primary degenerative myopathy”1. But there is evidence from studies of both human muscular dystrophy and animal models of muscular dystrophy that the muscle disease may have a neural basis2. The mechanism of the suspected neural disorder remains to be elucidated. Since there is independent evidence that in normal animals the trophic effect of nerve on muscle depends on intact axoplasmic transport3, we have initiated a study of axoplasmic transport in dystrophic mice. We have found a disturbance of axoplasmic transport of choline acetyltransferase activity in dystrophic mice.
Similar content being viewed by others
References
Walton, J. N., Br. Med. J., 1, 1271–1274, 1344–1348 (1967).
Gallup, B., and Dubowitz, V., Nature, 243, 287–289 (1973).
Albuquerque, E. X., Warnick, J. E., Tasse, J. R., and Sansone, F. M., Expl Neurol., 37, 607–634 (1972).
Hebb, C., Physiol. Rev., 52, 918–957 (1972).
Kása, P., Mann, S. P., and Hebb, C., Nature, 226, 814–816 (1970).
Hebb, C. O., and Waites, G. M. H., J. Physiol., Lond., 132, 667–671 (1956).
Hebb, C. O., and Silver, A., J. Physiol., Lond, 169, 41P–42P (1963).
Kása, P., Mann, S. P., Karcsu, S., Tóth, L., and Jordan, S., J. Neurochem., 21, 431–436 (1973).
Wooten, G. F., and Coyle, J. T., J. Neurochem., 20, 1361–1372 (1973).
Oesch, F., Otten, U., and Thoenen, H., J. Neurochem., 20, 1691–1706 (1973).
Saunders, N. R., Dziegielewska, K., Häggendal, C. J., and Dahlström, A. B., J. Neurobiol., 4, 95–103 (1973).
Michelson, A. M., Russell, E. S., and Harman, P. J., Proc. natn. Acad. Sci. U.S.A., 41, 1079–1084 (1955).
Brimijoin, S., J. Neurochem., 19, 2183–2193 (1972).
Lowry, O. H., Rosebrough, N. J., Farr, A. L., and Randall, R. J., J. biol. Chem., 193, 265–275 (1951).
Bradley, W. G., and Jaros, E., Brain, 96, 247–258 (1973).
McComas, A. J., and Mossawy, S. J., Research in Muscular Dystrophy (3rd Symposium on Muscular Dystrophy, London, 1965) pp. 317–341.
Harris, J. B., and Wilson, P., J. neurol. Neurosurg. Psychiat., 34, 512–520 (1971).
Harris, J. B., Wallace, C., and Wing, J., J. neurol. Sci., 15, 245–249 (1972).
Bradley, W. G., and Jenkison, M., J. neurol. Sci., 18, 227–247 (1973).
Salafsky, B., and Stirling, C. A., Nature, 246, 126–128 (1973).
Salafsky, B., Nature, 229, 270–273 (1971).
Fonnum, F., Frizell, M., and Sjöstrand, J., J. Neurochem., 21, 1109–1120 (1973).
Giller, E. J., jun., Schrier, B. K., Shainberg, A., Fisk, H. R., and Nelson, P. G., Science, 182, 588–589 (1973).
McCaman, M. W., Stafford, M. L., and Skinner, E. C., Am. J. Physiol., 212, 228–232 (1967).
Glover, V., and Green, D. P. L., J. Neurochem., 19, 2465–2466 (1972).
Feigenson, M. E., and Saelens, J. K., Biochem. Pharmac., 18, 1479–1486 (1969).
Potter, L. T., Glover, V. A. S., and Saelens, J. K., J. biol. Chem., 243, 3864–3870 (1968).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
JABLECKI, C., BRIMIJOIN, S. Reduced axoplasmic transport of choline acetyltransferase activity in dystrophic mice. Nature 250, 151–154 (1974). https://doi.org/10.1038/250151a0
Received:
Issue Date:
DOI: https://doi.org/10.1038/250151a0
- Springer Nature Limited
This article is cited by
-
Molecular biology and neurobiology of choline acetyltransferase
Molecular Neurobiology (1987)
-
Regeneration and reinnervation of the dystrophic mouse soleus muscle
Acta Neuropathologica (1983)
-
Choline acetyltransferase activity in human muscular diseases
Journal of Neurology (1976)
-
State of play in the neural hypothesis of muscular dystrophy
Nature (1974)