Skip to main content
Log in

Further studies on diurnal changes in small vesicles in sympathetic nerve endings in the mouse pineal and the effects of continuous light on the vesicles — Quantitative electron microscopic observations

  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Summary

Diurnal variations in the number of various types of small granulated and non-granulated vesicles as well as effects of continuous light on the vesicles in sympathetic nerve endings of the mouse pineal were investigated using quantitative electron microscopic techniques. Small granulated vesicles, 40 to 80 nm in diameter, were classified into two categories, type 1 or type 2, according to the size of the granule. Small non-granulated vesicles were also divided into two categories,i.e., spherical and elliptical. Nongranulated vesicles with the long diameter more than twice the shorter one (ranging from 50 to 90 nm in long diameter) were referred to as elliptical vesicles and the other (ranging from 40 to 80 nm in diameter) as spherical vesicles. The number of small vesicles, except for the non-granulated spherical vesicles, varied diurnally in relation to the daily photoperiod. The total vesicle density also exhibited diurnal changes. On the basis of these observations, possible relationships between small vesicles and noradrenaline or serotonin were discussed. Both the diurnal variation in small vesicles and that in the total vesicle density were completely abolished by continuous lighting. Continuous light exposure for various periods until 35 days provoked no apparent changes in small vesicles, except the type 2 granulated vesicles, which were increased in number in response to continuous lighting for about 1 to 3 days.

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

  • Bloom, F. E. The fine structural localization of biogenic monoamines in nervous tissue. Int. Rev. Neurobiol.13, 27–66 (1970).

    Google Scholar 

  • Brownstein, M., Axelrod, J. Pineal gland: 24-hour rhythm in norepinephrine turnover. Science184, 163–165 (1974).

    Google Scholar 

  • Jaim-Etcheverry, G., Zieher, L. M. Cytochemistry of 5-hydroxytryptamine at the electron microscope level. II. Localization in the autonomie nerves of the rat pineal gland. Z. Zellforsch.86, 393–400 (1968).

    Google Scholar 

  • Jaim-Etcheverry, G., Zieher, L. M. Ultrastructural cytochemistry and pharmacology of 5-hydroxytryptamine in adrenergic nerve endings. III. Selective increase of norepinephrine in the rat pineal gland consecutive to depletion of neuronal 5-hydroxytryptamine. J. Pharmacol. exp. Ther.178, 42–48 (1971).

    Google Scholar 

  • Matsushima, S., Ito, T. Diurnal changes in sympathetic nerve endings in the mouse pineal: Semiquantitative electron microscopic observations. J. Neural Transm.33, 275–288 (1972).

    Google Scholar 

  • Matsushima, S., Kachi, T., Mukai, S., Morisawa, Y. Functional relationships between sympathetic nerves and pinealocytes in the mouse pineal: Quantitative electron microscopic observations. Arch. histol. jap. (Suppl.)40, 279–291 (1977).

    Google Scholar 

  • Matsushima, S., Morisawa, Y., Mukai, S. Diurnal variation in large granulated vesicles in sympathetic nerve fibers of the mouse pineal-quantitative electron microscopic observations. J. Neural Transm.45, 63–73 (1979).

    Google Scholar 

  • Matsushima, S., Reiter, R. J. Fine structural features of adrenergic nerve fibers and endings in the pineal gland of the rat, ground squirrel and chinchilla. Am. J. Anat.148, 463–478 (1977).

    Google Scholar 

  • Pellegrino de Iraldi, A. Granulated vesicles in the pineal gland of the mouse. Z. Zellforsch.101, 408–418 (1969).

    Google Scholar 

  • Pellegrino de Iraldi, A., Gueudet, R. Catecholamine and serotonin in granulated vesicles of nerve endings in the pineal gland of the rat. Int. J. Neuropharmacol.8, 9–14 (1969).

    Google Scholar 

  • Quay, W. B. Circadian rhythm in rat pineal serotonin and its modifications by estrous cycle and photoperiod. Gen. comp. Endocrinol.3, 473–479 (1963).

    Google Scholar 

  • Romijn, H. J. Structure and innervation of the pineal gland of the rabbit,Oryctolagus cuniculus (L.). III. An electron microscopic investigation of the innervation. Cell Tiss. Res.157, 25–51 (1975).

    Google Scholar 

  • Snyder, S. H., Zweig, M., Axelrod, J., Fischer, J. E. Control of the circadian rhythm in serotonin content of the rat pineal gland. Proc. nat. Acad. Sci.53, 301–305 (1965).

    Google Scholar 

  • Spurr, A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res.26, 31–43 (1969).

    Google Scholar 

  • Weibel, E. R., Kistler, G. S., Scherle, W. F. Practical stereological methods for morphometric cytology. J. Cell Biol.30, 23–38 (1966).

    Google Scholar 

  • Wurtman, R. J., Axelrod, J., Sedvall, G., Moore, R. Y. Photic and neural control of the 24-hour norepinephrine rhythm in the rat pineal gland. J. Pharmacol. exp. Ther.157, 487–492 (1967).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Matsushima, S., Mukai, S. Further studies on diurnal changes in small vesicles in sympathetic nerve endings in the mouse pineal and the effects of continuous light on the vesicles — Quantitative electron microscopic observations. J. Neural Transmission 46, 123–137 (1979). https://doi.org/10.1007/BF01250334

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01250334

Key words

Navigation