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The pineal gland of the gerbil, Meriones unguiculatus

II. Morphometric analysis over a 24-hour period

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Summary

By means of morphometric analytical procedures, a diurnal rhythm in the cellular volume of gerbil pinealocytes was determined. This rhythm has been attributed primarily to a change in the cytoplasmic volume of the pinealocytes which is low during the daylight hours and increases to reach a peak during the middle of the dark period. At the ultrastructural level, six cytoplasmic components of the pinealocytes were found to exhibit a rhythm: free cytoplasm, smooth endoplasmic reticulum (SER), rough endoplasmic reticulum (RER) and ribosomes, secretory vesicles, microtubules, and mitochondria. The presumptive secretory vesicles and the microtubules reached a peak in volume one hour before lights-off. It is suggested that lights-on and lights-off both signal a decrease in size and/or number of the secretory vesicles. The SER and RER/ribosomes reached their peak volume one hour after lights-off which is interpreted as indicating a peak in indoleamine synthesis and protein synthesis, respectively. The volume of free cytoplasm exhibits two peaks; one occurs one hour before lights-off while the second peak occurs in the middle of the dark phase. It is suggested that, although part of the secretory product of the pinealocyte may be present in dense-cored vesicles, other locations could include the free cytoplasm and clear secretory vesicles.

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References

  • Ariëns Kappers, J.: Functional anatomy of the pineal: localization of indoleamine and protein synthesis in the mammalian pineal gland. J. Neural Transm., Suppl. 8, 6–11 (1978)

    Google Scholar 

  • Arstila, A.U., Kalimo, H.O., Hyyppa, M.: Secretory organelles of the rat pineal gland: electron microscopic and histochemical studies in vivo and in vitro. In: The Pineal Gland. A CIBA symposium (G.E.W. Wolstenholme and J. Knight, eds.), pp. 147–164. Edinburgh-London: Churchill Livingstone (1971)

    Google Scholar 

  • Benson, B., Krasovich, M.: Circadian rhythm in the number of granulated vesicles in the pinealocytes of mice: effects of sympathectomy and melatonin treatment. Cell Tissue Res. 184, 499–506 (1977)

    Google Scholar 

  • Glass, G.V., Peckham, P.D., Sanders, J.R.: Consequences of failure to meet assumptions underlying the fixed effects analyses of variance and covariance. Rev. Ed. Res. 42, 237–288 (1972)

    Google Scholar 

  • Hori, S., Kuroda, Y., Saito, K., Ohotani, S.: Subcellular localization of tryptophan-5-mono-oxygenase in pineal glands and raphe nuclei. J. Neurochem. 27, 911–914 (1976)

    Google Scholar 

  • Ito, T., Matsushima, S., Kachi, T.: Diurnal rhythm in the pineal: its morphological aspects. In: Biological Rhythms in Neuroendocrine Activity (M. Kawakami, ed.), pp. 338–348. Tokoyo: Igaku Shoin (1974)

    Google Scholar 

  • Karasek, M., Pawlikowski, M., Ariëns Kappers, J., Stepien, H.: Influence of castration followed by administration of LH-RH on the ultrastructure of rat pinealocytes. Cell Tissue Res. 167, 325–339 (1976)

    Google Scholar 

  • Kurumado, K., Mori, W.: A morphological study of the circadian cycle of the pineal gland of the rat. Cell Tissue Res. 182, 565–568 (1977)

    Google Scholar 

  • Lin, H.-S., Hwang, B.-H., Tseng, C.-Y.: Fine structural changes in the hamster pineal gland after blinding and superior cervical ganglionectomy. Cell Tissue Res. 158, 285–299 (1975)

    Google Scholar 

  • Louis, C.J., Kenny, G.C., Anderson, R.M.: Autoradiographic localization of 5-hydroxy-tryptamine in monkey pineal gland. Experientia 26, 756–757 (1970)

    Google Scholar 

  • Lukaszyk, A., Reiter, R.J.: Histophysiological evidence for the secretion of polypeptide by the pineal gland. Am. J. Anat. 143, 451–464 (1975)

    Google Scholar 

  • Lynch, H.J.: Diurnal oscillations in pineal melatonin content. Life Sci. 10, 791–795 (1971)

    Google Scholar 

  • Nir, I., Hirschmann, N., Sulman, F.G.: Diurnal rhythms of pineal nucleic acids and protein. Neuroendocrinology 7, 271–277 (1971)

    Google Scholar 

  • Pevet, P.: The pineal gland of the mole (Talpa europaea L.). IV. Effect of pronase on material present in cisternae of the granular endoplasmic reticulum of pinealocytes. Cell Tissue Res. 182, 215–219 (1977)

    Google Scholar 

  • Pevet, P., Ariëns Kappers, J., Nevo, E.: The pineal gland of the mole-rat (Spalax ehrenbergi, Nehring). I. The fine structure of pinealocytes. Cell Tissue Res. 174, 1–24 (1976)

    Google Scholar 

  • Pevet, P., Ariëns Kappers, J., Voûte, M.: The pineal gland of nocturnal mammals. I. The pinealocytes of the bat (Nyctalus noctula, Schreber). J. Neural Transm. 40, 47–68 (1977)

    Google Scholar 

  • Quay, W.B., Renzoni, A.: Twenty-four-hour rhythms in pineal mitotic activity and nuclear and nucleolar dimensions. Growth 20, 315–324 (1966)

    Google Scholar 

  • Reiter, R.J.: The Pineal — 1977. Montreal: Eden Press (1977)

    Google Scholar 

  • Romijn, H.J.: Structure and innervation of the pineal gland of the rabbit, Oryctolagus cuniculus. II. An electron microscopic investigation of the pinealocytes. Z. Zellforsch. 141, 545–560 (1973)

    Google Scholar 

  • Romijn, H.J.: The ultrastructure of the rabbit pineal gland after sympathectomy, parasympathectomy, continuous illumination, and continuous darkness. J. Neural Transm. 36, 183–194 (1975)

    Google Scholar 

  • Romijn, H.J., Gelsema, A.J.: Electron microscopy of the rabbit pineal organ in vitro: evidence of norepinephrine-stimulated secretory activity of the Golgi apparatus. Cell Tissue Res. 172, 365–377 (1976)

    Google Scholar 

  • Romijn, H.J., Mud, M.T., Wolters, P.S.: Diurnal variations in number of Golgi-dense core vesicles in light pinealocytes of the rabbit. J. Neural Transm. 38, 231–237 (1976)

    Google Scholar 

  • Sheridan, M.N., Reiter, R.J.: The fine structure of the hamster pineal gland. Am. J. Anat. 122, 357–376 (1968)

    Google Scholar 

  • Shibuya, H., Toru, M., Watanabe, S.: A circadian rhythm of tryptophan hydroxylase in rat pineals. Brain Res. 138, 364–368 (1978)

    Google Scholar 

  • Spurr, A.R.: A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26, 31–413 (1969)

    Google Scholar 

  • Trump, B.F., Bulger, R.E.: New ultrastructural characteristics of cells fixed in a glutaraldehyde-osmium tetroxide mixture. Lab. Invest. 15, 368–379 (1969)

    Google Scholar 

  • Vollrath, L.: Synaptic ribbons of a mammalian pineal gland. Circadian changes. Z. Zellforsch. 145, 171–183 (1973)

    Google Scholar 

  • Weibel, E.R., Bolender, R.P.: Stereological techniques for electron microscopic morphometry. In: Principles and Techniques of Electron Microscopy: Biological Applications, Vol. 3 (M.A. Hayat, ed.), pp. 237–296. New York: Van Nostrand Reinhold (1973)

    Google Scholar 

  • Welsh, M.G., Reiter, R.J.: The pineal gland of the gerbil, Meriones unguiculatus. I. An ultrastructural study. Cell Tissue Res. 193, 323–336 (1978)

    Google Scholar 

  • Williams, M.G., Adrian, E.K.: The use of elemental iodine to enhance staining of thin sections to be viewed in the electron microscope. Stain Technol. 52, 269–272 (1977)

    Google Scholar 

  • Wurtman, R.J., Axelrod, J., Kelly, D.E.: The Pineal. New York: Academic Press (1968)

    Google Scholar 

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Supported by NSF grant #PCM 77-05734

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Welsh, M.G., Cameron, I.L. & Reiter, R.J. The pineal gland of the gerbil, Meriones unguiculatus . Cell Tissue Res. 204, 95–109 (1979). https://doi.org/10.1007/BF00235167

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