Skip to main content
Log in

Hydrocortisone-induced increase in the number of small intensely fluorescent cells and their histochemically demonstrable catecholamine content in cultures of sympathetic ganglia of the newborn rat

  • Papers
  • Published:
The Histochemical Journal Aims and scope Submit manuscript

Synopsis

It is known that hydrocortisone causes a great increase in the number of small intensely fluorescent (SIF) cells in the sympathetic ganglia when injected into newborn rats. The effect of hydrocortisone on nervous tissuein vitro has not been studied previously.

Pieces of newborn rat sympathetic ganglia were cultivated in Rose chambers. Hydrocortisone was dissolved in the medium in concentrations of 1–9 mg/l. Both control and hydrocortisone-containing cultures were examined daily by phase-contrast microscopy, and the catecholamines were demonstrated histochemically by formaldehyde-induced fluorescence after 7 days in culture.

All cultures showed outgrowths of axons and supporting cells elements, although these were less extensive in the groups of cultures with hydrocortisone. After a week, SIF cells with a green fluorescence were observed in the control explants. In all cultures with hydrocortisone, a concentration-dependent increase was observed in the fluorescence intensity and the number of the SIF cells in the explant; numerous SIF cells were also seen in the outgrowth. Some SIF cells showed processes and the longest processes were seen in cultures with the highest concentration of hydrocortisone.

It is concluded that hydrocortisone causes an increased synthesis of catecholamines in the SIF cellsin vitro, and an increase in their number by affecting either their division or their differentiation from a more immature form, or both. This effect was a direct one and not mediated by any system other than the ganglion itself. Induction of enzyme synthesis by hydrocortisone is proposed as an explanation of the increase in catecholamine concentration.

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

  • Axelrod, J. (1966). Methylation reactions in the formation and metabolism of catecholamines and other biogenic amines.Pharmacol. Rev. 18, 95–113.

    Google Scholar 

  • Björklund, A., Cegrell, L., Falck, B., Ritzen, M. &Rosengren, E. (1970). Dopaminecontaining cells in sympathetic ganglia.Acta physiol. scand. 78, 334–8.

    Google Scholar 

  • Burnstock, G., Evans, B., Gannon, B. J., Heath, J. W. &James, V. (1971). A new method of destroying adrenergic nerves in adult animals using guanethidine.Br. J. Pharmacol. 43, 295–301.

    Google Scholar 

  • Chamley, J. H., Mark, G. E., Campbell, G. R. & Burnstock, G. (1972a). Sympathetic ganglia in culture. I. Neurons.Z. Zellforsch, mikrosk. Anat. (submitted for publication).

  • Chamley, J. H., Mark, G. E. & Burnstock, G. (1972b). Sympathetic ganglia in culture. II. Accessory cells.Z. Zellforsch. mikrosk. Anat. (submitted for publication).

  • Chaudhary, K. D., Lupien, P. J. &Hinse, C. (1969). Effect of ecdysone on glutamic decarboxylase in rat brain.Experientia 25, 250–1.

    Google Scholar 

  • Eränkö, L. & Eränkö, O. (1971a). Effect of hydrocortisone on histochemically demonstrable catecholamines in the sympathetic ganglia and extra-adrenal chromaffin tissue of the rat.Acta physiol. scand. (in press).

  • Eränkö, L. & Eränkö, O. (1971b). Effect of 6-hydroxydopamine on the ganglion cells and the small intensely fluorescent cells in the superior cervical ganglion of the rat.Acta physiol. scand. (in press).

  • Eränkö, L. & Eränkö, O. (1971c). Effect of guanethidine on nerve cells and small intensely fluorescent cells in sympathetic ganglia of newborn and adult rats.Acta pharmacol. et toxicol. (in press).

  • Eränkö, O. &Eränkö, L. (1971d). Small intensely fluorescent, granule-containing cells in the sympathetic ganglion of the rat.Progr. Brain Res. 34, 39–52.

    Google Scholar 

  • Eränkö, O. &Härkönen, M. (1963). Histochemical demonstration of fluorogenic amines in the cytoplasm of sympathetic ganglion cells of the rat.Acta physiol. scand. 58, 285–6.

    Google Scholar 

  • Eränkö, O. &Härkönen, M. (1965a). Monoamine-containing small cells in the superior cervical ganglion of the rat and an organ composed of them.Acta physiol. scand. 63, 511–12.

    Google Scholar 

  • Eränkö, O. &Härkönen, M. (1965b). Effect of axon division on the distribution of noradrenaline and acetylcholinesterase in sympathetic neurons of the rat.Acta physiol. scand. 63, 711–12.

    Google Scholar 

  • Eränkö, O., Lempinen, M. &Räisänen, L. (1966). Adrenaline and noradrenaline in the Organ of Zuckerkandl and adrenals of newborn rats treated with hydrocortisone.Acta physiol. scand. 66, 253–4.

    Google Scholar 

  • Grillo, M. A. (1966). Electron microscopy of sympathetic tissue.Pharmac. Rev. 18, 387–99.

    Google Scholar 

  • Hanks, J. H. &Wallace, R. E. (1949). Relation of oxygen and temperature in the preservation of tissues by refrigeration.Proc. Soc. exp. Biol. (NY).71, 196–200.

    Google Scholar 

  • Lempinen, M. (1964). Extra-adrenal chromaffin tissue of the rat and the effect of cortical hormones on it.Acta physiol. scand. 62, Suppl. 231.

    Google Scholar 

  • Matthews, M. R. &Raisman, G. (1969). The ultrastructure and somatic efferent synapses of small granule-containing cells in the superior cervical ganglion.J. Anat. 105, 255–82.

    Google Scholar 

  • Norberg, K.-A. & Hamberger, B. (1964). The sympathetic adrenergic neuron.Acta physiol. scand. 63, Suppl. 238.

    Google Scholar 

  • Ritzen, M. (1967). Cytochemical Identification and Quantitation of Biogenic Monoamines. Thesis, Stockholm, P.A. Norstedt & Söner, pp. 63.

    Google Scholar 

  • Rose, G. C. (1954). A separable and multipurpose tissue culture chamber.Tex. Rep. Biol. Med. 12, 1074–83.

    Google Scholar 

  • Salk, E. S., Youngner, J. S. &Ward, E. N. (1954). Use of color change of phenol red as the indicator in titrating poliomyelitis virus or its antibody in a tissue culture system. Appendix. Method of preparing medium 199.Amer. J. Hyg. 60, 214–30.

    Google Scholar 

  • Shelton, K. R. &Alfrey, V. G. (1970). Selective synthesis of a nuclear acidic protein in liver cells stimulated by cortisol.Nature, Lond. 228, 132–4.

    Google Scholar 

  • Van Orden, L. S., Burke, J. P., Geyer, M. &Lodeon, F. V. (1970). Localization of depletion-sensitive and depletion-resistant norepinephrine storage sites in autonomic ganglia.J. Pharmacol. exp. Ther. 174, 56–71.

    Google Scholar 

  • Williams, T. H. &Palay, S. L. (1969). Ultrastructure of the small neurons in the superior cervical ganglion.Brain Res. 15, 17–34.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

University of Melbourne Senior Research Fellow, September 1971-August 1972

Sunshine Foundation and Rowden White Trust Overseas Research Fellow in the University on Melbourne, September 1971-August 1972

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eränkö, O., Eränkö, L., Hill, C.E. et al. Hydrocortisone-induced increase in the number of small intensely fluorescent cells and their histochemically demonstrable catecholamine content in cultures of sympathetic ganglia of the newborn rat. Histochem J 4, 49–58 (1972). https://doi.org/10.1007/BF01005268

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01005268

Keywords

Navigation