Skip to main content
Log in

Immunocytochemical demonstration of peptidergic cells in the pond snail Lymnaea stagnalis with an antiserum to the molluscan cardioactive tetrapeptide FMRF-amide

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Summary

With an antiserum to the molluscan cardioactive tetrapeptide FMRF-amide immunoreactive perikarya and nerve fibers were identified in the central and peripheral nervous system of the pond snail Lymnaea stagnalis. Their localization is described. The same antiserum yielded reactive product in particular cells of the epithelium of the alimentary tract. The use of two different fixatives, glutaraldehyde, and a mixture of glutaraldehyde, picric acid, and acetic acid (GPA) showed that certain nerve cells can be identified only in material fixed with either the one or the other of these two fixatives, a result which indicates that in Lymnaea more than one FMRF-amide-like substance may occur.

“Positive” axon endings were found in the periphery of various nerves, i.e., in places where neurohormones are released into the blood. Other fibers were found to end, probably synaptically, on other neurons, on epithelial cells in the stomach, and between muscle cells in various parts of the body, e.g., in the heart. In these cases the FMRF-amide-like substance may function as a neurotransmitter or a neuromodulator.

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

  • Agarwal RA, Ligon PJB, Greenberg MJ (1972) The distribution of cardioactive agents among molluscan species and tissues. Comp Gen Pharmac 3:249–260

    Google Scholar 

  • Blanchi D, Noviello L, Libonati M (1973) A neurohormone of cephalopods with cardioexcitatory activity. Gen Comp Endocrinol 21:267–277

    Google Scholar 

  • Boer HH, Schot LPC, Roubos EW, Maat A ter, Lodder JC, Reichelt D, Swaab DF (1979) ACTH-like immunoreactivity in two electrotonically coupled giant neurons in the pond snail Lymnaea stagnalis. Cell Tissue Res 202:231

    Google Scholar 

  • Boer HH, Schot LPC, Veenstra JA, Reichelt D (1980) Immunocytochemical identification of neural elements in the central nervous system of a snail, some insects, a fish, and a mammal with an antiserum to the molluscan cardio-excitatory tetrapeptide FMRF-amide. Cell Tissue Res 213:21–27

    Google Scholar 

  • Cottrell GA (1978) Actions of a “molluscan cardioexcitatory neuropeptide” on identified 5-hydroxy-tryptamine-containing neurons and their follower neurons in Helix aspersa. J Physiol (Lond) 284:130–131

    Google Scholar 

  • Cottrell GA (1980) Voltage dependent and voltage independent actions of the molluscan neuropeptide Phe-Met-Arg-Phe-NH2 on a snail neurone. J Physiol (Lond) 300:41

    Google Scholar 

  • Dockray GJ, Vaillant C, Williams RC (1981) New vertebrate brain-gut peptide related to a molluscan neuropeptide and a opioidpeptide. Nature 292:656–657

    Google Scholar 

  • Elo JE (1938) Das Nervensystem von Lymnaea stagnalis (L.). Lam Ann Zool Vanamo 6:1–40

    Google Scholar 

  • Frontali N, Williams L, Welsh JH (1967) Heart excitatory and inhibitory substances in molluscan ganglia. Comp Biochem Physiol 22:833–841

    Google Scholar 

  • Geraerts WPM, Leeuwen JPThM van, Nuyt K, de With ND (1981) Cardioactive peptides of the CNS of the pulmonate snail Lymnaea stagnalis. Exp 37:1168–1169

    Google Scholar 

  • Greenberg MJ, Price DA (1979) FMRF amide, a cardioexcitatory neuropeptide of molluscs: An agent in search of a mission. Am Zool 19:163–174

    Google Scholar 

  • Greenberg MJ, Price DA (1980) Cardioregulatory peptides in molluscs. In: Bloom FE (ed) Peptides: Integrators of cell and tissue function. Raven Press, New York, pp 107–126

    Google Scholar 

  • Grimmelikhuijzen CJP, Dockray GJ, Schot LPC (1982) FMRF amide-like immunoreactivity in the nervous system of Hydra. Histochemistry 73:499–509

    CAS  PubMed  Google Scholar 

  • Hekstra GP, Lever J (1960) Some effects of ganglion extirpation in Lymnaea stagnalis. Proc Kon Ned Akad Wet C 63:271–282

    Google Scholar 

  • Lloyd PE (1978) Distribution and molecular characteristics of cardioactive peptides in the snail, Helix aspersa. J Comp Physiol 128:269–276

    Google Scholar 

  • Pearse AGE (1969) The cytochemistry and ultrastructure of polypeptide hormone producing cells of the APUD-series and the embryologie, physiologic and pathologic implications of the concept. J Histochem Cytochem 17:303–313

    Google Scholar 

  • Pearse AGE, Takor Takor T (1976) Neuroendocrine embryology and the APUD concept. Clin Endocrinol 5: Suppl: 229–244

    Google Scholar 

  • Plesch B (1977) An ultrastructural study of the innervation of the musculature of the pond snail, Lymnaea stagnalis (L.) with reference to peripheral neurosecretion. Cell Tissue Res 183:353–369

    Google Scholar 

  • Price DA, Greenberg MJ (1977) Purification and characterization of a cardio-excitatory neuropeptide from the central ganglia of a bivalve mollusc. Prep Biochem 7:50–62

    Google Scholar 

  • Scharrer B (1978) Peptidergic neurons: facts and trends. Gen Comp Endocrinol 34:50–62

    Google Scholar 

  • Schot LPC, Boer HH, Swaab DF, Noorden S van (1981) Immunocytochemical demonstration of peptidergic neurons in the central nervous system of the pond snail Lymnaea stagnalis with antisera raised to biologically active peptides of vertebrates. Cell Tissue Res 216:273–291

    Google Scholar 

  • Smock T, Arch S, Lloyd P (1978) Secretory sources of egg-laying induction also influence the isolated Aplysia heart. Neurosci Abstr 4:206

    Google Scholar 

  • Sternberger LA (1974) Immunocytochemistry foundation of immunology series (Oster A, Weiss L, eds). Prentice Hall Inc, Englewood Cliffs, New Jersey

  • Swaab DF, Pool CW (1975) Specificity of oxytocin and vasopressin immunofluorescence. J Endocrinol 66:263–272

    Google Scholar 

  • Swindale NV, Benjamin (1976) The anatomy of neurosecretory neurones in the pond snail Lymnaea stagnalis (L.). Phil Trans Roy Soc Lond B 274:169–202

    Google Scholar 

  • Wendelaar Bonga SE (1970) Ultrastructure and histochemistry of neurosecretory cells and neurohaemal areas in the pond snail Lymnaea stagnalis (L.). Z Zellforsch 108:190–224

    Google Scholar 

  • Wydenes J, Minnen J, van Boer HH (1980) A comparative study on neurosecretion demonstrated by the alcian blue — alcian yellow technique in three terrestrial pulmonates (Styllommatophora). Cell Tissue Res 210:47–56

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schot, L.P.C., Boer, H.H. Immunocytochemical demonstration of peptidergic cells in the pond snail Lymnaea stagnalis with an antiserum to the molluscan cardioactive tetrapeptide FMRF-amide. Cell Tissue Res. 225, 347–354 (1982). https://doi.org/10.1007/BF00214687

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00214687

Key words

Navigation