Reorganization of monoaminergic systems in the earthworm, Eisenia fetida, following brain extirpation.

The present study describes the major aspects of how monoaminergic (serotonin, dopamine) systems change in the course of regeneration of the brain in the earthworm (Eisenia fetida), investigated by immunocytochemistry, HPLC assay, and ligand binding. Following brain extirpation, the total regeneration time is about 80 days at 10 degrees C. On the 3rd postoperative day serotonin, and on the 11th postoperative day tyrosine hydroxylase-immunoreactive neurons can be observed in the wound tissue. Thereafter the number of the immunoreactive cells increases gradually, and by the 76th-80th postoperative days all serotonin- and tyrosine hydroxylase-immunopositive neurons can be found in their final positions, similarly to those observed in the intact brain. Labeled neurons located in the dorsal part of the regenerated brain appear earlier than the cells in lateral and ventral positions. Both serotonin- and tyrosine hydroxylase-immunoreactive neurons of the newly formed brain seem to originate from undifferentiated neuroblasts situated within and around the ventral ganglia and the pleura. Dopaminergic (tyrosine hydroxylase-immunoreactive) elements may additionally derive from the proliferation of neurons localized in the subesophageal ganglion and the pharyngeal nerve plexus. Following brain extirpation, both serotonin and dopamine levels, assayed by HPLC, first increase in the subesophageal ganglion; by the 25th day of regeneration, the monoamine content decreases in it and increases in the brain. Hence it is suggested that monoamines are at least partly transported from this ganglion to the regenerating brain. At the same time, (3)H-LSD binding can be detected in the regenerating brain from the 3rd postoperative day, showing a continuous increase until the 80th postoperative day, suggesting a guiding role of postsynaptic elements in the monoaminergic reinnervation of the newly formed brain.

[1]  M. Reuter,et al.  Neuronal signal substances in asexual multiplication and development in flatworms , 1996, Cellular and Molecular Neurobiology.

[2]  P. Zimmermann Fluoreszenzmikroskopische Studien über die Verteilung und Regeneration der Faserglia beiLumbricus terrestris L. , 1967, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[3]  T. Shinozawa,et al.  Inhibition of planarian regeneration by melatonin , 1991, Hydrobiologia.

[4]  H. Gras,et al.  Patterns of serotonin-immunoreactive neurons in the central nervous system of the earthworm Lumbricus terrestris L. , 1987, Cell and Tissue Research.

[5]  H. Gras,et al.  Patterns of serotonin-immunoreactive neurons in the central nervous system of the earthworm Lumbricus terrestris L. , 1987, Cell and Tissue Research.

[6]  J. C. Lodder,et al.  ACTH-Iike immunoreactivity in two electrotonically coupled giant neurons in the pond snail Lymnaea stagnalis , 1979, Cell and Tissue Research.

[7]  J. Burke Wound healing in Eisenia foetida (Oligochaeta) , 1974, Cell and Tissue Research.

[8]  H. Hartwig,et al.  The regeneration of the monoaminergic system in the cerebral ganglion of the earthworm, Allolobophora caliginosa , 1974, Cell and Tissue Research.

[9]  J. Kelemen Methode zur Imprägnation des in Paraffin eingebetteten Nervengewebes , 1965, Acta Neuropathologica.

[10]  G. Burnstock,et al.  5-Hydroxytryptamine-like immunoreactivity in the peripheral and central nervous systems of the leech Hirudo medicinalis , 2004, Cell and Tissue Research.

[11]  H. Myhrberg Monoaminergic mechanisms in the nervous system of Lumbricus terrestris (L.) , 2004, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[12]  A. Maule,et al.  Development of the nervous system in Dugesia tigrina during regeneration after fission and decapitation , 1996 .

[13]  K. Elekes,et al.  Octopamine in the central nervous system of Oligochaeta: an immunocytochemical and biochemical study , 1996, Cell and Tissue Research.

[14]  J. Hámori,et al.  The number of ganglion cells in the intact and regenerated nervous system in the earthworm (Lumbricus terrestris). , 1994, Acta biologica Hungarica.

[15]  G. Bittner,et al.  Axonal conduction and electrical coupling in regenerating earthworm giant axons , 1992, Experimental Neurology.

[16]  S. Kurabuchi,et al.  Effect of Delay in Anterior or Posterior Amputation on Regeneration of Short Fragments of PlanarialDevelopmental Biologyr , 1992 .

[17]  G. Bittner,et al.  Analysis of neuritic outgrowth from severed giant axons in Lumbricus terrestris , 1992, The Journal of comparative neurology.

[18]  B. Zipser,et al.  The segmentation of the leech nervous system is prefigured by myogenic cells at the embryonic midline expressing a muscle-specific matrix protein , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  C. R. Fourtner,et al.  Morphallaxis in an aquatic oligochaete, Lumbriculus variegatus: reorganization of escape reflexes in regenerating body fragments. , 1990, Developmental biology.

[20]  J. Garcia-Fernández,et al.  Growth, Degrowth and Regeneration as Developmental Phenomena in Adult Freshwater Planarians , 1990 .

[21]  R. Cole,et al.  Glial processes, identified through their glial‐specific 130 kD surface glycoprotein, are juxtaposed to sites of neurogenesis in the leech germinal plate , 1989, Glia.

[22]  G. Bittner,et al.  Developmental and other factors affecting regeneration of crayfish CNS axons , 1987, The Journal of comparative neurology.

[23]  S. Blackshaw Organisation and Development of the Peripheral Nervous System in Annelids , 1987 .

[24]  A. Bautz,et al.  Somatostatin-like peptide and regeneration capacities in planarians. , 1986, General and comparative endocrinology.

[25]  S. Palay,et al.  Serotonin neurons on the ventral brain surface. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[26]  K. McCarthy,et al.  In vivo and in vitro development of serotonergic neurons , 1982, Brain Research Bulletin.

[27]  C. Hulsebosch,et al.  Regeneration of axons and nerve cell bodies in the CNS of annelids , 1981, The Journal of comparative neurology.

[28]  J. Lauder,et al.  Maternal influences on tryptophan hydroxylase activity in embryonic rat brain. , 1981, Developmental neuroscience.

[29]  K. J. Muller,et al.  The morphological and physiological properties of a regenerating synapse in the C.N.S. of the leech , 1979, The Journal of comparative neurology.

[30]  I. Parnas,et al.  Destruction of a single cell in the central nervous system of the leech as a means of analysing its connexions and functional role , 1978, The Journal of physiology.

[31]  Nentwig Mr Comparative morphological studies of head development after decapitation and after fission in the planarian Dugesia dorotocephala. , 1978 .

[32]  H. Burden,et al.  Catecholamines and morphogenesis of the chick neural tube and notochord. , 1973, The American journal of anatomy.

[33]  R. Coggeshall,et al.  CHEMICAL AND ULTRASTRUCTURAL IDENTIFICATION OF 5-HYDROXYTRYPTAMINE IN AN IDENTIFIED NEURON , 1969, The Journal of cell biology.

[34]  S. Rude Monoamine‐containing neurons in the nerve cord and body wall of Lumbricus terrestris , 1966, The Journal of comparative neurology.

[35]  H. Barr Regeneration and Natural Selection , 1964, The American Naturalist.

[36]  E. Hibbard Regeneration in the severed spinal cord of chordate larvae of Petromyzon marinus , 1963 .