Skip to main content
Log in

Seasonal variation of serotonin content and nonassociative learning of swim induction in the leech Hirudo medicinalis

  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Summary

It is possible to obtain habituation of swim induction by stimulating the leech with repetitive light electrical trains. After obtaining this simple form of nonassociative learning, it is also possible to potentiate its response by a series of nociceptive skin brushings (dishabituation). Serotonin applied to the animal is the only neurotransmitter found to mimick dishabituation. We have observed that in the period April–June most animals did not exhibit potentiation of the swimming response after nociceptive stimulation while injection of serotonin mimicked dishabituation as in the animals treated in the period October–March. We have seen correlation between the changes in nonassociative learning and the seasonal variation of serotonin levels in segmental ganglia. This finding strengthens the hypothesis of serotonin as the neurotransmitter mediating dishabituation in swim induction of the leech.

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

Abbreviations

AHP :

afterhyperpolarization

HPLC :

high pressure liquid chromatography

References

  • Alkon DL, Naito S (1986) Biochemical mechanism of memory storage. J Physiol Paris 81:252–260

    Google Scholar 

  • Bagnoli P, Magni F (1975) Synaptic inputs to Retzius' cells in the leech. Brain Res 96:147–152

    Google Scholar 

  • Baylor DA, Nicholls JG (1969) After-effects of nerve impulses on signalling in the central nervous system of the leech. J Physiol Lond 203:571–589

    Google Scholar 

  • Belardetti F, Biondi C, Colombaioni L, Brunelli M, Trevisani A (1982) Role of serotonin and cAMP on facilitation of the fast conducting system activity in the leech, Hirudo medicinalis. Brain Res 246: 89–103

    Google Scholar 

  • Belardetti F, Biondi C, Brunelli M, Fabri M, Trevisani A (1983) Heterosynaptic facilitation and behavioral sensitization are inhibited by lowering endogenous cAMP in Aplysia. Brain Res 288:95–104

    Google Scholar 

  • Belardetti F, Brunelli M, Demontis G, Sonetti D (1984) Serotonin and Retzius cell depress the hyperpolarization following impulses of leech touch cell. Brain Res 300:91–102

    Google Scholar 

  • Boulis NM, Sahley CL (1988) A behavioral analysis of habituation and sensitization of shortening in the semi-intact leech. J Neurosci 8:4621–4627

    Google Scholar 

  • Brodfuehrer PD, Friesen WO (1986) Control of leech swimming activity by the cephalic ganglia. J Neurobiol 17:697–705

    Google Scholar 

  • Brunelli M, Demontis G, Traina G (1985) Role of serotonin and cAMP in short-term changes underlying simple forms of learning process. In: Will BE, Schmitt P, Dalrymple-Alford JC (ed) Brain plasticity, learning and memory. Plenum Publishing Corp., London, pp 97–106

    Google Scholar 

  • Brunelli M, Colombaioni L, Demontis, Traina G (1986) Role of serotonin on cellular mechanism of non associative learning in swim behavior of the leech Hirudo medicinalis. In: Biggio G, Spano PF, Toffano G, Gessa GL (eds) Modulation of central and peripheral transmitter function. Fidia Res Ser Symp Neurosci III. Liviana Press, Padova, pp 527–531

    Google Scholar 

  • Brunelli M, Colombaioni L, Traina G (1988) Mechanism of plasticity in short and long-term learning processes in invertebrates. In: Biggio G, Spano PF, Toffano G, Appel SH, Gessa GL (eds) Neuronal plasticity and trophic factors. Liviana Press, Padova, pp 129–132

    Google Scholar 

  • Coggeshall RE, Yaksta-Sauerland BA (1974) The localization of 5-hydroxytryptamine in chromaffin cells of the leech body wall. J Comp Neurol 156:459–470

    Google Scholar 

  • Debski EA, Friesen WO (1985) Habituation of swimming activity in the medicinal leech. J Exp Biol 116:169–188

    Google Scholar 

  • Debski EA, Friesen WO (1986) Role of central interneurons in habituation of swimming activity in the medicinal leech. J Neurophysiol 55:977–994

    Google Scholar 

  • Debski FA, Friesen WO (1987) Intracellular stimulation of sensory cells elicits swimming activity in the medicinal leech. J Comp Physiol A 160:447–457

    Google Scholar 

  • Della Corte L, Nistri A (1974) Amine oxidase activity in tissues of the leech Hirudo medicinalis. Br J Pharmacol 52:129P

  • Dickinson MH, Lent CM (1984) Feeding behavior of the medicinal leech, Hirudo medicinalis. J Comp Physiol A 154:449–455

    Google Scholar 

  • Kandel ER, Schwartz JH (1982) Molecular biology of learning: modulation of transmitter release. Science 218:433–443

    Google Scholar 

  • Kandel ER, Klein M, Castellucci VF, Schacher S, Goelet P (1986) Some principles emerging from the study of short- and long-term memory. Neurosci Res 3:498–520

    Google Scholar 

  • Kilts CD, Breese GR, Mailman RB (1981) Simultaneous quantification of dopamine, 5-hydroxytryptamine and four metabolically related compounds by means of reversed-phase high-performance liquid chromatography with electrochemical detection. J Chromatography 225:347–357

    Google Scholar 

  • Kristan WB (1983) The neurobiology of swimming in the leech. Trends Neurosci 6:84–88

    Google Scholar 

  • Kristan WB, McGirr SJ, Simpson GV (1982) Behavioural and mechanosensory neurone responses to skin stimulation in leeches. J Exp Biol 96:143–160

    Google Scholar 

  • Lent CM (1973) Retzius cells: neuroeffectors controlling mucus release by the leech. Science 179:693–696

    Google Scholar 

  • Lent CM (1982a) Fluorescent properties of monoamine neurons following glyoxylic acid treatment of intact leech ganglia. Histochemistry 75:77–89

    Google Scholar 

  • Lent CM (1982b) Serotonin-containing neurones within the segmental nervous system of the leech. In: Osborne NN, Wiley J (eds) Biology of serotonergic transmission. New York, pp 431–455

  • Lent CM (1984) Quantitative effects of a neurotoxin upon serotonin levels within tissue compartments of the medicinal leech. J Neurobiol 15:309–323

    Google Scholar 

  • Lent CM, Dickinson MH (1984) Serotonin integrates the feeding behavior of the medicinal leech. J Comp Physiol A 154:457–471

    Google Scholar 

  • Lent CM, Frazer BM (1977) Connectivity of the monoamine-containing neurones in the central nervous system of the leech. Nature 266:844–847

    Google Scholar 

  • Mason A, Kristan WB (1982) Neuronal excitation, inhibition and modulation of leech longitudinal muscle. J Comp Physiol 146:527–536

    Google Scholar 

  • Muller KJ, Nicholls JG, Stent G (eds) (1981) Neurobiology of the leech. Cold Spring Harbor Laboratory, New York

    Google Scholar 

  • Nusbaum MP, Kristan WB (1986) Swim initiation in the leech by serotonin containing interneurones, cells 21 and 61. J Exp Biol 122:277–302

    Google Scholar 

  • Nusbaum MP, Friesen WO, Kristan WB, Pearce RA (1987) Neural mechanisms generating the leech swimming rhythm: swim-initiator neurons excite the network of swim oscillator neurons. J Comp Physiol A 161:355–366

    Google Scholar 

  • Pearce RA, Friesen WO (1985a) Intersegmental coordination of the leech swimming rhythm. I. Roles of cyclic period gradient and coupling strength. J Neurophysiol 54:1444–1459

    Google Scholar 

  • Pearce RA, Friesen WO (1985b) Intersegmental coordination of the leech swimming rhythm. II. Comparison of long and short chains of ganglia. J Neurophysiol 54:1460–1472

    Google Scholar 

  • Sahley CL, Ready DF (1988) Associative learning modifies two behaviors in the leech Hirudo medicinalis. J Neurosci 8:4612–4620

    Google Scholar 

  • Sawyer RT (1986) Leech biology and behaviour. Clarendon Press, Oxford

    Google Scholar 

  • Stent GS, Kristan WB (1981) The swimming rhythm. In: Muller KJ, Nicholls JG, Stent GS (eds) Neurobiology of the leech. Cold Spring Harbor Laboratory, New York, pp 113–146

    Google Scholar 

  • Stenzel K, Neuhoff V (1976) Tryptophan metabolism and the occurrence of amino acids and serotonin in the leech (Hirudo medicinalis) nervous system. J Neurosci Res 2:1–9

    Google Scholar 

  • Stern-Tomlinson W, Nusbaum MP, Perez LE, Kristan WB (1986) A kinematic study of crawling behavior in the leech Hirudo medicinalis. J Comp Physiol A 158:593–603

    Google Scholar 

  • Willard AL (1981) Effects of serotonin on the generation of the motor program for swimming by the medicinal leech. J Neurosci 1:936–944

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Catarsi, S., Garcia-Gil, M., Traina, G. et al. Seasonal variation of serotonin content and nonassociative learning of swim induction in the leech Hirudo medicinalis . J Comp Physiol A 167, 469–474 (1990). https://doi.org/10.1007/BF00190817

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00190817

Key words

Navigation