Skip to main content
Log in

Parallel pathways coordinate crawling in the medicinal leech, Hirudo medicinalis

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

Abstract

Changes in the behavior of crawling leeches were investigated after various kinds of manipulations, including selective transection or inactivation of body parts, as well as partial or complete transection of the central nerve cord, using a frame-by-frame analysis of video tapes of the crawling animals. From these studies, we found that: 1. Leeches made rhythmic crawling cycles even after their suckers were prevented from contacting the substrate by covering them over with glue. Hence, engagement and disengagement of the suckers are not necessary links in the crawling cycle. 2. Cutting the small, medial connective (Faivre's nerve) had no influence on crawling, but contraction during the whole-body shortening reflex was interrupted. Thus two behaviors which use the same motor output (i.e., whole-body shortening and the contraction phase of crawling) are mediated by two different pathways. 3. Cutting all the connectives between two ganglia in the middle of the leech resulted in a loss of coordination between the parts of the animal on either side of the cut. Therefore, temporally coordinated sucker activity must be mediated through these connectives. 4. Pieces of leech bodies produced by complete transection produced rhythmic crawling cycles as long as the pieces included the head or tail plus 2–4 adjacent midbody segments. In all cases, the crawling movements progressed without delays as the movements reached the cut ends. Pieces of animals that included only midbody segments did not produce crawling movements. 5. These results can be explained by a model composed of intersegmental pathways for both elongation and contraction, circuits in the head and tail brains that switch between elongation and contraction, and both ascending and descending inhibitory influences that determine when the cycle switches from elongation to contraction and back again.

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

C1-C7 :

caudal segments 1 through 7 (comprise the tail sucker)

Circ. :

circular muscle(s)

CD :

circular element driver

CPG :

central pattern generator

ED :

elongation element driver

El :

elongation

El init :

initiation of elongation

FN :

Faivre's nerve

fs :

+ front sucker attachment

s—:

front sucker release

Long :

longitudinal muscle(s)

M1-M21 :

midbody segments 1 through 21

R1-R4 :

rostral segments 1 through 4 (comprise the head)

rs :

+ rear sucker attachment

rs :

rear sucker release

Sens :

sensory input

SR :

stretch receptors(s)

ti :

tonic inhibition

References

  • Baader A, Kristan WB Jr (1992) Monitoring neuronal activity during discrete behaviors: a crawling, swimming and shortening device for tethered leeches. J Neurosci Meth 43: 215–223

    Google Scholar 

  • Baylor DA, Nicholls JG (1968) Chemical and electrical synaptic connections between cutaneous mechanoreceptor neurones in the central nervous system of the leech. J Physiol (Lond) 203: 591–609

    Google Scholar 

  • Blackshaw SE (1993) Stretch receptors and body wall muscle in leeches. Comp Biochem Physiol 105: 643–652

    Google Scholar 

  • Blackshaw SE, Kristan WB Jr (1990) Input from single stretch receptor neurones influences the centrally generated swim motor pattern in the leech. J Physiol (Lond) 425: 93

    Google Scholar 

  • Blackshaw SE, Thompson SWN (1988) Hyperpolarizing responses to stretch in sensory neurones innervating leech body wall muscle. J Physiol (Lond) 396: 121–137

    Google Scholar 

  • Brodfuehrer PD, Friesen WO (1986) From stimulation to undulation: an identified pathway for the control of swimming activity in the leech. Science 234: 1002–1004

    Google Scholar 

  • Delcomyn, F (1980) Neural basis of rhythmic behavior in animals. Science 210: 492–498

    Google Scholar 

  • Friesen WO (1989) Neuronal control of leech swimming movements. In: Jack JW (ed.) Neuronal and cellular oscillators Marcel Dekker, Basel, pp 269–316

    Google Scholar 

  • Getting PA, Dekin MS (1985) Tritonia swimming: a model system for integration within rhythmic motor systems. In: AI Selverston (ed) Model neural networks and behavior Plenum, New York, pp 3–20

    Google Scholar 

  • Gray J, Lissman HW, Pumphrey RJ (1938) The mechanism of locomotion in the leech (Hirudo medicinalis Ray). J Exp Biol 15: 408–430

    Google Scholar 

  • Grillner S, Matsushima T (1991) The neural network underlying locomotion in lamprey — synaptic and cellular mechanisms. Neuron 7: 1–15

    Google Scholar 

  • Grillner S, Wallén P, Brodin L, Lansner A (1991) Neuronal network generating locomotor behavior in lamprey: Circuitry, transmitters, membrance properties, and behavior. Annu Rev Neurosci 14: 169–200

    Google Scholar 

  • Honjo I (1936) Zum nervoesen Mechanismus de Gehbewegungen beim Blutegel. Annot Zool Japon 15: 378–381

    Google Scholar 

  • Kretz JR, Stent GS, Kristan WB Jr (1976) Photosensory input pathways in the medicinal leech. J Comp Physiol 106: 1–37

    Google Scholar 

  • Kristan WB Jr, Calabrese RL (1976) Rhythmic swimming activity in neurons of the isolated nerve cord of the leech. J Exp Biol 65: 643–668

    Google Scholar 

  • Kristan WB Jr, Stent G (1974) Peripheral feedback in the leech swimming rhythm. Cold Spring Harbor Symp Quan Biol 65: 663–674

    Google Scholar 

  • Kristan WB Jr, Stent GS, Ort CA (1974) Neuronal control of swimming in the medicinal leech. I. Dynamics of the swimming rhythm. J Comp Physiol 94: 97–119

    Google Scholar 

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

    Google Scholar 

  • Kristan WB Jr, Wittenberg G, Nusbaum MP, Stern-Tomlinson W (1988) Multifunctional interneurons in behavioral circuits of the medicinal leech. Experientia 44: 383–389

    Google Scholar 

  • Pearson K (1985) Are there central pattern generators for walking and flight in insects? In: Barnes WPJ, Gladden M (eds) Feedback and motor control in invertebrates and vertebrates Croom Held, London, 307–316

  • Pearson KG, Rossingnol S (1991) Fictive motor patterns in chronic spinal cats. J Neurophysiol 66: 1874–1887

    Google Scholar 

  • Peterson EL (1983) Visual processing in the leech central nervous system. Nature 303: 240–242

    Google Scholar 

  • Robertson RM, Pearson KG (1985) Neural circuits in the flight system of the locust. J Neurophysiol 53: 110–128

    Google Scholar 

  • Rowell CHF (1988) Mechanisms of flight steering in locusts. Experientia 44: 389–395

    Google Scholar 

  • Sawyer RT (1986) Leech biology and behavior. Volume I. Anatomy, physiology and behavior. Oxford, Clearendon Press

    Google Scholar 

  • Schlüter E (1933) Die Bedeutung des Centralnervensystems von Hirudo medicinalis für Locomotion und Raumorientierung. Z Wiss Zool 143: 538–593

    Google Scholar 

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

    Google Scholar 

  • Von Uexküll J (1905) Studien über den Tonus, III. Die Blutegel. Z Biol 46: 372

    Google Scholar 

  • Weeks JC (1981) Neuronal basis of leech swimming: Separation of swim initiation, pattern generation, and intersegmental coordination by selective lesions. J Neurophysiol 45: 698–723

    Google Scholar 

  • Weeks JC (1982) Synaptic basis of swim initiation in the leech. I. Connections of a swim-initiating neuron (cell 204) with motor neurons and pattern-generating “oscillator” neurons. J Comp Physiol 148: 253–263

    Google Scholar 

  • Wilkinson JM, Coggeshall RE (1975) Axonal numbers and sizes in the connectives and peripheral nerves of the leech. J Comp Neurol 162: 87–396

    Google Scholar 

  • Wittenberg G, Kristan WB Jr (1992) Analysis and modeling of the multisegmental coordination of shortening behavior in the medicinal leech. 1. Motor output pattern. J Neurophysiol 68: 1683–1692

    Google Scholar 

  • Young SR, Dedwylder RD II, Friesen WO (1981) Responses of the medicinal leech to water waves. J Comp Physiol 144: 11–116

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Baader, A.P., Kristan, W.B. Parallel pathways coordinate crawling in the medicinal leech, Hirudo medicinalis . J Comp Physiol A 176, 715–726 (1995). https://doi.org/10.1007/BF00192620

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00192620

Key words

Navigation