Summary
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1.
Intracellular stimulation of each of three different types of mechanoreceptors, the T, P and N cells, evokes swimming behavior in leech preparations. Stimulation of an individual N cell or P cell evoked swimming in 75% and 53% respectively, of the preparations tested. Stimulation of an individual T cell was ineffective in eliciting swimming; however, simultaneous stimulation of two T cells evoked swimming in 59% of our preparations.
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2.
Stimulation of mechanosensory neurons elicited swimming activity for a limited number of trials; i.e. the response habituated. The number of swim episodes evoked before habituation to criterion did not differ significantly for the different types of mechanoreceptors.
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3.
The duration of swim episodes declined significantly over the course of N cell stimulation. The tendency for swim length to decline with repeated stimulation was present as well for swim episodes elicited by P or T cell stimulation.
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4.
Swim initiation recovered spontaneously following habituation resulting from T cell stimulation. Spontaneous recovery following N cell stimulation was not demonstrated. However, N cell stimulation evoked swimming again after DP nerve shock or to a limited extent, after cell 204 stimulation. Spontaneous recovery of swim initiation to P cell stimulation was not investigated.
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5.
A previous study detailed habituation of swimming activity to mechanical stimulation of the body wall (Debski and Friesen 1985). Only the T cells are activated significantly by this stimulus. Stimulation of sensory receptors other than mechanoreceptors was not effective in eliciting swimming in our preparation. We conclude that T cells mediate swim initiation elicited by stroking of the body wall and that the cessation of swimming to this stimulus is not due to sensory adaptation.
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References
Baylor DA, Nicholls JG (1969) Chemical and electrical synaptic connexions between cutaneous mechanoreceptor neurones in the central nervous system of the leech. J Physiol 203:591–609
Blackshaw SE, Nicholls JG, Parnas I (1982) Physiological responses, receptive fields and terminal arborizations of nociceptive cells in the leech. J Physiol 326:251–260
Brodfuehrer PD, Friesen WO (1984) A sensory system initiating swimming activity in the medicinal leech. J Exp Biol 108:341–355
Debski EA, Friesen WO (1985) Habituation of swimming activity in the medicinal leech. J Exp Biol 116:169–188
Debski EA, Friesen WO (1986) Role of central interneurons in habituation of swimming activity in the medicinal leech. J Neurophysiol 55:977–994
Friesen WO (1981) Physiology of water motion detection in the medicinal leech. J Exp Biol 92:255–275
Friesen WO (1985) Neuronal control of leech swimming movements: interactions between cell 60 and previously described oscillator neurons. J Comp Physiol A 156:231–242
Friesen WO, Poon M, Stent GS (1978) Neuronal control of swimming in the medicinal leech. IV. Identification of a network of oscillatory interneurones. J Exp Biol 75:25–43
Gillon JW, Wallace BG (1984) Segmental variation in the arborization of identified neurons in the leech central nervous system. J Comp Neurol 228:142–148
Johansen J, Hockfield S, McKay RDG (1984) Distribution and morphology of nociceptive cells in the CNS of three species of leeches. J Comp Neurol 226:263–273
Johansen J, Yang J, Kleinhaus AL (1984) Actions of procaine on specific nociceptive cells in leech central nervous system. J Neurosci 4:1253–1261
Kretz JR, Stent GS, Kristan WB Jr (1976) Photosensory input pathways in the medicinal leech. J Comp Physiol 106:1–37
Kristan WB Jr, Calabrese RL (1976) Rhythmic swimming activity in neurones of the isolated nerve cord of the leech. J Exp Biol 65:643–668
Kristan WB Jr, Stent GS (1976) Peripheral feedback in the leech swimming rhythm. Cold Spring Harbor Symp Quant Biol 40:663–674
Kristan WB Jr, McGirr SJ, Simpson GV (1982) Behavioral and mechanosensory neurone response to skin stimulation in leeches. J Exp Biol 96:143–160
Mann KM (1962) Leeches (Hirudinea). Their structure, physiology, ecology and embryology. Pergamon Press, New York, pp 79–100
McKay R, Hockfield S, Johansen J, Kleina L, Thompson I (1982) Monoclonal antibodies as probes of the leech nervous system. Soc Neurosci Abstr 8:714
Nicholls JG, Baylor DA (1968) Specific modalities and receptive fields of sensory neurons in the CNS of the leech. J Neurophysiol 31:740–756
Nusbaum MP, Kristan WB Jr (1986) Swim initiation in the leech by serotonin-containing interneurones, cells 21 and 61. J Exp Biol 122:277–302
Ort CA, Kristan WB Jr, Stent GS (1974) Neuronal control of swimming in the medicinal leech. II. Identification and connections of motor neurons. J Comp Physiol 94:121–154
Phillips CE, Friesen WO (1982) Ultrastructure of the watermovement-sensitive sensilla in the medicinal leech. J Neurobiol 13:473–486
Stent GS, Kristan WB Jr, Friesen WO, Ort CA, Poon M, Calabrese RL (1978) Neuronal generation of the leech swimming movement. Science 200:1348–1357
Weeks JC (1982) Synaptic basis of swim initiation in the leech. II. A pattern-generating neuron (cell 208) which mediates motor effects of swim-initiation neurons. J Comp Physiol 148:265–279
Weeks JC, Kristan WB Jr (1978) Initiation, maintenance and modulation of swimming in the medicinal leech by the activity of a single neurone. J Exp Biol 77:71–88
Willard A (1981) Effects of serotonin on the generation of the motor program for swimming by the medicinal leech. J Neurosci 1:936–944
Yau K-W (1976) Receptive fields, geometry and conduction block of sensory neurones in the central nervous system of the leech. J Physiol (Lond) 263:489–512
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Debski, E.A., Friesen, W.O. Intracellular stimulation of sensory cells elicits swimming activity in the medicinal leech. J. Comp. Physiol. 160, 447–457 (1987). https://doi.org/10.1007/BF00615078
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DOI: https://doi.org/10.1007/BF00615078