Functional alterations of cat abducens neurons after peripheral tetanus neurotoxin injection.

Tetanus neurotoxin (TeNT) cleaves synaptobrevin, a protein involved in synaptic vesicle docking and fusion, thereby preventing neurotransmitter release and causing a functional deafferentation. We injected TeNT into the lateral rectus muscle of adult cats at 0.5 or 5 ng/kg (low and high dose, respectively). In the periphery, TeNT slightly slowed motor axon conduction velocity, and at high doses, partially blocked neuromuscular transmission. TeNT peripheral actions displayed time courses different to the more profound and longer-lasting central actions. Central effects were first observed 2 days postinjection and reversed after 1 mo. The low dose induce depression of inhibitory inputs, whereas the high dose produce depression of both inhibitory and excitatory inputs. Simultaneous recordings of eye movement and neuronal firing revealed that low-dose injections specifically reduced inhibition of firing during off-directed saccadic movements, while high-dose injections of TeNT affected both inhibitory and excitatory driven firing patterns. Motoneurons and abducens interneurons were both affected in a similar way. These alterations resulted in modifications in all discharge characteristic analyzed such as background firing, threshold for recruitment, and firing sensitivities to both eye position and velocity during spontaneous movements or vestibulo-ocular reflexes. Removal of inhibition after low-dose injections also altered firing patterns, and although firing activity increased, it did not result in muscle tetanic contractions. Removal of inhibition and excitation by high-dose injections resulted in a decrease in firing modulation with eye movements. Our findings suggest that the distinct behavior of oculomotor and spinal motor output following TeNT intoxication could be explained by their different interneuronal and proprioceptive control.

[1]  W. Rall Distinguishing theoretical synaptic potentials computed for different soma-dendritic distributions of synaptic input. , 1967, Journal of neurophysiology.

[2]  A. Pastor,et al.  Discharge characteristics of axotomized abducens internuclear neurons in the adult cat , 2000, The Journal of comparative neurology.

[3]  A. Pastor,et al.  Effects of target depletion on adult mammalian central neurons: Morphological correlates , 1994, Neuroscience.

[4]  J. Mellanby,et al.  How does tetanus toxin act? , 1981, Neuroscience.

[5]  A. Schmitt,et al.  Different effects of botulinum A toxin and tetanus toxin on the transmitter releasing process at the mammalian neuromuscular junction , 1981, Neuroscience Letters.

[6]  L. Mendell Modifiability of spinal synapses. , 1984, Physiological reviews.

[7]  R. Cull Rôle of axonal transport in maintaining central synaptic connections , 1975, Experimental Brain Research.

[8]  M. Charlton,et al.  Retention of cleaved synaptosome-associated protein of 25 kDa (SNAP-25) in neuromuscular junctions: a new hypothesis to explain persistence of botulinum A poisoning. , 1999, Canadian journal of physiology and pharmacology.

[9]  W. E. Watson The response of motor neurones to intramuscular injection of botulinum toxin , 1969, The Journal of physiology.

[10]  M. Schwab,et al.  Electron microscopic evidence for a transsynaptic migration of tetanus toxin in spinal cord motoneurons: An autoradiographic and morphometric study , 1976, Brain Research.

[11]  K. Takano Neurophysiolocical aspects of tetanus toxin effects on the motor system , 1985, European Journal of Epidemiology.

[12]  M. Shahani,et al.  Neuropathy in tetanus , 1979, Journal of the Neurological Sciences.

[13]  Dale Purves,et al.  Trophic regulation of nerve cell morphology and innervation in the autonomic nervous system , 1988, Nature.

[14]  A. Pastor,et al.  Influence of the postsynaptic target on the functional properties of neurons in the adult mammalian central nervous system. , 1996 .

[15]  J. Lichtman,et al.  Axonal atrophy: The retraction reaction , 1999, Current Opinion in Neurobiology.

[16]  A. Pastor,et al.  Effects of botulinum neurotoxin type A on abducens motoneurons in the cat: alterations of the discharge pattern , 1997, Neuroscience.

[17]  D. H. Chen Qualitative and quantitative study of synaptic displacement in chromatolyzed spinal motoneurons of the cat , 1978, The Journal of comparative neurology.

[18]  J. M. Delgado-Garcia,et al.  Behavior of neurons in the abducens nucleus of the alert cat—I. Motoneurons , 1986, Neuroscience.

[19]  G. Bergey,et al.  Tetanus Toxin in Dissociated Spinal Cord Cultures: Long‐Term Characterization of Form and Action , 1986, Journal of neurochemistry.

[20]  B. Gustafsson,et al.  Effects of axotomy on the distribution of passive electrical properties of cat motoneurones. , 1984, The Journal of physiology.

[21]  H. Wellhöner,et al.  Electrical excitability of motoneurones in early local tetanus , 1979, Naunyn-Schmiedeberg's Archives of Pharmacology.

[22]  A. Pastor,et al.  Reversible deafferentation of abducens motoneurons and internuclear neurons with tetanus neurotoxin , 2001, Neuroreport.

[23]  R. de la Cruz Influence of the Postsynaptic Target on the Functional Properties of Neurons in the Adult Mammalian Central Nervous System , 1996, Reviews in the neurosciences.

[24]  J. Eccles,et al.  The action of tetanus toxin on the inhibition of motoneurones , 1957, The Journal of physiology.

[25]  R. Eckmiller Hysteresis in the static characteristics of eye position coded neurons in the alert monkey , 2004, Pflügers Archiv.

[26]  R Nowak Cell biologists get the message in New Orleans. , 1994, Science.

[27]  J. M. Delgado-García,et al.  Behavior of reticular, vestibular and prepositus neurons terminating in the abducens nucleus of the alert cat , 2004, Experimental Brain Research.

[28]  A. Pastor,et al.  Influence of afferent synaptic innervation on the discharge variability of cat abducens motoneurones , 2002, The Journal of physiology.

[29]  H. Wellhöner,et al.  Is there retrograde axonal transport of tetanus toxin in both α and γ fibres? , 1977, Nature.

[30]  M. Kuno,et al.  Differentiation of motoneurones and skeletal muscles in kittens. , 1975, The Journal of physiology.

[31]  E. Muñoz-Martínez,et al.  Differential reaction of fast and slow α‐motoneurones to axotomy , 1974 .

[32]  H. Henatsch,et al.  Tetanus toxin induced actions on spinal Renshaw cells and Ia-inhibitory interneurones during development of local tetanus in the cat , 1977, Experimental Brain Research.

[33]  G. Kreutzberg,et al.  Displacement of synaptic terminals from regenerating motoneurons by microglial cells , 2004, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[34]  D. Kernell,et al.  Effects of physiological amounts of high- and low-rate chronic stimulation on fast-twitch muscle of the cat hindlimb. I. Speed- and force-related properties. , 1987, Journal of neurophysiology.

[35]  A. Pastor,et al.  Correlation between CGRP immunoreactivity and firing activity in cat abducens motoneurons , 2002, The Journal of comparative neurology.

[36]  J. D. Porter,et al.  Structural organization of the extraocular muscles. , 1988, Reviews of oculomotor research.

[37]  A. Krassioukov,et al.  Changes in immunoreactivity for growth associated protein-43 suggest reorganization of synapses on spinal sympathetic neurons after cord transection , 1997, Neuroscience.

[38]  R. Burke Motor Units: Anatomy, Physiology, and Functional Organization , 1981 .

[39]  L. Landmesser,et al.  Axotomy Mimicked by Localized Colchicine Application , 1972, Science.

[40]  M. Meredith,et al.  Retractor bulbi muscle responses to oculomotor nerve and nucleus stimulation in the cat , 1981, Brain Research.

[41]  D. Robinson,et al.  Absence of a stretch reflex in extraocular muscles of the monkey. , 1971, Journal of neurophysiology.

[42]  T Gordon,et al.  Fast-to-slow conversion following chronic low-frequency activation of medial gastrocnemius muscle in cats. I. Muscle and motor unit properties. , 1997, Journal of neurophysiology.

[43]  R. Baker,et al.  Behavior of neurons in the abducens nucleus of the alert cat—II. Internuclear neurons , 1986, Neuroscience.

[44]  G K Bergey,et al.  Differential effects of tetanus toxin on inhibitory and excitatory synaptic transmission in mammalian spinal cord neurons in culture: a presynaptic locus of action for tetanus toxin. , 1987, Journal of neurophysiology.

[45]  J. Kellerth,et al.  Changes in synaptology of adult cat spinal α-motoneurons after axotomy , 1998, Experimental Brain Research.

[46]  A. Harvey,et al.  At least two mechanisms are involved in the death of retinal ganglion cells following target ablation in neonatal rats , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[47]  D. Faber,et al.  Axotomy-induced alterations in the electrophysiological characteristics of neurons , 1990, Progress in Neurobiology.

[48]  R Llinás,et al.  Enhancement of synaptic transmission by dendritic potentials in chromatolysed motoneurones of the cat , 1970, The Journal of physiology.

[49]  B LIBET,et al.  The behaviour of chromatolysed motoneurones studied by intracellular recording , 1958, The Journal of physiology.

[50]  J. Trontelj,et al.  Acetylcholinesterase mRNA Level and Synaptic Activity in Rat Muscles Depend on Nerve-Induced Pattern of Muscle Activation , 1998, The Journal of Neuroscience.

[51]  A. Pastor,et al.  Effects of botulinum neurotoxin type A on abducens motoneurons in the cat: ultrastructural and synaptic alterations , 1997, Neuroscience.

[52]  S. Waxman,et al.  Downregulation of Na+ channel mRNA in olfactory bulb tufted cells following deafferentiation , 1997, Neuroreport.

[53]  M. Matthews,et al.  Detachment of structurally intact nerve endings from chromatolytic neurones of rat superior cervical ganglion during the depression of synaptic transmission induced by post‐ganglionic axotomy. , 1975, The Journal of physiology.

[54]  Spencer Rf,et al.  Structural organization of the extraocular muscles. , 1988 .

[55]  A. Grantyn,et al.  Sources of direct excitatory and inhibitory inputs from the medial rhombencephalic tegmentum to lateral and medial rectus motoneurons in the cat , 2004, Experimental Brain Research.

[56]  R Llinás,et al.  Alterations of synaptic action in chromatolysed motoneurones of the cat , 1970, The Journal of physiology.

[57]  S. J. Goldberg,et al.  Extraocular motor units: type classification and motoneuron stimulation frequency-muscle unit force relationships , 1992, Brain Research.

[58]  A. Pastor,et al.  Response of abducens internuclear neurons to axotomy in the adult cat , 2000, The Journal of comparative neurology.

[59]  J. Munson,et al.  Fast-to-slow conversion following chronic low-frequency activation of medial gastrocnemius muscle in cats. II. Motoneuron properties. , 1997, Journal of neurophysiology.

[60]  L M Mendell,et al.  Connectivity changes of Ia afferents on axotomized motoneurons. , 1974, Brain research.

[61]  K. Kanda,et al.  Effect of tetanus toxin on the excitatory and the inhibitory post‐synaptic potentials in the cat motoneurone. , 1983, The Journal of physiology.

[62]  Niraj S. Desai,et al.  Plasticity in the intrinsic excitability of cortical pyramidal neurons , 1999, Nature Neuroscience.

[63]  H. Kretzschmar,et al.  Relations between the effect of tetanus toxin on the neuromuscular transmission and histological functional properties of various muscles of the rat , 2004, Experimental Brain Research.

[64]  N. Wallace,et al.  Axotomy-like changes in cat motoneuron electrical properties elicited by botulinum toxin depend on the complete elimination of neuromuscular transmission , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[65]  M. Dutia,et al.  Intrinsic excitability changes in vestibular nucleus neurons after unilateral deafferentation , 2001, Brain Research.

[66]  P. Calabresi,et al.  Selective depression of synaptic transmission by tetanus toxin: A comparative study on hippocampal and neostriatal slices , 1989, Neuroscience.

[67]  D. Kernell,et al.  Effects of physiological amounts of high- and low-rate chronic stimulation on fast-twitch muscle of the cat hindlimb. II. Endurance-related properties. , 1987, Journal of neurophysiology.

[68]  Reversible effects of low doses of tetanus toxin on synaptic inhibition in the substantia nigra and turning behaviour in the rat , 1980, Brain Research.

[69]  Gordon L. Ruskell,et al.  Extraocular muscle proprioceptors and proprioception , 1999, Progress in Retinal and Eye Research.

[70]  J. M. Delgado-Garcia,et al.  Behavior of neurons in the abducens nucleus of the alert cat—III. Axotomized motoneurons , 1988, Neuroscience.

[71]  L. Duchen,et al.  The effects of tetanus toxin on neuromuscular transmission and on the morphology of motor end‐plates in slow and fast skeletal muscle of the mouse , 1973, The Journal of physiology.

[72]  D. Purves Functional and structural changes in mammalian sympathetic neurones following colchicine application to post‐ganglionic nerves. , 1976, The Journal of physiology.

[73]  D. Price,et al.  Tetanus toxin: direct evidence for retrograde intraaxonal transport. , 1975, Science.

[74]  B. Barres,et al.  The relationship between neuronal survival and regeneration. , 2000, Annual review of neuroscience.

[75]  M. Poo,et al.  Retrograde signaling in the development and modification of synapses. , 1998, Physiological reviews.

[76]  J. Mellanby,et al.  Long‐term changes in hippocampal physiology and learning ability of rats after intrahippocampal tetanus toxin. , 1985, The Journal of physiology.

[77]  Ultrastructural study of vestibular and reticular projections to the abducens nucleus , 2004, Experimental Brain Research.

[78]  S. Salmons,et al.  Significance of impulse activity in the transformation of skeletal muscle type , 1976, Nature.

[79]  K. Takano,et al.  Gamma-bias of the muscle poisoned by tetanus toxin , 2004, Naunyn-Schmiedeberg's Archives of Pharmacology.