Chronic NMDA receptor blockade or muscimol inhibition of cerebellar cortical neuronal activity alters the development of spinocerebellar afferent topography.

The requirement for cerebellar cortical neuronal activity in the development of spinocerebellar afferent topography was investigated in neonatal rats. In adult rats lower thoracic-upper lumbar spinocerebellar projections are localized to sharply circumscribed patches in the granule cell layer of the cerebellar anterior lobe. In transverse sections these patches appear as sagittally oriented stripes. This pattern develops postnatally as many spinal axons which initially project between the incipient stripes are eliminated thereby sharpening the stripe boundaries. We attempted to alter cerebellar cortical neuronal activity in neonatal animals to study the effects of these changes on the development of spinocerebellar stripes. In some experiments glutaminergic excitatory synaptic transmission was chronically blocked with the N-methyl-D-aspartate (NMDA) receptor antagonist 2-aminophosphovaleric acid (APV). In other experiments postsynaptic activity was directly inhibited by the gamma-aminobutyric acid agonist muscimol. Chronic exposure to APV or to muscimol did not affect the initial development of spinocerebellar projections; many spinal axons were present in the anterior lobe and arranged in incipient stripes. Both the APV and the muscimol appeared to prevent the elimination of interstripe projections; consequently the boundaries of the stripes remained poorly defined. These findings suggest that cerebellar cortical neuronal activity is a necessary requirement for the refinement of spinal afferent topography in the anterior lobe.

[1]  E. Debski,et al.  N-methyl-D-aspartate receptor antagonist desegregates eye-specific stripes. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[2]  S B Udin,et al.  Formation of topographic maps. , 1988, Annual review of neuroscience.

[3]  A. Ganong,et al.  Excitatory amino acid neurotransmission: NMDA receptors and Hebb-type synaptic plasticity. , 1988, Annual review of neuroscience.

[4]  M. Stryker,et al.  Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents. , 1988, Science.

[5]  W M Cowan,et al.  Activity and the control of ganglion cell death in the rat retina. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[6]  G. Edelman,et al.  The NO hypothesis: possible effects of a short-lived, rapidly diffusible signal in the development and function of the nervous system. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[7]  Edward C. Cox,et al.  Axonal guidance in the chick visual system: Posterior tectal membanes induce collapse of growth cones from the temporal retina , 1990, Neuron.

[8]  J. Silver Studies on the factors that govern directionality of axonal growth in the embryonic optic nerve and at the chiasm of mice , 1984, The Journal of comparative neurology.

[9]  E. Joosten,et al.  Astrocytes and guidance of outgrowing corticospinal tract axons in the rat. An immunocytochemical study using anti-vimentin and anti-glial fibrillary acidic protein , 1989, Neuroscience.

[10]  James W. Fawcett,et al.  The role of electrical activity in the formation of topographic maps in the nervous system , 1985, Trends in Neurosciences.

[11]  M. Stryker,et al.  Neural plasticity without postsynaptic action potentials: less-active inputs become dominant when kitten visual cortical cells are pharmacologically inhibited. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[12]  J. Garthwaite,et al.  NMDA receptor activation induces nitric oxide synthesis from arginine in rat brain slices. , 1989, European journal of pharmacology.

[13]  M. Constantine-Paton,et al.  Patterned activity, synaptic convergence, and the NMDA receptor in developing visual pathways. , 1990, Annual review of neuroscience.

[14]  M. Constantine-Paton,et al.  Eye-specific segregation requires neural activity in three-eyed Rana pipiens , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  J. Garthwaite,et al.  Synaptic activation of N-methyl-d-aspartate and non-N-methyl-d-aspartate receptors in the mossy fibre pathway in adult and immature rat cerebellar slices , 1989, Neuroscience.

[16]  A. Rotter,et al.  Expression of GABAA/benzodiazepine receptor alpha 1-subunit mRNA and [3H]flunitrazepam binding sites during postnatal development of the mouse cerebellum. , 1991, Brain research. Developmental brain research.

[17]  J. Garthwaite,et al.  Nanomolar N(G)-nitroarginine inhibits NMDA-induced cyclic GMP formation in rat cerebellum. , 1990, European journal of pharmacology.

[18]  C. Sotelo,et al.  Development of the spinocerebellar system in the postnatal rat , 1985, The Journal of comparative neurology.

[19]  D. Tolbert,et al.  Lower thoracic-upper lumbar spinocerebellar projections in rats: A complex topography revealed in computer reconstructions of the unfolded anterior lobe , 1993, Neuroscience.

[20]  A. Rotter,et al.  The ontogeny of [3H]muscimol binding sites in the C57BL/6J mouse cerebellum. , 1987, Brain research.

[21]  J. Watkins,et al.  2-Amino-5-phosphonovalerate (2APV), a potent and selective antagonist of amino acid-induced and synaptic excitation , 1981, Neuroscience Letters.

[22]  M. Constantine-Paton,et al.  N-methyl-D-aspartate receptor antagonists disrupt the formation of a mammalian neural map. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[23]  C. Daniel,et al.  Elvax 40P implants: sustained, local release of bioactive molecules influencing mammary ductal development. , 1982, Developmental biology.

[24]  K D Miller,et al.  Visual responses in adult cat visual cortex depend on N-methyl-D-aspartate receptors. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[25]  M. Schwab,et al.  Channeling of developing rat corticospinal tract axons by myelin- associated neurite growth inhibitors , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  J. Changeux,et al.  Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks , 1976, Nature.

[27]  S. Rabacchi,et al.  Involvement of the N-methyl D-aspartate (NMDA) receptor in synapse elimination during cerebellar development. , 1992, Science.

[28]  W. Harris,et al.  Axonal pathfinding in the absence of normal pathways and impulse activity , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  J. Garthwaite,et al.  Excitatory Amino Acid Receptors Coupled to the Nitric Oxide/Cyclic GMP Pathway in Rat Cerebellum During Development , 1991, Journal of neurochemistry.

[30]  D. Steindler Glial boundaries in the developing nervous system. , 1993, Annual review of neuroscience.

[31]  Wilhelm Streinzer,et al.  Horseradish peroxidase histochemistry on mounted sections from embedded specimen: a simple method for serial reconstruction of neuronal projections , 1986, Journal of Neuroscience Methods.

[32]  R. Hawkes,et al.  Parasagittal organization of the rat cerebellar cortex: Direct comparison of purkinje cell compartments and the organization of the spinocerebellar projection , 1990, The Journal of comparative neurology.

[33]  J. Garthwaite,et al.  Selective loss of Purkinje and granule cell responsiveness to N-methyl-D-aspartate in rat cerebellum during development. , 1987, Brain research.

[34]  J. Garthwaite,et al.  Sources and targets of nitric oxide in rat cerebellum , 1992, Neuroscience Letters.

[35]  M. Cambray-Deakin,et al.  The expression of excitatory amino acid binding sites during neuritogenesis in the developing rat cerebellum. , 1990, Brain research. Developmental brain research.

[36]  M. Mesulam,et al.  Additional factors influencing sensitivity in the tetramethyl benzidine method for horseradish peroxidase neurohistochemistry. , 1980, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.