Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex.

1. Dual voltage recordings were made from pairs of adjacent, synaptically connected thick tufted layer 5 pyramidal neurones in brain slices of young rat (14‐16 days) somatosensory cortex to examine the physiological properties of unitary EPSPs. Pre‐ and postsynaptic neurones were filled with biocytin and examined in the light and electron microscope to quantify the morphology of axonal and dendritic arbors and the number and location of synaptic contacts on the target neurone. 2. In 138 synaptic connections between pairs of pyramidal neurones 96 (70%) were unidirectional and 42 (30%) were bidirectional. The probability of finding a synaptic connection in dual recordings was 0.1. Unitary EPSPs evoked by a single presynaptic action potential (AP) had a mean peak amplitude ranging from 0.15 to 5.5 mV in different connections with a mean of 1.3 +/‐ 1.1 mV, a latency of 1.7 +/‐ 0.9 ms, a 20‐80% rise time of 2.9 +/‐ 2.3 ms and a decay time constant of 40 +/‐ 18 ms at 32‐24 degrees C and ‐60 +/‐ 2 mV membrane potential. 3. Peak amplitudes of unitary EPSPs fluctuated randomly from trial to trial. The coefficient of variation (c.v.) of the unitary EPSP amplitudes ranged from 0.13 to 2.8 in different synaptic connections (mean, 0.52; median, 0.41). The percentage of failures of single APs to evoke a unitary EPSP ranged from 0 to 73% (mean, 14%; median, 7%). Both c.v. and percentage of failures decreased with increasing mean EPSP amplitude. 4. Postsynaptic glutamate receptors which mediate unitary EPSPs at ‐60 mV were predominantly of the L‐alpha‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionate (AMPA) receptor type. Receptors of the N‐methyl‐D‐aspartate (NMDA) type contributed only a small fraction (< 20%) to the voltage‐time integral of the unitary EPSP at ‐60 mV, but their contribution increased at more positive membrane potentials. 5. Branching patterns of dendrites and axon collaterals of forty‐five synaptically connected neurones, when examined in the light microscope, indicated that the axonal and dendritic anatomy of both projecting and target neurones and of uni‐ and bidirectionally connected neurones was uniform. 6. The number of potential synaptic contacts formed by a presynaptic neurone on a target neurone varied between four and eight (mean, 5.5 +/‐ 1.1 contacts; n = 19 connections). Synaptic contacts were preferentially located on basal dendrites (63%, 82 +/‐ 35 microns from the soma, n = 67) and apical oblique dendrites (27%, 145 +/‐ 59 microns, n = 29), and 35% of all contacts were located on tertiary basal dendritic branches. The mean geometric distances (from the soma) of the contacts of a connection varied between 80 and 585 microns (mean, 147 microns; median, 105 microns). The correlation between EPSP amplitude and the number of morphologically determined synaptic contacts or the mean geometric distances from the soma was only weak (correlation coefficients were 0.2 and 0.26, respectively). 7. Compartmental models constructed from camera lucida drawings of eight target neurones showed that synaptic contacts were located at mean electrotonic distances between 0.07 and 0.33 from the soma (mean, 0.13). Simulations of unitary EPSPs, assuming quantal conductance changes with fast rise time and short duration, indicated that amplitudes of quantal EPSPs at the soma were attenuated, on average, to < 10% of dendritic EPSPs and varied in amplitude up to 10‐fold depending on the dendritic location of synaptic contacts. The inferred quantal peak conductance increase varied between 1.5 and 5.5 nS (mean, 3 nS). 8. The combined physiological and morphological measurements in conjunction with EPSP simulations indicated that the 20‐fold range in efficacy of the synaptic connections between thick tufted pyramidal neurones, which have their synaptic contacts preferentially located on basal and apical oblique dendrites, was due to differences in transmitter release probability of the projecting neurones and, to a lesser extent, to differenc

[1]  J. Simpson THE RELEASE OF NEURAL TRANSMITTER SUBSTANCES , 1969 .

[2]  A. Peters,et al.  The small pyramidal neuron of the rat cerebral cortex. The perikaryon, dendrites and spines. , 1970, The American journal of anatomy.

[3]  J. Weakly,et al.  Correlation between nerve terminal size and transmitter release at the neuromuscular junction of the frog , 1971, The Journal of physiology.

[4]  E Henneman,et al.  Terminals of single Ia fibers: location, density, and distribution within a pool of 300 homonymous motoneurons. , 1971, Journal of neurophysiology.

[5]  L. Mendell,et al.  Analysis of pairs of individual Ia‐E.P.S.P.S in single motoneurones. , 1976, The Journal of physiology.

[6]  T. Wiesel,et al.  Morphology and intracortical projections of functionally characterised neurones in the cat visual cortex , 1979, Nature.

[7]  P. Schwindt,et al.  Negative slope conductance due to a persistent subthreshold sodium current in cat neocortical neurons in vitro , 1982, Brain Research.

[8]  A. Grinnell,et al.  Synaptic strength as a function of motor unit size in the normal frog sartorius. , 1983, The Journal of physiology.

[9]  A D Grinnell,et al.  The regulation of synaptic strength within motor units of the frog cutaneous pectoris muscle , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  H Korn,et al.  Probabilistic determination of synaptic strength. , 1986, Journal of neurophysiology.

[11]  F. Valverde,et al.  Intrinsic neocortical organization: Some comparative aspects , 1986, Neuroscience.

[12]  P. Schwindt,et al.  Anomalous rectification in neurons from cat sensorimotor cortex in vitro. , 1987, Journal of neurophysiology.

[13]  R. Miles,et al.  Variation in strength of inhibitory synapses in the CA3 region of guinea‐pig hippocampus in vitro. , 1990, The Journal of physiology.

[14]  B. Connors,et al.  Intrinsic firing patterns of diverse neocortical neurons , 1990, Trends in Neurosciences.

[15]  D. Prince,et al.  Burst generating and regular spiking layer 5 pyramidal neurons of rat neocortex have different morphological features , 1990, The Journal of comparative neurology.

[16]  A. Larkman,et al.  Correlations between morphology and electrophysiology of pyramidal neurons in slices of rat visual cortex. I. Establishment of cell classes , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  D. Faber,et al.  Applicability of the coefficient of variation method for analyzing synaptic plasticity. , 1991, Biophysical journal.

[18]  T. Bartol,et al.  Monte Carlo simulation of miniature endplate current generation in the vertebrate neuromuscular junction. , 1991, Biophysical journal.

[19]  W Zieglgänsberger,et al.  Voltage dependence of excitatory postsynaptic potentials of rat neocortical neurons. , 1991, Journal of neurophysiology.

[20]  K. Stratford,et al.  Synaptic transmission between individual pyramidal neurons of the rat visual cortex in vitro , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  B. Connors,et al.  Intrinsic oscillations of neocortex generated by layer 5 pyramidal neurons. , 1991, Science.

[22]  J. DeFelipe,et al.  The pyramidal neuron of the cerebral cortex: Morphological and chemical characteristics of the synaptic inputs , 1992, Progress in Neurobiology.

[23]  N. Spruston,et al.  Perforated patch-clamp analysis of the passive membrane properties of three classes of hippocampal neurons. , 1992, Journal of neurophysiology.

[24]  Bert Sakmann,et al.  Heteromeric NMDA Receptors: Molecular and Functional Distinction of Subtypes , 1992, Science.

[25]  B. Sakmann,et al.  Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus. , 1993, The Journal of physiology.

[26]  D. McCormick,et al.  Control of firing mode of corticotectal and corticopontine layer V burst-generating neurons by norepinephrine, acetylcholine, and 1S,3R- ACPD , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  Michael L. Hines,et al.  NEURON — A Program for Simulation of Nerve Equations , 1993 .

[28]  A. Thomson,et al.  Fluctuations in pyramid-pyramid excitatory postsynaptic potentials modified by presynaptic firing pattern and postsynaptic membrane potential using paired intracellular recordings in rat neocortex , 1993, Neuroscience.

[29]  K M Harris,et al.  Occurrence and three-dimensional structure of multiple synapses between individual radiatum axons and their target pyramidal cells in hippocampal area CA1 , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  J. Deuchars,et al.  Large, deep layer pyramid-pyramid single axon EPSPs in slices of rat motor cortex display paired pulse and frequency-dependent depression, mediated presynaptically and self-facilitation, mediated postsynaptically. , 1993, Journal of neurophysiology.

[31]  C Blakemore,et al.  Modulation of EPSP shape and efficacy by intrinsic membrane conductances in rat neocortical pyramidal neurons in vitro. , 1993, The Journal of physiology.

[32]  J. Deuchars,et al.  Temporal and spatial properties of local circuits in neocortex , 1994, Trends in Neurosciences.

[33]  C. Blakemore,et al.  Pyramidal neurons in layer 5 of the rat visual cortex. III. Differential maturation of axon targeting, dendritic morphology, and electrophysiological properties , 1994, The Journal of comparative neurology.

[34]  D. Faber,et al.  The one-vesicle hypothesis and multivesicular release. , 1994, Advances in second messenger and phosphoprotein research.

[35]  B. Sakmann,et al.  Quantal analysis of excitatory postsynaptic currents at the hippocampal mossy fiber-CA3 pyramidal cell synapse. , 1994, Advances in second messenger and phosphoprotein research.

[36]  H. Markram,et al.  Calcium transients in dendrites of neocortical neurons evoked by single subthreshold excitatory postsynaptic potentials via low-voltage-activated calcium channels. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[37]  J Deuchars,et al.  Relationships between morphology and physiology of pyramid‐pyramid single axon connections in rat neocortex in vitro. , 1994, The Journal of physiology.

[38]  C. Blakemore,et al.  Pyramidal neurons in layer 5 of the rat visual cortex. I. Correlation among cell morphology, intrinsic electrophysiological properties, and axon targets , 1994, The Journal of comparative neurology.

[39]  B. Sakmann,et al.  Differences in Ca2+ permeability of AMPA-type glutamate receptor channels in neocortical neurons caused by differential GluR-B subunit expression , 1994, Neuron.

[40]  B. Sakmann,et al.  Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons , 1995, Neuron.

[41]  B Sakmann,et al.  Fractional calcium currents through recombinant GluR channels of the NMDA, AMPA and kainate receptor subtypes. , 1995, The Journal of physiology.

[42]  S. Siegelbaum,et al.  Regulation of hippocampal transmitter release during development and long-term potentiation. , 1995, Science.

[43]  M. Raastad,et al.  Diversity of Postsynaptic Amplitude and Failure Probability of Unitary Excitatory Synapses between CA3 and CA1 Cells in the Rat Hippocampus , 1996, The European journal of neuroscience.

[44]  K. Martin,et al.  Excitatory synaptic inputs to spiny stellate cells in cat visual cortex , 1996, Nature.

[45]  R. Silver,et al.  Non‐NMDA glutamate receptor occupancy and open probability at a rat cerebellar synapse with single and multiple release sites. , 1996, The Journal of physiology.

[46]  S. Redman,et al.  Changes in quantal parameters of EPSCs in rat CA1 neurones in vitro after the induction of long‐term potentiation. , 1996, The Journal of physiology.

[47]  H. Markram,et al.  Frequency and Dendritic Distribution of Autapses Established by Layer 5 Pyramidal Neurons in the Developing Rat Neocortex: Comparison with Synaptic Innervation of Adjacent Neurons of the Same Class , 1996, The Journal of Neuroscience.

[48]  S. Redman,et al.  Statistical analysis of amplitude fluctuations in EPSCs evoked in rat CA1 pyramidal neurones in vitro. , 1996, The Journal of physiology.

[49]  B. Sakmann,et al.  Calcium influx and transmitter release in a fast CNS synapse , 1996, Nature.