Synaptic interactions in neocortical local circuits: dual intracellular recordings in vitro.
نویسندگان
چکیده
Properties of local synaptic connections in neocortex, studied with dual intracellular recordings in vitro and correlated with cell and synaptic morphology are summarized. The different durations and sensitivities to somatic membrane potential of pyramid-pyramid excitatory postsynaptic potentials (EPSPs) apparently reflect the positions of the synapses on the postsynaptic dendrites. Their time-, frequency- and voltage-dependent properties enable supra-linear summation of several low-frequency inputs arising in the same dendritic region, even if only loosely coincident, but they depress during repetitive firing in any one input. Pyramidal input to classical fast spiking and low threshold spiking interneurones are strikingly different. Here low presynaptic firing rates results in many transmission failures. EPSPs are brief and inputs must be near coincident for summation. However, these synapses display pronounced. frequency-dependent, incrementing facilitation at higher presynaptic frequencies. Once initiated by a brief high-frequency burst, this facilitation is maintained at lower frequencies. GABAA receptor-mediated inhibitory postsynaptic potentials (IPSPs) arising proximally are of very different durations depending on the type of interneurone activated and can prevent and subsequently synchronize firing in their many postsynaptic partners with very different delays (eg. 10-100 ms). Low threshold spiking interneurones, in contrast, generate brief IPSPs only in more distal dendritic regions and have little effect on somatic excitability acting to shunt input distally.
منابع مشابه
Network activity evoked by neocortical stimulation in area 36 of the guinea pig perirhinal cortex.
The perirhinal cortex is a key structure involved in memory consolidation and retrieval. In spite of the extensive anatomical studies that describe the intrinsic and extrinsic associative connections of the perirhinal cortex, the activity generated within such a network has been poorly investigated. We describe here the pattern of synaptic interactions that subtend the responses evoked in area ...
متن کاملA method to estimate synaptic conductances from membrane potential fluctuations.
In neocortical neurons, network activity can activate a large number of synaptic inputs, resulting in highly irregular subthreshold membrane potential (V(m)) fluctuations, commonly called "synaptic noise." This activity contains information about the underlying network dynamics, but it is not easy to extract network properties from such complex and irregular activity. Here, we propose a method ...
متن کاملSynaptic interactions underlying song-selectivity in the avian nucleus HVC revealed by dual intracellular recordings.
Stimulus-dependent synaptic interactions underlying selective sensory representations in neural circuits specialized for sensory processing and sensorimotor integration remain poorly understood. The songbird telencephalic nucleus HVC is a sensorimotor area essential to learned vocal control with one projection neuron (PN) type (HVC(RA)) innervating a song premotor pathway, another PN (HVC(X)) i...
متن کاملInnovative Methodology A Method to Estimate Synaptic Conductances From Membrane Potential Fluctuations
Rudolph, Michael, Zuzanna Piwkowska, Mathilde Badoual, Thierry Bal, and Alain Destexhe. A method to estimate synaptic conductances from membrane potential fluctuations. J Neurophysiol 91: 2884–2896, 2004; 10.1152/jn.01223.2003. In neocortical neurons, network activity can activate a large number of synaptic inputs, resulting in highly irregular subthreshold membrane potential (Vm) fluctuations,...
متن کاملEstimation of synaptic conductances and their variances from intracellular recordings of neocortical neurons in vivo
During intense network activity, neocortical neurons are in a “high-conductance” state. To estimate the respective contributions of excitatory and inhibitory conductances in generating such states, we combined computational models with intracellular recordings obtained in cat parietal cortex in vivo. Fitting a 6uctuating-conductance model to the recordings revealed that inhibitory conductances ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Cerebral cortex
دوره 7 6 شماره
صفحات -
تاریخ انتشار 1997