ترغب بنشر مسار تعليمي؟ اضغط هنا

How stochastic synchrony could work in cerebellar Purkinje cells

82   0   0.0 ( 0 )
 نشر من قبل Sergio Verduzco-Flores
 تاريخ النشر 2014
  مجال البحث علم الأحياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Simple spike synchrony between Purkinje cells projecting to a common neuron in the deep cerebellar nucleus is emerging as an important factor in the encoding of output information from cerebellar cortex. Stochastic synchronization is a viable mechanism through which this synchrony could be generated, but it has received scarce attention, perhaps because the presence of feedforward inhibition in the input to Purkinje cells makes insights difficult. This paper presents a method to account for feedforward inhibition so the usual mathematical approaches to stochastic synchronization can be applied. Three concepts (input correlation, heterogeneity, and PRC shape) are then introduced to facilitate an intuitive understanding of how different factors can affect synchronization in Purkinje cells. This is followed by a discussion of how stochastic synchrony could play a role in the cerebellar response under different assumptions.

قيم البحث

اقرأ أيضاً

Spike time response curves (STRCs) are used to study the influence of synaptic stimuli on the firing times of a neuron oscillator without the assumption of weak coupling. They allow us to approximate the dynamics of synchronous state in networks of n eurons through a discrete map. Linearization about the fixed point of the discrete map can then be used to predict the stability of patterns of synchrony in the network. General theory for taking into account the contribution from higher order STRC terms, in the approximation of the discrete map for coupled neuronal oscillators in synchrony is still lacking. Here we present a general framework to account for higher order STRC corrections in the approximation of discrete map to determine the domain of 1:1 phase locking state in the network of two interacting neurons. We begin by demonstrating that the effect of synaptic stimuli through a shunting synapse to a neuron firing in the gamma frequency band (20-80 Hz) last for three consecutive firing cycles. We then show that the discrete map derived by taking into account the higher order STRC contributions is successfully able predict the domain of synchronous 1:1 phase locked state in a network of two heterogeneous interneurons coupled through a shunting synapse.
In this paper we propose an $infty-$dimensional cerebellar model of neural controller for realistic human biodynamics. The model is developed using Feynmans action-amplitude (partition function) formalism. The cerebellum controller is acting as a sup ervisor for an autogenetic servo control of human musculo-skeletal dynamics, which is presented in (dissipative, driven) Hamiltonian form. The $infty-$dimensional cerebellar controller is closely related to entropic motor control. Keywords: realistic human biodynamics, cerebellum motion control, $infty-$dimensional neural network
Recordings from area V4 of monkeys have revealed that when the focus of attention is on a visual stimulus within the receptive field of a cortical neuron, two distinct changes can occur: The firing rate of the neuron can change and there can be an in crease in the coherence between spikes and the local field potential in the gamma-frequency range (30-50 Hz). The hypothesis explored here is that these observed effects of attention could be a consequence of changes in the synchrony of local interneuron networks. We performed computer simulations of a Hodgkin-Huxley type neuron driven by a constant depolarizing current, I, representing visual stimulation and a modulatory inhibitory input representing the effects of attention via local interneuron networks. We observed that the neurons firing rate and the coherence of its output spike train with the synaptic inputs was modulated by the degree of synchrony of the inhibitory inputs. The model suggest that the observed changes in firing rate and coherence of neurons in the visual cortex could be controlled by top-down inputs that regulated the coherence in the activity of a local inhibitory network discharging at gamma frequencies.
Grid cells in the entorhinal cortex are believed to establish their regular, spatially correlated firing patterns by path integration of the animals motion. Mechanisms for path integration, e.g. in attractor network models, predict stochastic drift o f grid responses, which is not observed experimentally. We demonstrate a biologically plausible mechanism of dynamic self-organization by which border cells, which fire at environmental boundaries, can correct such drift in grid cells. In our model, experience-dependent Hebbian plasticity during exploration allows border cells to learn connectivity to grid cells. Border cells in this learned network reset the phase of drifting grids. This error-correction mechanism is robust to environmental shape and complexity, including enclosures with interior barriers, and makes distinctive predictions for environmental deformation experiments. Our work demonstrates how diverse cell types in the entorhinal cortex could interact dynamically and adaptively to achieve robust path integration.
We use autoregressive hidden Markov models and a time-frequency approach to create meaningful quantitative descriptions of behavioral characteristics of cerebellar ataxias from wearable inertial sensor data gathered during movement. Wearable sensor d ata is relatively easily collected and provides direct measurements of movement that can be used to develop useful behavioral biomarkers. Sensitive and specific behavioral biomarkers for neurodegenerative diseases are critical to supporting early detection, drug development efforts, and targeted treatments. We create a flexible and descriptive set of features derived from accelerometer and gyroscope data collected from wearable sensors while participants perform clinical assessment tasks, and with them estimate disease status and severity. A short period of data collection ($<$ 5 minutes) yields enough information to effectively separate patients with ataxia from healthy controls with very high accuracy, to separate ataxia from other neurodegenerative diseases such as Parkinsons disease, and to give estimates of disease severity.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا