Collective Bursting in Populations of Intrinsically Nonbursting Neurons
نویسنده
چکیده
We describe a novel type of bursting that we observe in simulations of large recurrent networks of biophysically plausible, intrinsically non-bursting neurons. The mechanism responsible for the bursting is a combination of excitatory feedback received from neighbouring neurons, together with an activity-dependent adaptation mechanism that slows down spiking. During the bursting phases, the firing patterns are not repeated and the lengths of the interburst intervals are varying. We develop a simple phenomenological model that captures most qualitative aspects of the observed collective bursting. We compare the parameter range leading to bursting in the phenomenological model, with parameter estimates from cortical anatomy and physiology, and conjecture that the discovered new type of bursting should also be observable in biological neocortical networks.
منابع مشابه
Cycle-by-cycle assembly of respiratory network activity is dynamic and stochastic.
Rhythmically active networks are typically composed of neurons that can be classified as silent, tonic spiking, or rhythmic bursting based on their intrinsic activity patterns. Within these networks, neurons are thought to discharge in distinct phase relationships with their overall network output, and it has been hypothesized that bursting pacemaker neurons may lead and potentially trigger cyc...
متن کاملParticipation of a persistent sodium current and calcium-activated nonspecific cationic current to burst generation in trigeminal principal sensory neurons.
The properties of neurons participating in masticatory rhythmogenesis are not clearly understood. Neurons within the dorsal trigeminal principal sensory nucleus (dPrV) are potential candidates as components of the masticatory central pattern generator (CPG). The present study examines in detail the ionic mechanisms controlling burst generation in dPrV neurons in rat (postnatal day 8-12) brain s...
متن کاملSlow oscillatory firing: a major firing pattern of dopamine neurons in the ventral tegmental area.
Using spectral analysis and in vivo single-unit recording in rats, the present study revealed a pronounced slow oscillation (SO) in the firing activity of about half the dopamine (DA) neurons recorded in the ventral tegmental area. DA neurons in this group tended to fire repetitive spike clusters, making them appear to be rhythmic bursting cells. However, only some of these burst-like events me...
متن کاملMorphological characterization of the bursting and nonbursting neurones in the olfactory centre of the terrestrial slug limax marginatus
We investigated the morphological characteristics of physiologically characterized neurones in the procerebrum (PC) of the terrestrial slug Limax marginatus. The electrophysiological characteristics of the neurones were determined using the perforated patch recording technique. By comparing the shapes and sizes of somata, we found that the somata of bursting neurones were larger and had more ob...
متن کاملDynamics of propagating waves in the olfactory network of a terrestrial mollusk: an electrical and optical study.
1. The procerebral (PC) lobe of the terrestrial mollusk Limax maximus contains a highly interconnected network of local olfactory interneurons that receives ipsilateral axonal projections from superior and inferior noses. This network exhibits an approximately 0.7-Hz intrinsic oscillation in its local field potential (LFP). 2. Intracellular recordings show that the lobe contains at least two cl...
متن کامل