neuronal firing
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Author(s):  
Liang Guo ◽  
Shuai Zhang ◽  
Jiankang Wu ◽  
Xinyu Gao ◽  
Mingkang Zhao ◽  
...  

Transcranial magnetic-acoustic electrical stimulation (TMAES) is a new technology with ultrasonic waves and a static magnetic field to generate an electric current in nerve tissues to modulate neuronal firing activities. The existing neuron models only simulate a single neuron, and there are few studies on coupled neurons models about TMAES. Most of the neurons in the cerebral cortex are not isolated but are coupled to each other. It is necessary to study the information transmission of coupled neurons. The types of neuron coupled synapses include electrical synapse and chemical synapse. A neuron model without considering chemical synapses is not comprehensive. Here, we modified the Hindmarsh-Rose (HR) model to simulate the smallest nervous system—two neurons coupled electrical synapses and chemical synapses under TMAES. And the environmental variables describing the synaptic coupling between two neurons and the nonlinearity of the nervous system are also taken into account. The firing behavior of the nervous system can be modulated by changing the intensity or the modulation frequency. The results show that within a certain range of parameters, the discharge frequency of coupled neurons could be increased by altering the modulation frequency, and intensity of stimulation, modulating the excitability of neurons, reducing the response time of chemical postsynaptic neurons, and accelerating the information transferring. Moreover, the discharge frequency of neurons was selective to stimulus parameters. These results demonstrate the possible theoretical regulatory mechanism of the neurons' firing frequency characteristics by TMAES. The study establishes the foundation for large-scale neural network modeling and can be taken as the theoretical basis for TMAES experimental and clinical application.


2022 ◽  
Vol 14 ◽  
Author(s):  
Davide Warm ◽  
Jonas Schroer ◽  
Anne Sinning

Throughout early phases of brain development, the two main neural signaling mechanisms—excitation and inhibition—are dynamically sculpted in the neocortex to establish primary functions. Despite its relatively late formation and persistent developmental changes, the GABAergic system promotes the ordered shaping of neuronal circuits at the structural and functional levels. Within this frame, interneurons participate first in spontaneous and later in sensory-evoked activity patterns that precede cortical functions of the mature brain. Upon their subcortical generation, interneurons in the embryonic brain must first orderly migrate to and settle in respective target layers before they can actively engage in cortical network activity. During this process, changes at the molecular and synaptic level of interneurons allow not only their coordinated formation but also the pruning of connections as well as excitatory and inhibitory synapses. At the postsynaptic site, the shift of GABAergic signaling from an excitatory towards an inhibitory response is required to enable synchronization within cortical networks. Concomitantly, the progressive specification of different interneuron subtypes endows the neocortex with distinct local cortical circuits and region-specific modulation of neuronal firing. Finally, the apoptotic process further refines neuronal populations by constantly maintaining a controlled ratio of inhibitory and excitatory neurons. Interestingly, many of these fundamental and complex processes are influenced—if not directly controlled—by electrical activity. Interneurons on the subcellular, cellular, and network level are affected by high frequency patterns, such as spindle burst and gamma oscillations in rodents and delta brushes in humans. Conversely, the maturation of interneuron structure and function on each of these scales feeds back and contributes to the generation of cortical activity patterns that are essential for the proper peri- and postnatal development. Overall, a more precise description of the conducting role of interneurons in terms of how they contribute to specific activity patterns—as well as how specific activity patterns impinge on their maturation as orchestra members—will lead to a better understanding of the physiological and pathophysiological development and function of the nervous system.


Entropy ◽  
2021 ◽  
Vol 24 (1) ◽  
pp. 59
Author(s):  
Baihan Lin

Inspired by the adaptation phenomenon of neuronal firing, we propose the regularity normalization (RN) as an unsupervised attention mechanism (UAM) which computes the statistical regularity in the implicit space of neural networks under the Minimum Description Length (MDL) principle. Treating the neural network optimization process as a partially observable model selection problem, the regularity normalization constrains the implicit space by a normalization factor, the universal code length. We compute this universal code incrementally across neural network layers and demonstrate the flexibility to include data priors such as top-down attention and other oracle information. Empirically, our approach outperforms existing normalization methods in tackling limited, imbalanced and non-stationary input distribution in image classification, classic control, procedurally-generated reinforcement learning, generative modeling, handwriting generation and question answering tasks with various neural network architectures. Lastly, the unsupervised attention mechanisms is a useful probing tool for neural networks by tracking the dependency and critical learning stages across layers and recurrent time steps of deep networks.


2021 ◽  
Vol 13 ◽  
Author(s):  
Anna Regina Tröscher ◽  
Joachim Gruber ◽  
Judith N. Wagner ◽  
Vincent Böhm ◽  
Anna-Sophia Wahl ◽  
...  

Post-stroke Epilepsy (PSE) is one of the most common forms of acquired epilepsy, especially in the elderly population. As people get increasingly older, the number of stroke patients is expected to rise and concomitantly the number of people with PSE. Although many patients are affected by post-ischemic epileptogenesis, not much is known about the underlying pathomechanisms resulting in the development of chronic seizures. A common hypothesis is that persistent neuroinflammation and glial scar formation cause aberrant neuronal firing. Here, we summarize the clinical features of PSE and describe in detail the inflammatory changes after an ischemic stroke as well as the chronic changes reported in epilepsy. Moreover, we discuss alterations and disturbances in blood-brain-barrier leakage, astrogliosis, and extracellular matrix changes in both, stroke and epilepsy. In the end, we provide an overview of commonalities of inflammatory reactions and cellular processes in the post-ischemic environment and epileptic brain and discuss how these research questions should be addressed in the future.


2021 ◽  
Author(s):  
Aghil Abed Zadeh ◽  
Brandon David Turner ◽  
Nicole Calakos ◽  
Nicolas Brunel

GABA is canonically known as the principal inhibitory neurotransmitter in the nervous system, usually acting by hyper-polarizing membrane potential. However, GABAergic currents can also exhibit non-inhibitory effects, depending on the brain region, developmental stage or pathological condition. Here, we investigate the diverse effects of GABA on the firing rate of several single neuron models, using both analytical calculations and numerical simulations. We find that the relationship between GABAergic synaptic conductance and output firing rate exhibits three qualitatively different regimes as a function of GABA reversal potential, νGABA: monotonically decreasing for sufficiently low νGABA (inhibitory), monotonically increasing for νGABA above firing threshold (excitatory); and a non-monotonic region for intermediate values of νGABA. In the non-monotonic regime, small GABA conductances have an excitatory effect while large GABA conductances show an inhibitory effect. We provide a phase diagram of different GABAergic effects as a function of GABA reversal potential and glutamate conductance. We find that noisy inputs increase the range of νGABA for which the non-monotonic effect can be observed. We also construct a micro-circuit model of striatum to explain observed effects of GABAergic fast spiking interneurons on spiny projection neurons, including non-monotonicity, as well as the heterogeneity of the effects. Our work provides a mechanistic explanation of paradoxical effects of GABAergic synaptic inputs, with implications for understanding the effects of GABA in neural computation and development.


2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Nienke R. Wevers ◽  
Arya Lekshmi Nair ◽  
Tania M. Fowke ◽  
Maria Pontier ◽  
Dhanesh G. Kasi ◽  
...  

Abstract Background In ischemic stroke, the function of the cerebral vasculature is impaired. This vascular structure is formed by the so-called neurovascular unit (NVU). A better understanding of the mechanisms involved in NVU dysfunction and recovery may lead to new insights for the development of highly sought therapeutic approaches. To date, there remains an unmet need for complex human in vitro models of the NVU to study ischemic events seen in the human brain. Methods We here describe the development of a human NVU on-a-chip model using a platform that allows culture of 40 chips in parallel. The model comprises a perfused vessel of primary human brain endothelial cells in co-culture with induced pluripotent stem cell derived astrocytes and neurons. Ischemic stroke was mimicked using a threefold approach that combines chemical hypoxia, hypoglycemia, and halted perfusion. Results Immunofluorescent staining confirmed expression of endothelial adherens and tight junction proteins, as well as astrocytic and neuronal markers. In addition, the model expresses relevant brain endothelial transporters and shows spontaneous neuronal firing. The NVU on-a-chip model demonstrates tight barrier function, evidenced by retention of small molecule sodium fluorescein in its lumen. Exposure to the toxic compound staurosporine disrupted the endothelial barrier, causing reduced transepithelial electrical resistance and increased permeability to sodium fluorescein. Under stroke mimicking conditions, brain endothelial cells showed strongly reduced barrier function (35-fold higher apparent permeability) and 7.3-fold decreased mitochondrial potential. Furthermore, levels of adenosine triphosphate were significantly reduced on both the blood- and the brain side of the model (4.8-fold and 11.7-fold reduction, respectively). Conclusions The NVU on-a-chip model presented here can be used for fundamental studies of NVU function in stroke and other neurological diseases and for investigation of potential restorative therapies to fight neurological disorders. Due to the platform’s relatively high throughput and compatibility with automation, the model holds potential for drug compound screening.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hiroyuki Miyawaki ◽  
Brendon O. Watson ◽  
Kamran Diba
Keyword(s):  

2021 ◽  
Author(s):  
Pierce Mullen ◽  
Nadia Pilati ◽  
Charles H Large ◽  
Jim Deuchars ◽  
Susan A Deuchars

Autonomic parasympathetic preganglionic neurons (PGN) drive contraction of the bladder during micturition but remain quiescent during bladder filling. This quiescence is postulated to be due to recurrent inhibition of PGN by fast-firing adjoining interneurons. Here, we defined four distinct neuronal types within lamina VII of the lumbosacral spinal cord, where PGN are situated, by combining whole cell patch clamp recordings with k-means clustering of a range of electrophysiological parameters. Additional morphological analysis separated these neuronal classes into parasympathetic preganglionic populations (PGN) and a fast firing interneuronal population. Kv3 channels are voltage-gated potassium channels (Kv) that allow fast and precise firing of neurons. We found that blockade of Kv3 channels by tetraethylammonium (TEA) reduced neuronal firing frequency and isolated high-voltage-activated Kv currents in the fast-firing population but had no effect in PGN populations. Furthermore, Kv3 blockade potentiated the local and descending inhibitory inputs to PGN indicating that Kv3-expressing inhibitory neurons are synaptically connected to PGN. Taken together, our data reveal that Kv3 channels are crucial for fast and regulated neuronal output of a defined population that may be involved in intrinsic spinal bladder circuits that underpin recurrent inhibition of PGN.


2021 ◽  
Vol 11 (6) ◽  
pp. 159-166
Author(s):  
Archana B ◽  
Ravi Naik Mudavath ◽  
Vinay Enumula ◽  
N Ravali ◽  
Paka Sravan Kumar

The report used to be planned to analyze the antiepileptic activity of Cocos nucifera flowers against special experimentally induced convulsions in rats. In the present study, antiepileptic activity was assessed by following experimental models. Anti-convulsant in vivo models: Maximal electroshocks (MES) induced models in rats, Pentylenetetrazole (PTZ) induced in rats. Pretreatment of animals with Cocos nucifera flowers extract has reduced by half the general continuance of tonic hind leg extension, the most commonly used endpoint in assessing clonic convulsions. MES provokes repetitive neuronal firing indicates epileptic neurons. MES is the widely accepted model to demonstrate the antiepileptic property of a drug. This property is antagonistic of the plant extract could flow from to blockade of voltage-gated sodium channel or due to effect on NMDA receptors. The Cocos nucifera flowers extract was also demonstrated potential anticonvulsant activity in PTZ induced convulsions and this may be due to its agonistic activity on the GABAA receptor. This is further supported by an elevated level of GABA by the plant extract in the PTZ model. Methanolic extract of Cocos nucifera flowers has shown significant anticonvulsant activity against MES and Pentlylenetetrazole induced convulsion models. This observed activity could also be the referable presence of flavonoids and other phytochemical constituents found in the powerful extract. Keywords: Cocos nucifera, antiepileptic activity, Maximal electroshock, Pentlylenetetrazole, Flavonoids,


2021 ◽  
Vol 22 (23) ◽  
pp. 12770
Author(s):  
Annika Ahtiainen ◽  
Barbara Genocchi ◽  
Jarno M. A. Tanskanen ◽  
Michael T. Barros ◽  
Jari A. K. Hyttinen ◽  
...  

Astrocytes and neurons respond to each other by releasing transmitters, such as γ-aminobutyric acid (GABA) and glutamate, that modulate the synaptic transmission and electrochemical behavior of both cell types. Astrocytes also maintain neuronal homeostasis by clearing neurotransmitters from the extracellular space. These astrocytic actions are altered in diseases involving malfunction of neurons, e.g., in epilepsy, Alzheimer’s disease, and Parkinson’s disease. Convulsant drugs such as 4-aminopyridine (4-AP) and gabazine are commonly used to study epilepsy in vitro. In this study, we aim to assess the modulatory roles of astrocytes during epileptic-like conditions and in compensating drug-elicited hyperactivity. We plated rat cortical neurons and astrocytes with different ratios on microelectrode arrays, induced seizures with 4-AP and gabazine, and recorded the evoked neuronal activity. Our results indicated that astrocytes effectively counteracted the effect of 4-AP during stimulation. Gabazine, instead, induced neuronal hyperactivity and synchronicity in all cultures. Furthermore, our results showed that the response time to the drugs increased with an increasing number of astrocytes in the co-cultures. To the best of our knowledge, our study is the first that shows the critical modulatory role of astrocytes in 4-AP and gabazine-induced discharges and highlights the importance of considering different proportions of cells in the cultures.


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