Enhancement of synchronization in a hybrid neural circuit by spike timing dependent plasticity

Synchronization of neural activity is fundamental for many functions of the brain. We demonstrate that spike-timing dependent plasticity (STDP) enhances synchronization (entrainment) in a hybrid circuit composed of a spike generator, a dynamic clamp emulating an excitatory plastic synapse, and a chemically isolated neuron from the Aplysia abdominal ganglion. Fixed-phase entrainment of the Aplysia neuron to the spike generator is possible for a much wider range of frequency ratios and is more precise and more robust with the plastic synapse than with a nonplastic synapse of comparable strength. Further analysis in a computational model of HodgkinHuxley-type neurons reveals the mechanism behind this significant enhancement in synchronization. The experimentally observed STDP plasticity curve appears to be designed to adjust synaptic strength to a value suitable for stable entrainment of the postsynaptic neuron. One functional role of STDP might therefore be to facilitate synchronization or entrainment of nonidentical neurons

The malleable brain: plasticity of neural circuits and behavior: A review from students to students

One of the most intriguing features of the brain is its ability to be malleable, allowing it to adapt continually to changes in the environment. Specific neuronal activity patterns drive long-lasting increases or decreases in the strength of synaptic connections, referred to as long-term potentiation (LTP) and long-term depression (LTD) respectively. Such phenomena have been described in a variety of model organisms, which are used to study molecular, structural, and functional aspects of synaptic plasticity. This review originated from the first International Society for Neurochemistry (ISN) and Journal of Neurochemistry (JNC) Flagship School held in Alpbach, Austria (Sep 2016), and will use its curriculum and discussions as a framework to review some of the current knowledge in the field of synaptic plasticity. First, we describe the role of plasticity during development and the persistent changes of neural circuitry occurring when sensory input is altered during critical developmental stages. We then outline the signaling cascades resulting in the synthesis of new plasticity-related proteins, which ultimately enable sustained changes in synaptic strength. Going beyond the traditional understanding of synaptic plasticity conceptualized by LTP and LTD, we discuss system-wide modifications and recently unveiled homeostatic mechanisms, such as synaptic scaling. Finally, we describe the neural circuits and synaptic plasticity mechanisms driving associative memory and motor learning. Evidence summarized in this review provides a current view of synaptic plasticity in its various forms, offers new insights into the underlying mechanisms and behavioral relevance, and provides directions for future research in the field of synaptic plasticity.Fil: Schaefer, Natascha. University of Wuerzburg; AlemaniaFil: Rotermund, Carola. University of Tuebingen; AlemaniaFil: Blumrich, Eva Maria. Universitat Bremen; AlemaniaFil: Lourenco, Mychael V.. Universidade Federal do Rio de Janeiro; BrasilFil: Joshi, Pooja. Robert Debre Hospital; FranciaFil: Hegemann, Regina U.. University of Otago; Nueva ZelandaFil: Jamwal, Sumit. ISF College of Pharmacy; IndiaFil: Ali, Nilufar. Augusta University; Estados UnidosFil: García Romero, Ezra Michelet. Universidad Veracruzana; MéxicoFil: Sharma, Sorabh. Birla Institute of Technology and Science; IndiaFil: Ghosh, Shampa. Indian Council of Medical Research; IndiaFil: Sinha, Jitendra K.. Indian Council of Medical Research; IndiaFil: Loke, Hannah. Hudson Institute of Medical Research; AustraliaFil: Jain, Vishal. Defence Institute of Physiology and Allied Sciences; IndiaFil: Lepeta, Katarzyna. Polish Academy of Sciences; ArgentinaFil: Salamian, Ahmad. Polish Academy of Sciences; ArgentinaFil: Sharma, Mahima. Polish Academy of Sciences; ArgentinaFil: Golpich, Mojtaba. University Kebangsaan Malaysia Medical Centre; MalasiaFil: Nawrotek, Katarzyna. University Of Lodz; ArgentinaFil: Paid, Ramesh K.. Indian Institute of Chemical Biology; IndiaFil: Shahidzadeh, Sheila M.. Syracuse University; Estados UnidosFil: Piermartiri, Tetsade. Universidade Federal de Santa Catarina; BrasilFil: Amini, Elham. University Kebangsaan Malaysia Medical Centre; MalasiaFil: Pastor, Verónica. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia ; ArgentinaFil: Wilson, Yvette. University of Melbourne; AustraliaFil: Adeniyi, Philip A.. Afe Babalola University; NigeriaFil: Datusalia, Ashok K.. National Brain Research Centre; IndiaFil: Vafadari, Benham. Polish Academy of Sciences; ArgentinaFil: Saini, Vedangana. University of Nebraska; Estados UnidosFil: Suárez Pozos, Edna. Instituto Politécnico Nacional; MéxicoFil: Kushwah, Neetu. Defence Institute of Physiology and Allied Sciences; IndiaFil: Fontanet, Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia ; ArgentinaFil: Turner, Anthony J.. University of Leeds; Reino Unid

The spectro-contextual encoding and retrieval theory of episodic memory.

The spectral fingerprint hypothesis, which posits that different frequencies of oscillations underlie different cognitive operations, provides one account for how interactions between brain regions support perceptual and attentive processes (Siegel etal., 2012). Here, we explore and extend this idea to the domain of human episodic memory encoding and retrieval. Incorporating findings from the synaptic to cognitive levels of organization, we argue that spectrally precise cross-frequency coupling and phase-synchronization promote the formation of hippocampal-neocortical cell assemblies that form the basis for episodic memory. We suggest that both cell assembly firing patterns as well as the global pattern of brain oscillatory activity within hippocampal-neocortical networks represents the contents of a particular memory. Drawing upon the ideas of context reinstatement and multiple trace theory, we argue that memory retrieval is driven by internal and/or external factors which recreate these frequency-specific oscillatory patterns which occur during episodic encoding. These ideas are synthesized into a novel model of episodic memory (the spectro-contextual encoding and retrieval theory, or "SCERT") that provides several testable predictions for future research

Emergence of Spatio-Temporal Pattern Formation and Information Processing in the Brain.

The spatio-temporal patterns of neuronal activity are thought to underlie cognitive functions, such as our thoughts, perceptions, and emotions. Neurons and glial cells, specifically astrocytes, are interconnected in complex networks, where large-scale dynamical patterns emerge from local chemical and electrical signaling between individual network components. How these emergent patterns form and encode for information is the focus of this dissertation. I investigate how various mechanisms that can coordinate collections of neurons in their patterns of activity can potentially cause the interactions across spatial and temporal scales, which are necessary for emergent macroscopic phenomena to arise. My work explores the coordination of network dynamics through pattern formation and synchrony in both experiments and simulations. I concentrate on two potential mechanisms: astrocyte signaling and neuronal resonance properties. Due to their ability to modulate neurons, we investigate the role of astrocytic networks as a potential source for coordinating neuronal assemblies. In cultured networks, I image patterns of calcium signaling between astrocytes, and reproduce observed properties of the network calcium patterning and perturbations with a simple model that incorporates the mechanisms of astrocyte communication. Understanding the modes of communication in astrocyte networks and how they form spatial temporal patterns of their calcium dynamics is important to understanding their interaction with neuronal networks. We investigate this interaction between networks and how glial cells modulate neuronal dynamics through microelectrode array measurements of neuronal network dynamics. We quantify the spontaneous electrical activity patterns of neurons and show the effect of glia on the neuronal dynamics and synchrony. Through a computational approach I investigate an entirely different theoretical mechanism for coordinating ensembles of neurons. I show in a computational model how biophysical resonance shifts in individual neurons can interact with the network topology to influence pattern formation and separation. I show that sub-threshold neuronal depolarization, potentially from astrocytic modulation among other sources, can shift neurons into and out of resonance with specific bands of existing extracellular oscillations. This can act as a dynamic readout mechanism during information storage and retrieval. Exploring these mechanisms that facilitate emergence are necessary for understanding information processing in the brain.PHDApplied PhysicsUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.lib.umich.edu/bitstream/2027.42/111493/1/lshtrah_1.pd

STDP in Oscillatory Recurrent Networks: Theoretical Conditions for Desynchronization and Applications to Deep Brain Stimulation

Highly synchronized neural networks can be the source of various pathologies such as Parkinson's disease or essential tremor. Therefore, it is crucial to better understand the dynamics of such networks and the conditions under which a high level of synchronization can be observed. One of the key factors that influences the level of synchronization is the type of learning rule that governs synaptic plasticity. Most of the existing work on synchronization in recurrent networks with synaptic plasticity are based on numerical simulations and there is a clear lack of a theoretical framework for studying the effects of various synaptic plasticity rules. In this paper we derive analytically the conditions for spike-timing dependent plasticity (STDP) to lead a network into a synchronized or a desynchronized state. We also show that under appropriate conditions bistability occurs in recurrent networks governed by STDP. Indeed, a pathological regime with strong connections and therefore strong synchronized activity, as well as a physiological regime with weaker connections and lower levels of synchronization are found to coexist. Furthermore, we show that with appropriate stimulation, the network dynamics can be pushed to the low synchronization stable state. This type of therapeutical stimulation is very different from the existing high-frequency stimulation for deep brain stimulation since once the stimulation is stopped the network stays in the low synchronization regime

Relating macroscopic measures of brain activity to fast dynamic neuronal interactions

The aim of this thesis was to find a systematic relationship between neuronal synchrony and firing rates, that would enable us to make inferences about one given knowledge of the other. Functional neuroimaging techniques, such as functional magnetic resonance imaging (fMRI), are sensitive to changes in overall population synaptic activity, that can be interpreted in terms of rate coding for a particular stimulus or task. Characterising the relationship between synchrony and firing rates would facilitate inferences about fast neuronal interactions on the basis of macroscopic measures such as those obtained by fMRI. In this thesis, we used computer simulations of neuronal networks and fMRI in humans to investigate the relationship between mean synaptic activity and fast synchronous neuronal interactions. We found that the extent to which different neurons engage in fast dynamic interactions is largely dependent on the neuronal population firing rates and vice versa, i.e. as one metric changes (either activity or synchrony), so does the other. Additionally, as a result of the strong coupling between overall activity and neuronal synchrony, there is also a robust relationship between background activity and stimulus-evoked activity: Increased background activity increases the gain of the neurons, by decreasing effective membrane time constants, and enhancing stimulus-evoked population activity through the selection of fast synchronous dynamics. In concluding this thesis, we tested and confirmed, with fMRI in humans, that this mechanism may account for attentional modulation, i.e. the change in baseline neuronal firing rates associated with attention, in cell assemblies selectively responding to an attended sensory attribute, enhances responses elicited by presentation of that attribute

Attention Enhances the Retrieval and Stability of Visuospatial and Olfactory Representations in the Dorsal Hippocampus

Attention enhances the encoding and retrieval of olfactory and visuospatial representations by modulating place field stability, firing rate, and neuronal synchronization of pyramidal cells in the hippocampus

Oscillatory architecture of memory circuits

The coordinated activity between remote brain regions underlies cognition and memory function. Although neuronal oscillations have been proposed as a mechanistic substrate for the coordination of information transfer and memory consolidation during sleep, little is known about the mechanisms that support the widespread synchronization of brain regions and the relationship of neuronal dynamics with other bodily rhythms, such as breathing. During exploratory behavior, the hippocampus and the prefrontal cortex are organized by theta oscillations, known to support memory encoding and retrieval, while during sleep the same structures are dominated by slow oscillations that are believed to underlie the consolidation of recent experiences. The expression of conditioned fear and extinction memories relies on the coordinated activity between the mPFC and the basolateral amygdala (BLA), a neuronal structure encoding associative fear memories. However, to date, the mechanisms allowing this long-range network synchronization of neuronal activity between the mPFC and BLA during fear behavior remain virtually unknown. Using a combination of extracellular recordings and open- and closed-loop optogenetic manipulations, we investigated the oscillatory and coding mechanisms mediating the organization and coupling of the limbic circuit in the awake and asleep brain, as well as during memory encoding and retrieval. We found that freezing, a behavioral expression of fear, is tightly associated with an internally generated brain state that manifests in sustained 4Hz oscillatory dynamics in prefrontal-amygdala circuits. 4Hz oscillations accurately predict the onset and termination of the freezing state. These oscillations synchronize prefrontal-amygdala circuits and entrain neuronal activity to dynamically regulate the development of neuronal ensembles. This enables the precise timing of information transfer between the two structures and the expression of fear responses. Optogenetic induction of prefrontal 4Hz oscillations promotes freezing behavior and the formation of long-lasting fear memory, while closed-loop phase specific manipulations bidirectionally modulate fear expression. Our results unravel a physiological signature of fear memory and identify a novel internally generated brain state, characterized by 4Hz oscillations. This oscillation enables the temporal coordination and information transfer in the prefrontal-amygdala circuit via a phase-specific coding mechanism, facilitating the encoding and expression of fear memory. In the search for the origin of this oscillation, we focused our attention on breathing, the most fundamental and ubiquitous rhythmic activity in life. Using large-scale extracellular recordings from a number of structures, including the medial prefrontal cortex, hippocampus, thalamus, amygdala and nucleus accumbens in mice we identified and characterized the entrainment by breathing of a host of network dynamics across the limbic circuit. We established that fear-related 4Hz oscillations are a state-specific manifestation of this cortical entrainment by the respiratory rhythm. We characterized the translaminar and transregional profile of this entrainment and demonstrated a causal role of breathing in synchronizing neuronal activity and network dynamics between these structures in a variety of behavioral scenarios in the awake and sleep state. We further revealed a dual mechanism of respiratory entrainment, in the form of an intracerebral corollary discharge that acts jointly with an olfactory reafference to coordinate limbic network dynamics, such as hippocampal ripples and cortical UP and DOWN states, involved in memory consolidation. Respiration provides a perennial stream of rhythmic input to the brain. In addition to its role as the condicio sine qua non for life, here we provide evidence that breathing rhythm acts as a global pacemaker for the brain, providing a reference signal that enables the integration of exteroceptive and interoceptive inputs with the internally generated dynamics of the hippocampus and the neocortex. Our results highlight breathing, a perennial rhythmic input to the brain, as an oscillatory scaffold for the functional coordination of the limbic circuit, enabling the segregation and integration of information flow across neuronal networks

MUSCARINIC MODULATION OF BASOLATERAL AMYGDALA

The basolateral amygdala (BL) receives a dense cholinergic innervation from the basal forebrain. Despite the importance of muscarinic acetylcholine receptors (mAChRs) in fear learning, consolidation, and extinction, there have been no studies that have systematically investigated the functional role of mAChRs in regulating emotional processing in the BL. To address this critical knowledge gap we combined brain slice whole-cell recording, optogenetics, and immunohistochemistry to determine how muscarine, acting on mAChRs, regulates neuronal oscillations, synaptic transmission and plasticity in the BL. Neurons in the BL oscillate rhythmically during emotional processing, which are thought to be important to integrate sensory inputs, allow binding of information from different brain areas and facilitate synaptic plasticity in target downstream structures. We found that muscarine induced theta frequency rhythmic inhibitory postsynaptic potentials (IPSPs) in BL pyramidal neuron (PN). These IPSPs synchronized PN firing at theta frequencies. Recordings from neurochemically-identified interneurons revealed that muscarine selectively depolarized parvalbumin (PV)-containing, fast firing, but not PV, regular firing or somatostatin (SOM)-containing interneurons. This depolarization was mediated by M3 mAChRs. Dual cell recordings from connected interneuron-PN pair indicated that action potentials in fast firing, but not regular firing interneurons were strongly correlated with large IPSCs in BL PNs. Furthermore, selective blockade of M3, but not M1 mAChRs suppressed the rhythmic IPSCs in BL PNs. These findings suggest that muscarine induces rhythmic IPSCs in PNs by selectively depolarizing PV, fast firing interneurons through M3 mAChRs. Furthermore, we found that rhythmic IPSCs were highly synchronized between PNs throughout the BL. The BL receives extensive glutamatergic inputs from multiple brain regions and recurrent collaterals as well. They are important for fear learning and extinction, which are tightly regulated by local GABAergic inhibition. We found that mAChRs activation suppressed external glutamatergic inputs in a frequency dependent and pathway specific manner but kept recurrent glutamatergic transmission intact. In addition, muscarine disinhibited BL PNs by attenuating feedforward and GABAergic inhibition. In agreement with these observations, long term potentiation (LTP) induction was facilitated in the BL by mAChRs activation. Taken together, we provided mechanisms for cholinergic induction of thetaoscillations and facilitation of LTP in the BL