Impact of delays and rewiring on the dynamics of small-world neuronal networks with two types of coupling

We study synchronization transitions and pattern formation on small-world networks consisting of Morris-Lecar excitable neurons in dependence on the information transmission delay and the rewiring probability. In addition, networks formed via gap junctional connections and coupling via chemical synapses are considered separately. For gap-junctionally coupled networks we show that short delays can induce zigzag fronts of excitations, whereas long delays can further detriment synchronization due to a dynamic clustering anti-phase synchronization transition. For the synaptically coupled networks, on the other hand, we find that the clustering anti-phase synchronization can appear as a direct consequence of the prolongation of information transmission delay, without being accompanied by zigzag excitatory fronts. Irrespective of the coupling type, however, we show that an appropriate small-world topology can always restore synchronized activity if only the information transmission delays are short or moderate at most. Long information transmission delays always evoke anti-phase synchronization and clustering, in which case the fine-tuning of the network topology fails to restore the synchronization of neuronal activity.     

Delay-induced synchronization transitions in small-world neuronal networks with hybrid electrical and chemical synapses

We study the dependence of synchronization transitions in small-world networks of bursting neurons with hybrid electrical–chemical synapses on the information transmission delay, the probability of electrical synapses, and the rewiring probability. It is shown that, irrespective of the probability of electrical synapses, the information transmission delay can always induce synchronization transitions in small-world neuronal networks, i.e., regions of synchronization and nonsynchronization appear intermittently as the delay increases. In particular, all these transitions to burst synchronization occur approximately at integer multiples of the bursting period of individual neurons. In addition, for larger probability of electrical synapses, the intermittent synchronization transition is more profound, due to the stronger synchronization ability of electrical synapses compared with chemical ones. More importantly, chemical and electrical synapses can perform complementary roles in the synchronization of hybrid small-world neuronal networks: the larger the electrical synapse strength is, the smaller the chemical synapse strength needed to achieve burst synchronization. Furthermore, the small-world topology has a significant effect on the synchronization transition in hybrid neuronal networks. It is found that increasing the rewiring probability can always enhance the synchronization of neuronal activity. The results obtained are instructive for understanding the synchronous behavior of neural systems.     

小世界神经元网络随机共振现象:混合突触和部分时滞的影响

实际神经元网络中,信息传递时电突触和化学突触同时存在,并且有些神经元间的时滞很小可以忽略.本文构建了带有不同类型突触耦合的小世界网络,研究部分时滞、混合突触及噪声对随机共振的影响.结果表明:兴奋性和抑制性突触的比例影响共振的产生;在抑制性突触为主的网络里,几乎不产生随机共振.系统最佳噪声强度和化学突触比例大致呈线性递增关系;特别是在以化学耦合为主的混合突触网络里,仅当兴奋性突触与抑制性突触比例约为4:1时,噪声才可诱导网络产生共振行为.在此比例下,引入部分时滞发现时滞可诱导网络产生随机多共振,且随网络中时滞边比例的增加,系统响应强度达到最优水平的时滞取值区间逐渐变窄;同时发现,网络中含有的化学突触越多,部分时滞诱导产生的多共振行为越强.此外,当时滞为系统固有周期的整数倍时,时滞越大共振所对应的噪声区域越广;并且网络中时滞边越多,越容易促使噪声和时滞诱导其产生明显的共振行为.     

The influence of connectivity on the firing rate in a neuronal network with electrical and chemical synapses

We study the firing rate properties of a cellular automaton model for a neuronal network with chemical synapses. We propose a simple mechanism in which the nonlocal connections are included, through electrical and chemical synapses. In the latter case, we introduce a time delay which produces self-sustained activity. Nonlocal connections, or shortcuts, are randomly introduced according to a specified connection probability. There is a range of connection probabilities for which neuron firing occurs, as well as a critical probability for which the firing ceases in the absence of time delay. The critical probability for nonlocal shortcuts depends on the network size according to a power-law. We also compute the firing rate amplification factor by varying both the connection probability and the time delay for different network sizes.     

Stochastic resonance in hybrid scale-free neuronal networks

We study the phenomenon of stochastic resonance in a system of coupled neurons that are globally excited by a weak periodic input signal. We make the realistic assumption that the chemical and electrical synapses interact in the same neuronal network, hence constituting a hybrid network. By considering a hybrid coupling scheme embedded in the scale-free topology, we show that the electrical synapses are more efficient than chemical synapses in promoting the best correlation between the weak input signal and the response of the system. We also demonstrate that the average degree of neurons within the hybrid scale-free network significantly influences the optimal amount of noise for the occurrence of stochastic resonance, indicating that there also exists an optimal topology for the amplification of the response to the weak input signal. Lastly, we verify that the presented results are robust to variations of the system size.     

氧化锌/氧化钽双介质层忆阻器的突触特性分析

人工突触的开发是模拟人脑功能的关键。忆阻器由于具备独特的电阻记忆行为,在人工突触研究领域得到广泛的关注。氧化钽和氧化锌均是优良的忆阻器材料,鉴于有关ZnO/TaOx双介质忆阻器突触特性的研究较少,本文将氧化锌介质层引入Ti/TaOx/ITO忆阻器中拟改善其突触性能。研究发现,器件Ti/ZnO/TaOx/ITO在功耗和电导调制线性度方面皆有改善,并有着电阻渐变的行为,利于器件突触功能的实现及应用。为此对Ti/ZnO/TaOx/ITO双介质层器件进行了电压脉冲训练,并成功模拟了学习饱和、经验学习以及短时程记忆向长时程记忆转变等生物突触行为。     

Synthetic multivalent ligands as probes of signal transduction

Cell-surface receptors acquire information from the extracellular environment and coordinate intracellular responses. Many receptors do not operate as individual entities, but rather as part of dimeric or oligomeric complexes. Coupling the functions of multiple receptors may endow signaling pathways with the sensitivity and malleability required to govern cellular responses. Moreover, multireceptor signaling complexes may provide a means of spatially segregating otherwise degenerate signaling cascades. Understanding the mechanisms, extent, and consequences of receptor co-localization and interreceptor communication is critical; chemical synthesis can provide compounds to address the role of receptor assembly in signal transduction. Multivalent ligands can be generated that possess a variety of sizes, shapes, valencies, orientations, and densities of binding elements. This Review focuses on the use of synthetic multivalent ligands to characterize receptor function.