Vibrational Resonance and Electrical Activity Behavior of a Fractional-Order FitzHugh–Nagumo Neuron System

Making use of the numerical simulation method, the phenomenon of vibrational resonance and electrical activity behavior of a fractional-order FitzHugh–Nagumo neuron system excited by two-frequency periodic signals are investigated. Based on the definition and properties of the Caputo fractional derivative, the fractional L1 algorithm is applied to numerically simulate the phenomenon of vibrational resonance in the neuron system. Compared with the integer-order neuron model, the fractional-order neuron model can relax the requirement for the amplitude of the high-frequency signal and induce the phenomenon of vibrational resonance by selecting the appropriate fractional exponent. By introducing the time-delay feedback, it can be found that the vibrational resonance will occur with periods in the fractional-order neuron system, i.e., the amplitude of the low-frequency response periodically changes with the time-delay feedback. The weak low-frequency signal in the system can be significantly enhanced by selecting the appropriate time-delay parameter and the fractional exponent. In addition, the original integer-order model is extended to the fractional-order model, and the neuron system will exhibit rich dynamical behaviors, which provide a broader understanding of the neuron system.

New cell biological explanations for kinesin-linked axon degeneration

Axons are the slender, up to meter-long projections of neurons that form the biological cables wiring our bodies. Most of these delicate structures must survive for an organism's lifetime, meaning up to a century in humans. Axon maintenance requires life-sustaining motor protein-driven transport distributing materials and organelles from the distant cell body. It seems logic that impairing this transport causes systemic deprivation linking to axon degeneration. But the key steps underlying these pathological processes are little understood. To investigate mechanisms triggered by motor protein aberrations, we studied more than 40 loss- and gain-of-function conditions of motor proteins, cargo linkers or further genes involved in related processes of cellular physiology. We used one standardised Drosophila primary neuron system and focussed on the organisation of axonal microtubule bundles as an easy to assess readout reflecting axon integrity. We found that bundle disintegration into curled microtubules is caused by the losses of Dynein heavy chain and the Kif1 and Kif5 homologues Unc-104 and Kinesin heavy chain (Khc). Using point mutations of Khc and functional loss of its linker proteins, we studied which of Khc's sub-functions might link to microtubule curling. One cause was emergence of harmful reactive oxygen species through loss of Milton/Miro-mediated mitochondrial transport. In contrast, loss of the Kinesin light chain linker caused microtubule curling through an entirely different mechanism appearing to involve increased mechanical challenge to microtubule bundles through de-inhibition of Khc. The wider implications of our findings for the understanding of axon maintenance and pathology are discussed.

Mimetic Self-Reflexivity and Intersubjectivity in Complementary and Alternative Medicine Practices: The Mirror Neuron System in Breast Cancer Survivorship

This study examines complementary and alternative medicine (CAM) providers’ practices in the treatment of their breast cancer survivor (BCS) clients and interprets these practices within the context of existing neuroscientific research on the mirror neuron system (MNS). Purposive and snowball sampling was conducted to recruit CAM providers (N = 15) treating BCSs from integrative medicine centers, educational institutions, private practices, and professional medical associations across the United States. In-depth semi-structured interviewing (N = 252 single-spaced pages) and inductive qualitative content analysis reveal CAM therapeutic practices emphasize a diachronic form of mimetic self-reflexivity and a serendipitous form of mimetic intersubjectivity in BCS pain management to allow the providers to tune-in to their clients’ internal states over time and experience themselves as an embodied subject in an imaginative, shared space. By employing imagination and an intentional vulnerability in their embodied simulation of the others’ internal states, CAM providers co-create experiences of pain while recognizing what about the other remains an unknown. Although MNs provide the mechanism for imitation and simulation underlying empathy through a neuronally wired grasp of the other’s intentionality, the study suggests that examining mimetic self-reflexivity and intersubjectivity in the therapeutic space may allow for a shared simulation of participants’ subjective experiences of pain and potentially inform research on self-recognition and self-other discrimination as an index of self-awareness which implicates the MNS in embodied social cognition in imaginative ways.

Genetic dissection of the glutamatergic neuron system in cerebral cortex

Diverse types of glutamatergic pyramidal neurons mediate the myriad processing streams and output channels of the cerebral cortex1,2, yet all derive from neural progenitors of the embryonic dorsal telencephalon3,4. Here we establish genetic strategies and tools for dissecting and fate-mapping subpopulations of pyramidal neurons on the basis of their developmental and molecular programs. We leverage key transcription factors and effector genes to systematically target temporal patterning programs in progenitors and differentiation programs in postmitotic neurons. We generated over a dozen temporally inducible mouse Cre and Flp knock-in driver lines to enable the combinatorial targeting of major progenitor types and projection classes. Combinatorial strategies confer viral access to subsets of pyramidal neurons defined by developmental origin, marker expression, anatomical location and projection targets. These strategies establish an experimental framework for understanding the hierarchical organization and developmental trajectory of subpopulations of pyramidal neurons that assemble cortical processing networks and output channels.

Human mirror neuron system responsivity to unimodal and multimodal presentations of action

This study aims to clarify unresolved questions from two earlier studies (McGarry et al., 2012; Kaplan & Iacoboni, 2007) on human mirror neuron system (hMNS) responsivity to multimodal presentations of actions. These questions are: (1) whether the two frontal areas originally identified by Kaplan and Iacoboni (ventral premotor cortex [vPMC] and inferior frontal gyrus [IFG]) are both part of the hMNS (i.e., do they respond to execution as well as observation), (2) whether both areas yield effects of biologicalness (biological, control) and modality (audio, visual, audiovisual), and (3) whether the vPMC is preferentially responsive to multimodal input. To resolve these questions about the hMNS, we replicated and extended McGarry et al.’s electroencephalography (EEG) study, while incorporating advanced source localization methods. Participants were asked to execute movements (ripping paper) as well as observe those movements across the same three modalities (audio, visual, and audiovisual), all while 64-channel EEG data was recorded. Two frontal sources consistent with those identified in prior studies showed mu event-related desynchronization (mu-ERD) under execution and observation conditions. These sources also showed a greater response to biological movement than to control stimuli as well as a distinct visual advantage, with greater responsivity to visual and audiovisual compared to audio conditions. Exploratory analyses of mu-ERD in the vPMC under visual and audiovisual observation conditions suggests that the hMNS tracks the magnitude of visual movement over time.