Thermal cameras capture the infrared radiation emitted from a body in a contactless manner and can provide an indirect estimation of the autonomic nervous system (ANS) dynamics through the regulation of the skin temperature. This study investigates the contribution given by thermal imaging for an effective automatic stress detection with the perspective of a contactless stress recognition system. To this aim, we recorded both ANS correlates (cardiac, electrodermal, and respiratory activity) and thermal images from 25 volunteers under acute stress induced by the Stroop test. We conducted a statistical analysis on the features extracted from each signal, and we implemented subject-independent classifications based on the support vector machine model with an embedded recursive feature elimination algorithm. Particularly, we trained three classifiers using different feature sets: the full set of features, only those derived from the peripheral autonomic correlates, and only those derived from the thermal images. Classification accuracy and feature selection results confirmed the relevant contribution provided by the thermal features in the acute stress detection task. Indeed, a combination of ANS correlates and thermal features achieved 97.37% of accuracy. Moreover, using only thermal features we could still successfully detect stress with an accuracy of 86.84% in a contact-free manner.

Tissue clarification has been recently proposed to allow deep tissue imaging without light scattering. The clarification parameters are somewhat arbitrary and dependent on tissue type, source and dimension: every laboratory has its own protocol, but a quantitative approach to determine the optimum clearing time is still lacking. Since the use of transgenic mouse lines that express fluorescent proteins to visualize specific cell populations is widespread, a quantitative approach to determine the optimum clearing time for genetically labeled neurons from thick murine brain slices using CLARITY2 is described. In particular, as the main objective of the delipidation treatment is to clarify tissues, while limiting loss of fluorescent signal, the “goodness” of clarification was evaluated by considering the bulk tissue clarification index (BTCi) and the fraction of the fluorescent marker retained in the slice as easily quantifiable macroscale parameters. Here we describe the approach, illustrating an example of how it can be used to determine the optimum clearing time for 1 mm-thick cerebellar slice from transgenic L7GFP mice, in which Purkinje neurons express the GFP (green fluorescent protein) tag. To validate the method, we evaluated confocal stacks of our samples using standard image processing indices (i.e. the mean pixel intensity of neurons and the contrast-to-noise ratio) as figures of merit for image quality. The results show that detergent-based delipidation for more than five days does not increase tissue clarity but the fraction of GFP in the tissue continues to diminish. The optimum clearing time for 1 mm-thick slices was thus identified as five days, which is the best compromise between the increase in light penetration depth due to removal of lipids and a decrease in fluorescent signal as a consequence of protein loss: further clearing does not improve tissue transparency, but only leads to more protein removal or degradation. The rigorous quantitative approach described can be generalized to any clarification method to identify the moment when the clearing process should be terminated to avoid useless protein loss.

Objective: Most of the bodily functions are regulated by multiple interactions between the parasympathetic (PNS) and sympathetic (SNS) nervous system. In this study, we propose a novel framework to quantify the causal flow of information between PNS and SNS through the analysis of heart rate variability (HRV) and electrodermal activity (EDA) signals. Methods: Our method is based on a time-varying (TV) multivariate autoregressive model of EDA and HRV time-series and incorporates physiologically inspired assumptions by estimating the Directed Coherence in a specific frequency range. The statistical significance of the observed interactions is assessed by a bootstrap procedure purposely developed to infer causalities in the presence of both TV model coefficients and TV model residuals (i.e., heteroskedasticity). We tested our method on two different experiments designed to trigger a sympathetic response, i.e., a hand-grip task (HG) and a mental-computation task (MC). Results: Our results show a parasympathetic driven interaction in the resting state, which is consistent across different studies. The onset of the stressful stimulation triggers a cascade of events characterized by the presence or absence of the PNS-SNS interaction and changes in the directionality. Despite similarities between the results related to the two tasks, we reveal differences in the dynamics of the PNS-SNS interaction, which might reflect different regulatory mechanisms associated with different stressors. Conclusion: We estimate causal coupling between PNS and SNS through MVAR modeling of EDA and HRV time-series. Significance: Our results suggest promising future applicability to investigate more complex contexts such as affective and pathological scenarios.

Decoding the morphology and physical connections of all the neurons populating a brain is necessary for predicting and studying the relationships between its form and function, as well as for documenting structural abnormalities in neuropathies. Digitizing a complete and high-fidelity map of the mammalian brain at the micro-scale will allow neuroscientists to understand disease, consciousness, and ultimately what it is that makes us humans. The critical obstacle for reaching this goal is the lack of robust and accurate tools able to deal with 3D datasets representing dense-packed cells in their native arrangement within the brain. This obliges neuroscientist to manually identify the neurons populating an acquired digital image stack, a notably time-consuming procedure prone to human bias. Here we review the automatic and semi-automatic algorithms and software for neuron segmentation available in the literature, as well as the metrics purposely designed for their validation, highlighting their strengths and limitations. In this direction, we also briefly introduce the recent advances in tissue clarification that enable significant improvements in both optical access of neural tissue and image stack quality, and which could enable more efficient segmentation approaches. Finally, we discuss new methods and tools for processing tissues and acquiring images at sub-cellular scales, which will require new robust algorithms for identifying neurons and their sub-structures (e.g., spines, thin neurites). This will lead to a more detailed structural map of the brain, taking twenty-first century cellular neuroscience to the next level, i.e., the Structural Connectome.

Accurately digitizing the brain at the micro-scale is crucial for investigating brain structure-function relationships and documenting morphological alterations due to neuropathies. Here we present a new Smart Region Growing algorithm (SmRG) for the segmentation of single neurons in their intricate 3D arrangement within the brain. Its Region Growing procedure is based on a homogeneity predicate determined by describing the pixel intensity statistics of confocal acquisitions with a mixture model, enabling an accurate reconstruction of complex 3D cellular structures from high-resolution images of neural tissue. The algorithm’s outcome is a 3D matrix of logical values identifying the voxels belonging to the segmented structure, thus providing additional useful volumetric information on neurons. To highlight the algorithm’s full potential, we compared its performance in terms of accuracy, reproducibility, precision and robustness of 3D neuron reconstructions based on microscopic data from different brain locations and imaging protocols against both manual and state-of-the-art reconstruction tools.

Objective.The emotional response to olfactory stimuli implies the activation of a complex cascade of events triggered by structures lying in the limbic system. However, little is known about how this activation is projected up to cerebral cortex and how different cortical areas dynamically interact each other.Approach.In this study, we acquired EEG from human participants performing a passive odor-perception task with odorants conveying positive, neutral and negative valence. A novel methodological pipeline integrating global field power (GFP), independent component analysis (ICA), dipole source localization was applied to estimate effective connectivity in the challenging scenario of single-trial low-synchronized stimulation.Main results.We identified the brain network and the neural paths, elicited at different frequency bands, i.e. θ(4−7Hz) , α(8−12Hz) and β(13−30Hz) , involved in odor valence processing. This brain network includes the orbitofrontal cortex (OFC), the cingulate gyrus (CgG), the superior temporal gyrus (STG), the posterior cingulate cortex/precuneus (PCC/PCu) and the parahippocampal gyrus (PHG). It was analyzed using a time-varying multivariate autoregressive model to resolve time-frequency causal interactions. Specifically, the OFC acts as the main node for odor perception and evaluation of pleasant and unpleasant stimuli, whereas no specific path was observed for a neutral stimulus.Significance.The results introduce new evidences on the role of the OFC during hedonic perception and underpin its specificity during the odor valence assessment. Our findings suggest that, after the odor onset different, bidirectional interactions occur between the OFC and other brain regions associated with emotion recognition/categorization and memory according to the stimulus valence. This outcome unveils how the hedonic olfactory network dynamically changes based on odor valence.