Biology subjects

Tambalo, S.

Publications and source records attributed to Tambalo, S..

6 recordsLinked to original sources

bioRxiv2024

Multiscale excitation-inhibition balance dynamics: integrating metabolite kinetics with time-varying executive networks

The balance between neural excitation and inhibition (EIB) is an essential mechanism supporting cognitive processes. Yet, little is understood about how EIB shifts with cognitive load and its impact on functional connectivity dynamics. In this study, we investigate temporal profiles of the reciprocal modulation between EIB and functional network dynamics during working memory tasks, revealing that EIB prefrontal kinetics scale with increasing cognitive load. Notably, prefrontal EIB kinetics correlated with cognitive load, impacting stability of networks crucial for cognitive function. On one hand, brain dynamics adapt to meet increasing cognitive challenges with a shift towards more focused and sustained neural activity patterns in terms of connectivity. On the other, imbalances favouring excitation may hinder cognitive adaptability. Importantly, this experimental approach demonstrates a link between EIB kinetics, brain network dynamics and cognitive performance, defining the groundwork for exploring healthy and aberrant cognitive states. TeaserHighly focused or less responsive? Chemical signalling and network dynamics are coupled to produce persistent cognitive states.

neuroscience↗

bioRxiv2024

Advancing Thalamic Nuclei Segmentation: The Impact of Compressed Sensing and FastSurfer on MRI Processing

The thalamus is a collection of gray matter nuclei that play a crucial role in sensorimotor processing and modulation of cortical activity. Characterizing thalamic nuclei non-invasively with structural MRI is particularly relevant for patient populations with Parkinsons disease, epilepsy, dementia, and schizophrenia. However, severe head motion in these populations poses a significant challenge for in vivo mapping of thalamic nuclei. Recent advancements have leveraged the compressed sensing (CS) framework to accelerate structural MRI acquisition times in MPRAGE sequence variants, while fast segmentation tools like FastSurfer have reduced processing times in neuroimaging research. In this study, we evaluated thalamic nuclei segmentations derived from six different MPRAGE variants with varying degrees of CS acceleration (from about 9 to about 1 minute acquisitions), using both FreeSurfer and FastSurfer for segmentation. Our findings show minimal sequence effects with no systematic bias, and low volume variability across sequences for the whole thalamus and major thalamic nuclei. Notably, CS-accelerated sequences produced less variable volumes compared to non-CS sequences. Additionally, segmentations of thalamic nuclei by FreeSurfer and FastSurfer were highly comparable. We provide first evidence supporting that a good segmentation quality of thalamic nuclei with compressed sensing T1-weighted image acceleration in a clinical 3T MRI system is possible. Our findings encourage future applications of fast T1-weighted MRI to study deep gray matter. CS-accelerated sequences and rapid segmentation methods are promising tools for future studies aiming to characterize thalamic nuclei in vivo at 3T in both healthy individuals and clinical populations.

neuroscience↗

bioRxiv2024

Long-access heroin self-administration induces region specific reduction of grey matter volume and microglia reactivity in the rat.

In opioid use disorder (OUD) patients, a decrease in brain grey matter volume (GMV) has been reported. It is unclear whether this is the consequence of prolonged exposure to opioids or is a predisposing causal factor in OUD development. To investigate this, we conducted a structural MRI longitudinal study in NIH Heterogeneous Stock rats exposed to heroin self-administration and age-matched naive controls housed in the same controlled environment. Structural MRI scans were acquired before (MRI1) and after (MRI2) a prolonged period of long access heroin self-administration resulting in escalation of drug intake. Heroin intake resulted in reduced GMV in various cortical and sub-cortical brain regions. In drug-naive controls no difference was found between MRI1 and MRI2. Notably, the degree of GMV reduction in the medial prefrontal cortex (mPFC) and the insula positively correlated with the amount of heroin consumed and the escalation of heroin use. In a preliminary gene expression analysis, we identified a number of transcripts linked to immune response and neuroinflammation. This prompted us to hypothesize a link between changes in microglia homeostasis and loss of GMV. For this reason, we analyzed the number and morphology of microglial cells in the mPFC and insula. The number of neurons and their morphology was also evaluated. The primary motor cortex, where no GMV change was observed, was used as negative control. We found no differences in the number of neurons and microglia cells following heroin. However, in the same regions where reduced GMV was detected, we observed a shift towards a rounder shape and size reduction in microglia, suggestive of their homeostatic change towards a reactive state. Altogether these findings suggest that escalation of heroin intake correlates with loss of GMV in specific brain regions and that this phenomenon is linked to changes in microglial morphology.

neuroscience↗

bioRxiv2023

TR(acking) individuals down: exploring the effect of temporal resolution in resting-state functional MRI fingerprinting

Functional brain fingerprinting has emerged as an influential tool to quantify reliability in neuroimaging studies and to identify cognitive biomarkers in both healthy and clinical populations. Recent studies have revealed that brain fingerprints reside in the timescale-specific functional connectivity of particular brain regions. However, the impact of the acquisitions temporal resolution on fingerprinting remains unclear. In this study, we examine for the first time the reliability of functional fingerprinting derived from resting-state functional MRI (rs-fMRI) with different whole-brain temporal resolutions (TR = 0.5, 0.7, 1, 2, and 3 s) in a cohort of 20 healthy volunteers. Our findings indicate that subject identifiability within a fixed TR is successful across different temporal resolutions, with the highest identifiability observed at TR 0.5 and 3 s. We discuss this observation in terms of protocol-specific effects of physiological noise aliasing. We further show that, irrespective of TR, associative brain areas make substantial contributions to subject identifiability, whereas sensory-motor regions become influential only when integrating data from different TRs. We conclude that functional connectivity fingerprinting derived from rs-fMRI holds significant potential for multicentric studies also employing protocols with different temporal resolutions. However, it remains crucial to consider fMRI signals sampling rate differences in subject identifiability between data samples, in order to improve reliability and generalizability of both whole-brain and specific functional networks results. These findings contribute to a better understanding of the practical application of functional connectivity fingerprinting, and its implications for future neuroimaging research.

neuroscience↗

bioRxiv2023

Manganese Enhanced Magnetic Resonance Imaging reveals light-induced brain asymmetry in embryo

The idea that sensory stimulation to the embryo (in utero or in ovo) may be crucial for brain development is widespread. Unfortunately, up to now evidence was only indirect because imaging of embryonic brain activity in vivo was not viable. Here we applied for the first time Manganese Enhanced Magnetic Resonance Imaging (MEMRI) to the eggs of domestic chicks. We revealed light-induced brain asymmetry by comparing embryonic brain activity in vivo of eggs that were stimulated by light or maintained in the darkness. Our protocol paves the way to investigation of the effects of a variety of sensory stimulations on brain activity in embryo. SignificanceSensory stimulation in embryo may be crucial for many aspects of brain and behavioral development (e.g., mother language in humans). However, direct evidence of this is lacking because imaging of embryonic brain activity in vivo is not viable. Here we established a new protocol for measuring embryonic brain activity in vivo in domestic chick eggs. We were able to visualize in vivo the effect of light stimulation on the development of structural brain asymmetries of the embryo. The protocol established paves the way for collecting further evidence on the effects of sensory stimulation on embryonic brain activity.

neuroscience↗

bioRxiv2022

Head motion correction shapes functional network estimates: evidence from healthy and Parkinson's disease cohorts

An open discussion in studies of intrinsic brain functional connectivity is the mitigation of head motion-related artifacts, particularly in the presence of peculiar symptomatology such as in Parkinsons disease (PD). Previous studies show that Independent Component Analysis (ICA) denoising improves the reproducibility of functional connectivity findings by detecting sources of non-neural signals. However, there is still no consensus about which pre-processing pipeline should be applied in natural high motion populations such as PD, particularly in relation to novel functional network descriptions derived from dynamic connectivity analyses. In this study, we investigated how different pre-processing pipelines affect intrinsic brain connectivity metrics, both static and dynamic, derived from a group of young healthy controls (HC) and a group of PD participants. A total of 20 HC and 20 PD subjects participated in this 3 T MRI study. Resting-state functional MRI images were used to test the effects of the pre-processing pipeline of static (sFC) and temporal-varying functional connectivity (dFC) estimations. Both MRI datasets were pre-processed using three different workflows differing in the motion correction approach: (i) standard motion realignment (mc); (ii) motion outlier detection and deweighting based on image intensity change estimations (DVARS) and (iii) ICA-based noise removal using reference noise features (AROMA). Furthermore, the PD dataset was also processed with a fourth method by applying an ICA-based denoising (FIX), previously trained on the HC group. sFC analysis was performed using Group ICA, by temporally concatenating different pre-processing types in pairs of different runs. Two types of dFC analyses were considered: innovation-driven co-activation patterns (iCAPs) and co-activation patterns (CAPs). CAPs allow dFC estimations that do not require the deconvolution of the hemodynamic response function and its derivative, thus potentially being less sensitive to head-motion related noise. We found that regardless of substantial head motion differences in the two groups, sFC results were consistent across denoising strategies. Conversely, dFC was extremely sensitive to denoising strategies, particularly for the PD group with the transient-based dFC analyses. Indeed, the use of the peak-based dFC framework enables the detection of time-varying networks but in a way that is highly dependent on the motion correction pipeline. In conclusion, we show that dynamic functional network representations are highly sensitive to both head motion and to fMRI denoising methods. These findings stress the importance of considering and reporting these experimental aspects to help with the reproducibility and interpretation of different studies. Future work is needed to further investigate transient-based dFC strategies that are more robust to head motion.

neuroscience↗