Biology subjects

Arshamian, A.

Publications and source records attributed to Arshamian, A..

14 recordsLinked to original sources

bioRxiv2026

Recurrent beta-gamma interactions between olfactory bulb and piriform cortex support cross-sniff perceptual continuity in humans

Olfactory perception relies on active sampling, with successive inhalations providing discrete sensory inputs that in humans can be separated by several seconds. Yet odors are perceived as continuous and stable, raising the question of how the brain integrates sensory information across these temporal gaps. Here, we used electrobulbogram (EBG) recordings in 48 participants to demonstrate that successive sniffs are not processed independently but are linked through recurrent oscillatory dynamics between the olfactory bulb (OB) and piriform cortex (PC). Specifically, first-sniff alpha/beta activity in the OB and OB-PC functional connectivity predicted second-sniff gamma power, while transfer entropy indicated a directional temporal dependence from first-sniff alpha/beta to second-sniff gamma dynamics. In parallel, second-sniff gamma activity selectively tracked subjective odor valence prior to inhalation onset. At the network level, the PC exhibited stronger alpha/beta-band connectivity with orbitofrontal, insular, and prefrontal regions during the first sniff than during the second, suggesting that early evaluative processing provides a contextual signal that is carried forward to shape subsequent sensory representations. These results demonstrate that the human OB-PC circuit carries evaluative information across inhalations through directed alpha/beta-to-gamma interactions, providing a mechanism for maintaining perceptual continuity in a sensory system defined by temporally discrete sampling.

neuroscience↗

bioRxiv2026

Precision measurement of non-conscious avoidance reactions using 3D tracking: Validation across olfaction and vision

One of our sensory systems key functions is to detect threats in the environment. Sensory information eliciting negative emotions, such as fear or disgust, triggers instinctive avoidance reactions. This core survival mechanism is believed to be expressed as subtle non-conscious postural reactions, even when participants are instructed to stand still. Such avoidance behavior has mainly been studied using indirect measures that make participants aware of their posture (e.g. force-plate based methods) or measures that depend on explicit cognitive tasks, like moving a joystick to indicate an urge to approach or avoid the stimulus; experimental tasks with limited ecological validity and generalizability. Therefore, despite the importance of this basic survival strategy, its underlying mechanisms are still poorly understood. Here, we used a novel 3D-camera-based method allowing direct but implicit measures of postural reactions with high precision. Participants are aware that they are being filmed but, crucially, are not informed that distance measures are obtained. We assessed this ecologically valid measure of approach/avoidance responses in two different sensory modalities: olfaction and vision. Participants were standing upright while exposed to either olfactory or visual stimuli and verbally rating their perceived valence in each trial. In response to subjectively unpleasant odors and images, participants moved away from the stimulus source, as compared to pleasant stimuli. These results demonstrate a putative modality-independent early proxy for avoidance behavior in response to perceived negative valence. Considering its face validity and general applicability, this novel experimental method presents new possibilities for assessing non-conscious approach-avoidance responses in humans.

neuroscience↗

bioRxiv2025

The olfactory bulb reflects structural plasticity within a genetically stable olfactory network

The olfactory bulb (OB), the first central relay of the olfactory pathway, plays a critical role in odor perception and exhibits remarkable structural plasticity shaped by environmental influences. This raises a fundamental question about the extent to which the structure of the OB is genetically determined. While both OB volume and function have been implicated in a range of neurodegenerative and neuropsychiatric disorders, such as Parkinsons disease, schizophrenia, and depression, all of which involve known genetic risk factors, the heritability of the OB structure remains poorly understood. Here, we investigated the heritability of OB volume and the broader olfactory network architecture in a large sample of healthy young adults (n = 941; aged 22-35 years), including monozygotic and dizygotic twin pairs. Using a deep learning-based segmentation model, we first automatically segmented OB volumes and then employed a support vector machine framework to classify zygosity based on within-pair morphological similarity. The OB volume alone showed weak classification performance in distinguishing between monozygotic and dizygotic twins, suggesting limited heritability. However, integrating OB volume with morphometric features from olfactory-associated brain regions, including the hippocampus, parahippocampal gyrus, entorhinal cortex, and medial orbitofrontal cortices, substantially improved classification performance. This effect was specific to the olfactory network, underscoring the distributed nature of genetic influence in this system. These findings suggest that the OB, despite being a highly plastic and environmentally responsive structure, is embedded within a genetically coordinated neural network.

neuroscience↗

bioRxiv2025

Methodological determinants of signal quality in electrobulbogram recordings

The electrobulbogram (EBG) is a new, non-invasive method for measuring the functional activity of the human olfactory bulb (OB). To date, the EBG has been used to assess how the OB process odor identity, valence, intensity, and it has shown promise as an early biomarker for Parkinsons disease. However, current implementation of the EBG method depends on several methodological components, including subject specific co-registration of electrode positions through neuronavigation and EEG source reconstruction, which may limit accessibility for many research groups. In this study, we test the quality and reliability of the OB signal under different configurations to potentially remedy this. Specifically, we compare six EBG setups that vary in the use of subject-specific T1 scans versus a template head model, co-registered versus template electrode positions, and individualized versus template-based OB location. Our results indicate that strongest EBG signals are obtained when using subject-specific T1 scans in combination with co-registered electrode positions. However, we obtained significant EBG activity even when using a fully template-based configuration. Our anatomical analysis of OB location of 941 individuals reveals that in 86% of cases, the OB is centered within the spatial resolution bounds of the EEG source dipole, supporting the feasibility of detecting olfactory bulb signals without precise individual anatomical mapping using template coordinates. These findings suggest that while subject-specific configurations enhance signal quality, the EBG method remains robust enough to yield meaningful results even with less complex setups. This enables a broader adoption of the EBG method in both clinical and research settings.

neuroscience↗

bioRxiv2025

Olfactory bulb and cortex activity reflects subjective odor intensity perception rather than concentration

Understanding stimulus intensity processing is fundamental in sensory science, yet this question remains largely unexplored in human olfaction. We investigated how the human olfactory bulb (OB) and piriform cortex (PC) process odor concentration versus subjective perceived intensity. We demonstrate that OB-PC network oscillatory dynamics are predominantly driven by perceived intensity, not physical concentration. The OB initially processes and communicates perceived intensity to the PC via early gamma-band oscillations (bottom-up feedback). The PC then refines and sends this percept back to the OB via later beta-band oscillations (top-down feedback), updating the OBs gamma activity for subsequent odorants. Critically, analyses of phase-amplitude coupling and beta burst activity demonstrate that transient beta patterns from the PC update OB gamma activity, providing the OB with an updated internal representation of the odor percept. These results reveal an oscillatory mechanism by which the olfactory system maintains perceptual constancy and adaptability despite fluctuations in environmental odor concentrations.

neuroscience↗

bioRxiv2024

The Respiratory-Pupillary Phase Effect: Pupils size is smallest around inhalation onset and largest during exhalation

The prevailing view in the study of animal and human pupillary function has been that pupils dilate and are largest during inhalation and constrict and are smallest during exhalation. However, this notion has recently been challenged. Here, we systematically address this question by conducting a study encompassing three experiments (two resting tasks and one visual perception task), with the latter two being pre-registered. Collectively, across nasal and oral breathing, resting, and task conditions, our experiments consistently and robustly demonstrate that pupil size is smallest around inhalation onset and largest around peak exhalation. This phenomenon, which we term the Respiratory-Pupillary Phase Effect (RPPE), directly contradicts the long-held notion that pupils are largest during inhalation and smallest during exhalation. Notably, the dilation and constriction processes overlap with both phases. The observed consistency and significance of the RPPE across various conditions underscore the need for further investigation into its underlying mechanisms and potential impact on human behavior.

physiology↗

bioRxiv2023

The how, when, and what of odor valence communication between the olfactory bulb and piriform cortex

A core function of the olfactory system is to determine an odors valence. The central processing of odor valence is initiated in the olfactory bulb, but the neural mechanisms by which this important information is communicated to, and from, the olfactory cortex (piriform cortex) in humans are not known. To assess communication between the two nodes, we simultaneously measured odor-dependent neural activity in the olfactory bulb and piriform cortex from human participants while obtaining trial-by-trial valence ratings. We determined when valence information was communicated, what kind of information was transferred, and how the information was transferred (i.e., in which frequency band). Support vector machine learning on the coherence spectrum and frequency-resolved Granger causality were used to identify valence-dependent differences in functional and effective connectivity between the olfactory bulb and piriform cortex. We found that the olfactory bulb communicates odor valence to the piriform cortex in the gamma band shortly after odor onset, while the piriform cortex subsequently feeds valence-related information back to the olfactory bulb in the beta band. Decoding accuracy was better for negative than positive valence, suggesting negative valence superiority. Critically, we replicated these findings in an independent dataset using other odors across a larger perceived valence range. Combined, these results demonstrate that the olfactory bulb and piriform cortex communicate levels of odor pleasantness across multiple frequencies, at specific time-points and in a direction-dependent pattern in accordance with the two-stage model of odor processing. It also provides further evidence that odor valence should be viewed as two perceptual dimensions and not one continuous.

neuroscience↗

bioRxiv2023

Metabolic state modulates neural processing of odors in the human olfactory bulb

The olfactory and endocrine systems have recently been shown to reciprocally shape the homeostatic processes of energy intake. As demonstrated in animal models, the individuals metabolic state dynamically modulates how the olfactory bulb process odor stimuli using a range of endocrine signals. Here we aimed to determine whether the neural processing of odors in human olfactory bulb is modulated by metabolic state. Participants were exposed to food-associated odors, in separate sessions being hungry and sated, while neural responses from the olfactory bulb was obtained using electrobulbogram. We found significantly higher gamma power activity (51-100Hz) in the OBs response to odors during the Hunger compared to Sated condition. Specifically, EBG gamma power were elevated while hungry already at 100ms after odor onset, thereby suggesting intra-bulbar modulation according to metabolic state. These results demonstrate that, akin to other animal models, hunger state affects OB activity in humans. Moreover, we show that the EBG method has the potential to measure internal metabolic states and, as such, could be used to study specificities in olfactory processing of individuals suffering from pathologies such as obesity or anorexia.

neuroscience↗

bioRxiv2021

ODOR IDENTITY CAN BE EXTRACTED FROM THE RECIPROCAL CONNECTIVITY BETWEEN OLFACTORY BULB AND PIRIFORM CORTEX IN HUMANS

Neuronal oscillations route external and internal information across brain regions. In the olfactory system, the two central nodes--the olfactory bulb (OB) and the piriform cortex (PC)--communicate with each other via neural oscillations to shape the olfactory percept. Communication between these nodes have been well characterized in non-human animals but less is known about their role in the human olfactory system. Using a recently developed and validated EEG-based method to extract signals from the OB and PC sources, we show in healthy human participants that there is a bottom-up information flow from the OB to the PC in the beta and gamma frequency bands, while top-down information from the PC to the OB is facilitated by delta and theta oscillations. Importantly, we demonstrate that there was enough information to decipher odor identity above chance from the low gamma in the OB-PC oscillatory circuit as early as 100ms after odor onset. These data further our understanding of the critical role of bidirectional information flow in human sensory systems to produce perception. However, future studies are needed to determine what specific odor information is extracted and communicated in the information exchange.

neuroscience↗

bioRxiv2021

The perception of odor pleasantness is shared across cultures

Human sensory experience varies across the globe. Nonetheless, all humans share sensory systems with a common anatomical blueprint. In olfaction, it is unknown to what degree sensory perception, in particular the perception of odor pleasantness, is dictated by universal biological principles versus sculpted by culture. To address this issue, we asked 235 individuals from 9 diverse non-western cultures to rank the hedonic value of monomolecular odorants. We observed substantial global consistency, with molecular identity explaining 41% of the variance in individual pleasantness rankings, while culture explained only 6%. These rankings were predicted by the physicochemical properties of out-of-sample molecules and out-of-sample pleasantness ratings given by a separate group of industrialized western urbanites, indicating human olfactory perception is strongly constrained by universal principles.

animal behavior and cognition↗

bioRxiv2021

The human olfactory bulb process odor valence representation and initiate motor avoidance behavior

Determining the valence of an odor to provide information to guide rapid approach-avoidance behavior is thought to be one of the core tasks of the olfactory system, yet little is known of its initial neural mechanisms or subsequent behavioral manifestation in humans. In two experiments, we measured the functional processing of odor valence perception in the human olfactory bulb (OB)--the first processing stage of the olfactory system--using a non-invasive method as well as assessed subsequent motor avoidance response. We demonstrate that odor valence perception is associated with both gamma and beta activity in the human OB. Moreover, we show that negative, but not positive, odors initiate an early beta response in the OB, a response that is linked to a preparatory neural motor response in motor cortex. Finally, in a separate experiment we show that negative odors trigger a full-body motor avoidance response, manifested as a rapid leaning away from the odor, in the time period predicted by the OB results. Taken together, these results demonstrate that the human OB processes odor valence in a sequential manner in both the gamma and beta frequency bands and suggest that early processing of unpleasant odors in the OB might underlie rapid approach-avoidance decisions.

neuroscience↗

bioRxiv2021

Acquired olfactory loss alters functional connectivity and morphology

Removing function from a developed and functional sensory system is known to alter both cerebral morphology and functional connections. To date, a majority of studies assessing sensory-dependent plasticity have focused on effects from either early onset or long-term sensory loss and little is known how the recent sensory loss affects the human brain. With the aim of determining how recent sensory loss affects cerebral morphology and functional connectivity, we assessed differences between individuals with acquired olfactory loss (duration 7-36 months, n=20) and matched healthy controls (n=23) in their grey matter volume, using multivariate pattern analyses, and functional connectivity, using dynamic connectivity analyses, within and from the olfactory cortex. Our results demonstrate that acquired olfactory loss alters grey matter volume in, among others, posterior piriform cortex, a core olfactory processing area, as well as the inferior frontal gyrus and angular gyrus. In addition, compared to controls, individuals with acquired anosmia displayed significantly stronger dynamic functional connectivity from the posterior piriform cortex to, among others, the angular gyrus, a known multisensory integration area. No significantly stronger connectivity in healthy control participants were demonstrated. When assessing differences in dynamic functional connectivity from the angular gyrus, individuals with acquired anosmia had stronger connectivity from the angular gyrus to areas primary responsible for basic visual and taste processing. These results demonstrate that recently acquired sensory loss alters both cerebral morphology within core olfactory areas and increase dynamic functional connectivity from olfactory cortex to cerebral areas processing multisensory integration.

neuroscience↗

bioRxiv2020

Differentiating ADHD subtypes and simulation of in silico therapeutic neuronal excitation in a whole-brain nonlinear dynamic modelling frame-work

Recent advances in non-linear computational and dynamical modelling have opened up the possibility to param etrize dynamic neural mechanisms that drive complex behavior. Importantly, building models of neuronal processes is of key importance to fully understand disorders of the brain as it may provide a quantitative platform that is capable of binding multiple neurophysiological processes to phenotype profiles. In this study, we apply a newly developed adaptive frequency-based model of whole-brain oscillations to resting-state fMRI data acquired from healthy controls and a cohort of attention deficit hyperactivity disorder (ADHD) subjects. As expected, we found that healthy control subjects differed from ADHD in terms of attractor dynamics. However, we also found a marked dichotomy in neural dynamics within the ADHD cohort. Next, we classified the ADHD group according to the level of distance of each individuals empirical network from the two model-based simulated networks. Critically, the model was mirrored in the empirical behavior data with the two ADHD subgroups displaying distinct behavioral phenotypes related to emotional instability (i.e., depression and hypomanic personality traits). Finally, we investigated the applicability and feasibility of our whole-brain model in a therapeutic setting by conducting in silico excitatory stimulations to parsimoniously mimic clinical neuro-stimulation paradigms in ADHD. We tested the effect of stimulating any individual brain region on the key network measures derived from the simulated brain network and its contribution in rectifying the brain dynamics to that of the healthy brain, separately for each ADHD subgroup. This showed that this was indeed possible for both subgroups. However, the current effect sizes were small suggesting that the stimulation protocol needs to be tailored at the individual level. These findings demonstrate the potential of this new modelling framework to unveil hidden neurophysiological profiles and establish tailored clinical interventions.

neuroscience↗

bioRxiv2019

Non-invasive recording from the human olfactory bulb

Current methods can, in a non-invasive manner, assess neural activity in all areas of the human brain but the olfactory bulb (OB). The OB is intimately involved in a long list of olfactory tasks, has been suggested to fulfill a role comparable to that of V1 and the thalamus in the visual system, and have been closely linked to a wide range of neuropathologies. Here we present a method for non-invasive recording of signals from the human OB with millisecond precision. We demonstrate that signals obtained via recordings from EEG electrodes at the nasal bridge represent responses from the olfactory bulb - recordings we term Electrobulbogram (EBG). The EBG is localized to the OB, is reliable, and follows response patterns demonstrated in non-human animal models. The EBG will aid future olfactory-related translational work but can also easily be implemented as an everyday clinical tool to detect pathology-related changes in human central olfactory processing in neurodegenerative diseases.

neuroscience↗