bioRxiv Science⌕ Search

Biology subjects

Murty, D. V. P. S.

Publications and source records attributed to Murty, D. V. P. S..

5 recordsLinked to original sources

Disentangling value, arousal and valence systems in approach-avoidance behaviors in humans using functional magnetic resonance imaging

Appetitive and aversive stimuli evoke approach and avoidance behaviors essential for survival and well-being. While affective processing has been extensively examined in terms of arousal and valence, the extent to which value processing is independent from arousal and valence processing in naturalistic contexts remains unclear. We addressed this gap using a naturalistic approach-avoidance task. Ninety-one human participants underwent functional MRI scanning while engaging in approach-avoidance tasks involving two levels of threat (mild or aversive electrical stimulation) and reward (monetary gains). We estimated effect sizes (Cohens D) across subjects for increasing levels of threat, reward and arousal; for valence (negative vs positive); and for valence-arousal interactions. Effect sizes for threat and reward were strongly positively correlated across brain voxels (r = 0.82), suggesting a strong influence of a shared factor. Spatial independent component analysis decomposed these effect sizes into two independent latent factors, one that represented arousal processing and another that exhibited characteristics of value processing. Importantly, we predicted that valence-arousal interaction effects would increase with latent value effects across voxels, since both valence and arousal contribute to our overall valuation process. We indeed found this to be true. Furthermore, sizable latent value effects were observed in dorsolateral prefrontal cortex, fusiform gyrus and middle temporal gyrus, areas also involved in attention and executive control. Thus, our findings revealed a value system in the human brain that could operate independently of arousal and valence systems during naturalistic approach-avoidance behaviors, providing new insights into the neural mechanisms of affective processing. Significance statementUnderstanding how the human brain processes affective stimuli is crucial for unraveling the neural underpinnings of behavior. Traditional models often conflate arousal and valence with subjective value, making it challenging to disentangle their independent contributions during naturalistic behaviors. In our study, we revealed independent neural correlates of value in diverse regions previously implicated in emotional processing, attention and executive control. These findings advance our comprehension of affective processing and have implications for developing targeted interventions in neuropsychiatric conditions where affective processing is disrupted.

neuroscience↗

Threat and reward imminence processing in the human brain

In the human brain, aversive and appetitive processing have been studied with controlled stimuli in rather static settings. In addition, the extent to which aversive- and appetitive-related processing engage distinct or overlapping circuits remains poorly understood. Here, we sought to investigate the dynamics of aversive and appetitive processing while male and female participants engaged in comparable trials involving threat-avoidance or reward-seeking. A central goal was to characterize the temporal evolution of responses during periods of threat or reward imminence. For example, in the aversive domain, we predicted that the bed nucleus of the stria terminalis (BST), but not the amygdala, would exhibit anticipatory responses given the role of the former in anxious apprehension. We also predicted that the periaqueductal gray (PAG) would exhibit threat-proximity responses based on its involvement in proximal-threat processes, and that the ventral striatum would exhibit threat-imminence responses given its role in threat escape in rodents. Overall, we uncovered imminence-related temporally increasing ("ramping") responses in multiple brain regions, including the BST, PAG, and ventral striatum, subcortically, and dorsal anterior insula and anterior midcingulate, cortically. Whereas the ventral striatum generated anticipatory responses in the proximity of reward as expected, it also exhibited threat-related imminence responses. In fact, across multiple brain regions, we observed a main effect of arousal. In other words, we uncovered extensive temporally-evolving, imminence-related processing in both the aversive and appetitive domain, suggesting that distributed brain circuits are dynamically engaged during the processing of biologically relevant information irrespective of valence, findings further supported by network analysis. Significance StatementIn the human brain, aversive and appetitive processing have been studied with controlled stimuli in rather static settings. Here, we sought to investigate the dynamics of aversive/appetitive processing while participants engaged in trials involving threat-avoidance or reward-seeking. A central goal was to characterize the temporal evolution of responses during periods of threat or reward imminence. We uncovered imminence-related temporally increasing ("ramping") responses in multiple brain regions, including the bed nucleus of the stria terminalis, periaqueductal gray, and ventral striatum, subcortically, and dorsal anterior insula and anterior midcingulate, cortically. Overall, we uncovered extensive temporally-evolving, imminence-related processing in both the aversive and appetitive domain, suggesting that distributed brain circuits are dynamically engaged during the processing of biologically relevant information irrespective of valence.

neuroscience↗

Distributed and multifaceted effects of threat and safety

Sustained anticipation of unpredictable aversive events generates anticipatory processing that is central to anxiety. In the present functional Magnetic Resonance Study (fMRI) study, we examined how sustained threat is processed in the human brain. We used a relatively large sample (N = 109) and employed a Bayesian multilevel analysis approach to contrast threat and safe periods. Our analyses demonstrated that the effect of sustained threat is heterogeneous and distributed across the brain. Thus, the impact of threat is widespread, and not restricted to a small set of putatively emotion-related regions, such as the amygdala and the bed nucleus of the stria terminalis. Both transient and sustained, and increased and decreased responses during threat were observed. Our study reveals that transitioning between threat and safe states, and vice versa, leads to a widespread switch in brain responding that involves most of the brain.

neuroscience↗

Stimulus-induced narrowband gamma oscillations are test-retest reliable in healthy elderly in human EEG

Visual stimulus-induced narrowband gamma oscillations in electroencephalogram (EEG) recordings have been recently shown to be compromised in subjects with Mild Cognitive Impairment or Alzheimers Disease (AD), suggesting that gamma could be an inexpensive and easily accessible biomarker for early diagnosis of AD. However, to use gamma as a biomarker, its characteristics should remain consistent across multiple recordings, even when separated over long intervals. Previous magnetoencephalography studies in young subjects have reported that gamma power remains consistent over recordings separated by a few weeks to months. Here, we assessed the consistency of slow (20-35 Hz) and fast gamma (36-66 Hz) oscillations induced by static full-field gratings in male (N=20) and female (N=20) elderly subjects (>49 years) in EEG recordings separated by more than a year, and tested the consistency in the magnitude of gamma power, its temporal evolution and spectral profile. Gamma oscillations had distinct spectral and temporal characteristics across subjects, which remained consistent across recordings (average intraclass correlation, ICC of [~]0.7). Alpha oscillations (8-12 Hz) and steady-state-visually-evoked-potentials (SSVEPs) were also found to be reliable. We further tested how EEG features can be used to identify two recordings as belonging to the same versus different subjects and found high classifier performance (area under ROC curve of [~]0.89), with the temporal evolution of slow gamma and spectral profile emerging as the most informative features. These results suggest that EEG gamma oscillations are reliable across recordings and can be used as a clinical biomarker as well as a potential tool for subject identification. Significance statementWe demonstrate the reliability of stimulus-induced gamma oscillations in elderly humans for the first time in EEG. Since gamma has recently been shown to be compromised in patients with Mild Cognitive Impairment or early Alzheimers Disease (AD), together these results mark the first steps towards an EEG based clinical biomarker for early diagnosis of AD. We observed high reliability in the power spectrum, gamma power and its temporal characteristics, within the test-retest period of one year. Alpha and steady-state-visually-evoked potential power were also found to be reliable. These spectral and temporal features could also be used to identify EEG recordings as belonging to the same versus different subjects with high performance, suggesting a potentially key role in subject identification also.

neuroscience↗

Fast gamma oscillations weaken with age in healthy elderly in human EEG

Gamma rhythms ([~]20-70 Hz) have been reported to be abnormal in mental disorders such as autism and schizophrenia in humans, and Alzheimers disease (AD) models in rodents. However, the effect of normal aging on these oscillations is not known, especially for elderly subjects (>49 years) for which AD is most prevalent. In a first large-scale (236 subjects; 104 females) electroencephalogram (EEG) study on gamma oscillations on elderly subjects (aged 50-88 years), we presented full-screen Cartesian gratings that induced two distinct gamma oscillations (slow: 20-34 Hz and fast: 36-66 Hz). Power and centre frequency significantly decreased with age for both slow and fast gamma, but not alpha (8-12 Hz). Reduction was more salient for fast gamma than slow. These results were independent of microsaccades and pupillary reactivity to stimulus, as well as variations in power spectral density with age. Steady-state visual evoked potentials (SSVEPs) also reduced with age. These results are crucial first steps towards using gamma/SSVEPs as biomarkers of cognitive decline in elderly.\n\nSignificance statementNo study in humans has examined visual narrow-band gamma oscillations with healthy aging in elderly subjects. In a first large-scale (236 subjects) EEG study on stimulus-induced narrow band gamma in cognitively normal elderly (>49 years) humans, we show that both power and centre frequency of slow and fast gamma (20-34 Hz and 36-66 Hz respectively) decrease with age, but alpha power does not. Steady-state visual evoked potential (SSVEPs) in gamma range also decrease with age. Any EEG-based biomarker is accessible and affordable to patients of a wide socio-economic spectrum. Our results are important steps for developing such screening/diagnostic tests for aging-related diseases, like Alzheimers disease.

neuroscience↗