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Caspi, Y.

Publications and source records attributed to Caspi, Y..

3 recordsLinked to original sources

Beta bursts carry a graded signal of semantic updating during naturalistic narrative comprehension

Comprehending a narrative requires continuously updating a model of the discourse, and beta-band activity is thought to signal when that model should be held versus changed. Whether beta also grades how much to update, and whether that index is carried by discrete bursts beyond sustained power, is unknown for naturalistic comprehension. We recorded MEG from 61 human participants (22 men, 39 women) while they listened to naturalistic Hebrew narratives, detected beta bursts in the continuous signal, and quantified the semantic shift between successive sentences from sentence embeddings. Beta burst rate decreased after sentence boundaries, and regression-based deconvolution separated a pre-onset maintenance phase from a graded post-onset response whose magnitude scaled with semantic shift (peak ~0.9 s). This response was independent of lexical surprisal, the acoustic envelope, and referent introduction, largely robust to dependency structure, though it shared variance with propositional quantity. Burst occurrence carried a component of the effect beyond the accompanying amplitude change: applying that change as a pure gain to each participant's envelope and re-running the identical detection predicts only 75% of the observed burst-rate reduction (excess p = .038), the effect survived an amplitude-invariant threshold, and a Poisson model reproduced it as a graded reduction in burst-initiation rate. The effect held in both participant groups, which heard differently framed narratives, and was decisively supported (BF10 > 250). Beta bursts thus provide a graded signal of semantic updating during continuous comprehension, expressed in the rate of burst occurrence over and above the accompanying change in sustained power.

neuroscience↗

Structural plasticity of axon initial segment in spinal cord neurons underlies inflammatory pain

Activity-dependent structural plasticity of axon initial segment (AIS) regulates neuronal excitability, thus fine-tuning neuronal and overall network output. Here using behavioral, immunohistochemical, electrophysiological and computational approaches, we describe the structural plasticity of AIS in rats superficial spinal cord dorsal horn (SDH) neurons, which underlies inflammatory pain. We show an inflammation-mediated distal shift of the AIS away from the soma in inhibitory but not excitatory SDH neurons, concomitant with the peak of inflammatory pain. This AIS translocation was accompanied by a decrease in excitability of the inhibitory neurons. Following recovery from inflammatory hyperalgesia, the AIS location and neuronal excitability reversed to baseline levels. The computational model of SDH inhibitory neurons predicts that the distal shift of AIS is sufficient to decrease the intrinsic excitability of these neurons. Our results provide evidence of differential inflammation-mediated AIS plasticity, reducing the excitability of inhibitory but not excitatory SDH neurons and contributing to inflammatory hyperalgesia.

neuroscience↗

Changes in the intracranial volume from early adulthood to the sixth decade of life: A longitudinal study

Normal brain-aging occurs at all structural levels. Excessive pathophysiological changes in the brain, beyond the normal one, are implicated in the etiology of brain disorders such as severe forms of the schizophrenia spectrum and dementia. To account for brain-aging in health and disease, it is critical to study the age-dependent trajectories of brain biomarkers at various levels and among different age groups. The intracranial volume (ICV) is a key biological marker, and changes in the ICV during the lifespan can teach us about the biology of development, aging, and gene X environment interactions. However, whether ICV changes with age in adulthood is not resolved. Applying a semi-automatic in-house-built algorithm for ICV extraction on T1w MR brain scans in the Dutch longitudinal cohort (GROUP), we measured ICV changes. Individuals between the ages of 16 and 55 years were scanned up to three consecutive times with 3.32{+/-}0.32 years between consecutive scans (N=482, 359, 302). Using the extracted ICVs, we calculated ICV longitudinal aging-trajectories based on three analysis methods; direct calculation of ICV differences between the first and the last scan, fitting all ICV measurements of individuals to a straight line and applying a global linear mixed model fitting. We report statistically significant increases in the ICV in adulthood until the fourth decade of life (average change +0.03%/y, or about 0.5 ml/y, at age 20), and decreases in the ICV afterward (-0.09%/y, or about -1.2 ml/y, at age 55). To account for previous cross-sectional reports of ICV changes, we analyzed the same data using a cross-sectional approach. Our cross-sectional analysis detected ICV changes consistent with the previously reported cross-sectional effect. However, the reported amount of cross-sectional changes within this age range was significantly larger than the longitudinal changes. We attribute the cross-sectional results to a generational effect. In conclusion, the human intracranial volume does not stay constant during adulthood but instead shows a small increase during young adulthood and a decrease thereafter from the fourth decade of life. The age-related changes in the longitudinal setup are smaller than those reported using cross-sectional approaches and unlikely to affect structural brain imaging studies correcting for intracranial volume considerably. As to the possible mechanisms involved, this awaits further study, although thickening of the meninges and skull bones have been proposed, as well as a smaller amount of brain fluids addition above the overall loss of brain tissue.

neuroscience↗