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Lepsien, J.

Publications and source records attributed to Lepsien, J..

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Multi-Echo Investigations of Positive and Negative CBF and Concomitant BOLD Changes

Unlike the positive blood oxygenation level-dependent (BOLD) response (PBR), commonly taken as an indication of an activated brain region, the physiological origin of negative BOLD signal changes (i.e. a negative BOLD response, NBR), also referred to as deactivation is still being debated. In this work, an attempt was made to gain a better understanding of the underlying mechanism by obtaining a comprehensive measure of the contributing cerebral blood flow (CBF) and its relationship to the NBR in the human visual cortex, in comparison to a simultaneously induced PBR in surrounding visual regions. To overcome the low signal-to-noise ratio (SNR) of CBF measurements, a newly developed multi-echo version of a center-out echo planar-imaging (EPI) readout was employed with pseudo-continuous arterial spin labeling (pCASL). It achieved very short echo and inter-echo times and facilitated a simultaneous detection of functional CBF and BOLD changes at 3 T with improved sensitivity. Evaluations of the absolute and relative changes of CBF and the effective transverse relaxation rate, [Formula], the coupling ratios, and their dependence on CBF at rest, CBFrest, indicated differences between activated and deactivated regions. Analysis of the shape of the respective functional responses also revealed faster negative responses with more pronounced post-stimulus transients. Resulting differences in the flow-metabolism coupling ratios were further examined for potential distinctions in the underlying neuronal contributions. HighlightsO_LIIntroduction of multi-echo center-out EPI for investigating concomitant CBF and BOLD changes in regions of positive (PBR) and negative BOLD response (NBR). C_LIO_LI{Delta}CBF timecourses closely follow those of [Formula] with negative signals exhibiting faster responses and more pronounced post-stimulus transients. C_LIO_LIDecreases in CBF appear to warrant a larger change in NBR than CBF increases in PBR regions. C_LIO_LIConsideration of baseline CBF values is important in comparisons of relative coupling ratios ({delta}sBOLD/{delta}cbf) between brain regions. C_LIO_LIDiscussion of potential excitatory and inhibitory neuronal feed forward control of CBF and CMRO2 in PBR and NBR. C_LI

neuroscience↗

Distributed networks for auditory memory contribute differentially to recall precision

Re-directing attention to objects in working memory can enhance their representational fidelity. However, how this attentional enhancement of memory representations is implemented across distinct, sensory and cognitive-control brain network is unspecified. The present fMRI experiment leverages psychophysical modelling and multivariate auditory- pattern decoding as behavioral and neural proxies of mnemonic fidelity. Listeners performed an auditory syllable pitch-discrimination task and received retro-active cues to selectively attend to a to-be-probed syllable in memory. Accompanied by increased neural activation in fronto-parietal and cingulo-opercular networks, valid retro-cues yielded faster and more perceptually sensitive responses in recalling acoustic detail of memorized syllables. Information about the cued auditory object was decodable from hemodynamic response patterns in superior temporal sulcus (STS), fronto-parietal, and sensorimotor regions. However, among these regions retaining auditory memory objects, neural fidelity in the left STS and its enhancement through attention-to-memory best predicted individuals gain in auditory memory recall precision. Our results demonstrate how functionally discrete brain regions differentially contribute to the attentional enhancement of memory representations.

neuroscience↗