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The importance of the excitatory-inhibitory (E/I) balance in a wide range of cognitive and behavioral processes has prompted a commensurate interest in methods for reliably quantifying it. Proton Magnetic Resonance Spectroscopy ( 1 H-MRS) remains the only method capable of safely and non-invasively measuring the concentrations of the brain's major excitatory (glutamate) and inhibitory (γ-aminobutyric-acid, GABA) neurotransmitters in-vivo. MRS relies on spectral Mescher-Garwood (MEGA) editing techniques at 3T to distinguish GABA from its overlapping resonances. However, with the increased spectral resolution at ultrahigh field strengths of 7T and above, non-edited spectroscopic techniques become potential viable alternatives to MEGA based approaches, and also address some of their shortcomings, such as signal loss, sensitivity to transmitter inhomogeneities and temporal resolution. We present a comprehensive comparison of both edited and non-edited strategies at 7T for simultaneously quantifying glutamate and GABA from the dorsal anterior cingulate cortex (dACC), and evaluate their reproducibility and relative bias. The combined root-mean-square test-retest reproducibility of Glu and GABA (CV E/I ) was as low as 13.3% for unedited MRS at TE=80 ms using SemiLASER localization, while edited MRS at TE=80 ms yielded CV E/I =20% and 21% for asymmetric and symmetric MEGA editing, respectively. An unedited SemiLASER acquisition using a shorter echo time of TE=42 ms yielded CV E/I as low as 24.9%. Our results show that non-edited sequences at an echo time of 80 ms provide better reproducibility than either edited sequences at the same TE, or non-edited sequences at a shorter TE of 42 ms. This is supported by numerical simulations and is driven in part by a pseudo-singlet appearance of the GABA multiplets at TE=80 ms, and the excellent spectral resolution at 7T. Our results uphold a transition to non-edited MRS for monitoring the E/I balance at ultrahigh fields, and stress the importance of using a properly-optimized echo time., (Copyright © 2021. Published by Elsevier Inc.)

Human brain imaging typically employs structured and controlled tasks to avoid variable and inconsistent activation patterns. Here we expand this assumption by showing that an extremely open-ended, high-level cognitive task of thinking about an abstract content, loosely defined as "abstract thinking" - leads to highly consistent activation maps. Specifically, we show that activation maps generated during such cognitive process were precisely located relative to borders of well-known networks such as internal speech, visual and motor imagery. The activation patterns allowed decoding the thought condition at >95%. Surprisingly, the activated networks remained the same regardless of changes in thought content. Finally, we found remarkably consistent activation maps across individuals engaged in abstract thinking. This activation bordered, but strictly avoided visual and motor networks. On the other hand, it overlapped with left lateralized language networks. Activation of the default mode network (DMN) during abstract thought was similar to DMN activation during rest. These observations were supported by a quantitative neuronal distance metric analysis. Our results reveal that despite its high level, and varied content nature - abstract thinking activates surprisingly precise and consistent networks in participants' brains., (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)

In the absence of a task, the human brain enters a mode of slow spontaneous fluctuations. A fundamental, unresolved question is whether these fluctuations are ongoing and thus persist during task engagement, or alternatively, are quenched and replaced by task-related activations. Here, we examined this issue in the human visual cortex, using fMRI. Participants were asked to either perform a recognition task of randomly appearing face and non-face targets (attended condition) or watch them passively (unattended condition). Importantly, in approximately half of the trials, all sensory stimuli were absent. Our results show that even in the absence of stimuli, spontaneous fluctuations were suppressed by attention. The effect occurred in early visual cortex as well as in fronto-parietal attention network regions. During unattended trials, the activity fluctuations were negatively linked to pupil diameter, arguing against attentional fluctuations as underlying the effect. The results demonstrate that spontaneous fluctuations do not remain unchanged with task performance, but are rather modulated according to behavioral and cognitive demands., (Copyright © 2017 Elsevier Inc. All rights reserved.)

The interfacial interactions and their effects on electrical properties are reported for thermally grown SiO(2)-Parylene-C laminar composites. The segmental chain mobility of the interfacial Parylene-C was found to be enhanced in the composites. TSDC (thermally stimulated depolarization current) measurements showed the presence of dipolar interfacial energy states in these laminar composites. Functionalization of the oxide surface with 3-aminopropyltriethoxysilane (APTES) created dipolar energy states with larger activation energy at the interface between Parylene-C and SiO(2). In addition to the modification of interfacial states, incorporation of APTES interfacial layer also increased polarizability (real part of permittivity) and reduced the quasi-DC conductivity of laminar composites. The systematic changes in interfacial characteristics with thickness of APTES layer were explained based on structural orientation and cross linking of silane molecules.

Solid tumors often develop high interstitial fluid pressure (IFP) as a result of increased water leakage and impaired lymphatic drainage, as well as changes in the extracellular matrix composition and elasticity. This high fluid pressure forms a barrier to drug delivery and hence, resistance to therapy. We have developed techniques based on contrast enhanced magnetic resonance imaging for mapping in tumors the vascular and transport parameters determining the delivery efficiency of blood borne substances. Sequential images are recorded during continuous infusion of a Gd-based contrast agent and analyzed according to a new physiological model, yielding maps of microvascular transfer constants, as well as outward convective interstitial transfer constants and steady state interstitial contrast agent concentrations both reflecting IFP distribution. We further demonstrated in non small cell human lung cancer xenografts the capability of our techniques to monitor in vivo collagenase induced increase in contrast agent delivery as a result of decreased IFP. These techniques can be applied to test drugs that affect angiogenesis and modulate interstitial fluid pressure and has the potential to be extended to cancer patients for assessing resistance to drug delivery.