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Nasuto, S. J.

Publications and source records attributed to Nasuto, S. J..

3 recordsLinked to original sources

Dissociable thalamic oscillatory mechanisms support motor sequence learning

The ventrointermediate nucleus of the thalamus (VIM) is implicated in motor sequence learning, yet the underlying neural mechanisms remain unclear. We recorded intracranial activity from the human VIM during a serial reaction time task to determine how neural dynamics support learning. Participants responded faster during repeating than randomized sequences. Beta-to-low-gamma activity was greater during repeating sequences and elevated relative to the prestimulus baseline, consistent with emergence and stabilization of learned motor representations. In contrast, beta-phase modulation of high-frequency activity decreased progressively from rest to random to repeated sequence execution. Stronger phase-amplitude coupling was associated with faster responses, reaching significance in the random condition. These findings reveal a dissociation between power and cross-frequency coupling. Together they suggest that thalamic dynamics contribute to motor learning through multiple mechanisms: beta-band power reflects the emergence of learned motor representations, whereas beta-high-frequency coupling is enhanced when the context is less predictable.

neuroscience↗

The anti-cancer drug trametinib suppresses angiotensin-induced cardiac remodelling in mice but is detrimental to function

Aims. Echocardiography is used widely in preclinical mouse studies, but the emphasis remains the histological/pathological/biochemical changes in the myocardium. Analysis/reporting of cardiac function is generally limited, often relying on M-mode assessment of a single plane across the left ventricle. The aim was to determine if global/segmental endocardial speckle-tracking (strain) has greater potential to assess function by distinguishing between mouse lines and identifying regional effects of different drugs. Methods and results. Echocardiograms from male C57Bl/6J (commercially-available) or C57Bl/6(R) (bred in-house) mice treated with vehicle or angiotensin II (AngII; 0.8 mg/kg/d, 7 d) were analysed. Global strain demonstrated different degrees of hypertrophy induced by AngII in the different lines, and variation in function (e.g. stroke volume/cardiac output were reduced in C57Bl/6J mice only, with no effect on global longitudinal strain). For C57Bl/6J mice, segmental strain (radial/longitudinal peak displacement/velocity/strain/strain rate) and frame-to-frame analysis of radial/longitudinal displacement identified more significant effects of AngII in the basal/mid-regions of the left ventricle. Thus, speckle-tracking distinguished between responses in different mouse lines. The methodology was applied to studies of anti-cancer drugs that inhibit extracellular signal-regulated kinase 1/2 signalling. Dabrafenib and/or trametinib inhibited AngII-induced cardiac hypertrophy, but dabrafenib alone caused abnormalities in endocardial movement whilst, for trametinib with AngII, more abnormalities were detected than with AngII alone. For both, the dominant effect was in the basal/mid-regions of the left ventricle. Conclusion. Echocardiography in preclinical studies can be exploited using endocardial segmental strain for greater insight into how drugs affect cardiac function in different regions of the left ventricle.

physiology↗

Ventrointermediate thalamic stimulation improves motor learning in humans

Ventrointermediate thalamic stimulation (VIM-DBS) modulates oscillatory activity in a cortical network including primary motor cortex, premotor cortex, and parietal cortex. Here we show that, beyond the beneficial effects of VIM-DBS on motor execution, this form of invasive stimulation facilitates production of sequential finger movements that follow a fixed sequence but not when the sequence is selected at random. These results highlight the role of thalamo-cortical activity in motor learning.

neuroscience↗