Behavioural brain research
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Inhibitory processes play a significant role in the control of goal-directed actions. To increase insights into these mechanisms as a function of handedness, we measured the transient inhibition of volitional motor activity induced by single pulse transcranial magnetic stimulation during bimanual isometric contractions with symmetrical and asymmetrical force demands. Here, we assess the cortical silent period (cSP), which associates with intrahemispheric inhibition, and the ipsilateral silent period (iSP), which provides an estimation of interhemispheric inhibition. ⋯ In particular, right-handers demonstrated increased inhibitory processing that favoured control of the dominant (left) hemisphere whereas both motor cortices exhibited equal capabilities in left-handers. These observations were specific to the bimanual nature of the task. The present results underline distinct organisational mechanisms of coordinated behaviour in right- and left-handers.
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Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is effectively used to treat motor symptoms in Parkinson's disease (PD). Recently more attention has been paid to behavioral disturbances caused by PD itself and by STN DBS. In the 6-hydroxydopamine (6-OHDA) PD rat model we investigated the effect of STN DBS on deficient prepulse inhibition (PPI) induced by the dopamine (DA) receptor agonist apomorphine, which is an operative measure for disturbed sensorimotor gating seen in certain neuropsychiatric disturbances. ⋯ Furthermore, in lesioned rats the startle reaction was marginally enhanced without effect of stimulation or apomorphine treatment. These data suggest that STN DBS interacts with dopaminergic action. With respect to functional neurosurgery, STN DBS alone may improve certain aspects of psychiatric disturbances, but may have a different impact when combined with dopaminergic medication.
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The tricyclic antidepressant amitriptyline binds with high affinity to N-methyl-d-aspartate receptors (NMDARs) and inhibits NMDAR-mediated events. Activation of the postsynaptic density protein-95 (PSD-95)/NMDAR-mediated downstream signaling cascade, including neuronal nitric oxide synthase (nNOS) and protein kinase gamma (PKCγ), has been shown to be involved in morphine tolerance. The present study examined the potential effect of amitriptyline on chronic morphine infusion-induced spinal PSD-95/NMDAR/nNOS/PKCγ signaling in morphine tolerance. ⋯ Furthermore, amitriptyline co-infusion significantly inhibited morphine-induced PKCγ expression in both the cytosol and membrane of spinal neurons. These findings suggest that the attenuation of morphine tolerance caused by amitriptyline is due to downregulation of NMDAR NR1 subunit expression in the synaptosomal membrane accompanied by decreased expression of the scaffolding protein PSD-95. The effects of amitriptyline in attenuating astrocyte activation and reversing tolerance to morphine may be due, at least in part, to inhibition of the PSD-95/NMDAR NR1/nNOS/PKCγ signaling cascade.
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The fundamental cognitive-control function of inhibitory control over motor behavior has been extensively investigated using the Stop-signal task. The critical behavioral parameter describing stopping efficacy is the Stop-signal response time (SSRT), and correlations with estimates of this parameter are commonly used to establish that other variables (e.g., other behavioral measures or brain activity measures) are closely related to inhibitory motor control. Recently, however, it has been argued that SSRT estimates can be strongly distorted if participants strategically slow down their responses over the course of the experiment, resulting in the SSRT no longer reliably representing response-inhibition efficacy. ⋯ Concerning brain-behavior correlations, only the left anterior insula was found to be significantly correlated with the SSRT within the set of areas tested here. Interestingly, this brain-behavior correlation differed little for the different SSRT-estimation procedures. In sum, the current results highlight that different SSRT-estimation procedures can strongly influence the distribution of SSRT values across subjects, which in turn can ramify into correlational analyses with other parameters.
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It is well known that elite athletes have higher performance in perception, planning, and execution in sports activities relative to novices. It remains controversial, however, whether any differences in basic cognitive functions between experts and novices exist. Furthermore, few studies have directly used functional magnetic resonance imaging (fMRI) to investigate neural activation and deactivation differences between experts and novices while performing visuospatial working memory (WM) tasks. ⋯ With regard to brain activation, archery experts displayed higher activation in cortical areas associated with visuospatial attention and working memory, including the middle frontal cortex, supplemental motor area, and dorsolateral prefrontal cortex than that of the novices during the performance of the JLO task. With regard to brain deactivation, archery experts exhibited stronger task-related deactivation in cortical areas, such as the paracentral cortex/precuneus and the anterior and posterior cingulate cortex related to the default network, than that of the novices. These results suggest that the archery experts have a strategy that demands greater use of neural correlates associated with visuospatial working memory and attention in addition to greater use of DMN in visuospatial working memory task not directly tied to their domain of expertise.