Department of Psychology, Royal Holloway, University of London, Egham TW20 0EX, UK.
Published: January 2006
AI Article Synopsis
Article Abstract
Throughout the visual areas of the brain, the sensory response to a stimulus is enhanced by attending to the stimulus. Neurophysiological studies in primates show that such enhancement is marked in posterior parietal cortex and some anterior occipital areas, but much more modest in the earliest processing stages, such as the primary visual cortex (V1). In contrast, human fMRI studies show large and robust attentional modulation in all visual areas, including V1. We investigate the possibility that, in the case of fMRI, the BOLD (blood oxygen level dependent) response may be increased not only by local attention-related increases in neural activity, but also by local blood-flow increases caused by remote control systems that anticipate an impending need for oxygen at the attended location. Such changes could be much more rapid than the rather slow response to oxygenation change that typifies the BOLD response. We have employed a paradigm that isolates the component of the BOLD response due to attentional modulation and the component due to the mere presence of a visual stimulus. The results show that the temporal profiles of the BOLD responses in human V1 to the onset of a stimulus and to the onset of attention are extremely similar. The time-course of the attention-related BOLD response is not consistent with the action of remote, anticipatory control mechanisms and suggests that the modulatory effect of attention seen in human V1 with fMRI probably reflects genuine changes in local neural activity that are considerably larger than in non-human primates.
Individuals with borderline personality disorder (BPD) often hold pervasive and negative self-views and experience feelings of low connectedness toward others despite effective treatment. This study aimed to identify neural and affective mechanisms of identity disturbance in BPD that contribute to difficulties in relating to others. Participants diagnosed with BPD ( = 34) and nonclinical controls (NCC; = 35) completed a within-subject social feedback task inside a magnetic resonance imaging scanner.
In functional magnetic resonance imaging, the hemodynamic response function (HRF) is a stereotypical response to local changes in cerebral hemodynamics and oxygen metabolism due to briefly (< 4 s) evoked neural activity. Accordingly, the HRF is often used as an impulse response with the assumption of linearity in data analysis. In cognitive aging studies, it has been very common to interpret differences in brain activation as age-related changes in neural activity.
The present studies were undertaken to understand the effects of the commonly used nutraceutical PEA on brain function and lipid chemistry. These studies using MRI and broad-scale lipidomics are without precedent in animal or human research. During the MRI scanning session awake rats were given one of three doses of PEA (3, 10, or 30 mg/kg) or vehicle and imaged for changes in BOLD signal and functional connectivity.
Objective: To examine the blood oxygen level-dependent (BOLD) responses in the default mode network (DMN) and subcortical regions in relation to epileptic events in scalp EEG and intracranial EEG (iEEG).
Methods: We retrospectively compared BOLD responses in the DMN and subcortical regions to interictal epileptiform discharge (IED) characteristics of the scalp and iEEG in consecutive patients with focal epilepsy. All voxels were used as the denominator to assess the positive and negative BOLD ratios in each region, and the percentage of voxels with significant activation or deactivation was assessed.
Deciding between a pair of familiar items is thought to rely on a comparison of their subjective values. When the values are similar, decisions take longer, and the choice may be inconsistent with stated value. These regularities are thought to be explained by the same mechanism of noisy evidence accumulation that leads to perceptual errors under conditions of low signal to noise.
