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Bengtsson, F.

Publications and source records attributed to Bengtsson, F..

3 recordsLinked to original sources

D-amphetamine alters the dynamic ECoG activity distribution patterns in the rat neocortex

Amphetamine has widespread effects on multiple neurotransmitter systems, potentially altering the physiological connectivity and network dynamics across various regions of the brain. In this study, we investigated the effects of D-amphetamine using our previously published approach where electrocorticogram (ECoG) recordings from eight cortical areas provided a coarse estimation of the global activity distribution patterns across sets of neuron populations. Changes in these activity distribution patterns were quantified with Principal Component Analysis (PCA) and k-Nearest Neighbors (kNN) classification. We found that D-amphetamine significantly altered the activity distribution patterns both for spontaneous activity and for activity recorded during ongoing tactile stimulation. It also reduced the difference between spontaneous activity and activity during ongoing tactile stimulation, which suggests that amphetamine reduced the organization in the network activity and could potentially explain hallucinations under the influence of amphetamine. Each of these changes were distributed approximately evenly across each dimension of the principal component space. This indicates that amphetamine impacts cortical network dynamics broadly and in multifaceted ways, compatible with the system-wide presence of the receptors that amphetamine interferes with. Our data indicates that relatively low doses of D-amphetamine can induce changes in brain activity distributions that are measurable potentially also by non-invasive EEG electrodes.

neuroscience↗

EEG covariance patterns detects global cortical activity distribution following weak tactile input

Many studies have suggested that the neocortex operates as a global network of functionally interconnected neurons, indicating that any sensory input could shift activity distributions across the whole brain. A tool assessing the activity distribution across cortical regions with high temporal resolution could then potentially detect subtle changes that may pass unnoticed in regionalized analyses. We used eight-channel, distributed electrocorticogram (ECoG) recordings to analyze changes in global activity distribution caused by single pulse electrical stimulations of the paw. We analyzed the temporally evolving covariance patterns of the activity distributions using principal component analysis (PCA). We found that localized tactile stimulation caused clearly measurable changes in global ECoG activity distribution. These changes in signal covariance patterns were detectable across a small number of ECoG channels, even when not including the somatosensory cortex, suggesting that the method has high sensitivity, potentially making it applicable to human EEG for detection of pathological changes.

neuroscience↗

Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons in the adult cat in vivo

The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity for muscular, tendon and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical segments. Using low noise intracellular whole cell recordings in the decerebrated, nonanesthetized cat in vivo, we could define mono-, di-, trisynaptic inputs as well as the weights of each input. Whereas each neuron had a highly specific input, and each indirect input could moreover be explained by inputs in other recorded neurons, we unexpectedly also found the input connectivity of the spinal interneuron population to form a continuum. Our data hence contrasts with the currently widespread notion of distinct classes of interneurons. We argue that this suggested diversified physiological connectivity, which likely requires a major component of circuitry learning, implies a more flexible functionality. 1. Graphical Abstract O_FIG_DISPLAY_L [Figure 1] M_FIG_DISPLAY C_FIG_DISPLAY 2. HighlightsO_LIIn vivo whole cell, intracellular recording of spinal interneurons. C_LIO_LIPatterns of input from Ia, Ib and cutaneous afferents is highly diversified. C_LIO_LILearning appears to be a defining factor of spinal interneuron connectivity. C_LI

neuroscience↗