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Missault, S.

Publications and source records attributed to Missault, S..

4 recordsLinked to original sources

Selective cholinergic stimulation of the medial septum-diagonal band of Broca via DREADDs improves spatial learning in healthy rats

The septohippocampal pathway plays an important role in learning and memory. It projects from the medial septum-vertical limb of the diagonal band of Broca (MSDB) to the hippocampus and provides the latter with its main cholinergic innervation. To assess the importance of cholinergic selectivity and timing of MSDB stimulation in modulating learning and memory, we directly compared the effects of several MSDB stimulation strategies in healthy rats. We evaluated the effects of DREADD-mediated selective cholinergic neuronal MSDB stimulation and nonselective neuronal MSDB stimulation on spatial learning and memory in the appetitive radial arm maze and on resting-state brain networks using resting-state functional MRI. DREADDs were activated with the novel DREADD agonist J60. Selective cholinergic MSDB stimulation during - but not after - radial arm maze training improved spatial learning compared with J60-treated sham rats and had no effect on working memory or reversal learning. J60-treated sham rats had a worse working memory than saline-treated sham rats during the reversal phase of the radial arm maze task, suggesting an adverse effect of chronic use of J60. Nonselective MSDB stimulation during training resulted in a loss of appetite and exclusion from the radial arm maze training. Acute selective cholinergic and nonselective MSDB stimulation induced decreased functional connectivity (FC) in the default mode-like network. In addition, acute nonselective MSDB stimulation resulted in increased intrahippocampal FC, while selective cholinergic MSDB stimulation led to globally increased FC with the nucleus accumbens. While the combined effect of radial arm maze learning and the necessary chronic food restriction with or without chronic MSDB stimulation had no observable effect on resting-state networks, chronic food restriction alone globally increased FC in the brain.

neuroscience↗

Chemogenetic silencing of neurons in the mouse anterior cingulate area modulates neuronal activity and functional connectivity

The anterior cingulate area (ACA) is an integral part of the prefrontal cortex in mice and has been implicated in several cognitive functions. Previous anatomical and functional imaging studies demonstrated that the ACA is highly interconnected with numerous brain regions acting as a hub region in functional networks. However, the importance of the ACA in regulating functional network activity and connectivity remains to be elucidated. Recently developed neuromodulatory techniques, such as Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) allow for precise control of neuronal activity. In this study, we used an inhibitory kappa-opioid receptor DREADDs (KORD) to temporally inhibit neuronal firing in the right ACA of mice and assessed functional network activity and connectivity using non-invasive functional MRI. We demonstrated that KORD-induced inhibition of the right ACA induced blood oxygenation-level dependent (BOLD) signal decreases and increases in connected brain regions throughout of hemispheres. Furthermore, these modulations in neuronal activity were associated with decreased intra- and interhemispheric functional connectivity. These results demonstrate that the combination of the DREADD technology and non-invasive functional imaging methods is a valuable tool for unraveling the underlying mechanisms of network function and dysfunction.

neuroscience↗

Bottom-up sensory processing can decrease activity and functional connectivity in the default mode like network in rats.

The default mode network is a large-scale brain network that is active during rest and internally focused states and deactivates as well as desynchronizes during externally oriented (top-down) attention demanding cognitive tasks. However, it is not sufficiently understood if unpredicted salient stimuli, able to trigger bottom-up attentional processes, could also result in similar reduction of activity and functional connectivity in the DMN. In this study, we investigated whether bottom-up sensory processing could influence the default mode like network (DMLN) in rats. DMLN activity was examined using block-design visual functional magnetic resonance imaging (fMRI) while its synchronization was investigated by comparing functional connectivity during a resting versus a continuously stimulated brain state by unpredicted light flashes. We demonstrated that activity in DMLN regions was decreased during visual stimulus blocks and increased during blanks. Furthermore, decreased inter-network functional connectivity between the DMLN and visual networks as well as decreased intra-network functional connectivity within the DMLN was observed during the continuous visual stimulation. These results suggest that triggering of bottom-up attention mechanisms in anesthetized rats can lead to a cascade similar to top-down orienting of attention in humans and is able to deactivate and desynchronize the DMLN.

neuroscience↗

The Effect of Acute Pharmacological Inhibition of Urokinase Plasminogen Activator and Neuropsin Extracellular Proteases on Neuronal Networks in vitro

Neuronal networks are surrounded by the extracellular matrix (ECM), which functions both as a scaffold and as a regulator of neuronal function. The ECM is in turn dynamically altered through the action of serine proteases, which break down its constituents. This pathway has been implicated in the regulation of synaptic plasticity and of intrinsic excitability. Here, we determined the effects of acutely inhibiting two important regulators of the ECM, Urokinase Plasminogen Activator and Neuropsin, selectively and potently with the inhibitor UAMC-01162. Spontaneous electrophysiological activity was recorded from in vitro primary rat cortical cultures using microelectrode arrays. While inhibition at a low dosage had no significant effect, at elevated concentrations network bursting dynamics and functional connectivity were drastically altered. These results indicate that the serine protease inhibition affects neuronal and synaptic properties, likely through their actions on the ECM. We propose that in the acute phase, a transient increase of excitatory synaptic efficacy is compensated for by a downregulation of single-cell excitability.

neuroscience↗