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fens.org

Federating numerous pan-European single discipline and national neuroscience societies from across 33 European countries, FENS represents European neuroscience from basic to clinical research.

jneurosci.org

While transient changes in synaptic strength occurring during the repetitive firing of primary afferent inputs to the spinal superficial dorsal horn (SDH) are predicted to strongly influence the fidelity with which nociceptive signals are transmitted through the SDH network, little is known about whether the properties of short-term plasticity (STP) at sensory synapses depend on the identity of the postsynaptic target or whether STP is under the control of neuromodulators such as dopamine. Here we investigate these issues using ex vivo patch-clamp recordings from identified lamina I spinoparabrachial neurons, inhibitory interneurons (VGAT+), and putative excitatory interneurons (VGAT−) in spinal cord slices from adult mice of both sexes. Repeated activation of A-fiber inputs to the SDH evoked short-term depression (STD) across all major subtypes of SDH neurons, although the magnitude of STD was greatest in projection neurons with high-frequency stimulation. Meanwhile, repetitive activation of C-fiber synapses onto GABAergic interneurons evoked more pronounced STD compared with excitatory neurons across a range of stimulation frequencies. Both A-fiber and C-fiber synapses recovered from STD at a similar rate across the different SDH cell types examined. Dopamine (20 µM) significantly depressed the overall glutamatergic drive, and reduced afferent-evoked firing, selectively in spinoparabrachial neurons and excitatory interneurons without changes in the properties of STP. Collectively, these findings reveal novel potential mechanisms by which the efficacy of the spinal inhibitory “gate,” and thus the gain of ascending nociceptive transmission to the brain, may be rapidly altered during periods of strong sensory input to the SDH network.

thejns.org

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brainproducts.com

Skip to main content Search our resources Tip: Start typing in the input box for immediate search results from our Support Resources Knowledge Base. For a more comprehensive search, use the site search in the main menu above. < All Topics Main Browse by product Electrodes & Caps LiveCap How can I customize my electrode cap? Customizing caps To customize most caps, please discuss your specifications/montage with your local distributor.   Configuring caps for LiveAmp 8 or LiveAmp 16 When ordering a LiveAmp 8 or a LiveAmp 16 with active or passive gel electrodes, please complete the respective form and forward it to your local distributor or us along with your order. PostedJanuary 12, 2022UpdatedOctober 23, 2023Tags: LiveCapactiCHampLiveAmpBrainCap MRactiCAPBrainAmp MR Table of Contents

eneuro.org

Recently developed probes for extracellular electrophysiological recordings have large numbers of electrodes on long linear shanks. Linear electrode arrays, such as Neuropixels probes, have hundreds of recording electrodes distributed over linear shanks that span several millimeters. Because of the length of the probes, linear probe recordings in rodents usually cover multiple brain areas. Typical studies collate recordings across several recording sessions and animals. Neurons recorded in different sessions and animals thus have to be aligned to each other and to a standardized brain coordinate system. Here, we evaluate two typical workflows for localization of individual electrodes in standardized coordinates. These workflows rely on imaging brains with fluorescent probe tracks and warping 3D image stacks to standardized brain atlases. One workflow is based on tissue clearing and selective plane illumination microscopy (SPIM), whereas the other workflow is based on serial block-face two-photon (SBF2P) microscopy. In both cases electrophysiological features are then used to anchor particular electrodes along the reconstructed tracks to specific locations in the brain atlas and therefore to specific brain structures. We performed groundtruth experiments, in which motor cortex outputs are labeled with ChR2 and a fluorescence protein. Light-evoked electrical activity and fluorescence can be independently localized. Recordings from brain regions targeted by the motor cortex reveal better than 0.1-mm accuracy for electrode localization, independent of workflow used.

painresearchforum.org

Register here Senescence of Primary Sensory Neurons: A Novel Perspective on Pain in Aging Dr. Lauren Donovan is a Senior Research Scientist at Stanford University’s Department of Anesthesiology, Perioperative, and…

snacc.org

society for neuroscience in anesthesiology and critical care