Journal: Frontiers in Psychology

Article Title: A Comparison of the Affectiva iMotions Facial Expression Analysis Software With EMG for Identifying Facial Expressions of Emotion

doi: 10.3389/fpsyg.2020.00329

Figure Lengend Snippet: Three-dimensional scatter plot of mean difference scores between the Affectiva scores for smile and brow furrow and the difference scores between “joy” and “anger,” as well as between the EMG amplitudes for zygomaticus mayor and corrugator supercilii activity. Note that the difference score is computed to be more negative (closer to –1) if the respective measure indicates a more negative (i.e. angry) expression and more positive (closer to 1) if the measure indicated a positive (i.e. happy) expression. Red dots indicate the difference scores in the angry condition, green dots in the happy condition and blue dots in the neutral condition. Difference scores of all three types were significantly positive (close to 1) in the happy condition and significantly negative (close to –1) in the angry condition.

Article Snippet: , Joy/Anger – Zygo/Curro , Affectiva/EMG – EMG , 1.13 , 19 , 0.272 , 0.136 , 0.25.

Techniques: Activity Assay, Expressing

Journal: Frontiers in Psychology

Article Title: A Comparison of the Affectiva iMotions Facial Expression Analysis Software With EMG for Identifying Facial Expressions of Emotion

doi: 10.3389/fpsyg.2020.00329

Figure Lengend Snippet: Descriptive statistics for the different outcome measures.

Article Snippet: , Joy/Anger – Zygo/Curro , Affectiva/EMG – EMG , 1.13 , 19 , 0.272 , 0.136 , 0.25.

Techniques:

Journal: Frontiers in Psychology

Article Title: A Comparison of the Affectiva iMotions Facial Expression Analysis Software With EMG for Identifying Facial Expressions of Emotion

doi: 10.3389/fpsyg.2020.00329

Figure Lengend Snippet: Three-dimensional scatter plot of mean difference scores between the Affectiva scores for smile and brow furrow and the scores for “joy” and “anger” during the EMG condition, as well as the EMG amplitudes for zygomaticus mayor and corrugator supercilii activity. Note that the difference score is computed to be more negative (closer to –1) if the respective measure indicates a more negative (i.e., angry) expression and more positive (closer to 1) if the measure indicated a positive (i.e., happy) expression. Red dots indicate the difference scores in the angry condition, green dots in the happy condition and blue dots in the neutral condition.

Article Snippet: , Joy/Anger – Zygo/Curro , Affectiva/EMG – EMG , 1.13 , 19 , 0.272 , 0.136 , 0.25.

Techniques: Activity Assay, Expressing

Journal: Frontiers in Psychology

Article Title: A Comparison of the Affectiva iMotions Facial Expression Analysis Software With EMG for Identifying Facial Expressions of Emotion

doi: 10.3389/fpsyg.2020.00329

Figure Lengend Snippet: Dependent sample t -tests comparing the Affectiva Scores during EMG testing between conditions.

Article Snippet: , Joy/Anger – Zygo/Curro , Affectiva/EMG – EMG , 1.13 , 19 , 0.272 , 0.136 , 0.25.

Techniques:

Journal: Frontiers in Psychology

Article Title: A Comparison of the Affectiva iMotions Facial Expression Analysis Software With EMG for Identifying Facial Expressions of Emotion

doi: 10.3389/fpsyg.2020.00329

Figure Lengend Snippet: Comparison of mean difference scores between the three different methods (Affectiva, Affectiva with attached EMG electrodes and EMG amplitudes) within each of the three emotion conditions (happy, angry, neutral).

Article Snippet: , Joy/Anger – Zygo/Curro , Affectiva/EMG – EMG , 1.13 , 19 , 0.272 , 0.136 , 0.25.

Techniques: Comparison

Journal: The Journal of Neuroscience

Article Title: Dynamic Network Activation of Hypothalamic MCH Neurons in REM Sleep and Exploratory Behavior

doi: 10.1523/JNEUROSCI.0305-19.2019

Figure Lengend Snippet: Deep-brain imaging of MCH neurons. A, Schematic of transfection of MCH neurons in MCH-Cre mice with AAV-DIO-GCaMP6 followed by placement of the GRIN lens in region transfected with GCaMP6 (slow or medium). The miniscope is attached to the GRIN lens via a baseplate on the skull. B, Photomicrograph depicts the location of the GRIN lens (outlined in dashed lines) atop the body of GCaMP6s containing neurons in the hypothalamus in a representative MCH-Cre mouse. The brain region containing the GRIN lens was sectioned along the coronal axis of the brain, and tissue containing the GCaMP6s neurons were identified. f, Fornix. Scale bar, 300 μm. C, Immunohistochemistry revealed that GCaMP6s-infected neurons (green) were also immunopositive for MCH. The coronal sections were incubated with the MCH antibody and visualized using a Leica confocal microscope. Scale bar, 80 μm. D, The field of view of the GRIN lens with fluorescence (ΔF/F0) in somata and processes during REM sleep in neurons extracted automatically by PCA-ICA analysis. We have labeled the three neurons (labeled 1, 2, and 3) whose Ca2+ fluorescence is plotted in E. E, GCaMP6s fluorescence (ΔF/F0) in MCH neurons is associated with REM sleep. Ca2+ imaging was performed simultaneously with recording of cortical EEG and EMG activity in the nuchal muscles. Behavioral video recordings were obtained and examined to identify behaviors such as walking, eating, grooming, or eating. Activity in the EEG (depicted as power spectra, 0.3–15 Hz) and the EMG is used to identify wake, NREM, and REM sleep states (labeled as hypnogram). The traces depict the change in fluorescence (ΔF/F) during wake–sleep bouts of the three neurons identified in D. In each neuron, the ΔF/F0 (expressed as a z-score) varies with the wake–sleep state of the animal, with peak fluorescence associated with REM sleep. The hypnogram categorizes the sleep–wake states in the following colors: purple, active wake; blue, quiet wake; green, NREM; yellow, pre-REM sleep; red, REM sleep. F, The same field of view as in D, but this image shows the PCA-ICA extracted neurons (ΔF/F0) while the mouse was engaged in exploring novel objects placed in its home cage. This image shows that some neurons that were evident in REM sleep (D) were also activated during exploratory behavior. However, some neurons in D were not evident during exploratory behavior, indicating selective activation of these neurons during REM sleep (D). Thirty percent of the neurons were activated during REM sleep but not during exploratory behavior, indicating that a subset of MCH neurons is selectively active in REM sleep. G, GCaMP6s fluorescence in MCH neurons while exploring novel objects. The traces are from the same neurons represented in REM sleep (E). Note that the GCaMP6s has a rapid response and a slow rate of decay, which makes it difficult to infer whether the imaged neuron fired as single spikes or in clusters.

Article Snippet: The sleep–wake states were identified based on EEG, EMG and video data (Neuroexplorer; Plexon).

Techniques: Imaging, Transfection, Immunohistochemistry, Infection, Incubation, Microscopy, Fluorescence, Labeling, Activity Assay, Muscles, Activation Assay

Journal: PLoS ONE

Article Title: Mild Transient Hypercapnia as a Novel Fear Conditioning Stimulus Allowing Re-Exposure during Sleep

doi: 10.1371/journal.pone.0067435

Figure Lengend Snippet: Shock-induced electrical artifact is evident in EEG and EMG tracings (top two traces marked by horizontal arrow). Heart rate and blood pressure were analyzed for the 10 sec prior to initiation of the conditioning stimulus (Pre), for the 10 sec immediately prior to footshock (End) and the 10 sec immediately after footshock (Post), and are marked by the short horizontal bars on the inspired CO 2 tracing. Note the presence of bradycardia during exposure to each episode of mtHC (the transient artifact in the heart rate tracing at time of foot shock did not affect the determination of End and Post heart rate and blood pressure values).

Article Snippet: The EEG, EMG and EKG electrodes were inserted into a pedestal (MS363, Plastics One) and secured to the skull with dental acrylic.

Techniques:

Journal: ACS chemical neuroscience

Article Title: A Rodent Model of Traumatic Stress Induces Lasting Sleep and Quantitative Electroencephalographic Disturbances

doi: 10.1021/cn500342u

Figure Lengend Snippet: Experimental design for EEG studies and tissue collection. In cohort 1, continuous EEG, EMG, and temperature data were telemetrically recorded from chronically implanted rats throughout successive 24 h light-dark cycles (ON, 6:00 am; OFF, 6:00 pm) before (BL) and several days after (days 0, 1, 2, and 7) either single prolonged stress (SPS) or SHAM treatment. Both treatments were performed within the first 6 h of the light phase on day 0, during which recording was not possible; EEG data from this day was reinitiated when each animal was returned to its home cage. In cohort 2, nonimplanted aged-matched rats underwent either SPS or SHAM treatment. SPS rats were sacrificed either 1 h (day 0), 1 day (day 1), or 7 days (day 7) later; SHAM rats were sacrificed 7 days later.

Article Snippet: Sleep Staging EEG, EMG, and temperature data were collected with Dataquest A.R.T.

Techniques: