Hearing VS. Listening: Attention Changes the Neural Representations of Auditory Percepts

Making sense of acoustic environments is a challenging task. At any moment, the signals from distinct auditory sources arrive in the ear simultaneously, forming an acoustic mixture. The brain must represent distinct auditory objects in this complex scene and prioritize processing of relevant stimuli while maintaining the capability to react quickly to unexpected events. The present studies explore neural representations of temporal modulations and the effects of attention on these representations. Temporal modulation plays a significant role in speech perception and auditory scene analysis. To uncover how temporal modulations are processed and represented is potentially of great importance for our general understanding of the auditory system. Neural representations of compound modulations were investigated by magnetoencephalography (MEG). Interaction components are generated by near rather than distant modulation rhythms, suggesting band-limited modulation filter banks operating in the central stage of the auditory system. Furthermore, the slowest detectable neural oscillation in the auditory cortex corresponds to the perceived oscillation of the auditory percept. Interactions between stimulus-evoked and goal-related neural responses were investigated in simultaneous behavioral-neurophysiological studies, in which we manipulate subjects' attention to different components of an auditory scene. Our experimental results reveal that attention to the target correlates with a sustained increase in the neural target representation, beyond well-known transient effects. The enhancement of power and phase coherence presumably reflects increased local and global synchronizations in the brain. Furthermore, the target's perceptual detectability improves over time (several seconds), correlating strongly with the target representation's neural buildup. The change in cortical representations can be reversed in a short time-scale (several minutes) by various behavioral goals. These aforementioned results demonstrate that the neural representation of the percept is encoded using the feature-driven mechanisms of sensory cortex, but shaped in a sustained manner via attention-driven projections from higher-level areas. This adaptive neural representations occur on multiple time scales (seconds vs. minutes) and multiple spatial scales (local vs. global synchronization). Such multiple resolutions of adaptation may underlie general mechanisms of scene organization in any sensory modality and may contribute to our highly adaptive behaviors

White dwarf-main sequence binaries from LAMOST: the DR1 catalogue

Context. White dwarf-main sequence (WDMS) binaries are used to study several different important open problems in modern astrophysics. Aims. The Sloan Digital Sky Survey (SDSS) identified the largest catalogue of WDMS binaries currently known. However, this sample is seriously affected by selection effects and the population of systems containing cool white dwarfs and early-type companions is under-represented.Here we search for WDMS binaries within the spectroscopic data release 1 of the LAMOST (Large sky Area Multi-Object fiber Spectroscopic Telescope) survey. LAMOST and SDSS follow different target selection algorithms. Hence, LAMOST WDMS binaries may be drawn from a different parent population and thus help in overcoming the selection effects incorporated by SDSS on the current observed population. Methods. We develop a fast and efficient routine based on the wavelet transform to identify LAMOST WDMS binaries containing a DA white dwarf and a M dwarf companion, and apply a decomposition/fitting routine to their LAMOST spectra to estimate their distances and measure their stellar parameters, namely the white dwarf effective temperatures, surface gravities and masses, and the secondary star spectral types. Results. We identify 121 LAMOST WDMS binaries, 80 of which are new discoveries, and estimate the sample to be \sim90 per cent complete. The LAMOST and SDSS WDMS binaries are found to be statistically different. However, this result is not due to the different target selection criteria of both surveys, but likely a simple consequence of the different observing conditions. Thus, the LAMOST population is found at considerably shorter distances (\sim50-450 pc) and is dominated by systems containing early-type companions and hot white dwarfs. (abridged)Comment: 14 pages, 8 figures, accepted for publication in A&

The Milky Way's rotation curve out to 100 kpc and its constraint on the Galactic mass distribution

The rotation curve (RC) of the Milky Way out to $\sim$ 100 kpc has been constructed using $\sim$ 16,000 primary red clump giants (PRCGs) in the outer disk selected from the LSS-GAC and the SDSS-III/APOGEE survey, combined with $\sim$ 5700 halo K giants (HKGs) selected from the SDSS/SEGUE survey. To derive the RC, the PRCG sample of the warm disc population and the HKG sample of halo stellar population are respectively analyzed using a kinematical model allowing for the asymmetric drift corrections and re-analyzed using the spherical Jeans equation along with measurements of the anisotropic parameter $\beta$ currently available. The typical uncertainties of RC derived from the PRCG and HKG samples are respectively 5-7 km/s and several tens km/s. We determine a circular velocity at the solar position, $V_c (R_0)$ = 240 $\pm$ 6 km/s and an azimuthal peculiar speed of the Sun, $V_{\odot}$ = 12.1 $\pm$ 7.6 km/s, both in good agreement with the previous determinations. The newly constructed RC has a generally flat value of 240 km/s within a Galactocentric distance $r$ of 25 kpc and then decreases steadily to 150 km/s at $r$ $\sim$ 100 kpc. On top of this overall trend, the RC exhibits two prominent localized dips, one at $r$ $\sim$ 11 kpc and another at $r$ $\sim$ 19 kpc. From the newly constructed RC, combined with other constraints, we have built a parametrized mass model for the Galaxy, yielding a virial mass of the Milky Way's dark matter halo of $0.90^{+0.07}_{-0.08} \times 10^{12}$ ${\rm M}_{\odot}$ and a local dark matter density, $\rho_{\rm \odot, dm} = 0.32^{+0.02}_{-0.02}$ GeV cm$^{-3}$.Comment: MNRAS accepted, 18 pages, 15 figures, 4 table

Cis-regulatory functions of overlapping HIF-1alpha/E-box/AP-1-like sequences of CD164

<p>Abstract</p> <p>Background</p> <p>CD164 (also known as MGC-24v or endolyn) is a sialomucin which has been suggested to participate in regulating the proliferation, cell adhesion and differentiation of hematopoietic stem and progenitor cells. CD164 is also involved in the development of cancer. The functions of cis-regulatory elements of CD164 remain relatively unknown.</p> <p>Methods</p> <p>In this study, we investigated the function of cis-regulatory elements within the promoter of CD164. We fused the 5'-flanking region of CD164 to a luciferase reporter vector. The minimal promoter region was confirmed by luciferase reporter assay. Using <it>in silico </it>analysis, we found the presence of one HIF-1alpha (HIF-1A) motif (5_-RCGTG-3_) overlapping E-box (CACGTG) and two AP-1-like binding sites (CGCTGTCCC, GTCTGTTG), one of which is also overlapped with HIF-1alpha sequence. Dual-luciferase assay was performed to examine the transcriptional activity of AP-1 and HIF-1alpha of CD164 promoter. Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) was performed to measure CD164 expression. Chromatin Immunoprecipitation was used to confirm the binding of HIF-1alpha and CD164.</p> <p>Results</p> <p>Co-transfection of c-jun, HIF-1alpha and minimal promoter region construct demonstrated that c-jun and HIF-1alpha bound the CD164 promoter and promoted CD164 expression. Hypoxia treatment also led to the up-regulation of CD164 expression. The mutation of overlapping sequences resulted in the reduced expression of CD164 induced by HIF-1alpha. Chromatin Immunoprecipitation demonstrated that the HIF-1alpha bound the minimal promoter region.</p> <p>Conclusions</p> <p>Determination of the optimal promoter region and transcription factors governing CD164 expression is useful in understanding CD164 functions. These results suggest that cis-regulatory elements of CD164 overlapping HIF-1alpha/E-box/AP-1-like sequences may play important regulatory roles.</p

A nomogram for prediction of deep venous thrombosis risk in elderly femoral intertrochanteric fracture patients: A dual-center retrospective study

ObjectiveDeep venous thrombosis (DVT) of the lower extremity is a common perioperative complication of femoral intertrochanteric fracture. This study aimed to identify the risk factors of lower extremity deep vein thrombosis (DVT) in elderly femoral intertrochanteric fracture patients and establish a nomogram model.MethodsFrom August 2014 to June 2021, a total of 1,652 femoral intertrochanteric fracture patients over the age of 65 were enrolled in our study. We distinguished independent risk factors by univariate and multivariate Cox analyses. A nomogram model was then built, and the discriminative and calibration of the model was evaluated through receiver operating characteristics (ROC) and calibration plots.ResultsA total of 378 patients developed DVT (292 in the training group, 86 in the validation group) while the remaining patients did not. According to the univariate and multivariate Cox analyses results, age (OR = 1.07, 95% CI: 1.04–1.10), fibrinogen (OR = 2.09, 95% CI: 1.68–2.60), D-dimer (OR = 1.33, 95% CI: 1.27–1.40), time from injury to admission (OR = 1.78, 95% CI: 1.55–2.05), functional status (OR = 4.21, 95% CI: 2.86–6.20), and diabetes (OR = 1.65, 95% CI: 1.10–2.48) were identified as independent risk factors of DVT. The ROC values for DVT of the training and validation group were 0.862 and 0.912, and the P-value of the Hosmer-Lemeshow calibration test was 0.767.ConclusionThis nomogram model can be used to predict the probability of preoperative DVT in elderly patients with femoral intertrochanteric fracture and guide physician in perioperative thrombosis management

Phytohormone Abscisic Acid Improves Spatial Memory and Synaptogenesis Involving NDR1/2 Kinase in Rats

The abscisic acid (ABA) is a phytohormone involved in plant growth, development and environmental stress response. Recent study showed ABA can also be detected in other organisms, including mammals. And it has been reported that ABA can improve learning and memory in rats. In this study, we attempted to investigate the effects of ABA on the alternation of dendritic spine morphology of pyramidal neurons in developmental rats, which may underlie the learning and memory function. Behavior tests showed that ABA significantly improved spatial memory performance. Meanwhile, Golgi-Cox staining assay showed that ABA significantly increased the spine density and the percentage of mushroom-like spines in pyramidal neurons of hippocampus, indicating that ABA increased dendritic spine formation and maturation, which may contribute to the improvement of spatial memory. Furthermore, ABA administration increased the protein expression of NDR1/2 kinase, as well as mRNA levels of NDR2 and its substrate Rabin8. In addition, NDR1/2 shRNA prohibited the ABA-induced increases in the expression of NDR1/2 and spine density. Together, our study indicated that ABA could improve learning and memory in rats and the effect are possibly through the regulation of synaptogenesis, which is mediated via NDR1/2 kinase pathway

MODIFIED YUPINGFENG FORMULA FOR THE TREATMENT OF STABLE CHRONIC OBSTRUCTIVE PULMONARY DISEASE: A SYSTEMATIC REVIEW OF RANDOMIZED CONTROLLED TRIALS

Background: Chronic obstructive pulmonary disease (COPD), is a very common disease of respiratory system. An increasing number of clinical trials on Yupingfeng formula in the management of stable COPD have been performed. However, the evidence base for it remains unknown. This review aims at assessing the efficacy, and safety of modified Yupingfeng formula in the treatment of stable COPD through a systematic review of all available randomized controlled trials. Materials and Methods: Literature retrieval was conducted using four English databases (CENTRAL, PubMed, EMBASE, and ISI Web of Science), and four Chinese databases (CBM, CNKI, VIP, and WANFANG), from respective inception to January 2013, and supplemented with a manual search. Review authors independently extracted the trial data, and assessed the quality of each trial. Methodological quality was assessed by Cochrane risk of bias and Jadad’s scale. The following outcomes were evaluated: (1) lung function; (2) 6-minute walk distance (6MWD); (3) effective rate; (4) serum levels of IgA, IgG and IgE; and (5) adverse events. Data were analyzed using STATA 12.0 software. Results: A total of nine studies involving 660, stable COPD patients were identified. Patients from all studies included in this review were randomized to receive Yupingfeng formula combined with Western medications in comparison with Western medications. In general, the methodological quality of the included trials was poor. The results of this systematic review indicates that, compared with Western medications alone, the use of Yupingfeng formula, if combined with Western medications could significantly improve FEV1 (WMD = 0.30L; 95%CI: 0.19, 0.42), FEV1/FVC ratio (SMD = 0.69; 95%CI: 0.48, 0.91), 6MWD (WMD = 31.73m; 95% CI: 19.29, 44.17), and effective rate (RR = 1.24; 95% CI: 1.10, 1.41), and increase the serum levels of IgA (WMD = 0.25; 95%CI: 0.16, 0.34) and IgG (WMD = 1.10; 95%CI: 0.53, 1.68), but no difference was found in the serum IgE levels (WMD = 0.47; 95%CI: -0.32, 1.27) between the two groups. No serious adverse events were reported. Conclusions: Within the limitations of this systematic review, we may conclude that compared with Western medications alone, Yupingfeng formula, when combined with Western medications can provide more benefits for patients with stable COPD, without any serious adverse reactions being identified. However, these benefits need to be further confirmed through high-quality prospective placebo-controlled trials that should be strictly conducted in accordance with methodological principles and procedures