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BACKGROUND: Studies have found that the use of clinically approved caffeine and modafinil can alleviate cognitive impairment due to sleep deprivation (SD) to some extent. However, the neural mechanisms by which these two cognitive enhancers work to counteract the effects of SD on cognitive impairment remain unclear. METHODS: A double-blind within-subjects experiment using resting-state functional magnetic resonance imaging (rs-fMRI) was designed. Participants underwent three 36-h SD trials, each of which involved taking 200 mg of caffeine, modafinil, or placebo at the 28th and 32 nd h of SD. Sixteen subregions of the thalamus were selected as the regions of interest and changes in functional connectivity (FC) between the thalamus and the other brain regions were explored after the participants took caffeine or modafinil. RESULTS: The subjective sleepiness of the participants increased with the duration of SD. compared with placebo, modafinil and caffeine had insignificant effects on wakefulness or sleepiness. However, in terms of neural FC, we found varying degrees of attenuation or enhancement of the FC between the thalamus and other regions. Taking caffeine during SD weakened the FC between the right rostral temporal thalamus (rTtha) subregion and the left lingual gyrus compared with placebo. Caffeine enhanced the FC between three subregions of the thalamus, namely the left sensory thalamus, the left rTtha, and the right lateral pre-frontal thalamus, and the right inferior temporal, left orbitofrontal, and right superior occipital gyris. Modafinil weakened the FC between the right posterior parietal thalamus and left middle temporal gyrus, and enhanced the FC between the left medial pre-frontal thalamus, left rTtha, and right occipital thalamus and left middle frontal gyrus. CONCLUSIONS: After 36 h of total SD, modafinil and caffeine administration enhanced or attenuated the time-domain correlations between various subregions of the thalamus and brain regions of the frontal and temporal lobes in healthy adults, compared with placebo. These results provide valuable evidence for further unraveling the neuropharmacological mechanisms of caffeine and modafinil, as well as important insights for exploring effective pharmacological intervention strategies against SD.
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Cafeína , Imageamento por Ressonância Magnética , Modafinila , Privação do Sono , Tálamo , Humanos , Cafeína/farmacologia , Cafeína/administração & dosagem , Cafeína/uso terapêutico , Modafinila/farmacologia , Modafinila/uso terapêutico , Privação do Sono/tratamento farmacológico , Privação do Sono/complicações , Privação do Sono/fisiopatologia , Método Duplo-Cego , Tálamo/efeitos dos fármacos , Tálamo/diagnóstico por imagem , Masculino , Projetos Piloto , Adulto , Feminino , Estimulantes do Sistema Nervoso Central/farmacologia , Estimulantes do Sistema Nervoso Central/uso terapêutico , Promotores da Vigília/farmacologia , Promotores da Vigília/uso terapêutico , Adulto JovemRESUMO
The development of novel near-infrared (NIR) materials with extremely small energy gaps and high stability is highly desirable in bioimaging and phototherapy. Here we report an effective strategy for narrowing the energy gaps of porphyrins by synergistic regulation of meso/ß substituents. The novel NIR absorbing/emitting meso-alkynyl naphthoporphyrins (Zn-TNP and Pt-TNP) are synthesized via the retro-Diels-Alder reaction. X-ray crystallography analysis confirms the highly distorted structures of the complexes. Both compounds exhibit intense Q bands around 800 nm, while Zn-TNP shows deep NIR fluorescence at 847 nm. Pt-TNP displays NIR-II room temperature phosphorescence peaking at 1106 nm with an extremely large Stokes shift of 314 nm, which are the longest wavelengths observed among the reported platinum porphyrinoids. Furthermore, Pt-TNP shows remarkable photostability and a notable capacity for synchronous singlet oxygen and heat generation under NIR light irradiation, demonstrating potential in combined photodynamic/photothermal therapy. A theoretical analysis reveals the progressive lifting of the HOMO by the ß-fused benzene ring, the decrease of the LUMO upon meso-alkynyl substitution, and energy-releasing pathways varying with metal ions. This dual regulation approach demonstrates great promise in designing innovative multifunctional NIR porphyrin materials.
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This study explores the impact of postharvest storage temperatures (4 °C and 25 °C) on starch metabolism and textural attributes of glutinous lotus root. While starch metabolism is a well-known factor influencing texture, changes in powdery and sticky qualities have remained unexplored. Our research reveals that storing lotus roots at 4 °C delays water dissipation, amylopectin reduction, and the decline in textural elements such as hardness, adhesiveness, springiness, gumminess, and resilience. Lower temperatures postpone amylopectin reduction and sugar interconversion, thereby preserving the sticky texture. Additionally, they suppress starch formation, delay starch metabolism, and elevate the expression of genes involved in starch metabolism. The correlation between gene expression and root texture indicates the critical role of gene regulation in enzyme activity during storage. Overall, low-temperature storage extends lotus root preservation by regulating metabolite content, enzyme activities, and the corresponding genes involved in starch metabolism, preserving both intrinsic and external root quality.
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Armazenamento de Alimentos , Nelumbo , Raízes de Plantas , Amido , Raízes de Plantas/metabolismo , Raízes de Plantas/química , Raízes de Plantas/genética , Amido/metabolismo , Amido/química , Nelumbo/química , Nelumbo/metabolismo , Nelumbo/genética , Temperatura , Amilopectina/metabolismo , Amilopectina/química , Proteínas de Plantas/metabolismo , Proteínas de Plantas/genéticaRESUMO
A practical synthetic method for the synthesis of vinyl sulfonyl fluorides through copper-promoted direct fluorosulfonylation has been developed. The reaction of the vinylboronic acids with DABSO and then NFSI is performed under mild reaction conditions. This transformation efficiently affords aryl or alkyl vinyl sulfonyl fluorides with good reaction yields, exclusive E-configuration, broad substrate scope, excellent compatibility, and operational simplicity.
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BACKGROUND AND AIM: Patients with autism spectrum disorder (ASD) commonly experience aberrant skin sensation sensitivity; however, the causal relationship is not yet clear. This study uses a bidirectional Mendelian randomization (MR) method to explore the relationship between disturbance of skin sensation (DSS) and ASD. METHODS: Single-nucleotide polymorphisms (SNPs) extracted from the summary data of genome-wide association studies were used as genetic instruments. MR was performed using the inverse-variance-weighted method, with alternate methods (e.g., weighted median, MR-Egger, simple mode, weighted mode, and MR-pleiotropy residual sum and outlier) and multiple sensitivity analyses to assess horizontal pleiotropy and remove outliers. RESULTS: The results of the analysis using six SNPs as genetic instruments showed that the DSS is associated with an increased risk of ASD (odds ratio = 1.126, 95% confidence interval = 1.029-1.132; p = .010). The results of the sensitivity analyses were robust with no evidence of pleiotropy. The reverse MR analyses showed no causal effects of ASD on DSS. CONCLUSION: This study's findings suggest that DSS has potential causal effects on ASD, whereas ASD has no effect on DSS. Thus, skin sensitivity may represent a behavioral marker of ASD, by which some populations could be subtyped in the future.
This study examines whether disturbance of skin sensation (DSS) has potential causal effects on autism spectrum disorder (ASD) using the bidirectional Mendelian randomization method. We believe our study makes a significant contribution to the literature because it provides more evidence of the causal effect of skin sensory abnormalities, such as touch, temperature, and tactile sensation, in ASD. Additionally, the findings are a reminder that the discovery of DSS as a biomarker in some ASD patients provides an objective and quantifiable indicator of the clinically relevant course of ASD, which can help to identify targets for intervention or treatment.
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Transtorno do Espectro Autista , Humanos , Transtorno do Espectro Autista/genética , Estudo de Associação Genômica Ampla , Análise da Randomização Mendeliana , Pele , SensaçãoRESUMO
Sleep deprivation leads to reduced inhibitory control in individuals. However, the underlying neural mechanisms are poorly understood. Accordingly, this study aimed to investigate the effects of total sleep deprivation (TSD) on inhibitory control and their neuroelectrophysiological mechanisms from the perspective of the time course of cognitive processing and brain network connectivity, using event-related potential (ERP) and resting-state functional connectivity techniques. Twenty-five healthy male participants underwent 36 h of TSD (36-h TSD), completing Go/NoGo tasks and resting-state data acquisition before and after TSD; their behavioral and electroencephalogram data were recorded. Compared to baseline, participants' false alarms for NoGo stimuli increased significantly (t = -4.187, p < 0.001) after 36-h TSD. ERP results indicated that NoGo-N2 negative amplitude increased and latency was prolonged (t = 4.850, p < 0.001; t = -3.178, p < 0.01), and NoGo-P3 amplitude significantly decreased and latency was prolonged (t = 5.104, p < 0.001; t = -2.382, p < 0.05) after 36-h TSD. Functional connectivity analysis showed that the connectivity of the default mode and visual networks in the high alpha band was significantly reduced after TSD (t = 2.500, p = 0.030). Overall, the results suggest that the negative amplitude increase in N2 after 36-h TSD may reveal that more attention and cognitive resources are invested after TSD; the significant decrease in P3 amplitude may indicate the impairment of advanced cognitive processing. Further functional connectivity analysis indicated impairment of the brain's default mode network and visual information processing after TSD.
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Encéfalo , Privação do Sono , Humanos , Masculino , Adulto , Privação do Sono/complicações , Eletroencefalografia , Potenciais Evocados , Cognição/fisiologiaRESUMO
BACKGROUND: Previous studies revealed that sleep deprivation (SD) impairs risk perception and leads to poor decision-making efficiency. However, how risk perception is related to brain regions' communication after SD has not been elucidated. In this study, we investigated the neuropsychological mechanisms of SD-impaired risk perception. METHODS: Nineteen healthy male adults were recruited and underwent resting-state functional magnetic resonance imaging during a state of rested wakefulness and after nearly 36 h of total SD. They then completed the balloon analog risk task, which was used to measure the risk perception ability of risky decision-making. Regional homogeneity (ReHo) and voxel-wise functional connectivity were used to investigate neurobiological changes caused by SD. Correlation analysis was used to investigate the relationship between changes in ReHo, function, and risk perception. RESULTS: At the behavioral level, risk perception decreased after 36 h of SD. At the neural level, SD induced a significant increase in ReHo in the right postcentral gyrus and was positively correlated with risk perception changes. The functional connectivity between the right postcentral gyrus, left medial temporal gyrus, and right inferior temporal gyrus was enhanced. Critically, increased right postcentral gyrus and right inferior temporal gyrus connectivity positively correlated with changes in risk perception. CONCLUSIONS: SD impairs the risk perception associated with altered postcentral connectivity. The brain requires more energy to process and integrate sensory and perceptual information after SD, which may be one possible reason for decreased risk perception ability after SD.
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Monocrystalline silicon-based, n-type front and back contact (nFAB) solar cells are gradually attracting more interest from the photovoltaic industry, due to their good bifaciality and high efficiency potentials. To further improve the conversion efficiency, nFAB solar cells need to make better use of the solar spectrum. Conventional single-layer SiNx antireflection coating (ARC) tends to have a high reflection loss for ultraviolet photons. Thus, in this work, we prepare a double-layer ARC structure made of SiNx/SiOx stack, deposited by the plasma-enhanced chemical vapor deposition method. We investigate the effects of double-layer ARC through simulation and experimental studies by fabricating bifacial nFAB cells. The results show that the implementation of a double-layer ARC helps to greatly reduce front reflection in short wavelength, and thus allow for improvement of the photocurrent by up to 0.3 mA/cm2. As a result, the average cell efficiency of nFAB solar cells increases by absolute â¼0.2%.
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Superconductivity that spontaneously breaks time-reversal symmetry (TRS) has been found, so far, only in a handful of three-dimensional (3D) crystals with bulk inversion symmetry. We report an observation of spontaneous TRS breaking in a 2D superconducting system without inversion symmetry: the epitaxial bilayer films of bismuth and nickel. The evidence comes from the onset of the polar Kerr effect at the superconducting transition in the absence of an external magnetic field, detected by the ultrasensitive loop-less fiber-optic Sagnac interferometer. Because of strong spin-orbit interaction and lack of inversion symmetry in a Bi/Ni bilayer, superconducting pairing cannot be classified as singlet or triplet. We propose a theoretical model where magnetic fluctuations in Ni induce the superconducting pairing of the [Formula: see text] orbital symmetry between the electrons in Bi. In this model, the order parameter spontaneously breaks the TRS and has a nonzero phase winding number around the Fermi surface, thus making it a rare example of a 2D topological superconductor.
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A systematic theoretical study of the structural and magnetic properties of small transition metal oxide clusters TM(n)O(m) (TM = Sc, Ti, V, Cr and Mn; n = 1, 2; m = 1-6) has been carried out by using an ab initio density functional theory approach. The O atoms are partly molecularly adsorbed in O-rich and few-valence electron TM oxide clusters like ScO(3), TiO(3), Sc(2)O(4-6), Ti(2)O(5-6), and V(2)O(6). The binding energy increases monotonously with increasing O atoms and decreases with the appearance of the peroxide unit, with the exception of ScO(3). The Sc-, Ti- and V- oxide clusters have a stronger binding than the Cr- and Mn-oxide ones. The magnetic properties are dependent on the TM element and on the density of O. The successive addition of an O atom to Mn(2) induces an odd-even magnetic oscillation from antiferromagnetic to ferrimagnetic and to nonmagnetic state. In the V-, Cr- and Mn-oxide clusters, the O atoms play a negligible role in the magnetism and they are generally antiferromagnetic when coupled with TM atoms, while the O atoms possess large magnetic moments in some Sc- and Ti- oxide clusters.