Insomnia and stress: the mediating roles of frontoparietal network.

Insomnia is a widespread health problem among adults, and it impairs cognitive control and emotional regulation functions. Stress and insomnia are positively correlated, and their vicious cycle has been widely reported. In this study, we explore the neural biomarkers of insomnia from the perspective of whole-brain functional connectivity and investigate the neural mechanisms underlying the association between stress and insomnia. The current study was conducted on a cross-sectional sample (N = 430). First, we investigated the correlation between perceived stress and insomnia. Second, we applied connectome-based predictive modeling (CPM) to determine the neuromarkers of insomnia. Finally, we explored the neural basis underlying the association between perceived stress and insomnia. A significant positive correlation was found between perceived stress and insomnia in the present research. Results of CPM revealed the following as the neural substrates supporting insomnia: the emotion regulation circuit involving repetitive negative thinking and the cognitive control circuit involving attention control. According to further results from mediation analysis, the frontoparietal network supporting cognitive emotion regulation is an important neural mechanism that maintains the correlation between stress and insomnia. The present study offers a profound insight into the alterations of brain activity related to insomnia, and it further investigates the neural underpinnings of the robust association between stress and insomnia. This study also opens new avenues for neural interventions to alleviate stress-related insomnia.

Cinnamaldehyde promotes the defense response in postharvest citrus fruit inoculated with Penicillium digitatum and Geotrichum citri-aurantii.

Induced resistance in harvested fruit and vegetables is a superior strategy to reduce postharvest decay. In the present study, Cinnamaldehyde (CA) was applied to investigate for its induced resistance against Penicillium digitatum and Geotrichum citri-aurantii. The results showed that 5250 mg CA/L wax was effective concentration in inducing the resistance of citrus fruit to green mold and sour rot. Wax+ CA (WCA) reduced significantly green mold and sour rot incidences at different exposure times, with 24 h being the optimal exposure time. The host reactions under infection with different pathogens were similar. During initial exposure, treatment with 5250 mg CA/L wax enhanced significantly the activities of phenylalanine ammonia-lyase (PAL), peroxidase (POD), polyphenol oxidase (PPO), ß-1, 3-glucanase (GLU) and chitinase (CHT) in the presence of direct contact with the pathogen. Simultaneously, WCA induced an increase in total phenolic, flavanone and dihydroflavonol, flavone and flavonol, and lignin contents. Thus, our results suggest that treatment using 5250 mg CA/L wax can be applied early to control diseases by provoking response reactions in citrus fruit.

Inhibited enzyme activities in soil macroaggregates contribute to enhanced soil carbon sequestration under afforestation in central China.

The fate of soil organic carbon (SOC) sequestered by afforestation is crucial for the mitigation of the anthropogenic climate change but remains largely unclear. This lack of knowledge is particularly true for SOC turnover driven by enzyme activity. Here we measured hydrolase (including ß-glucosidase, α-glucosidase, cellobiohydrolase and xylanase) and oxidase (including polyphenol oxidase and peroxidase) activities in soil aggregates following 30-year afforestation in central China. We also analyzed the relationships of enzyme activities with SOC concentrations, soil C:nitrogen (N) ratios and δ13C values of soil organic pool (removing any carbonates by acid hydrolysis) and stable pool (NaOCl-resistant). Afforestation significantly enhanced soil ß-glucosidase, α-glucosidase and xylanase activities in bulk soil, as well as SOC concentrations in bulk soil and all aggregate fractions compared to those in the open area and cropland. In particular, the woodland increased SOC concentration in >2000 µm macroaggregates by 4.2- and 3.2-fold, compared to the open area and cropland, respectively. Soil hydrolase activities were generally lower but SOC concentrations were higher in >2000 µm macroaggregates compared with those in other aggregate fractions following afforestation. Hydrolase activities were negatively correlated with SOC and C:N ratios in soil aggregate fractions following afforestation. Results of structural equation modeling indicated that the increasingly inhibited hydrolase activities with increasing soil aggregate size indirectly promoted SOC sequestration following afforestation. In addition, both hydrolase and oxidase were positively correlated with δ13C values in the stable pool of the afforested soils, confirming the essential role of enzymes for SOC turnover in soil aggregates following afforestation. Overall, our results highlight the importance of unevenly distributed enzyme activities among soil aggregates in regulating SOC sequestration following afforestation.

Supramolecular self-assembly of monoend-functionalized methoxy poly(ethylene glycol) and α-cyclodextrin: from micelles to hydrogel.

An effective strategy was developed to fabricate a supramolecular hydrogel with the complexation of α-cyclodextrins (α-CDs) and monoend-functionalized low molecular weight methoxy poly(ethylene glycol) (mPEG, Mn=2000) micelles. Hydrophobic cinnamic acid was immobilized on methoxy poly(ethylene glycol) via L-lysine as linker to prepare amphiphilic mPEG. The monoend-functionalized mPEG self-assembled micelles in aqueous solution. The size and size distribution of the micelles were tested by dynamic laser scattering (DLS). The morphology of the micelles was observed by SEM, TEM and AFM. The critical micelle concentration (CMC) was tested and it was 42.5 mg/L. The monodisperse micelles had core-shell structure and the mean diameter was around 40 nanometers. α-cyclodextrins were added in the suspension of micelles to form supramolecular hydrogel with the polypseudorotaxanes complexation. Hydrophilic drug doxorubicin hydrochloride was used as model drug to study the release profile. The results showed that the hydrogel was a promising carrier for drug delivery.