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Object: Obsessive–compulsive disorder (OCD) is a mental disease in which people experience uncontrollable and repetitive thoughts or behaviors. Clinical diagnosis of OCD is achieved by using neuropsychological assessment metrics, which are often subjectively affected by psychologists and patients. In this study, we propose a classification model for OCD diagnosis using functional MR images. Methods: Using functional connectivity (FC) matrices calculated from brain region of interest (ROI) pairs, a novel Riemann Kernel principal component analysis (PCA) model is employed for feature extraction, which preserves the topological information in the FC matrices. Hierarchical features are then fed into an ensemble classifier based on the XGBoost algorithm. Finally, decisive features extracted during classification are used to investigate the brain FC variations between patients with OCD and healthy controls. Results: The proposed algorithm yielded a classification accuracy of 91.8%. Additionally, the well‐known cortico–striatal–thalamic–cortical (CSTC) circuit and cerebellum were found as highly related regions with OCD. To further analyze the cerebellar‐related function in OCD, we demarcated cerebellum into three subregions according to their anatomical and functional property. Using these three functional cerebellum regions as seeds for brain connectivity computation, statistical results showed that patients with OCD have decreased posterior cerebellar connections. Conclusions: This study provides a new and efficient method to characterize patients with OCD using resting‐state functional MRI. We also provide a new perspective to analyze disease‐related features. Despite of CSTC circuit, our model‐driven feature analysis reported cerebellum as an OCD‐related region. This paper may provide novel insight to the understanding of genetic etiology of OCD. [ABSTRACT FROM AUTHOR]

Phthalimide can be formed from either the degradation of folpet and phosmet, or reaction of phthalic anhydride with primary amino groups. Consequently, the sum of phthalimide and folpet, expressed as folpet‐residue definition, is highly prone to false‐positive levels of folpet in tea. An analytical method is thus urgently needed to investigate the residue level and source of phthalimide in tea. In this work, we developed an accurate method of determining phthalimide and phthalic acid (the indicator of phthalic anhydride) by acetonitrile extraction and 3‐bromopropyltrimethylammonium bromide derivatization coupled with ultra high performance liquid chromatography and high‐resolution mass spectrometry. The method was validated, and linearity (correlation coefficients > 0.99) was obtained. Satisfactory recoveries at 10, 20, 50, and 100 μg/kg ranged from 76 to 117%, and the intra‐ and interday accuracies were <23%. The limit of quantification for phthalimide and phthalic acid was 10 μg/kg. The developed method was further successfully used to determine phthalimide and phthalic acid in some tea samples. The positive rate of phthalimide and phthalic acid detected in the tea samples ranged from 30–75 and 50–90%, respectively. [ABSTRACT FROM AUTHOR]

An active and stable photocatalyst to directly split water is desirable for solar-energy conversion. However, it is difficult to accomplish overall water splitting without sacrificial electron donors. Herein, we demonstrate a strategy via constructing a single site to simultaneously promote charge separation and catalytic activity for robust overall water splitting. A single Co1-P4 site confined on g-C3N4 nanosheets was prepared by a facile phosphidation method, and identified by electron microscopy and X-ray absorption spectroscopy. This coordinatively unsaturated Co site can effectively suppress charge recombination and prolong carrier lifetime by about 20 times relative to pristine g-C3N4, and boost water molecular adsorption and activation for oxygen evolution. This single-site photocatalyst exhibits steady and high water splitting activity with H2 evolution rate up to 410.3 μmol h−1 g−1, and quantum efficiency as high as 2.2 % at 500 nm. [ABSTRACT FROM AUTHOR]

An active and stable photocatalyst to directly split water is desirable for solar-energy conversion. However, it is difficult to accomplish overall water splitting without sacrificial electron donors. Herein, we demonstrate a strategy via constructing a single site to simultaneously promote charge separation and catalytic activity for robust overall water splitting. A single Co1-P4 site confined on g-C3N4 nanosheets was prepared by a facile phosphidation method, and identified by electron microscopy and X-ray absorption spectroscopy. This coordinatively unsaturated Co site can effectively suppress charge recombination and prolong carrier lifetime by about 20 times relative to pristine g-C3N4, and boost water molecular adsorption and activation for oxygen evolution. This single-site photocatalyst exhibits steady and high water splitting activity with H2 evolution rate up to 410.3 μmol h−1 g−1, and quantum efficiency as high as 2.2 % at 500 nm. [ABSTRACT FROM AUTHOR]

The histamine H3 receptor (H3R), abundantly expressed in the central and the peripheral nervous system, has been recognized as a promising target for the treatment of various important CNS diseases including narcolepsy, Alzheimer's disease, and attention deficit hyperactivity disorder. The H3R acts via Gi/o-proteins to inhibit adenylate cyclase activity and modulate MAPK activity. However, the underlying molecular mechanisms for H3R mediation of the activation of extracellular signal-regulated kinases 1 and 2 ( ERK1/2) remain to be elucidated. In this study, using HEK293 cells stably expressing human H3R and mouse primary cortical neurons endogenously expressing mouse H3R, we found that the H3R-mediated activation of ERK1/2 was significantly blocked by both the pertussis toxin and the MEK1/2 inhibitor U0126. Upon stimulation by H3R agonist histamine or imetit, H3R was shown to rapidly induce ERK1/2 phosphorylation via PLC/ PKC-, PLDs-, and epidermal growth factor receptor ( EGFR) transactivation-dependent pathways. Furthermore, it was also indicated that while the βγ-subunits play a key role in H3R-activated ERK1/2 phosphorylation, β-arrestins were not required for ERK1/2 activation. In addition, when the cultured mouse cortical neurons were exposed to oxygen and glucose deprivation conditions ( OGD), imetit exhibited neuroprotective properties through the H3R. Treatment of cells with the inhibitor UO126 abolished these protective effects. This suggests a possible neuroprotective role of the H3R-mediated ERK1/2 pathway under hypoxia conditions. These observations may provide new insights into the pharmacological effects and the physiological functions modulated by the H3R-mediated activation of ERK1/2. [ABSTRACT FROM AUTHOR]

DOI: 10.1002/jssc.201801128 The cover picture shows an accurate method of determining phthalimide (PI) and phthalic acid (PA) in tea by acetonitrile extraction and 3‐bromopropyltrimethylammonium bromide derivatization coupled with ultraperformance liquid chromatography high resolution mass spectrometry. The method was validated, and satisfactory linearity, recovery, repeatability values were obtained. Then, the developed method was further successfully used to determine PI and PA in different tea matrices. All these observations provided crucial information and an analytical method to further study the sources and the related pathway of PI generation in tea. [ABSTRACT FROM AUTHOR]