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In this study, we examined the changes in high-sensitivity C-reactive protein (Hs-CRP) and homocysteine (HCY) levels, two of the risk factors, during the acute period of ischemic stroke (IS) and evaluated the relationship between these two factors and long-term post-stroke depression (PSD). In this study, 259 patients with IS had finished the follow-up and were included. Based on the symptoms, diagnoses of depression were made in accordance with DSM-IV criteria for depression at 1 year after stroke. The influence of Hs-CRP/CHY levels on PSD was performed by binary logistic regression analysis and receiver operating characteristic curves (ROC). Totally, 94 out of the 259 patients were diagnosed as PSD (36.3%; 95% CI 30.4–42.1%). In multivariate logistic regression analysis, the third and fourth quartiles of Hs-CRP or HCY were significantly associated with PSD during the observation period compared to the first quartile group ( P  < 0.05). In addition, patients with depression were older and more frequently were female, living with offspring, widowhood, higher initial stroke severity, and BMI. HCY improved the ability of Hs-CRP [0.72 (95% CI 0.66–0.79)] to diagnose PSD (AUC of the combined model 0.76; 95% CI 0.69–0.82; P  = 0.021). The patient group with higher levels of both Hs-CRP and HCY (> median) had an OR of 6.05 (95 % CI 3.13–10.15; P  < 0.001) for PSD compared with patients with lower levels of both factors (< median). The data suggests that elevated serum levels of Hs-CRP and HCY were associated with the risk of developing PSD 1 year after the stroke onset, and those two factors combined to add prognostic information in the early evaluation of PSD.

ObjectivesAiming to uncover the genetic basis of abdominal obesity, we performed a genome-wide association study (GWAS) meta-analysis of trunk fat mass adjusted by trunk lean mass (TFMadj) and followed by a series of functional investigations.SubjectsA total of 11,569 subjects from six samples were included into the GWAS meta-analysis.MethodsMeta-analysis was performed by a weighted fixed-effects model. In silico replication analysis was performed in the UK-Biobank (UKB) sample (N = 331,093) and in the GIANT study (N up to 110,204). Cis-expression QTL (cis-eQTL) analysis, dual-luciferase reporter assay and electrophoresis mobility shift assay (EMSA) were conducted to examine the functional relevance of the identified SNPs. At last, differential gene expression analysis (DGEA) was performed.ResultsWe identified an independent SNP rs12409479 at 1p21 (MAF = 0.07, p = 7.26 × 10−10), whose association was replicated by the analysis of TFM in the UKB sample (one-sided p = 3.39 × 10−3), and was cross-validated by the analyses of BMI (one-sided p = 0.03) and WHRadj (one-sided p = 0.04) in the GIANT study. Cis-eQTL analysis demonstrated that allele A at rs12409479 was positively associated with PTBP2 expression level in subcutaneous adipose tissue (N = 385, p = 4.15 × 10−3). Dual-luciferase reporter assay showed that the region repressed PTBP2 gene expression by downregulating PTBP2 promoter activity (p < 0.001), and allele A at rs12409479 induced higher luciferase activity than allele G did (p = 4.15 × 10−3). EMSA experiment implied that allele A was more capable of binding to unknown transcription factors than allele G. Lastly, DGEA showed that the level of PTBP2 expression was higher in individuals with obesity than in individuals without obesity (N = 20 and 11, p = 0.04 and 9.22 × 10−3), suggesting a regulatory role in obesity development.ConclusionsTaken together, we hypothesize a regulating path from rs12409479 to trunk fat mass development through its allelic specific regulation of PTBP2 gene expression, thus providing some novel insight into the genetic basis of abdominal obesity.

Cu-Nb microcomposite wire was successfully prepared by a groove rolling process. The effects of groove rolling on the diffraction peaks, microstructure, and properties of the Cu-Nb microcomposite were investigated and the microstructure evolutions and strengthening mechanism were discussed. The tensile strength of the Cu-Nb microcomposite wire with a diameter of 2.02 mm was greater than 1 GPa, and its conductivity reached 68% of the International Annealed Copper Standard, demonstrating the Cu-Nb microcomposite wire with high tensile strength and high conductivity after groove rolling. The results show that an appropriate groove rolling method can improve the performance of the Cu-Nb microcomposite wire.

FeSe superconducting bulks were prepared with high energy ball milling (HEBM) aided sintering process, within which process, tetragonal β-FeSe superconducting phase could be formed directly with one step sintering process, and the formation of hexagonal δ-FeSe non-superconducting phase was effectively avoided. The influences of HEBM time on the sintering process of FeSe bulks were systematically investigated. With different HEBM time, the phase composition and morphology of precursor powders changed correspondingly, which thus influenced the final phase composition and superconducting properties of FeSe superconducting bulks. Due to the formation of FeSe bulks with larger tetragonal phase content and higher superconducting transition temperature, HEBM time of 6.0 h was recognized as the optimal parameter. Shorter HEBM time could lead to the insufficient decrease of particle size and low density. While longer HEBM time caused the formation of amorphous hexagonal δ-FeSe, which crystallized during sintering process. Thus no more tetragonal FeSe could be obtained. The FeSe superconducting bulk with the critical temperature Tc(onset) of 8.0 K was obtained with the HEBM time of 6 h, and sintering temperature of 700 oC for 12 h.

Biological signal encoding is shaped by the underlying neural circuitry. In Drosophila melanogaster, the mushroom body (MB) houses thousands of Kenyon cells (KCs) that process olfactory signals from hundreds of projection neurons (PNs). Previous studies debated the connectivity between PNs and KCs (random vs. structured). Our multiscale analysis of electron microscopic data revealed a hybrid network with diverse synaptic connection preferences and input divergence across different KC classes. Using MB connectome data, our simulation model, validated via functional imaging, accurately predicted distinct chemical sensitivities in the major KC classes. The model suggests that the hybrid network excels in detecting food odors while maintaining precise odor discrimination in different KC classes. These findings underscore the computational advantages of this hybrid network.Competing Interest StatementThe authors have declared no competing interest.

Objective To observe the efficacy of superselective trans⁃microcatheter intra⁃anterior inferior cerebellar artery thrombolytic therapy with urokinase for patients with sudden vascular deafness. Methods Seventy ⁃ four cases of sudden vascular deafness were randomly treated by transarterial or transvenous urokinase thrombolytic therapy. After thrombolysis, low molecular weight heparin subcutaneous injection of 0.40 ml (2 times/d) and aspirin 100 mg oral (1 time/d) were given continuously for 7 days. Electric audiometry was performed at day 1, 3, 6, 10 to assess the efficacy. Results At day 10, the total effective rate of patients given with transarterial thrombolysis (intra⁃arterial group) was 84.21% (32/38), and the patients given with transvenous thrombolysis (intra⁃venous group) was 58.33% (21/36), the difference between two groups was significant (χ2 = 6.091, P = 0.014). The results of electric audiometry at different time points in intra⁃arterial group were all better than those in intra⁃venous group, the differences were all significant (P < 0.01, for all). Conclusion Superselective intra⁃arterial urokinase thrombolysis is probably an effective therapy for sudden vascular deafness.

Aim： To investigate the effects of the wingless-related MMTV integration site 3A （Wnt3a） signaling on the proliferation, migration, and the myogenic and adipogenic differentiation of rat bone marrow mesenchymal stem cells （rMSC）. Methods： Primary MSC were isolated and cultured from Sprague-Dawley rats and characterized by flow cytometry. Mouse L cells were transfected with Wnt3a cDNA, and conditioned media containing active Wnt3a proteins were prepared. Cell proliferation was evaluated by cell count and 5-bromodeoxyuridine incorporation assay. The migration of rMSC was performed by using a transwell migration and wound healing assay. The myogenic and adipogenic differentiation in rMSC were examined by light microscopy, immunofluorescence, and RT-PCR at different time points after myogenic or adipogenic introduction. Results： Wnt3a signaling induced β-catenin nuclear translocation and activated the Writ pathway in rMSC. In the presence of Wnt3a, rMSC proliferated more rapidly than the control cells, keeping their differentiation potential. Moreover, Wnt3a signaling induced 2.62% and 3.76% of rMSC-expressed desmin and myosin heavy chain after being cultured in myogenic medium. The myogenic differentiation genes, including Pax7, MyoD, Myf5, Myf4, and myogenin, were activated after Wnt3a treatment. On the other hand, Wnt3a inhibited the adipogenic differentiation in rMSC through the downregulated expression of CCAAT/enhancer-binding protein alpha （C/EBPalpha） and peroxisome proliferator-activated receptor gamma （PPARgamma）. Furthermore, Wnt3a promoted the migration capacity of rMSC. Conclusion： The results indicate that Wnt3a signaling can induce myogenic differentiation in rMSC. Wnt3a signaling is also involved in the regulation of the proliferation and migration of rMSC. These results could provide a rational foundation for cell-based tissue repair in humans.

Using nanoscale electrical-discharge-induced rapid Joule heating, we developed a method for ultrafast shape change and joining of small-volume materials. Shape change is dominated by surface-tension-driven convection in the transient liquid melt, giving an extremely high strain rate of N106 s-1. In addition, the heat can be dissipated in small volumes within a few microseconds through thermal conduction, quenching the melt back to the solid state with cooling rates up to 108 K.s-1. We demonstrate that this approach can be utilized for the ultrafast welding of small-volume crystalline Mo （a refractory metal） and amorphous Cu49Zr51 without introducing obvious microstructural changes, distinguishing the process from bulk welding.

Recent studies on cerebral ischemic stroke have demonstrated the importance of the inflammatory response. Ongoing inflammatory insults have been implicated as a secondary mechanism underlying neuronal injury induced by ischemia, and anti-inflammatory strategies have gained considerable interest. Selenoprotein S (SelS), which is an endoplasmic reticulum resident protein, is known to promote cell survival by regulating inflammation. Moreover, SelS has been shown to be responsive to ischemia in cultured astrocytes. A Finnish report revealed that a variation in the SelS gene locus is associated with a higher predisposition to ischemic stroke in humans, suggesting a crucial role for SelS in protection against brain ischemia. However, the time-course of SelS expression following cerebral ischemia in vivo remains unknown. In the present study, we show, for the first time, differential SelS expression from 3 h to 7 days after reperfusion in rats with transient focal cerebral ischemia induced by a 1-h middle cerebral artery occlusion. We found that the SelS protein level decreased in the ischemic core 3–7 days after reperfusion. Furthermore, SelS expression was upregulated in the ischemic penumbra adjacent to the ischemic core 3–7 days after reperfusion and is matched by reactive astrogliosis. Thus, we propose that the upregulation of Sels represents a reaction of astrocytes against inflammatory stimuli, and the findings of this study open a new chapter in the research of the interrelationships between SelS and cerebral ischemic stroke.

The major ingredients of grassleaf sweetflag rhizome are β-asarone and eugenol, which can cross the blood-brain barrier and protect neurons. This study aimed to observe the neuroprotective effects and mechanisms of β-asarone and eugenol, components of the Chinese herb grassleaf sweetflag rhizome, on PC12 cells. First, PC12 cells were cultured with different concentrations（between 1 × 10–10 M and 1 × 10–5 M） of β-asarone and eugenol. Survival rates of PC12 cells were not significantly affected. Second, PC12 cells incubated with amyloid-beta42, which reduced cell survival, were cultured under the same conditions（1 × 10–6 M β-asarone and eugenol）. The survival rates of PC12 cells significantly increased, while expression levels of the m RNAs for the pro-apoptotic protein Bax decreased, and those for the anti-apoptotic protein Bcl m RNA increased. In addition, the combination of β-asarone with eugenol achieved better results than either component alone. Our experimental findings indicate that both β-asarone and eugenol protect PC12 cells through inhibiting apoptosis, and that the combination of the two is better than either alone.