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Since the 1987 democratic reform, regional attitudes toward the two southern provinces have been regarded as the most significant determinant of South Korean voters' political preferences. In recent years, however, many scholars have speculated that regional animus is losing its ground as a basis for political judgment and will eventually be replaced by other politically relevant factors such as political ideology and issue preference. Others raise questions about the validity of this kind of \"revisionist\" argument, noting that election outcomes remain regionally divided. Adopting the implicit association test (IAT) as a measure of regional attitudes, we provide an empirical test to measure the effects of the emergence of new generations and geographical mobility in South Korean voters' regional attitudes. Our results show that younger Korean voters are less regionally biased toward either of the two southern provinces. The only exception was the younger generation in the Honam region: they held even higher levels of animus toward Yeongnam than their older counterparts. Geographical mobility also seems to decrease regional bias. Those who have relocated to other provinces showed less regional bias when compared with the natives of Yeongnam and Honam still residing in their respective regions. Likewise, our results show that the inter-generational transfer of regional animus is not overwhelming. For the descendants of Yeongnam or Honam natives residing in another province, their family's region of origin mattered little. In short, our findings suggest that changing generational composition and geographical mobility are likely to lessen the severity of regional animus and the political significance of regional attitudes will wane.

Manganese (Mn)‐based cathode materials have garnered huge research interest for rechargeable aqueous zinc‐ion batteries (AZIBs) due to the abundance and low cost of manganese and the plentiful advantages of manganese oxides including their different structures, wide range of phases, and various stoichiometries. A novel in situ generated Mn‐deficient ZnMn2O4@C (Mn‐d‐ZMO@C) nanoarchitecture cathode material from self‐assembly of ZnO‐MnO@C for rechargeable AZIBs is reported. Analytical techniques confirm the porous and crystalline structure of ZnO‐MnO@C and the in situ growth of Mn deficient ZnMn2O4@C. The Zn/Mn‐d‐ZMO@C cell displays a promising capacity of 194 mAh g−1 at a current density of 100 mA g−1 with 84% of capacity retained after 2000 cycles (at 3000 mA g−1 rate). The improved performance of this cathode originates from in situ orientation, porosity, and carbon coating. Additionally, first‐principles calculations confirm the high electronic conductivity of Mn‐d‐ZMO@C cathode. Importantly, a good capacity retention (86%) is obtained with a year‐old cell (after 150 cycles) at 100 mA g−1 current density. This study, therefore, indicates that the in situ grown Mn‐d‐ZMO@C nanoarchitecture cathode is a promising material to prepare a durable AZIB. A novel battery consisting of zinc anode and Mn deficient ZnMn2O4@C cathode has been developed by immersing ZnO‐MnO@C electrode in 2 m ZnSO4 + 0.2 m MnSO4. The in situ formation of a reversible ZnMn2‐xO4@C with Zn4(OH)6(SO4).xH2O surface layer exhibits extraordinary cycle performance.

A metabolomic investigation of depression and chronic fluoxetine treatment was conducted using a chronic unpredictable mild stress model with C57BL/6N mice. Establishment of the depressive model was confirmed by body weight measurement and behavior tests including the forced swim test and the tail suspension test. Behavioral despair by depression was reversed by four week-treatment with fluoxetine. Hippocampus, serum, and feces samples collected from four groups (control + saline, control + fluoxetine, model + saline, and model + fluoxetine) were subjected to metabolomic profiling based on ultra-high performance liquid chromatography-quadrupole-time-of-flight mass spectrometry. Alterations in the metabolic patterns were evident in all sample types. The antidepressant effects of fluoxetine appeared to involve various metabolic pathways including energy metabolism, neurotransmitter synthesis, tryptophan metabolism, fatty acid metabolism, lipid metabolism, and bile acid metabolism. Predictive marker candidates of depression were identified, including β-citryl-L-glutamic acid (BCG) and docosahexaenoic acid (DHA) in serum and chenodeoxycholic acid and oleamide in feces. This study suggests that treatment effects of fluoxetine might be differentiated by altered levels of tyramine and BCG in serum, and that DHA is a potential serum marker for depression with positive association with hippocampal DHA. Collectively, our comprehensive study provides insights into the biochemical perturbations involved in depression and the antidepressant effects of fluoxetine.

Psoriasis is an immune-mediated inflammatory skin disease. IL-22, a proinflammatory cytokine, is implicated in psoriasis pathogenesis; however, there is currently no established biological treatment targeting IL-22 or its receptor, IL-22Rα. Alloferon is a short peptide that has an antiinflammatory effect on skin disorders; however, little is known about its anti-inflammatory activity in psoriasis. We investigated the regulatory role of alloferon in the development of psoriasis in an imiquimod (IMQ)-induced psoriasis model through the regulation of IL-22Rα expression. The expression of IL-22Rα was analyzed by immunofluorescence staining in primary human keratinocytes. The effect of alloferon on the development of psoriasis was investigated in IMQ-induced wild-type and IL-22Rα KO mice. We found that alloferon decreased the expression of IL-22Rα in psoriasis-like keratinocytes treated with TNF-α, while epidermal hyperplasia was observed in IMQ-induced wild-type and IL-22Rα KO mice. In addition, the expression of IL-1β, IL-19, and IL-33 was suppressed when IL-22Rα KO mice were treated with alloferon. The findings of this study indicate that alloferon could be an effective potential drug for the treatment of psoriasis by interrupting IL-22 signaling and factors related to skin inflammation.

Background and Objectives: The attentional bias and information processing model explained that individuals who interpret pain stimuli as threatening may increase their attention toward pain-related information. Previous eye tracking studies found pain attentional bias among individuals with chronic pain; however, those studies investigated this phenomenon by using only one stimulus modality. Therefore, the present study investigated attentional engagement to pain-related information and the role of pain catastrophizing on pain attentional engagement to pain-related stimuli among chronic pain patients by utilizing both linguistic and visual stimulus. Materials and Methods: Forty chronic pain patients were recruited from the rehabilitation center, the back pain clinic, and the rheumatology department of Chung-Ang University Hospital in Seoul, Korea. Patients observed pictures of faces and words displaying pain, presented simultaneously with neutral expressions, while their eye movements were measured using the eye tracking system. A t-test and ANOVA were conducted to compare stimulus pairs for the total gaze duration. Results: Results revealed that chronic pain patients demonstrated attentional preference toward pain words but not for pain faces. An ANOVA with bias scores was conducted to investigate the role of pain catastrophizing on attentional patterns. Results indicated that chronic pain patients with high pain catastrophizing scores gazed significantly longer at pain- and anger-related words than neutral words compared to those with low pain catastrophizing scores. The same patterns were not observed for the facial expression stimulus pairs. Conclusions: The results of the present study revealed attentional preference toward pain-related words and the significant role of pain catastrophizing on pain attentional engagement to pain-related words. However, different patterns were observed between linguistic and visual stimuli. Clinical implications related to use in pain treatment and future research suggestions are discussed.

TAPL is a lysosomal ATP-binding cassette transporter that translocates a broad spectrum of polypeptides from the cytoplasm into the lysosomal lumen. Here we report that, in addition to its well-known role as a peptide translocator, TAPL exhibits an ATP-dependent phosphatidylserine floppase activity that is the possible cause of its high basal ATPase activity and of the lack of coupling between ATP hydrolysis and peptide efflux. We also present the cryo-EM structures of mouse TAPL complexed with (i) phospholipid, (ii) cholesteryl hemisuccinate (CHS) and 9-mer peptide, and (iii) ADP·BeF 3 . The inward-facing structure reveals that F449 protrudes into the cylindrical transport pathway and divides it into a large hydrophilic central cavity and a sizable hydrophobic upper cavity. In the structure, the peptide binds to TAPL in horizontally-stretched fashion within the central cavity, while lipid molecules plug vertically into the upper cavity. Together, our results suggest that TAPL uses different mechanisms to function as a peptide translocase and a phosphatidylserine floppase. In this work, the authors report an ATP-dependent phosphatidylserine floppase activity for the lysosomal ATP-binding cassette transporter TAPL. In addition, they report the cryo-EM structures of mouse TAPL complexed with (i) phospholipid, (ii) cholesteryl hemisuccinate (CHS) and 9-mer peptide, and (iii) ADP·BeF3. Together, their results suggest that TAPL uses different mechanisms to function as a peptide translocase and a phosphatidylserine floppase.

Recently, a novel electrochemical regulation associated with a deposition/dissolution reaction on an electrode surface has been proven to show superiority in large-scale energy storage systems (ESSs). Hence, in the search for high-performance electrodes showcasing these novel regulations, we utilized a low-cost ZnO microsphere electrode to construct aqueous rechargeable batteries (ARBs) that supplied a harvestable and storable charge through electrochemical deposition/dissolution via a reversible manganese oxidation reaction (MOR)/manganese reduction reaction (MRR), respectively, induced by the inherent formation/dissolution of zinc basic sulfate in a mild aqueous electrolyte solution containing 2 M ZnSO4 and 0.2 M MnSO4.

Inositol hexakisphosphate kinase (IP6K) is an important mammalian enzyme involved in various biological processes such as insulin signalling and blood clotting. Recent analyses on drug metabolism and pharmacokinetic properties on TNP (N 2 -(m-trifluorobenzyl), N 6 -(p-nitrobenzyl)purine), a pan-IP6K inhibitor, have suggested that it may inhibit cytochrome P450 (CYP450) enzymes and induce unwanted drug-drug interactions in the liver. In this study, we confirmed that TNP inhibits CYP3A4 in type I binding mode more selectively than the other CYP450 isoforms. In an effort to find novel purine-based IP6K inhibitors with minimal CYP3A4 inhibition, we designed and synthesised 15 TNP analogs. Structure-activity relationship and biochemical studies, including ADP-Glo kinase assay and quantification of cell-based IP7 production, showed that compound 9 dramatically reduced CYP3A4 inhibition while retaining IP6K-inhibitory activity. Compound 9 can be a tool molecule for structural optimisation of purine-based IP6K inhibitors.

Highly dispersive molybdenum disulfide nanoflakes (MoS2 NFs), without any phase transition during the exfoliation process, are desirable for full utilization of their semiconductor properties in practical applications. Here, we demonstrate an innovate approach for fabricating MoS2 NFs by using hydrazine-assisted ball milling via the synergetic effect of chemical intercalation and mechanical exfoliation. The NFs obtained have a lateral size of 600–800 nm, a thickness less than 3 nm, and high crystallinity in the 2H semiconducting phase. They form a stable dispersion in various solvents, which will be helpful for many applications, due to the oxygen functional group. To investigate production of a two-dimensional (2D) photodetector, 2D semiconducting MoS2, MoS2–p-Si vertical devices were fabricated, and their optical properties were characterized. The photodiode exhibited consistent responses with excellent photo-switching characteristics with wavelengths of 850, 530, and 400 nm.

Background Combined decoction (CD)—boiling multiple herbs together—is a fundamental preparation method in Traditional Asian Medicine. While biological synergies are well documented, chemical interactions during the decoction process itself remain largely unexplored. Understanding these preparation-dependent chemical modifications is crucial for standardizing and modernizing traditional herbal medicines. Methods We developed a systematic analytical framework combining theoretical additive modeling with structural similarity analysis to investigate structure-dependent extraction in CD. Using Palmijihwang-tang as a proof-of-concept model, we used liquid chromatography–quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) to compare chemical profiles of CD with predicted profiles from individual decoctions (ID). We then predicted drug-likeness and bioactivity in silico and validated our findings with cell-based assays. Results CD systematically modified compound extraction based on structural features, selectively enhancing certain structural groups while suppressing others. These distinct extraction patterns correlated with the compounds' physicochemical properties, structural complexity, and predicted therapeutic properties—suggesting an empirically optimized process. Cell-based assays confirmed these chemical alterations lead to measurable biological differences between CD and ID preparations. Conclusions Our findings suggest that CD selectively modifies the chemical composition of herbal formulations through structure-dependent extraction, providing a preliminary chemical basis for better understanding traditional decoction practices. This highlights the critical importance of considering preparation methodology in herbal medicine standardization. Our analytical framework opens new avenues for investigating these CD effects across a wider range of traditional prescriptions. We believe this approach may ultimately contribute to the improved understanding and standardization of this fundamental method in Traditional Asian Medicine.