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Aquaporin 2 (AQP2) contributes to water reabsorption and urine concentration by migrating to the luminal surface of the collecting ducts in an anti-diuretic hormone-stimulated manner, and the signaling pathway involved in AQP2 subcellular localization is a target for arginine vasopressin receptor antagonists (aquaretics). This study investigated the involvement of AQP2 in the diuretic effect and mechanisms of Goreisan (GRS), a traditional Japanese Kampo medicine used to treat conditions such as edema in patients with decreased urination. GRS exerted diuretic effects on desmopressin (DDAVP)-induced decreases in urine output and the level of AQP2 phosphorylated at Serine269 (pSer269-AQP2) in the renal tissues of mice. Furthermore, GRS inhibited the accumulation of pSer269-AQP2 to the luminal side following forskolin stimulation using a 3D culture model of the kidney collecting duct cell line mIMCD-3. GRS induced a transient increase in the intracellular Ca 2+ concentration via the calcium-sensing receptor (CaSR) and suppressed the forskolin-stimulated increase in cAMP production. These results suggest that GRS regulates urine volume by modulating the subcellular localization of AQP2 via CaSR.

Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in a mouse model of influenza infection. On the fifth day of oral administration to mice intranasally infected with influenza virus [A/PR/8/34 (H1N1)], maoto significantly improved survival rate, decreased viral titer, and ameliorated the infection-induced phenotype as compared with control mice. Analysis of the lung and plasma transcriptome and lipid mediator metabolite profile showed that maoto altered the profile of lipid mediators derived from ω-6 and ω-3 fatty acids to restore a normal state, and significantly up-regulated the expression of macrophage- and T-cell-related genes. Collectively, these results suggest that maoto regulates the host’s inflammatory response by altering the lipid mediator profile and thereby ameliorating the symptoms of influenza.

Although the importance of the host tissue microenvironment in cancer progression and metastasis has been established, the spatiotemporal process establishing a cancer metastasis‐prone tissue microenvironment remains unknown. In this study, we aim to understand the immunological character of a metastasis‐prone microenvironment in a murine 4T1 breast tumor model, by using the activation of nuclear factor‐κb (NF‐κB) in cancer cells as a sensor of inflammatory status and by monitoring its activity by bioluminescence imaging. By using a 4T1 breast cancer cell line stably expressing an NF‐κB/Luc2 reporter gene (4T1 NF‐κB cells), we observed significantly increased bioluminescence approximately 7 days after metastasis‐prone orthotopic mammary fat‐pad inoculation but not ectopic s.c. inoculation of 4T1 NF‐κB cells. Such in vivo NF‐κB activation within the fat‐pad 4T1 tumor was diminished in immune‐deficient SCID or nude mice, or T cell‐depleted mice, suggesting the requirement of host T cell‐mediated immune responses. Given the fat‐pad 4T1 tumor expressed higher inflammatory mediators in a T cell‐dependent mechanism compared to the s.c. tumor, our results imply the importance of the surrounding tissue microenvironment for inflaming tumors by collaborating with T cells to instigate metastatic spread of 4T1 breast cancer cells. In this study, we aim to understand the immunological character of a metastasis‐prone microenvironment in a murine 4T1 breast tumor model, by utilizing the activation of nuclear factor‐κb (NF‐κB) in cancer cells as a sensor of inflammatory status and by monitoring its activity by bioluminescence imaging. By using a 4T1 breast cancer cell line stably expressing an NF‐κB/Luc2 reporter gene, we observed significantly increased bioluminescence around 7 days after metastasis‐prone orthotopic mammary fat‐pad inoculation but not ectopic subcutaneous inoculation. Such in vivo NF‐κB activation within the fat‐pad 4T1 tumor was diminished in immune‐deficient SCID or nude mice, or T cell‐depleted mice, suggesting the requirement of host T cell‐mediated immune responses. Given the fat‐pad 4T1 tumor expressed higher inflammatory mediators in T cell‐dependent mechanism as compared to the subcutaneous tumor, our results imply the importance of the surrounding tissue microenvironment for inflaming tumors by collaborating with T cells to instigate metastatic spread of 4T1 breast cancer cells.

Objectives: This study investigated the potential of Hounsfield unit (HU) values obtained from computed tomography (CT) scans as predictors of mechanical complications (MCs) in patients undergoing long-segment spinal fusion involving the pelvis. Additionally, it identified a threshold HU value associated with an increased risk of MCs. Methods: We conducted a retrospective, multicenter review of patients who underwent long-segment spinal fusion involving the pelvis, with a minimum follow-up period of two years. Patients were categorized based on the presence or absence of postoperative MCs. Both preoperative and postoperative radiographic parameters were analyzed, and HU values were quantified from CT images. Logistic regression modeling was used to identify independent risk factors for MCs. Results: Among 129 patients, 33 (25.6%) developed MCs, including proximal and distal junctional failures, rod fractures, and cases necessitating re-operation. The HU values were significantly lower in the MC group, whereas conventional bone mineral density (BMD) measurements showed no significant difference. Global alignment parameters, such as the sagittal vertical axis (SVA) and global tilt (GT), were consistently higher in patients with MCs. Receiver operating characteristic analysis identified 131 HU as the optimal cut-off, yielding a sensitivity of 56.4% and a specificity of 69.7%. Multivariate analysis confirmed that lower HU values were independently associated with the occurrence of MCs. Conclusions: Lower HU values and larger radiological global alignment parameters are significant predictors of MCs in patients undergoing surgery for adult spinal deformity. These findings underscore the importance of CT-based quantitative assessments in preoperative planning.

Chemotherapy-induced peripheral neuropathy is a major dose-limiting side effect of commonly used chemotherapeutic agents. However, there are no effective strategies to treat the neuropathy. We examined whether Goshajinkigan, a herbal medicine, would prevent paclitaxel-induced allodynia without affecting the anticancer action in mice. Murine breast cancer 4T1 cells were inoculated into the mammary fat pad. Paclitaxel (10 and 20 mg/kg, intraperitoneal, alternate day from day 7 postinoculation) inhibited the tumor growth, and Goshajinkigan (1 g/kg, oral, daily from day 2 postinoculation) did not affect the antitumor action of paclitaxel. Mechanical allodynia developed in the inoculated region due to tumor growth and in the hind paw due to paclitaxel-induced neuropathy. Paclitaxel-induced allodynia was markedly prevented by Goshajinkigan, although tumor-associated allodynia was not inhibited by Goshajinkigan. These results suggest that Goshajinkigan prevents paclitaxel-induced peripheral neuropathy without interfering with the anti-cancer action of paclitaxel.

Purpose To determine the most valid bone health parameter to predict mechanical complications (MCs) following surgery for adult spinal deformity (ASD). Methods This multicenter study retrospectively examined the records of patients who had undergone fusion of three or more motion segments, including the pelvis, with a minimum two-year follow-up period. Patients with moderate and severe global alignment and proportion scores were included in the study and divided into two groups: those who developed MCs and those who did not. Bone mineral density (BMD) of the lumbar spine and femoral neck was measured using dual-energy X-ray absorptiometry, and Hounsfield units (HUs) were measured in the lumbar spine on computed tomography. Radiographic parameters were evaluated preoperatively, immediately after surgery, and at final follow-up. Results Of 108 patients, 30 (27.8%) developed MCs, including 26 cases of proximal junctional kyphosis/failure, 2 of distal junctional failure, 6 of rod fracture, and 11 reoperations. HUs were significantly lower in patients who experienced MCs (113.7 ± 41.1) than in those who did not (137.0 ± 46.8; P  = 0.02). BMD did not differ significantly between the two groups. The preoperative and two-year postoperative global tilt, as well as the immediately postoperative sagittal vertical axis, were significantly greater in patients who developed MCs than in those who did not ( P  = 0.02, P  < 0.01, and P  = 0.01, respectively). Conclusion Patients who experienced MCs following surgery for ASD had lower HUs than those who did not. HUs may therefore be more useful than BMD for predicting MCs following surgery for ASD.

d-serine administration prevents kidney damage in murine models of acute kidney injury, and risperidone inhibits the activity of d-amino acid oxidase, which regulate plasma d-amino acid levels. This pilot randomized controlled trial investigated the effects of risperidone on glucose, amino acid metabolism, and kidney function in healthy adults. Healthy adults with a homeostasis model assessment of insulin resistance (HOMA-IR) of ≥ 1.6 and estimated glomerular filtration rate (eGFR) of ≥ 60 mL/min/1.73m2 were randomly assigned to the risperidone and control groups. The risperidone group received 0.5 mg/day risperidone for 4 days. The primary outcome was mean change in HOMA-IR on day 5, and the secondary outcomes were changes in d-amino acid levels, eGFR, and urinary albumin. Seven participants were randomized to the risperidone and control groups. The changes in HOMA-IR, eGFR, and urinary albumin on day 5 were not significantly different between the two groups (all p > 0.05). Mean changes in plasma d-serine level and urinary d-serine/creatinine ratio were significantly higher in the risperidone group than in the control group (0.2 vs. -0.3 nmol/mL, p = 0.03 and 38.2 vs. -25.8 nmol/mL, p = 0.01, respectively). Short-term risperidone affects d-serine metabolism without instigating acute adverse effects on kidney or glucose homeostasis in healthy individuals. Clinical Trial Registry number: This study was registered with the Japan Registry for Clinical Trials (jRCTs041210165).

The FeMo-cofactor of nitrogenase, a metal–sulfur cluster that contains eight transition metals, promotes the conversion of dinitrogen into ammonia when stored in the protein. Although various metal–sulfur clusters have been synthesized over the past decades, their use in the activation of N 2 has remained challenging, and even the FeMo-cofactor extracted from nitrogenase is not able to reduce N 2 . Herein, we report the activation of N 2 by a metal–sulfur cluster that contains molybdenum and titanium. An N 2 moiety bridging two [Mo 3 S 4 Ti] cubes is converted into NH 3 and N 2 H 4 upon treatment with Brønsted acids in the presence of a reducing agent. Nitrogenase—whose cofactor consists of a metal–sulfur cluster—catalyzes the production of NH 3 from N 2 , but designing metal–sulfur complexes capable of promoting this conversion remains challenging. Here, the authors report on the activation of N 2 by a metal–sulfur cluster containing [Mo 3 S 4 Ti] cubes, demonstrating NH 3 and N 2 H 4 production.

The FeMo-cofactor of nitrogenase, a metal-sulfur cluster that contains eight transition metals, promotes the conversion of dinitrogen into ammonia when stored in the protein. Although various metal-sulfur clusters have been synthesized over the past decades, their use in the activation of N has remained challenging, and even the FeMo-cofactor extracted from nitrogenase is not able to reduce N . Herein, we report the activation of N by a metal-sulfur cluster that contains molybdenum and titanium. An N moiety bridging two [Mo S Ti] cubes is converted into NH and N H upon treatment with Brønsted acids in the presence of a reducing agent.

Water at interfaces plays crucial roles in various natural phenomena and in the material sciences. Therefore, understanding the structure and hydrogen-bonding network at such interfaces is essential. Recent advances in porous crystalline materials, combined with single-crystal X-ray diffraction techniques, have enabled the visualization of molecular structures on pore surfaces at atomic resolution. Herein, we report the formation of a supramolecular porous crystal composed of a resorcin[4]arene and a rigid cationic coordination complex, stabilized by hydrogen bonds and noncovalent interactions. This specific arrangement creates a porous framework with anisotropic, information-rich surfaces, accommodating water molecules to form multi-layered water channels. The analysis reveals clustering motifs and hydrogen-bonding patterns in the water molecules at interfaces, supported by molecular dynamics simulations and spectroscopy studies. These findings advance our understanding of the structure–property relationship of water at interfaces in low-entropy crystalline materials, offering insights into their behavior on complex surfaces. Water at interfaces plays crucial roles in various natural phenomena and in material sciences. Here, the authors report the formation of a supramolecular crystal forming a porous framework with anisotropic, information-rich surfaces, accommodating water molecules to form multi-layered water channels.