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A longstanding goal in regenerative medicine is to reconstitute functional tissues or organs after injury or disease. Attention has focused on the identification and relative contribution of tissue specific stem cells to the regeneration process. Relatively little is known about how the physiological process is regulated by other tissue constituents. Numerous injury models are used to investigate tissue regeneration, however, these models are often poorly understood. Specifically, for skeletal muscle regeneration several models are reported in the literature, yet the relative impact on muscle physiology and the distinct cells types have not been extensively characterised. We have used transgenic Tg:Pax7nGFP and Flk1GFP/+ mouse models to respectively count the number of muscle stem (satellite) cells (SC) and number/shape of vessels by confocal microscopy. We performed histological and immunostainings to assess the differences in the key regeneration steps. Infiltration of immune cells, chemokines and cytokines production was assessed in vivo by Luminex®. We compared the 4 most commonly used injury models i.e. freeze injury (FI), barium chloride (BaCl2), notexin (NTX) and cardiotoxin (CTX). The FI was the most damaging. In this model, up to 96% of the SCs are destroyed with their surrounding environment (basal lamina and vasculature) leaving a \"dead zone\" devoid of viable cells. The regeneration process itself is fulfilled in all 4 models with virtually no fibrosis 28 days post-injury, except in the FI model. Inflammatory cells return to basal levels in the CTX, BaCl2 but still significantly high 1-month post-injury in the FI and NTX models. Interestingly the number of SC returned to normal only in the FI, 1-month post-injury, with SCs that are still cycling up to 3-months after the induction of the injury in the other models. Our studies show that the nature of the injury model should be chosen carefully depending on the experimental design and desired outcome. Although in all models the muscle regenerates completely, the trajectories of the regenerative process vary considerably. Furthermore, we show that histological parameters are not wholly sufficient to declare that regeneration is complete as molecular alterations (e.g. cycling SCs, cytokines) could have a major persistent impact.

Ion leaching from pure-phase oxygen-evolving electrocatalysts generally exists, leading to the collapse and loss of catalyst crystalline matrix. Here, different from previous design methodologies of pure-phase perovskites, we introduce soluble BaCl 2 and SrCl 2 into perovskites through a self-assembly process aimed at simultaneously tuning dual cation/anion leaching effects and optimizing ion match in perovskites to protect the crystalline matrix. As a proof-of-concept, self-assembled hybrid Ba 0.35 Sr 0.65 Co 0.8 Fe 0.2 O 3- δ (BSCF) nanocomposite (with BaCl 2 and SrCl 2 ) exhibits the low overpotential of 260 mV at 10 mA cm -2 in 0.1 M KOH. Multiple operando spectroscopic techniques reveal that the pre-leaching of soluble compounds lowers the difference of interfacial ion concentrations and thus endows the host phase in hybrid BSCF with abundant time and space to form stable edge/face-sharing surface structures. These self-optimized crystalline structures show stable lattice oxygen active sites and short reaction pathways between Co–Co/Fe metal active sites to trigger favorable adsorption of OH − species. Water oxidation catalysis may provide the electrons needed for sustainable fuel production, but catalysts often degrade under working conditions. Here, authors introduce soluble species into perovskites to exert positive ion leaching effects for enhancing perovskite stability and activity.

There is an increasing public awareness of the relatively new and expanded industrial barium uses which are potential sources of human exposure (e.g., a shale gas development that causes an increased awareness of environmental exposures to barium). However, absorption of barium in exposed humans and a full spectrum of its health effects, especially among chronically exposed to moderate and low doses of barium populations, remain unclear. We suggest a systematic literature review (from 1875 to 2014) on environmental distribution of barium, its bioaccumulation, and potential and proven health impacts (in animal models and humans) to provide the information that can be used for optimization of future experimental and epidemiological studies and developing of mitigative and preventive strategies to minimize negative health effects in exposed populations. The potential health effects of barium exposure are largely based on animal studies, while epidemiological data for humans, specifically for chronic low-level exposures, are sparse. The reported health effects include cardiovascular and kidney diseases, metabolic, neurological, and mental disorders. Age, race, dietary patterns, behavioral risks (e.g., smoking), use of medications (those that interfere with absorbed barium in human organism), and specific physiological status (e.g., pregnancy) can modify barium effects on human health. Identifying, evaluating, and predicting the health effects of chronic low-level and moderate-level barium exposures in humans is challenging: Future research is needed to develop an understanding of barium bioaccumulation in order to mitigate its potential health impacts in various exposured populations. Further, while occupationally exposed at-risk populations exist, it is also important to identify potentially vulnerable subgroups among non-occupationally exposed populations (e.g., elderly, pregnant women, children) who are at higher risk of barium exposure from drinking water and food.

Barium chloride (BaCl2), a known environmental pollutant, induces organ-specific oxidative stress through disruption of redox homeostasis. This study evaluated the protective effects and safety profile of sodium copper chlorophyllin (SCC) and ascorbic acid (ASC) against BaCl2-induced oxidative damage in the liver and brain of mice using a two-phase experimental protocol. Animals received either SCC (40 mg/kg), ASC (160 mg/kg), or their combination for 14 days prior to BaCl2 exposure (150 mg/L in drinking water for 7 days), allowing evaluation of both preventive and therapeutic effects. Toxicological and behavioral assessments confirmed the absence of systemic toxicity or neurobehavioral alterations following supplementation. Body weight, liver and kidney indices, and biochemical markers (Aspartate Aminotransferase (ASAT), Alanine Aminotransferase (ALAT), creatinine) remained within physiological ranges, and no anxiogenic or locomotor effects were observed. In the brain, BaCl2 exposure significantly increased SOD (+49%), CAT (+66%), GPx (+24%), and GSH (+26%) compared to controls, reflecting a robust compensatory antioxidant response. Although lipid peroxidation (MDA) showed a non-significant increase, SCC, ASC, and their combination reduced MDA levels by 42%, 37%, and 55%, respectively. These treatments normalized antioxidant enzyme activities and GSH, indicating an effective neuroprotective effect. In contrast, the liver exhibited a different oxidative profile. BaCl2 exposure increased MDA levels by 80% and GSH by 34%, with no activation of SOD, CAT, or GPx. Histological analysis revealed extensive hepatocellular necrosis, vacuolization, and inflammatory infiltration. SCC significantly reduced hepatic MDA by 39% and preserved tissue architecture, while ASC alone or combined with SCC exacerbated inflammation and depleted hepatic GSH by 71% and 78%, respectively, relative to BaCl2-exposed controls. Collectively, these results highlight a differential, organ-specific response to BaCl2-induced oxidative stress and the therapeutic potential of SCC and ASC. SCC emerged as a safer and more effective agent, particularly in hepatic protection, while both antioxidants demonstrated neuroprotective effects when used individually or in combination.

Synthesis is a major challenge in the discovery of new inorganic materials. Currently, there is limited theoretical guidance for identifying optimal solid-state synthesis procedures. We introduce two selectivity metrics, primary and secondary competition, to assess the favorability of target/impurity phase formation in solid-state reactions. We used these metrics to analyze 3520 solid-state reactions in the literature, ranking existing approaches to popular target materials. Additionally, we implemented these metrics in a data-driven synthesis planning workflow and demonstrated its application in the synthesis of barium titanate (BaTiO3). Using an 18-element chemical reaction network with first-principles thermodynamic data from the Materials Project, we identified 82985 possible BaTiO3 synthesis reactions and selected 9 for experimental testing. Characterization of reaction pathways via synchrotron powder X-ray diffraction reveals that our selectivity metrics correlate with observed target/impurity formation. We discovered two efficient reactions using unconventional precursors (BaS/BaCl2 and Na2TiO3) that produce BaTiO3 faster and with fewer impurities than conventional methods, highlighting the importance of considering complex chemistries with additional elements during precursor selection. Our framework provides a foundation for predictive inorganic synthesis, facilitating the optimization of existing recipes and the discovery of new materials, including those not easily attainable with conventional precursors.

The objective of this work is to investigate the interaction of turbulence with the nonlinear processes of particle nucleation and growth that occur in reaction crystallisation, also known as precipitation. A validated methodology for coupling the population balance equation with direct numerical simulation of turbulent flows is employed for simulating an experiment conducted by Schwarzer et al. (Chem. Engng Sci., vol. 61, no. 1, 2006, pp. 167–181), where barium sulphate nanoparticles are formed by mixing and reaction of barium chloride and sulphate acid in a T-mixer, with the spatial resolution resolved down to the Kolmogorov scale. A unity Schmidt number is assumed, since at present it is not possible to resolve the Batchelor scale for realistic Schmidt numbers (order of 1000 or more). The probability density function, filtered averages and spatial distribution of time and length scales are all examined in order to shed light on the interplay of turbulence and precipitation. Separate Damköhler numbers are defined for nucleation and growth and both are found to be close to unity, indicating that the process is neither mixing nor kinetics controlled. The nucleation length scales are also evaluated and compared with the Kolmogorov scale to show the importance of resolving nucleation bursts. In addition, zones of different rate-determining mechanisms are identified. The ultimate aim of precipitation is to obtain control over the product particle size distribution, and the present study elucidates the synergistic or competing roles of mixing, nucleation and growth on the process outcome and discusses the implications for modelling.

Considering the current absence of adequate equipment at home and abroad to directly detect the ion content of formation water under high temperature and pressure conditions. A static experiment was established to examine the solubility of ions in fluids. The effect of cations on the solubility of CaCO 3 at different temperatures and pressures was investigated through experiments, and the variation law of ion content and its internal relationship under high temperature and pressure conditions were studied. In solution of barium chloride and magnesium chloride, the solubility of CaCO 3 increases gradually as the level of its concentration. At the same concentration, the solubility of CaCO 3 show decreases first and then increases trend as the level of temperature. In the solution of strontium chloride, as the level of strontium chloride concentration, and the solubility of CaCO 3 was progressively reduced. At the same concentration, the solubility of CaCO 3 decreases first and then increases as the level of temperature. under the influence of carbon dioxide, the solubility of CaCO 3 gradually decreases with increasing temperature. influence of pressure on the solubility of CaCO 3 at low temperature is larger. The solubility of CaCO 3 exhibits minimal variation as the level of PCO 2 at higher temperature. However, when the pressure reaches a certain degree (above 3MPa), the a downward trend in solubility was observed.

BaTiS 3 , a quasi-1D complex chalcogenide, has gathered considerable scientific and technological interest due to its giant optical anisotropy and electronic phase transitions. However, the synthesis of high-quality BaTiS 3 crystals, particularly those featuring crystal sizes of millimeters or larger, remains a challenge. Here, we investigate the growth of BaTiS 3 crystals utilizing a molten salt flux of either potassium iodide, or a mixture of barium chloride and barium iodide. The crystals obtained through this method exhibit a substantial increase in volume compared to those synthesized via the chemical vapor transport method, while preserving their intrinsic optical and electronic properties. Our flux growth method provides a promising route toward the production of high-quality, large-scale single crystals of BaTiS 3 , which will greatly facilitate advanced characterizations of BaTiS 3 and its practical applications that require large crystal dimensions. Additionally, our approach offers an alternative synthetic route for other emerging complex chalcogenides. Graphical Abstract

Pepsinogen is an inactive enzyme (proenzyme) secreted by chief cells in the stomach. One source is the stomach of catfish, a by-product of fisheries that has not been fully utilized. The study aimed to characterize the pepsinogen precipitate from the stomach of Clarias sp. The research method involved partially purifying pepsinogen precipitate from catfish stomachs using 30% ammonium sulfate. The study also characterized pepsinogen, including its optimal temperature, optimal pH, effect of metal ions, and enzyme kinetics. Results showed that catfish pepsinogen had an optimum temperature of 50°C (341.92±24.17 U/mL) and an optimum pH of 5 (364.42±28.60 U/mL). Relative activity toward metal ions NaCl, MgCl 2 , BaCl 2 , CuCl 2 , ZnCl 2 , and FeCl 3 was 182.50±13.65 U/mL, 190.67±13.79 U/mL, 164.58±0.57 U/mL, 301.92±14.74 U/mL, 259.75±41.42 U/mL, and 643.50±0.00 U/mL, respectively. The addition of FeCl 3 metal ions increased the reaction rate. Other metal ions decreased the reaction rate. Catfish stomach pepsinogen had Vmax and Km values of 83.33 mmol/s and 0.62 mM, respectively.