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Industrially, NH3 production mainly relies on the energy-intensive Haber–Bosch process with the release of a large amount of CO2. Electrochemical fixation of N2 to NH3 under ambient conditions is an environmentally friendly and sustainable alternative, but the N2 reduction reaction (NRR) requires stable and efficient electrocatalysts. In this work, we report that the electrocatalytic NRR activity of Pd nanoparticles can be improved by surface modification with oxygen-rich tannic acid. The electrochemical test results in 0.1 M Na2SO4 suggest that such a catalyst achieves a large NH3 yield of 24.12 μg h−1 mgcat.−1 and a high faradaic efficiency of 9.49% at −0.45 V vs. the reversible hydrogen electrode (RHE), rivaling the performances of most of the reported aqueous-based NRR electrocatalysts. In addition, it also shows strong long-term electrochemical stability. [ABSTRACT FROM AUTHOR]

The interaction of chemokine (C-X-C motif) ligand 10 (CXCL10) with its receptor (CXCR3) is a critical process in recruiting donor reactive T cells to a graft and alloantigen-specific memory T (Tm) cells exert a principal function in promoting graft dysfunction during accelerated cardiac rejection. However, whether CXCL10 chemokine exerts any effects on acute accelerated rejection mediated by CD8+ Tm cells in a re-transplant model has remained elusive. The present study established a cardiac transplant model by advanced microsurgery technology and improved organ storage. A novel rat model of cardiac re-transplantation was established at 40 days following primary heart transplant. The experiment included two parts, and when models were established, the rats were divided into two groups: Primary cardiac transplant (HTx) and re-transplantation without treatment (HRTx). In part 1, recipients from part 2, including re-transplantation without treatment (HRTx+NS) and re-transplantation treated with anti-CXCL10 antibodies (500 µg every other day by intraperitoneal injection; HRTx+CXCL10 Abs group). The graft survival time was observed and graft infiltration by inflammatory cells was assessed via histology of cardiac graft sections; in addition, the gene expression and the serum concentration of CXCL10 in each group was assessed. Indexes such as rejection-associated cytokines were assayed by reverse-transcription quantitative PCR and ELISA kits, and flow cytometry of splenocytes was used to detect Tm cells in the re-transplantation groups. The results demonstrated that level of CXCL10 was significantly increased and the graft mean survival time was shortened accompanied with aggravated lymphocyte cell infiltration in the HRTx group when compared that in the HTx group; in addition, the serum levels and mRNA expression of interleukin (IL)-2 and interferon (IFN)-γ were increased, while transforming growth factor (TGF)-β was decreased in the HRTx group. Furthermore, neutralization of CXCL10 prolonged the graft mean survival time and delayed accelerated rejection. Compared with that in the HRTx+NS group, serum levels and graft tissue mRNA expression of IFN-γ and IL-2 were decreased in the HRTx+CXCL10 Abs group, while TGF-β mRNA was significantly increased but the serum concentration was not significantly affected. In addition, there was no difference in IL-10 between the two groups, while delayed accelerated rejection paralleled with inflammatory cell infiltration decreased and the proliferation and differentiation of CD8+ Tm cells in secondary lymphoid organs were reduced in the HRTx+CXCL10 Abs group vs. those in the HRTx+NS group. The present study demonstrated that CXCL10 had a crucial role in cardiac transplantation and re-transplantation, and that treatment with CXCL10 antibodies delays accelerated acute rejection mediated by Tm cells in a rat model of cardiac re-transplantation. [ABSTRACT FROM AUTHOR]

With climate change, significant fluctuations in wildfires have been observed on the Mongolian Plateau. The ability to predict the distribution of wildfires in the context of climate change plays a critical role in wildfire management and ecosystem maintenance. In this paper, Ripley's K function and a Random Forest (RF) model were applied to analyse the spatial patterns and main influencing factors affecting the occurrence of wildfire on the Mongolian Plateau. The results showed that the wildfires were mainly clustered in space due to the combination of influencing factors. The distance scale is less than 1/2 of the length of the Mongolian Plateau; that is, it does not experience boundary effects in the study area and it meets the requirements of Ripley's K function. Among the driving factors, the fraction of vegetation coverage (FVC), land use degree (La), elevation, precipitation (pre), wet day frequency (wet), and maximum temperature (tmx) had the greatest influences, while the aspect had the lowest influence. The likelihood of fire was mainly concentrated in the northern, eastern, and southern parts of the Mongolian Plateau and in the border area between the Inner Mongolia Autonomous Region (Inner Mongolia) and Mongolian People's Republic (Mongolia), and wildfires did not occur or occurred less frequently in the hinterland area. The fitting results of the RF model showed a prediction accuracy exceeding 90%, which indicates that the model has a high ability to predict wildfire occurrences on the Mongolian Plateau. This study can provide a reference for predictions and decision-making related to wildfires on the Mongolian Plateau. [ABSTRACT FROM AUTHOR]

Background: Previous observational studies have investigated the association between educational attainment and sepsis, pneumonia, and urinary tract infections (UTIs). However, their findings have been susceptible to reverse causality and confounding factors. Furthermore, no study has examined the effect of educational level on the risk of infections of the skin and subcutaneous tissue (SSTIs). Thus, we aimed to evaluate the causal relationships between educational level and the risk of four infectious diseases using Mendelian randomisation (MR) techniques., Methods: We used univariable MR analysis to investigate the causal associations between educational attainment (years of schooling (n = 766 345) and holding college or university degree (n = 334 070)) and four infectious diseases (sepsis (n = 486 484), pneumonia (n = 486 484), UTIs (n = 463 010), and SSTIs (n = 218 792)). We included genetic instrumental variables with a genome-wide significance (P < 5 × 10 -8 ) in the study. We used inverse variance-weighted estimation in the primary analysis and explored the stability of the results using multivariable MR analysis after adjusting for smoking, alcohol consumption, and body mass index., Results: Genetically predicted years of schooling were associated with a reduced risk of sepsis (odds ratio (OR) = 0.763; 95% confidence interval (CI) = 0.668-0.870, P = 5.525 × 10 -5 ), pneumonia (OR = 0.637; 95% CI = 0.577-0.702, P = 1.875 × 10 -19 ), UTIs (OR = 0.995; 95% CI = 0.993-0.997, P = 1.229 × 10 -5 ), and SSTIs (OR = 0.696; 95% CI = 0.605-0.801, P = 4.034 × 10 -7 ). We observed consistent results for the correlation between qualifications and infectious diseases. These findings remained stable in the multivariable MR analyses., Conclusions: Our findings suggest that increased educational attainment may be causally associated with a decreased risk of sepsis, pneumonia, UTIs, and SSTIs., Competing Interests: Disclosure of interest: The authors completed the ICMJE Disclosure of Interest Form (available upon request from the corresponding author) and declare no conflicts of interest., (Copyright © 2024 by the Journal of Global Health. All rights reserved.)

The interaction of chemokine (C-X-C motif) ligand 10 (CXCL10) with its receptor (CXCR3) is a critical process in recruiting donor reactive T cells to a graft and alloantigen-specific memory T (Tm) cells exert a principal function in promoting graft dysfunction during accelerated cardiac rejection. However, whether CXCL10 chemokine exerts any effects on acute accelerated rejection mediated by CD8 + Tm cells in a re-transplant model has remained elusive. The present study established a cardiac transplant model by advanced microsurgery technology and improved organ storage. A novel rat model of cardiac re-transplantation was established at 40 days following primary heart transplant. The experiment included two parts, and when models were established, the rats were divided into two groups: Primary cardiac transplant (HTx) and re-transplantation without treatment (HRTx). In part 1, recipients from part 2, including re-transplantation without treatment (HRTx+NS) and re-transplantation treated with anti-CXCL10 antibodies (500 µg every other day by intraperitoneal injection; HRTx+CXCL10 Abs group). The graft survival time was observed and graft infiltration by inflammatory cells was assessed via histology of cardiac graft sections; in addition, the gene expression and the serum concentration of CXCL10 in each group was assessed. Indexes such as rejection-associated cytokines were assayed by reverse-transcription quantitative PCR and ELISA kits, and flow cytometry of splenocytes was used to detect Tm cells in the re-transplantation groups. The results demonstrated that level of CXCL10 was significantly increased and the graft mean survival time was shortened accompanied with aggravated lymphocyte cell infiltration in the HRTx group when compared that in the HTx group; in addition, the serum levels and mRNA expression of interleukin (IL)-2 and interferon (IFN)-γ were increased, while transforming growth factor (TGF)-β was decreased in the HRTx group. Furthermore, neutralization of CXCL10 prolonged the graft mean survival time and delayed accelerated rejection. Compared with that in the HRTx+NS group, serum levels and graft tissue mRNA expression of IFN-γ and IL-2 were decreased in the HRTx+CXCL10 Abs group, while TGF-β mRNA was significantly increased but the serum concentration was not significantly affected. In addition, there was no difference in IL-10 between the two groups, while delayed accelerated rejection paralleled with inflammatory cell infiltration decreased and the proliferation and differentiation of CD8 + Tm cells in secondary lymphoid organs were reduced in the HRTx+CXCL10 Abs group vs. those in the HRTx+NS group. The present study demonstrated that CXCL10 had a crucial role in cardiac transplantation and re-transplantation, and that treatment with CXCL10 antibodies delays accelerated acute rejection mediated by Tm cells in a rat model of cardiac re-transplantation.