Association between urinary sodium and circulating lipid levels: a Mendelian randomization study

BackgroundUrinary sodium was indicated to be associated with dyslipidemia, but inconsistent conclusions for this association exist across the present observational studies.ObjectivesThis study aimed to evaluate the causal association between urinary sodium and circulating lipid levels [low-density lipoprotein cholesterol (LDL-C), triglycerides, and high-density lipoprotein cholesterol (HDL-C)] through Mendelian randomization.MethodsUnivariable Mendelian randomization (UVMR) and multivariable Mendelian randomization (MVMR) with pleiotropy-resistant methods were performed. Data for urinary sodium were obtained from the genome-wide association study (GWAS) from 446,237 European individuals. Data for lipid profiles were extracted from GWAS based on the UK Biobank (for the discovery analysis) and the Global Lipids Genetics Consortium (for the replication analysis).ResultsIn the discovery analysis, UVMR provided evidence that per 1-unit log-transformed genetically increased urinary sodium was associated with a lower level of HDL-C level (beta = −0.32; 95% CI: −0.43, −0.20; p = 7.25E−08), but not with LDL-C and triglycerides. This effect was still significant in the further MVMR when considering the effect of BMI or the other two lipid contents. In contrast, higher genetically predicted triglycerides could increase urinary sodium in both UVMR (beta = 0.030; 95% CI: 0.020, −0.039; p = 2.12E−10) and MVMR analyses (beta = 0.029; 95% CI: 0.019, 0.037; p = 8.13E−10). Similar results between triglycerides and urinary sodium were found in the replication analysis.ConclusionIncreased urinary sodium may have weak causal effects on decreased circulating HDL-C levels. Furthermore, genetically higher triglyceride levels may have independent causal effects on increased urinary sodium excretion

Analysis of changes in bacterial diversity in healthy and bacterial wilt mulberry samples using metagenomic sequencing and culture-dependent approaches

IntroductionMulberry bacterial wilt is a serious destructive soil-borne disease caused by a complex and diverse group of pathogenic bacteria. Given that the bacterial wilt has been reported to cause a serious damage to the yield and quality of mulberry, therefore, elucidation of its main pathogenic groups is essential in improving our understanding of this disease and for the development of its potential control measures.MethodsIn this study, combined metagenomic sequencing and culture-dependent approaches were used to investigate the microbiome of healthy and bacterial wilt mulberry samples.ResultsThe results showed that the healthy samples had higher bacterial diversity compared to the diseased samples. Meanwhile, the proportion of opportunistic pathogenic and drug-resistant bacterial flora represented by Acinetobacter in the diseased samples was increased, while the proportion of beneficial bacterial flora represented by Proteobacteria was decreased. Ralstonia solanacearum species complex (RSSC), Enterobacter cloacae complex (ECC), Klebsiella pneumoniae, K. quasipneumoniae, K. michiganensis, K. oxytoca, and P. ananatis emerged as the main pathogens of the mulberry bacterial wilt.DiscussionIn conclusion, this study provides a valuable reference for further focused research on the bacterial wilt of mulberry and other plants

Geochemical Insights from Clinopyroxene Phenocrysts into the Magma Evolution of an Alkaline Magmatic System from the Sanshui Basin, South China

The Sanshui Basin is located at the northern continental margin of the South China Sea and characterized by a continental rift basin. The bimodal volcanic rocks in Sanshui Basin record the early Cenozoic magmatic activity in the South China Block, but the magmatic evolution that produced the bimodal volcanic rocks is poorly understood. Clinopyroxenes in bimodal volcanic rocks in the Sanshui Basin provide an opportunity to investigate magma during magma ascent. In this work, we classified nine types of clinopyroxene phenocrysts according to composition and texture in cogenetic basalt-trachyandesite-comenditic trachyte, while the composition of unzoned clinopyroxene have an evolution sequence of diopside-hedenbergite-aegirine along with an increase in trace element contents with a decrease of Mg#, indicating that the genesis of clinopyroxene was dominated by fractional crystallization in a closed magma system. However, the clinopyroxenes with reversed zoning and multiple zoning record the process of magma mixing and recharge indicating an open magma system. While fractional crystallization is the dominant process, magma mixing, recharge, and crystal settling were also found to influence magma evolution. Thermobarometric calculations showed that clinopyroxene crystallized a several structural levels in the crust during magma ascent. In this study, we established a magma plumbing system that provides new constraints for the magma evolution in the Sanshui Basin

Geochemical Insights from Clinopyroxene Phenocrysts into the Magma Evolution of an Alkaline Magmatic System from the Sanshui Basin, South China

The Sanshui Basin is located at the northern continental margin of the South China Sea and characterized by a continental rift basin. The bimodal volcanic rocks in Sanshui Basin record the early Cenozoic magmatic activity in the South China Block, but the magmatic evolution that produced the bimodal volcanic rocks is poorly understood. Clinopyroxenes in bimodal volcanic rocks in the Sanshui Basin provide an opportunity to investigate magma during magma ascent. In this work, we classified nine types of clinopyroxene phenocrysts according to composition and texture in cogenetic basalt-trachyandesite-comenditic trachyte, while the composition of unzoned clinopyroxene have an evolution sequence of diopside-hedenbergite-aegirine along with an increase in trace element contents with a decrease of Mg#, indicating that the genesis of clinopyroxene was dominated by fractional crystallization in a closed magma system. However, the clinopyroxenes with reversed zoning and multiple zoning record the process of magma mixing and recharge indicating an open magma system. While fractional crystallization is the dominant process, magma mixing, recharge, and crystal settling were also found to influence magma evolution. Thermobarometric calculations showed that clinopyroxene crystallized a several structural levels in the crust during magma ascent. In this study, we established a magma plumbing system that provides new constraints for the magma evolution in the Sanshui Basin

Comparative Membrane Proteomics Reveals a Nonannotated E. coli Heat Shock Protein

Recent advances in proteomics and genomics have enabled discovery of thousands of previously nonannotated small open reading frames (smORFs) in genomes across evolutionary space. Furthermore, quantitative mass spectrometry has recently been applied to analysis of regulated smORF expression. However, bottom-up proteomics has remained relatively insensitive to membrane proteins, suggesting they may have been underdetected in previous studies. In this report, we add biochemical membrane protein enrichment to our previously developed label-free quantitative proteomics protocol, revealing a never-before-identified heat shock protein in Escherichia coli K12. This putative smORF-encoded heat shock protein, GndA, is likely to be ∼36–55 amino acids in length and contains a predicted transmembrane helix. We validate heat shock-regulated expression of the <i>gndA</i> smORF and demonstrate that a GndA-GFP fusion protein cofractionates with the cell membrane. Quantitative membrane proteomics therefore has the ability to reveal nonannotated small proteins that may play roles in bacterial stress responses

Comparative Membrane Proteomics Reveals a Nonannotated E. coli Heat Shock Protein

Recent advances in proteomics and genomics have enabled discovery of thousands of previously nonannotated small open reading frames (smORFs) in genomes across evolutionary space. Furthermore, quantitative mass spectrometry has recently been applied to analysis of regulated smORF expression. However, bottom-up proteomics has remained relatively insensitive to membrane proteins, suggesting they may have been underdetected in previous studies. In this report, we add biochemical membrane protein enrichment to our previously developed label-free quantitative proteomics protocol, revealing a never-before-identified heat shock protein in Escherichia coli K12. This putative smORF-encoded heat shock protein, GndA, is likely to be ∼36–55 amino acids in length and contains a predicted transmembrane helix. We validate heat shock-regulated expression of the <i>gndA</i> smORF and demonstrate that a GndA-GFP fusion protein cofractionates with the cell membrane. Quantitative membrane proteomics therefore has the ability to reveal nonannotated small proteins that may play roles in bacterial stress responses

Enhancing effect of vitexin on osteogenic activity of murine pre-osteoblastic MC3T3-E1 cells

Vitexin (5,7,4-trihydroxyflavone-8-glucoside), a natural flavone present in a variety of plants, is well known for its rich pharmacological properties. However, its osteogenic activity remains unclear to date. The purpose of this study was to explore the effects of vitexin on osteogenic activity in murine pre-osteoblastic MC3T3-E1 cells using the MTT assay for cell proliferation, alkaline phosphatase (ALP) activity assay for cell differentiation, and Von Kossa staining for cell mineralization. Quantitative real-time PCR was used for the detection of osteocalcin (OCN) mRNA expression in cells. Furthermore, effects of vitexin on the differentiation and matrix mineralization of dexamethasone (DEX)- suppressed cells was also investigated. The results showed vitexin could significantly enhance cell proliferation in a low concentration range of 10-10-10-6 μg mL-1. ALP activity was significantly increased after the cells were treated with vitexin at 10-8 and 10-6 μg mL-1. The expression levels of the osteogenic OCN gene in cells treated with vitexin at 10-6, 10- 8, and 10-10 μg mL-1 were improved by 3.1-fold, 5.8-fold, and 4.2-fold over the control, respectively. Additionally, vitexin (10-8 μg mL-1) significantly alleviated the inhibitory effect of osteoblast differentiation and mineralization induced by DEX. Collectively, our findings suggest vitexin could enhance cell proliferation and osteogenic differentiation of MC3T3-E1 cells, as well as rescue the inhibitory effect of cell differentiation and matrix mineralization induced by DEX. Therefore, vitexin may be useful as a promising therapeutic agent for bone disease and plays an important role in the prevention of glucocorticoid-induced osteoporosis

Synthesis of <i>Meso</i>-Halogenated BODIPYs and Access to <i>Meso</i>-Substituted Analogues

8-Halogenated boradiaza-<i>s</i>-indacenes can be efficiently prepared from dipyrrylketones. The new dyes react smoothly with nucleophiles to yield N-, O-, and S-substituted chromophores, as well as transition-metal-catalyzed cross-coupling reactions. The nature of the new substitutent has a strong influence on the spectral properties of the dyes

Similarities and differences between post-traumatic stress disorder and major depressive disorder: Evidence from task-evoked functional magnetic resonance imaging meta-analysis

Background: Post-traumatic stress disorder (PTSD) and major depressive disorder (MDD) are psychiatric disorders that can present with overlapping symptoms and shared risk factors. However, the extent to which these disorders share common underlying neuropathological mechanisms remains unclear. To investigate the similarities and differences in task-evoked brain activation patterns between patients with PTSD and MDD.// Methods: A coordinate-based meta-analysis was conducted across 35 PTSD studies (564 patients and 543 healthy controls) and 125 MDD studies (4049 patients and 4170 healthy controls) using anisotropic effect-size signed differential mapping software.// Results: Both PTSD and MDD patients exhibited increased neural activation in the bilateral inferior frontal gyrus. However, PTSD patients showed increased neural activation in the right insula, left supplementary motor area extending to median cingulate gyrus and superior frontal gyrus (SFG), and left fusiform gyrus, and decreased neural activation in the right posterior cingulate gyrus, right middle temporal gyrus, right paracentral lobule, and right inferior parietal gyrus relative to MDD patients.// Conclusion: Our meta-analysis suggests that PTSD and MDD share some similar patterns of brain activation, but also have distinct neural signatures. These findings contribute to our understanding of the potential neuropathology underlying these disorders and may inform the development of more targeted and effective treatment and intervention strategies. Moreover, these results may provide useful neuroimaging targets for the differential diagnosis of MDD and PTSD

A Blue-Light-Emitting BODIPY Probe for Lipid Membranes

Here we describe a new BODIPY-based membrane probe (1) that provides an alternative to dialkylcarbocyanine dyes, such as DiI-C18, that can be excited in the blue spectral region. Compound 1 has unbranched octadecyl chains at the 3,5-positions and a meso-amino function. In organic solvents, the absorption and emission maxima of 1 are determined mainly by solvent acidity and dipolarity. The fluorescence quantum yield is high and reaches 0.93 in 2-propanol. The fluorescence decays are well fitted with a single-exponential in pure solvents and in small and giant unilamellar vesicles (GUV) with a lifetime of ca. 4 ns. Probe 1 partitions in the same lipid phase as DiI-C18(5) for lipid mixtures containing sphingomyelin and for binary mixtures of dipalmitoylphosphatidylcholine (DPPC) and dioleoylphosphatidylcholine (DOPC). The lipid phase has no effect on the fluorescence lifetime but influences the fluorescence anisotropy. The translational diffusion coefficients of 1 in GUVs and OLN-93 cells are of the same order as those reported for DiI-C18. The directions of the absorption and emission transition dipole moments of 1 are calculated to be parallel. This is reflected in the high steady-state fluorescence anisotropy of 1 in high ordered lipid phases. Molecular dynamic simulations of 1 in a model of the DOPC bilayer indicate that the average angle of the transition moments with respect to membrane normal is ca. 70°, which is comparable with the value reported for DiI-C18.status: publishe