cis-Tetra­aqua­bis­{5-[4-(1H-imidazol-1-yl-κN 3)phen­yl]tetra­zolido}manganese(II) dihydrate

In the title compound, [Mn(C10H7N6)2(H2O)4]·2H2O, the complex unit comprises an Mn2+ ion, coordinated by two imidazole N atoms from cis-related monodentate 5-[4-(imidazol-1-yl)phen­yl]tetra­zolide ligands and four water mol­ecules, together with two water mol­ecules of solvation. The Mn2+ ion lies on a twofold rotation axis and has a slightly distorted octa­hedral geometry. The mol­ecules are connected by O—H⋯N and O—H⋯O hydrogen bonds involving both coordinated and solvent water mol­ecules, generating a three-dimensional structure. Two C atoms of the imidazole ring of the ligand are each disordered over two sites with occupancy factors of 0.75 and 0.25

Analysis of morphological differences in five large yellow croaker (<em>Larimichthys crocea</em>) populations

To explore the morphological and phenotypic characteristics and differences among different populations of Larimichthys crocea, traditional morphological measurements were carried out on three wild populations from Zhoushan, Xiamen and Zhanjiang and two farmed populations from Ningde and Wenzhou. Seven morphological parameters of five L. crocea populations were compared and analyzed. The results of one-way ANOVA showed significant differences in trunk and caudal stalk among the five populations. The contribution rates of the first five principal components to the total difference among different populations were 29.984%, 18.462%, 17.234%, 12.167%, and 9.904%, respectively, and the cumulative contribution rates were 87.751%. Trunk can be used to distinguish different geographic populations best. The cluster analysis results showed that the distance between wild populations was the closest, while the distance between farmed populations was far. The step discriminant method established the classification discriminant function of 5 populations. The discriminant accuracy P1 was 78.3%-92.7%, the discriminant accuracy P2 was 76.4%-96.5%, and the comprehensive recognition rate was 99.3%. The discriminant accuracy of this method was high, and it could provide a reference for the differentiation of different populations of L. crocea. This study provided basic morphological data for identifying a large yellow croaker population, protecting germplasm resources, and breeding improved varieties

catena-Poly[[(2,2′-bipyridine)­manganese(II)]-μ3-4,4′-sulfonyl­dibenzoato]

In the title compound, [Mn(C14H8O6S)(C10H8N2)]n, the MnII ion is coordinated by four O atoms from three 4,4′-sulfonyl­dibenzoate (sdba) ligands and two N atoms from one 2,2′-bipyridine (2,2′-bipy) ligand in a distorted octa­hedral geometry. The manganese atoms are alternately bridged either by two sdba ligands, with an Mn⋯Mn separation of 12.284 (1) Å, or by two carboxyl­ate groups from two sdba ligands, with an Mn⋯Mn separation of 4.064 (1) Å, thus producing polymeric chains propagated in [101]. Weak inter­molecular C—H⋯O hydrogen bonds and π–π inter­actions [centroid–centroid distance of 3.730 (3) Å between the aromatic rings of neighbouring polymeric chains] further stabilize the crystal packing

Transcriptome analysis of the allometric growth of golden pompano (<em>Trachinotus ovatus</em>) following soybean meal feed

Golden pompano (*Trachinotus ovatus*) is a marine fish of great commercial value. It was selected for a study on allometric growth using fermented soybean meal (SBM) as the primary protein source during an 8-week culture period. By comparing the gene expression levels of different individuals in the fermented soybean meal group, we discovered that 1026 genes exhibited significant changes in slow and fast-growth individuals. Among these genes, 358 showed high expression levels, while 668 showed low ones. Subsequently, we conducted go function annotation and KEGG pathway enrichment analysis on all the significantly differentially expressed genes. This analysis revealed that many of these genes were associated with oxidative phosphorylation, steroid biosynthesis, glyceride metabolism, alanine, aspartic acid, and glutamate metabolism. Identifying these differentially expressed genes is a foundation for unraveling the molecular mechanisms behind growth and development. Additionally, it provides valuable gene data for future studies on the cloning and expression of growth-related genes and offers insights for subsequent biological research

Analysis of morphological differences among different populations of golden pompano (<em>Trachinotus ovatus</em>)

To explore the external morphological differences of golden pompano in different geographical populations, eight quantitative traits of 210 samples from seven golden pompano populations were measured. Multivariate statistical methods, such as principal component analysis, discriminant analysis, cluster analysis, and One-way ANOVA, were used to compare morphological differences among the populations. Principal component analysis extracted the top five principal components with a cumulative contribution rate of 85.79%, of which the first three principal components could explain seven morphological features. The principal component scatter plot showed that the NH, CH, and LL populations had similar morphology. Using the stepwise discriminant method to establish the classification and discrimination functions of the seven populations, the discrimination accuracy of the DL population was 93.3% for P1 and 87.5% for P2, which was the highest, and the comprehensive discrimination rate was 71.4%. The clustering relationship diagram showed that the populations were divided into three branches, and the CH and NH populations were closest. In contrast, the DL and HF populations were farthest from the other populations. One-way ANOVA showed significant differences (P<0.05) among all traits of the populations, and the morphological differences between the HX and DL populations were the largest. The results of this study showed specific differences in the external morphology of golden pompano among different populations

The Transcriptional Factor PPARαb Positively Regulates Elovl5 Elongase in Golden Pompano Trachinotus ovatus (Linnaeus 1758)

The nuclear peroxisome proliferator-activated receptors (PPARs) regulate the transcription of elongases of very long-chain fatty acids (Elovl), which are involved in polyunsaturated fatty acid (PUFA) biosynthesis in mammals. In the present study, we first characterized the function of Elovl5 elongase in Trachinotus ovatus. The functional study showed that ToElovl5 displayed high elongation activity toward C18 and C20 PUFA. To investigate whether PPARαb was a regulator of Elovl5, we also reported the sequence of T. ovatus PPARαb (ToPPARαb). The open reading frame (ORF) sequence encoded 469 amino acids possessing four typical characteristic domains, including an N-terminal hypervariable region, a DNA-binding domain (DBD), a flexible hinge domain and a ligand-binding domain (LBD). Thirdly, promoter activity experiments showed that the region from PGL3-basic-Elovl5-5 (-146 bp to +459 bp) was defined as the core promoter by progressive deletion mutation of Elovl5. Moreover, PPARαb overexpression led to a clear time-dependent enhancement of ToElovl5 promoter expression in HEK 293T cells. Fourth, the agonist of PPARαb prominently increased PPARαb and Elovl5 expression, while PPARαb depletion by RNAi or an inhibitor was correlated with a significant reduction of Elovl5 transcription in T. ovatus caudal fin cells (TOCF). In conclusion, the present study provides the first evidence of the positive regulation of Elovl5 transcription by PPARαb and contributes to a better understanding of the transcriptional mechanism of PPARαb in fish

Anti-Neuroinflammatory Effects of the Calcium Channel Blocker Nicardipine on Microglial Cells: Implications for Neuroprotection

Background/Objective Nicardipine is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension following events such as ischemic stroke, traumatic brain injury, and intracerebral hemorrhage. However, accumulating evidence suggests that inflammatory processes in the central nervous system that are mediated by microglial activation play important roles in neurodegeneration, and the effect of nicardipine on microglial activation remains unresolved. Methodology/Principal Findings In the present study, using murine BV-2 microglia, we demonstrated that nicardipine significantly inhibits microglia-related neuroinflammatory responses. Treatment with nicardipine inhibited microglial cell migration. Nicardipine also significantly inhibited LPS plus IFN-γ-induced release of nitric oxide (NO), and the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Furthermore, nicardipine also inhibited microglial activation by peptidoglycan, the major component of the Gram-positive bacterium cell wall. Notably, nicardipine also showed significant anti-neuroinflammatory effects on microglial activation in mice in vivo. Conclusion/Significance The present study is the first to report a novel inhibitory role of nicardipine on neuroinflammation and provides a new candidate agent for the development of therapies for inflammation-related neurodegenerative diseases

A simulation study on the measurement of D0-D0bar mixing parameter y at BES-III

We established a method on measuring the \dzdzb mixing parameter $y$ for BESIII experiment at the BEPCII $e^+e^-$ collider. In this method, the doubly tagged $\psi(3770) \to D^0 \overline{D^0}$ events, with one $D$ decays to CP-eigenstates and the other $D$ decays semileptonically, are used to reconstruct the signals. Since this analysis requires good $e/\pi$ separation, a likelihood approach, which combines the $dE/dx$, time of flight and the electromagnetic shower detectors information, is used for particle identification. We estimate the sensitivity of the measurement of $y$ to be 0.007 based on a $20fb^{-1}$ fully simulated MC sample.Comment: 6 pages, 7 figure

Construction of a cross-species cell landscape at single-cell level.

Individual cells are basic units of life. Despite extensive efforts to characterize the cellular heterogeneity of different organisms, cross-species comparisons of landscape dynamics have not been achieved. Here, we applied single-cell RNA sequencing (scRNA-seq) to map organism-level cell landscapes at multiple life stages for mice, zebrafish and Drosophila. By integrating the comprehensive dataset of > 2.6 million single cells, we constructed a cross-species cell landscape and identified signatures and common pathways that changed throughout the life span. We identified structural inflammation and mitochondrial dysfunction as the most common hallmarks of organism aging, and found that pharmacological activation of mitochondrial metabolism alleviated aging phenotypes in mice. The cross-species cell landscape with other published datasets were stored in an integrated online portal-Cell Landscape. Our work provides a valuable resource for studying lineage development, maturation and aging