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In this paper, firstly, on the basis of Marx’s theory of intersubjectivity, we use the concept of teachers and students as the main body of each other to construct the interactive teaching mode and mechanism of teachers and students in Civics courses and actively explore the path and prospect of interactive teaching of Civics in courses in the new era. Then we use the pure strategy game in game theory to determine the performance production function, and then we use Nash equilibrium to obtain the teacher utility function and student utility function on the basis of the performance production function so as to further construct the game model of teacher-student behavior in the teaching process of Civics courses, and analyze the teacher-student interaction in the Civics of higher education courses by using the game model. The results show that in the pure strategy game analysis of teacher-student behavior, 0.3872 teachers will choose to reduce teaching inputs, while the other 0.6128 teachers will choose to reduce teaching inputs to “almost no” or “very little”, i.e., the optimal choice strategy is “no” or “very little”, i.e., the optimal choice strategy is “no” or “very little”. The optimal choice strategy is “no reduction in instructional inputs”. In the Nash equilibrium analysis of teacher-student behavior, the equilibrium value of the teacher-student behavior game is (42.22% and 64.59%), and teachers and students need to continuously improve their behavioral strategy choices in order to achieve the maximum utility value of each other. This study improves the quality of teaching and ultimately achieves the objective of Civic Education.

Metallabenzenes are recognized as a unique class of aromatic compounds, not only of structural and theoretical interest but also as platforms to design powerful transformations. Here, we report the successful transmutation of a metallabenzene for pyridine synthesis. This ‘metal-to-nitrogen swapping’ process utilizes readily available ruthenabenzene phosphonium salts and commercially available 2-aminopyridines under mild conditions. The isolation of ruthena-azepines, containing a planar seven-membered aza-metallacycle, along with DFT calculations, supports the nitrogen insertion/metal deletion cascade driven by aromatization. Additionally, we investigate the tunable photophysical properties of the resulting pyridine phosphonium salts. Metallabenzenes are recognized as a unique class of aromatic compounds, not only of structural and theoretical interest but also as platforms to design powerful transformations. Here, the authors report the successful transmutation of a metallabenzene for pyridine synthesis.

Fluoride, a geochemical element, can damage the brain and result in dysfunction of the central nervous system. In recent years, fluoride-induced neurotoxicity has become one of research focuses of environmental toxicology. Our previous study showed that fluoride could induce the structural damages of the cerebral cortex and reduce the learning and memory abilities of mice offspring. However, the underlying mechanisms of these effects remain unclear. In this study, primary neurons were isolated from the cerebral cortices of postnatal 1-day SD rats. The primary cultured cerebral cortical neurons were adherent and the cellular network was obvious. Neurons were identified by Nissl’s staining and were used for experiments. Different concentrations of sodium fluoride (0.5, 1.0, 1.5, 2.0 and 2.5 mM) were chosen to explore its toxic effects on neuron of SD rats in vitro. Results showed that neuronal morphology was obviously damaged in 2.0 and 2.5 mM, but was not adversely affected in 0.5 and 1 mM. Further studies revealed that the neurites of neuron were shrunken and even became fractured with the increase in NaF dose, which have been detected by scanning electron microscopy (SEM). Meanwhile, TEM showed marginated chromatin, widened nuclear gaps, damaged nuclei and swollen or even absent mitochondria in 1.5, 2 and 2.5 mM group. The cytoskeletal staining was consistent with the above results. The number of neurites of cerebral cortical neuron significantly decreased after fluoride exposure by immunofluorescent assay. In summary, high fluoride (1.5, 2 and 2.5 mM) concentrations exerted a significant toxic effect on the cellular morphologies and neural formation of primary cultured cortical neurons. These findings provide new insights into the roles of NaF in neuronal damage and can contribute to an improved understanding of fluoride-induced neurotoxicity.

In this study, biochar was generated from chicken manure by using a tube furnace under different temperatures (300, 500, and 700 °C), and the treatments were noted as J300, J500, and J700, respectively. In comparison, another type of biochar was prepared under 500 °C with a muffle furnace, and the treatment was noted as JM500. Biochar in treatment group J500 was subsequently modified with HNO 3 and NaOH, and the treatments were noted as J500-HNO 3 and J500-NaOH, respectively. The sorption efficiencies of naphthalene by the above six types of biochar were evaluated. Characteristic results showed that the surface pores of the biochar were improved with the increase of temperature, and biochar under the treatments J300, J500, J700, and JM500 experienced a high speed of adsorption within 1 h after the naphthalene adsorption started. The adsorption capacity of naphthalene increased with the increase of the initial concentration of naphthalene. Treatment J700 exhibited the largest adsorption capacity since its biochar surface pore structure was more fully developed with a crystal structure formed, and its specific surface area was increased by about 20 times compared to the original chicken manure. After biochar modification using HNO 3 and NaOH, the infrared spectrum changed, and the adsorption active sites were increased. The biochar modification by HNO 3 had a high naphthalene adsorption efficiency compared to NaOH. The order of adsorption capacity was as follows: J500 ≈ JM500 < J300 < J500-NaOH < J500-HNO 3 < J700.

Objective: Coat color is an important characteristic and economic trait in domestic sheep. In this study, we explored the potential mechanisms and the signaling pathways involved in coat color regulation for sheep.Methods: Isobaric tags for relative and absolute quantification (iTRAQ) technology was used to catalog global protein expression profiles in skin of sheep with black versus white coat color. Immunofluorescence was used to observe the expression localization of differential protein. Western blot and quantitative real time polymerase chain reaction (qRT-PCR) were used to evaluate their role in the coat color formation of sheep.Results: A total of 136 differential proteins were obtained in different coat colors, including 101 up-regulated and 35 down-regulated. Pigmentation function entries were enriched through gene ontology annotation. Tyrosine metabolism and platelet activation signaling pathway were extracted by Kyoto encyclopedia of genes and genomes analysis. Apolipoprotein A-1 (APOA1) and fibrinogen alpha chain (FGA) were found to be critical differential proteins by the interaction of differential proteins in the direct-interaction network diagram. Strikingly, twenty candidate differential proteins were screened, from which beta-actin (ACTB) protein showed higher expression in white sheep skin, while albumin (ALB), APOA1, MAOA (amine oxidase) and FGA proteins showed higher expression in black sheep skin, which was validated by immunofluorescence, western blot, and qRT-PCR.Conclusion: This study identified several novel proteins that may be involved in the coat color formation of sheep. The white and black sheep skin proteome profiles obtained provide a valuable resource for future research to understand the network of protein expression controlling skin physiology and melanogenesis in sheep.

Objective: Pigment production and distribution are controlled through multiple proteins, resulting in different coat color phenotypes of sheep.Methods: The expression distribution of vimentin (VIM) and transthyretin (TTR) in white and black sheep skins was detected by liquid chromatography–electrospray ionization tandem MS (LC–ESI–MS/MS), gene ontology (GO) statistics, immunohistochemistry, Western blot, and quantitative real time polymerase chain reaction (qRT-PCR) to evaluate their role in the coat color formation of sheep.Results: LC–ESI–MS/MS results showed VIM and TTR proteins in white and black skin tissues of sheep. Meanwhile, GO functional annotation analysis suggested that VIM and TTR proteins were mainly concentrated in cellular components and biological process, respectively. Further research confirmed that VIM and TTR proteins were expressed at significantly higher levels in black sheep skins than in white sheep skins by Western blot, respectively. Immunohistochemistry notably detected VIM and TTR in hair follicle, dermal papilla, and outer root sheath of white and black sheep skins. qRT-PCR results also revealed that the expression of VIM and TTR mRNAs was higher in black sheep skins than in white sheep skins.Conclusion: The expression of VIM and TTR were higher in black sheep skins than in white sheep skins and the transcription and translation were unanimous in this study. VIM and TTR proteins were expressed in hair follicles of white and black sheep skins. These results suggested that VIM and TTR were involved in the coat color formation of sheep.

Pareuchiloglanis longicauda, a Sisorid fish that is distributed in the upper Pearl River. In this study, the complete mitogenome of P. longicauda was sequenced using traditional Sanger sequencing approach. The 16,588 bp genome was consisted of 2 rRNAs, 22tRNAs, 13 protein-coding genes (PCGs) and 1 control region. The 13 PCGs started with a traditional ATG and end with stop codon TAA, TAG, TGA, TA or a single T base. Phylogenetic analysis based on 13 PCGs from 22 species using maximum-likelihood method produced three major clades (Clade I, II and III). Unexpectedly, our mitogenome exhibited only 92.12% identity to the previously published one (GenBank accession no. KP872693) with differences mainly located in the gene region. Furthermore, Pareuchiloglanis did not form a monophyletic genus and P. longicauda had the closest relationship with P. macrotrema. The result suggested that more complete mitogenomes are needed to reveal the phylogenetic placement of Pareuchiloglanis in the family Sisoridae.

An automatic tensioner that consists of a torsional spring and friction damping elements is widely used in belt drive system. The relation of the applied torque versus the imposed angle of tensioner during loading and unloading processes is described as a hysteretic loop. An analytical model is established for estimating the hysteretic behavior of a tensioner, and measurements for hysteretic loop in quasi-static and dynamic excitation are carried out to validate the analytical model. Taking one engine timing belt drive system as a studying example, the method and the procedure for estimating vibration responses of the nonlinear tensioner are given. An iterative algorithm for predicting the accurate equivalent viscous damping of tensioner is carried out in analyzing a belt drive system. The vibration responses of tensioner are validated by the measurement of timing belt drive system. The developed method presented in this article is useful for predicting the hysteretic behavior of tensioner, vibration responses, and the parameters optimization of a belt drive system.

Florfenicol (FLO), which is widely used in veterinary clinics and aquaculture, can disrupt the protein synthesis of bacteria and mitochondria and, thus, lead to antibacterial and toxic effects in plants, insects, and mammals. FLO was found to repress chicken embryonic development and induce early embryonic death previously, but the underlying mechanism is not fully understood. Clarifying the mechanism of FLO-induced embryonic toxicity is important to the research and development of new drugs and the rational use of FLO to ensure human and animal health and ecological safety. In this study, the effects of FLO on pluripotency, proliferation, and differentiation were investigated in P19 stem cells (P19SCs). We also identified differentially expressed genes and performed bioinformatics analysis to obtain hub genes and conducted some functional analysis. FLO inhibited the proliferation and pluripotency of P19SCs and repressed the formation of embryoid bodies derived from P19SCs. A total of 2,396 DEGs were identified using RNA-Seq in FLO-treated P19SCs, and these genes were significantly enriched in biological processes, such as angiogenesis, embryonic organ development, and morphogenesis of organs. Kyoto encyclopedia of genes and genome-based pathway analysis also showed that five relevant pathways, especially the canonical Wnt pathway, were engaged in FLO-induced toxicity of pluripotent stem cells. We further analyzed modules and hub genes and found the involvement of ubiquitin-mediated proteolysis, DNA replication, and cell cycle machinery in regulating the pluripotency and proliferation of FLO-treated P19SCs. In summary, our data suggest that FLO disrupts the signaling transduction of pathways, especially the canonical Wnt pathway, and further inhibits the expression of target genes involved in regulating DNA replication, cell cycle, and pluripotency. This phenomenon leads to the inhibition of proliferation and differentiation in FLO-treated P19SCs. However, further experiments are required to validate our findings and elucidate the potential mechanisms underlying FLO-induced embryonic toxicity.

Florfenicol (FLO) has been shown to elicit diverse toxic effects in plants, insects, and mammals. Previously, our investigations revealed that FLO induced abnormal cardiac development and early embryonic mortality in chicken embryos. However, the effect of FLO on mitochondrial responses in stem cells remains unclear. In this study, we show that FLO significantly diminishes proliferation viability and obstructs the directed differentiation of P19 stem cells (P19SCs) into cardiomyocytes. Proteomic analysis revealed 148 differentially expressed proteins in response to FLO. Functional analysis has pinpointed FLO interference with biological processes associated with oxidative phosphorylation within the mitochondria. In alignment with the results of proteomic analysis, we confirmed that FLO inhibits the expression of both nuclear DNA-encoded and mitochondrial DNA-encoded subunits of the electron transport chain. Subsequent experiments demonstrated that FLO disrupts mitochondrial dynamics and induces the mitochondrial unfolded protein response to maintain mitochondrial homeostasis. These findings collectively highlight the significance of mitochondrial dynamics and the mitochondrial unfolded protein response to mediate the decreased proliferation viability and directed differentiation potential in P19SCs treated with FLO. In conclusion, this study provides a comprehensive overview of mitochondrial responses to FLO-induced cytotoxicity and enhances our understandings of the molecular mechanisms underlying FLO-induced embryonic toxicity.