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ABSTRACT Background Azvudine (FNC) is a novel small molecule antiviral drug for treating COVID‐19 that is available only on the Chinese market. Despite being recommended for treating COVID‐19 by the Chinese guidelines, its efficacy and safety are still unclear. This study aimed to evaluate the protective effect of FNC on COVID‐19 outcomes and its safety. Methods We followed the PRISMA 2020 guidelines and searched the PubMed, Embase, Web of Science, Scopus, and China National Knowledge Infrastructure (CNKI) databases to evaluate studies on the effectiveness of FNC in treating COVID‐19 in China, focusing on mortality and overall outcomes. Additionally, its impact on the length of hospital stay (LOHS), time to first nucleic acid negative conversion (T‐FNANC), and adverse events was evaluated. The inclusion criterion was that the studies were published from July 2021 to April 10, 2024. This study uses the ROBINS‐I tool to assess bias risk and employs the GRADE approach to evaluate the certainty of the evidence. Results The meta‐analysis included 24 retrospective studies involving a total of 11 830 patients. Low‐certainty evidence revealed no significant difference in mortality (OR = 0.91, 95% CI: 0.76–1.08) or LOHS (WMD = −0.24, 95% CI: −0.83 to 0.35) between FNC and Paxlovid in COVID‐19 patients. Low‐certainty evidence shows that the T‐FNANC was longer (WMD = 1.95, 95% CI: 0.36–3.53). Compared with the Paxlovid group, low‐certainty evidence shows the FNC group exhibited a worse composite outcome (OR = 0.77, 95% CI: 0.63–0.95) and fewer adverse events (OR = 0.63, 95% CI: 0.46–0.85). Compared with supportive treatment, low certainty shows FNC significantly reduced the mortality rate in COVID‐19 patients (OR = 0.61, 95% CI: 0.51–0.74) and decreased the composite outcome (OR = 0.67, 95% CI: 0.50–0.91), and very low certainty evidence shows significantly decreased the T‐FNANC (WMD = −4.62, 95% CI: −8.08 to −1.15). However, in very low certainty, there was no significant difference in LOHS (WMD = −0.70, 95% CI: −3.32 to 1.91) or adverse events (OR = 1.97, 95% CI: 0.48–8.17). Conclusions FNC appears to be a safe and potentially effective treatment for COVID‐19 in China, but further research with larger, high‐quality studies is necessary to confirm these findings. Due to the certainty of the evidence and the specific context of the studies conducted in China, caution should be exercised when considering whether the results are applicable worldwide. Trial Registration PROSPERO number: CRD42024520565

In response to the challenges posed by complex background textures and limited hardware resources in fabric defect detection, this study proposes a lightweight fabric defect detection algorithm based on an improved GSL-YOLOv8n model. Firstly, to reduce the parameter count and complexity of the YOLOv8n network, the GhostNet concept is used to construct the C2fGhost module, replacing the conventional convolution layers in the YOLOv8n structure with Ghost convolutions. Secondly, the SimAM parameter-free attention mechanism is embedded at the end of the backbone network to eliminate redundant background, enhance semantic information for small targets, and improve the network’s feature extraction capability. Lastly, a lightweight shared convolution detection head is designed, employing the scale layer to adjust features, ensuring the lightweight nature of the model while minimizing precision loss. Compared to the original YOLOv8n model, the improved GSL-YOLOv8n algorithm increases the mAP@0.5 by 0.60% to 98.29% and reduces model size, computational load, and parameter count by 66.7%, 58.0%, and 67.4%, respectively, meeting the application requirements for fabric defect detection in textile industry production.

Introduction: Dopamine is one of the most significant neurotransmitters and plays an important role in the management of cognitive functions such as learning, memory, and behavior. The disorder of dopamine is associated with many major mental diseases. It is necessary to develop selective methods for the detection of dopamine.Methods: In this work, carbon dots (CDs) were synthesized by a solvothermal route using glutathione, L-histidine, and formamide as sources.Results: Under light irradiation, The CDs convert dissolved oxygen to singlet oxygen (1O2), which could oxidize TMB. When reduced dopamine was present, it suppressed the catalysis of CDs, then the absorption of the CDs-coupled TMB complex at 652 nm was diminished. Furthermore, it was revealed that the surface groups including hydroxyl, amino, carbonyl, and carboxyl groups of CDs were related to their light-responsive catalytic activity by surface modification. In the range of 0.5-15 μM, the CDs could afford a LOD of 0.25 μM for dopamine detection with fine linearity, also showing good selectivity.Discussion: The results from fetal bovine serum indicated the good applicability of the CDs in the determination of dopamine.

Several studies have shown that the level of trust between agents is a determinant of financial decisions. This paper studies this issue further by analyzing whether the trust distance between two countries can explain bilateral stock market correlations among emerging countries. One finding is that a smaller trust distance among nations is related to a higher stock market correlation. This effect seems to be more pronounced in active-trading countries than thin-trading countries. Finally, we confirm the effect of trust distance upon stock market correlations by excluding extreme observations. Keywords: International financial markets, Stock market correlation, Trust distance, JEL classification: G15, F15, D31, G11

In the past few decades, how to reduce the computational complexity of dealing with $k$ -valued logical networks (LNs) has become a heated research topic. This paper firstly presents a brief survey on the recent efforts of dealing with large-scale LNs, including approximation of LNs, network aggregation approach, and logical matrix factorization technique. Then, by using the network aggregation approach, the stability of large-scale network pairing problem is studied. The network aggregation approach is also used to study probabilistic logical networks (PLNs). Finally, an illustrative example is given to demonstrate the effectiveness of the obtained results.

Background/Aims: Ginsenoside Rb1 (GS-Rb1) is one of the most important active pharmacological extracts of the Traditional Chinese Medicine ginseng, with extensive evidence of its cardioprotective properties. Mir-208 has been shown to act as a biomarker of acute myocardial infarction in vivo studies including man. However the impact of miR-208 on the protective effect of GS-Rb1 in hypoxia/ischemia injured cardiomyocytes remains unclear. The current study aims to investigate the target gene of miR-208 and the impact on the protective effect of GS-Rb1 in hypoxia/ischemia (H/I) injuried cardiomyocytes. Materials and Methods: Primary cultures of neonatal rat cardiomyocytes (NRCMs) was subjected to the H/I conditions with or without GS-Rb1. Cell viability was calculated by MTT assay and confirmed by flow cytometry analysis. Mir-208 was then detected by qRT-PCR. Luciferase reporter assay was carried out to detect the target gene of Mir-208. Then the NRCMs were transfected with miR-208 mimics and inhibitors to evaluate the impact on cardioprotective properties of Rb1. Results: The miR-208 expression level was clearly upregulated in the H/I treated NRCMs accompanied by the percentage of the apoptotic cells which could be reversed by GS-Rb1 pretreatment. The nemo-like kinase (NLK) mRNA and protein expression levels were decreased in H/I group measured by RT-PCR and western blotting. Luciferase activity assay was then carried out to identify that NLK may be a direct target of mir-208. MTT assay showed that miR-208 inhibitor slightly decreased the protective effect of Rb1 on the H/I impaired NRCMs. However, results showed no statistical difference. Conclusions: These findings proved that NLK was a direct target of mir-208 and miR-208 act indirectly during Rb1 protecting H/I impaired NRCMs and further researches were needed to explore the relationship that microRNAs and other signal pathways in the protective effect of GS-Rb1 on the hypoxia/ischemia injuries in cardiomyocytes.

Background: This study aims to uncover the potential correlation between LTC4S -444 A>C polymorphism and susceptibility to asthma. Methods: Literatures reporting the correlation between LTC4S -444 A>C polymorphism and susceptibility to asthma published before 1st June, 2019 were searched in PubMed, Embase, Cochrane, Wanfang and CNKI. Eligible literatures were enrolled and their data were extracted. OR and its 95% Cl were calculated for assessing the correlation between LTC4S -444 A>C polymorphism and susceptibility to asthma. The included data were weighted by an inverse variance and then analyzed by a fixed or random effects model. Heterogeneity test and sensitivity analysis were performed on the enrolled reports. STATA12.1 and TSA (trial sequential analysis) were utilized for analyses. Results: Fifteen studies involving 3,791 asthma patients and 2,185 healthy controls were enrolled. No significant correlation was found between the LTC4S -444 A> C polymorphism and susceptibility to asthma according to the results of different models ((Dominant model (D): OR=1.10, 95% Cl=0.98-1.23; Recessive model (R): 1.07, 0.84-1.36; Homozygous model (Homo): 1.11, 0.87-1.41; Heterozygous model (Hetero): 1.10, 0.98-1.24; Allele model (A): 1.07, 0.98-1.18). Subgroup analyses carried out in Asian and Caucasian population, as well as in population-based and hospital-based controls obtained the same conclusions. Conclusion: No significant correlation is identified between the LTC4S -444 A>C polymorphism and susceptibility to asthma. Researches with high-quality and large sample size are required for further validation in multi-center hospital. [ABSTRACT FROM AUTHOR]

The goal of this study was to investigate the impact of coriander root extract on the migration and proliferation of the BGC-823 gastric cancer cell line, as well as to establish a theoretical and experimental foundation for the prevention and treatment of gastric cancer using coriander root. Clonal formation of BGC-823 cells was significantly reduced and cell proliferation was inhibited by coriander root extract; The invasion number of gastric cancer cells was reduced, the scratch healing ability was significantly reduced, and the cell migration ability was inhibited. The results showed that coriander root extract could inhibit the EMT process. After the action of coriander root extract, β-catenin and TGF-β/SMAD pathway genes like P-GSK-3β, TGF-β, and P-SMAD2/3 were decreased; The increased expression of SMAD2/3 and Gsk-3β suggested that coriander root extract may be mediated by βCatenin and TGF-β/SMAD pathway regulated the proliferation and migration of BGC-823 cell of gastric cancer. Further analysis found that α- The human gastric cancer cell line BGC-823's growth and invasion were reduced by linalool. Coriander root extract, especially α-Linalool, which can be mediated by β-Catenin and TGF-β/SMAD pathway, inhibited the proliferation and migration of gastric cancer BGC-823 cells. [ABSTRACT FROM AUTHOR]

Ginsenoside (GS-Rb1) is one of the most important active compounds of ginseng, with extensive evidence of its cardioprotective properties. However, the miRNA mediated mechanism of GS-Rb1 on cardiomyocytes remains unclear. Here, the roles of miRNAs in cardioprotective activity of GS-Rb1 were investigated in hypoxic- and ischemic-damaged cardiomyocytes. Neonatal rat cardiomyocytes (NRCMs) were first isolated, cultured, and then incubated with or without GS-Rb1 (2.5-40 µM) in vitro under conditions of hypoxia and ischemia. Cell growth, proliferation, and apoptosis were detected by MTT and flow cytometry. Expressions of various microRNAs were analyzed by real-time PCR. Compared with that of the control group, GS-Rb1 significantly decreased cell death in a dose-dependent manner and expressions of mir-1, mir-29a, and mir-208 obviously increased in the experimental model groups. In contrast, expressions of mir-21 and mir-320 were significantly downregulated and GS-Rb1 could reverse the differences in a certain extent. The miRNAs might be involved in the protective effect of GS-Rb1 on the hypoxia/ischemia injuries in cardiomyocytes. The effect might be based on the upregulation of mir-1, mir-29a, and mir-208 and downregulation of mir-21 and mir-320. This might provide us a new target to explore the novel strategy for ischemic cardioprotection. [ABSTRACT FROM AUTHOR]

Aim. To investigate the effect of Ginsenoside Rb1 (GS-Rb1) on hypoxia/ischemia (H/I) injury in cardiomyocytes in vitro and the mitochondrial apoptotic pathway mediated mechanism. Methods. Neonatal rat cardiomyocytes (NRCMs) for the H/I groups were kept in DMEM without glucose and serum, and were placed into a hypoxic jar for 24 h. GS-Rb1 at concentrations from2.5 to 40 μM was given during hypoxic period for 24 h. NRCMs injury was determined by MTT and lactate dehydrogenase (LDH) leakage assay. Cell apoptosis, ROS accumulation, and mitochondrial membrane potential (MMP) were assessed by flow cytometry. Cytosolic translocation ofmitochondrial cytochrome c and Bcl-2 family proteins were determined byWestern blot. Caspase-3 and caspase-9 activities were determined by the assay kit. Results. GS-Rb1 significantly reduced cell death and LDH leakage induced by H/I. It also reduced H/I induced NRCMs apoptosis induced by H/I, in accordance with a minimal reactive oxygen species (ROS) burst. Moreover,GS-Rb1markedly decreased the translocation of cytochrome c from themitochondria to the cytosol, increased the Bcl-2/ Bax ratio, and preserved mitochondrial transmembrane potential (ΔΨm). Its administration also inhibited activities of caspase-9 and caspase-3. Conclusion. Administration of GS-Rb1 during H/I in vitro is involved in cardioprotection by inhibiting apoptosis, which may be due to inhibition of the mitochondrial apoptotic pathway. [ABSTRACT FROM AUTHOR]

Background. Licorice has long been used to treat many ailments including cardiovascular disorders in China. Recent studies have shown that the cardiac actions of licorice can be attributed to its active component, glycyrrhetinic acid (GA). However, the mechanism of action remains poorly understood. Aim. The effects of GA on the delayed rectifier potassium current (IK), the rapidly activating (iKr) and slowly activating (iKs) components of iK, and the HERG K+ channel expressed in HEK-293 cells were investigated. Materials and Methods. Single ventricular myocytes were isolated from guinea pig myocardium using enzymolysis. The wild type HERG gene was stably expressed in HEK293 cells. Whole-cell patch clamping was used to record IK (iKr, IKs) and the HERG K+ current. Results. GA (1,5, and 10 ΜM) inhibited IK (iKr, IKs) and the HERG K+ current in a concentration-dependent manner. Conclusion. GA significantly inhibited the potassium currents in a dose- and voltage-dependent manner, suggesting that it exerts its antiarrhythmic action through the prolongation of APD and ERP owing to the inhibition of IK (iKr, IKs)) and HERG K+ channel. [ABSTRACT FROM AUTHOR]