OBJECTIVE To explore the mechanism of Chaiqi yigan granules （CQYG） against liver cancer through the ferroptosis pathway. METHODS Network pharmacology combined with ferroptosis-related database was used to screen key targets and main effective components of CQYG against liver cancer via regulating ferroptosis； molecular docking technology was employed to analyze the binding ability of main active components to key targets. Human liver Huh-7 cells were divided into blank serum control （CON） group， CQYG drug-containing serum （CQYGKL） group， ferroptosis inducer （RSL3） group， mammalian target of rapamycin complex 1 （mTORC1） inhibitor （RMC-5552） group， mTORC1 agonist （CCT007093） group， and CCT007093+CQYGKL group. The levels of Fe 2+ ， malondialdehyde （MDA）， and glutathione （GSH） in the cells were detected in the former three groups； mRNA expressions of mammalian target of rapamycin （mTOR）， sterol regulatory element-binding protein 1 （SREBP1）， and stearoyl-CoA desaturase 1 （SCD1）， protein expressions of SREBP1 and SCD1 as well as phosphorylation levels of mTOR and ribosomal S6 kinase （S6K） proteins were detected in all groups. RESULTS Key targets of CQYG for anti-liver cancer through the ferroptosis pathway were mTOR， SREBP1， SCD1，etc. The main active components included quercetin， tanshinone Ⅱ A ， baicalein， etc. The binding energies of main active components to key targets were all less than －5 kJ/mol. Compared with CON group， the levels of Fe 2+ and MDA in the cells in CQYGKL group and RSL3 group were significantly increased， while the levels of GSH were significantly decreased （ P ＜0.05）. mRNA expressions of mTOR， SREBP1 and SCD1， protein expressions of SREBP1 and SCD1， as well as the phosphorylation levels of mTOR and S6K proteins were significantly decreased in the CQYGKL group， RSL3 group， and RMC-5552 group， whereas all the above indicators were significantly increased in the CCT007093 group （ P ＜0.05）. Compared with CCT007093 group， the changes in all the above indicators were significantly suppressed in the CCT007093+CQYGKL group （ P ＜0.05）. CONCLUSIONS CQYG may induce ferroptosis by inhibiting mTORC1/SREBP1/SCD1 axis， thereby exerting anti-liver cancer effects.

In recent years, the incidence of liver metastasis from colorectal cancer has continued to rise, posing a significant threat to human health and life.Although traditional treat-ments such as surgery and chemotherapy have shown some efficacy in certain patients, options remain limited for those who are not surgical candidates or are resistant to chemotherapy.Yttrium-90 microsphere selective internal radiation therapy, as an innovative local treatment, has fully demons-trated its effectiveness and safety in treating colorectal cancer liver metastasis patients. The authors review the research background, mechanisms, and principles of yttrium-90 microsphere selective internal radiation therapy in the field of colorectal cancer liver metastasis, and to explore its applica-tion progress in clinical practice, aiming to provide clinical doctors with more comprehensive and detailed reference information, with the goal of improving treatment outcomes and quality of life for colorectal cancer liver metastasis patients.

Objective:To assess the effects of probiotic supplementation following bariatric surgery on weight loss outcomes, glycemic and lipid metabolism profiles, and nutritional status.Methods:Searches were conducted across China National Knowledge Infrastructure (CNKI), WanFang, VIP, Web of Science, and PubMed using Chinese or English search words including probiotics, morbid obesity, severe obesity, bariatric surgery, sleeve gastrectomy, Roux-en-Y gastric bypass, SG, and RYGB up to May 31, 2024. Meta-analysis was performed using Review Manager 5.3. Study quality was evaluated using Cochrane risk of bias tool.Results:In the 12 randomized controlled trials (RCTs) containing 663 severely obese patients who underwent bariatric surgery, 329 were in the probiotic group (receiving probiotic supplementation following bariatric surgery) and 334 in the control group (using placebo). Compared with the control group, the probiotic group had significantly lower fasting blood glucose ( WMD=-4.42 mg/dL, 95% CI: -7.71–-1.13, P=0.009) and triglyceride ( WMD=-18.75 mg/dL, 95% CI: -35.83–-1.67, P=0.03) and significantly increased vitamin B 12 ( SMD=0.52, 95% CI: 0.02–1.02, P=0.04). However, the two groups showed no significant differences in body mass index, waist circumference, weight, % excess weight loss, hemoglobin A1c, insulin, homeostasis model assessment of insulin resistance, total cholesterol, low-density lipoprotein, high-density lipoprotein, or vitamin D levels (all P>0.05). Conclusion:Supplementing probiotics after bariatric surgery can improve glucose and lipid metabolism and increase vitamin B 12 absorption, whereas its potential effect on weight loss remains unclear.

Objective To investigate the forensic toxicological characteristics associated with etomidate abuse.Methods Blood and urine samples from six cases of etomidate abuse were quantitatively analyzed for etomidate and its metabolite etomidate acid.Relevant literature on etomidate abuse and poisoning was reviewed to summarize the pharmacological and toxicological effects of etomidate and case data.Results In the cases examined,the blood concentrations of etomidate and its metabolite,etomidate acid,were relatively low,ranging from 1.97～187.61 ng/mL and 12.29～316.31 ng/mL,respectively.Urine samples offered a broader detection window,with etomidate concentrations ranging from 1.65 to 700.89 ng/mL and etomidate acid concentrations from 295.26～214 483.52 ng/mL.Notably,in a sexual assault case,the victims's blood concentration of etomidate acid dropped below 6.98 ng/mL eight hours post-ingestion,while urinary concentration was still above 59 449.02 ng/mL.Conclusion Abuse of electronic cigarettes containing etomidate can result in severe overdoses.Given that etomidate is rapidly metabolized in vivo,it is essential to collect and analyze biological samples promptly,with a particular emphasis on detecting its metabolite,etomidate acid.

Objective To explore the clinical efficacy of using 3D patches to repair inguinal hernia in laparoscopic transabdominal preperitoneal inguinal hernia repair(TAPP).Methods A retrospective study was conducted on 102 patients with inguinal hernia.All the patients were treated with laparoscopic TAPP.The patients were divided into two groups based on the different patch methods used after the surgery.The patients who used ordinary patches were in the ordinary patch group(n=50),and the patients who used 3D patches were in the 3D patch group(n=52).The surgery-related conditions,postoperative pain,postoperative complications and recurrence of the two groups of patients were compared.Results The 3D patch group had shorter surgery time,first exhaust time,got out of bed mobility time,less hospital stay and intraoperative bleeding volume than those in the ordinary patch group,the differences were statistically significant(P<0.05).On the 1,3,and 5 d after surgery,the visual analogue scale(VAS)scores of patients in the 3D patch group were lower than those in the ordinary patch group,the differences were statistically significant(P<0.05).The total complications rate in the 3D patch group was 5.77%,which was significantly lower than the 20.00%in the ordinary patch group,the difference was statistically significant(P<0.05).There was no statistically significant difference in the postoperative recurrence rate between the two groups of patients(P>0.05).Conclusion For patients with inguinal hernia,administering 3D hernia patches during laparoscopic TAPP can reduce intraoperative bleeding volume,alleviate postoperative pain,and lower the complications rate such as postoperative urinary retention,scrotal edema,and seroma.It is worthy of clinical promotion and application.

For middle-aged and elderly patients with conditions such as spinal fractures and degenerative spinal diseases, spinal internal fixation is a core surgical procedure for reconstructing spinal stability, heavily relying on the biomechanical stability provided by pedicle screw systems. Whereas, these patients are often complicated by osteoporosis that can significantly compromise the stability of the bone-pedicle screw interface, leading to a marked increase in pedicle screw loosening and surgical failure rates. The bone cement-augmented pedicle screw technique, which involves injecting bone cement into the vertebral body or screw trajectory to optimize the mechanical properties of the bone-pedicle screw composite, has been proven to significantly enhance fixation strength and effectively prevent screw-related failures, thereby reducing the incidence of internal fixation failure in high-risk populations undergoing spinal fusion. However, the widespread clinical application of this technique has faced challenges such as inaccurate clinical decision-making (indication and contraindication selection), non-standardized operative practices, and insufficient awareness of complication prevention, resulting in considerable variability in clinical outcomes and even severe complications. To address this, Prof. Luo Fei from First Affiliated Hospital of Army Medical University initiated the project and the Chinese Association Orthopaedic Surgeons organized relevant experts to develop the Evidence-based clinical practice guideline for bone cement-augmented pedicle screw technique ( version 2025), based on current evidence. The guidelines put forward 8 recommendations regarding the clinical value, scope of application, and operational standards of the technique, aiming to provide evidence-based medical support and technical standardization for clinical decision-making.

For middle-aged and elderly patients with conditions such as spinal fractures and degenerative spinal diseases, spinal internal fixation is a core surgical procedure for reconstructing spinal stability, heavily relying on the biomechanical stability provided by pedicle screw systems. Whereas, these patients are often complicated by osteoporosis that can significantly compromise the stability of the bone-pedicle screw interface, leading to a marked increase in pedicle screw loosening and surgical failure rates. The bone cement-augmented pedicle screw technique, which involves injecting bone cement into the vertebral body or screw trajectory to optimize the mechanical properties of the bone-pedicle screw composite, has been proven to significantly enhance fixation strength and effectively prevent screw-related failures, thereby reducing the incidence of internal fixation failure in high-risk populations undergoing spinal fusion. However, the widespread clinical application of this technique has faced challenges such as inaccurate clinical decision-making (indication and contraindication selection), non-standardized operative practices, and insufficient awareness of complication prevention, resulting in considerable variability in clinical outcomes and even severe complications. To address this, Prof. Luo Fei from First Affiliated Hospital of Army Medical University initiated the project and the Chinese Association Orthopaedic Surgeons organized relevant experts to develop the Evidence-based clinical practice guideline for bone cement-augmented pedicle screw technique ( version 2025), based on current evidence. The guidelines put forward 8 recommendations regarding the clinical value, scope of application, and operational standards of the technique, aiming to provide evidence-based medical support and technical standardization for clinical decision-making.

Objective: To screen and identify the key active molecules, signaling pathways, and therapeutic targets of Shuxuening (SXN) injection for treating liver cirrhosis (LC) and to evaluate its therapeutic potential using a mouse model. Methods: Target genes of SXN and LC were retrieved from public databases, and enrichment analysis was performed. A protein–protein interaction (PPI) network was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING), and hub genes were identified using Molecular Complex Detection (MCODE). LC was induced in rats and mice via intraperitoneal injections of diethylnitrosamine and carbon tetrachloride (CCl4) for 12 weeks. Starting at week 7, SXN was administered intraperitoneally to the mice in the treatment group. Serum and liver tissues of the mice were collected for the detection of indicators, pathological staining, and expression analysis of hub targets using quantitative real-time polymerase chain reaction (qRT-PCR). Results: We identified 368 overlapping genes (OLGs) between SXN and LC targets. These OLGs were subsequently used to build a PPI network and to screen for hub genes. Enrichment analysis showed that these genes were associated with cancer-related pathways, including phosphoinositide-3-kinase/Akt and mitogen-activated protein kinase signaling and various cellular processes, such as responses to chemicals and metabolic regulation. In vivo experiments demonstrated that SXN treatment significantly improved liver function and pathology in CCl4-induced LC mice by reducing inflammation and collagen deposition. Furthermore, qRT-PCR demonstrated that SXN regulated the expression of MAPK8, AR and CASP3 in the livers of LC mice. Conclusion This study highlighted the therapeutic effects of SXN in alleviating LC using both bioinformatics and experimental methods. The observed effect was associated with modulation of hub gene expression, particularly MAPK8, and CASP3.

Diabetic nephropathy is the most serious complication of diabetes and a major cause of end-stage renal disease worldwide.Although hyperglycaemia is widely considered to be the main driving force for the progression of diabetic nephropathy to end-stage renal disease,inflammatory signaling pathways and inflammatory cells also play important roles in the pathogenesis and progression of the disease.Therefore,treatment strategies targeting the inflammation-related intracellular signaling pathways may become a new direction for the treatment of diabetic nephropathy.Currently,the development of anti-inflammatory drugs for diabetic nephropathy is also underway,and they have shown promising results in experimental models.This article focuses on the connection between inflammatory cells and inflammatory signaling pathways and diabetic nephropathy,as well as the current research progress on targeted anti-inflammatory treatment.

Objective To explore the clinical efficacy of using 3D patches to repair inguinal hernia in laparoscopic transabdominal preperitoneal inguinal hernia repair(TAPP).Methods A retrospective study was conducted on 102 patients with inguinal hernia.All the patients were treated with laparoscopic TAPP.The patients were divided into two groups based on the different patch methods used after the surgery.The patients who used ordinary patches were in the ordinary patch group(n=50),and the patients who used 3D patches were in the 3D patch group(n=52).The surgery-related conditions,postoperative pain,postoperative complications and recurrence of the two groups of patients were compared.Results The 3D patch group had shorter surgery time,first exhaust time,got out of bed mobility time,less hospital stay and intraoperative bleeding volume than those in the ordinary patch group,the differences were statistically significant(P<0.05).On the 1,3,and 5 d after surgery,the visual analogue scale(VAS)scores of patients in the 3D patch group were lower than those in the ordinary patch group,the differences were statistically significant(P<0.05).The total complications rate in the 3D patch group was 5.77%,which was significantly lower than the 20.00%in the ordinary patch group,the difference was statistically significant(P<0.05).There was no statistically significant difference in the postoperative recurrence rate between the two groups of patients(P>0.05).Conclusion For patients with inguinal hernia,administering 3D hernia patches during laparoscopic TAPP can reduce intraoperative bleeding volume,alleviate postoperative pain,and lower the complications rate such as postoperative urinary retention,scrotal edema,and seroma.It is worthy of clinical promotion and application.