Objective To study the potential molecular biological mechanism of Wuzi decoction on polycystic ovary syndrome(PCOS)by using network pharmacology and molecular docking technology.Methods TCMSP database and literature survey were used to screen the active ingredients of Wuzi decoction and related target proteins,and the target protein names were translated into target gene names.Key genes of PCOS disease were queried in the database,cross analysis of genes and visual networks were generated.The interaction network between drugs and disease targets were establish,key target proteins were conducted by gene ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)analysis,and molecular docking validation of the proteins were encoded by the active components and the selected core target genes.Results According to the set conditions,81 active ingredients were found from the drug Wuzi decoction and a total of 221 targets genes were detected.A total of 151 TCM and disease interaction targets were obtained by using PCOS as the search term.The target genes were compared and analyzed,and the number of main core targets was 93.NPM1,HSPA5,YWHAZ,HNRNPA1,HNRNPK,MCM2,HSPA8,EEF1A1,VCP,and HSP90AB1 may be the main core targets for the treatment of PCOS.GO was used for analysis,and 376 enrichment results were obtained.A total of 102 related pathways were identified in the KEGG analysis.Corresponding active drug ingredient was docked with the core target protein molecule and shows good.Conclusion Wuzi decoction can play a role in the prevention and control of PCOS,and the mechanism of action involves multiple targets and signaling pathways.

Objective:To analyze the influencing factors for special interests in rheumatology diseases in residents after their completion of standardized residency training.Methods:A questionnaire survey was conducted among general practitioners who participated in residential training in the base from September 1, 2011 to June 30, 2024, and the possible influencing factors were collected and analyzed.Results:Eighty-six cases (63.2%) of general practitioners expressed interest in rheumatology. A higher proportion of physicians showed interest in rheumatology when they engaged in the following activities: taking rheumatology as a subspecialty in practice on rheumtic diseases [16.3% (14/86) vs. 0 (0/50), χ2=15.93, P<0.001], taking night shifts during rheumatology rotation [57.0%(49/86) vs. 20% (10/50), χ2=17.60, P<0.001], studying with mentors of rheumatogy[89.5%(77/86) vs. 54.0%(27/50), χ2=22.19, P<0.001], participating in research on rheamatic diseases[16.3% (14/86) vs. 2.0% (1/50), χ2=6.57, P=0.010], involved in rheumatology outpatient teaching sessions [33.7%(29/86) vs. 8.0% (4/50), χ2=11.38, P<0.001], and receiving career guidance on mentors of rheumatology[39.5%(34/86) vs. 18.0% (9/50), χ2=6.78, P=0.012]. Multivariate logistic analysis revealed that the following were independent promoting factors for developing interest in rheumatology: taking rheumatology as a subspecialty in practice [ OR(95% CI) =3.82 (1.5,9.7), P=0.005], taking night shifts during rheumatology rotation [ OR(95% CI) =3.41 (1.25,9.28), P=0.017], and studying with mentors of rheumatology[ OR(95% CI) =6.44 (2.18,19.08), P<0.001]. Conclusion:Most residents expressed interest in rheumatology. Taking rheumatology as a practice sub-specialty, taking night shifts and during rotation and learning from mentors have a positive impact on residents interest in rheumatology after their completion of residency.

OBJECTIVE To investigate the mechanism by which aloin （ALO） ameliorates atherosclerosis （AS）. METHODS Eight C57BL/6J mice were assigned to the control group （CON group） and fed a standard diet； thirty-two apolipoprotein E-knockout （APOE－/－） mice were randomly divided into model group （MOD group）， ALO low-dose and high-dose groups [ALO-L group， ALO-H group， 20， 40 mg/（kg·d）]， and atorvastatin positive control group [ATO group， 4 mg/（kg·d）]， with 8 mice in each group， establishing the AS model through feeding with a high-fat diet. The mice were administered the drug via gavage or given an equal volume of deionized water for 8 consecutive weeks. The lipid levels in the serum of mice were measured， and the pathological structural changes in their aortas were observed. The expressions of macrophage polarization markers （CD86+ ， CD206+） in the aorta were determined， along with the mRNA expressions of inducible nitric oxide synthase （iNOS）， tumor necrosis factor-α （TNF-α）， arginase-1 （Arg-1）， and interleukin-10 （IL-10）， as well as the protein expressions of iNOS and Arg- 1， and the phosphorylation levels of nuclear factor κB p65 （NF-κB p65） and signal transduction and activator of transcription 3 （STAT3） proteins. Additionally， a macrophage polarization model was established using lipopolysaccharide （LPS）-induced RAW264.7 cells， and the effect of ALO （400 μmol/L） on the cellular polarization phenotype was investigated. RESULTS Compared with the MOD group， administration groups all showed significant improvement in dyslipidemia （except for high-density lipoprotein cholesterol in the serum of ALO-L group） （P＜0.05）； aortic intimal structure improved significantly， plaque area was reduced significantly （P＜0.01）； the CD86+ relative fluorescence intensity in the aorta decreased significantly， the CD206+relative fluorescence intensity increased significantly （P＜0.01）， while the expressions of iNOS and TNF-α mRNA were down-regulated significantly （P＜0.05）； mRNA expressions of Arg-1 and IL-10， and protein expression of Arg-1 were increased significantly in ALO-H group and ATO group （P＜0.05）； the protein expressions of iNOS， and the phosphorylation levels of NF-κB p65 and STAT3 protein were decreased significantly （P＜0.05）. In vitro experiments further confirmed that ALO significantly reduced the proportion of LPS-induced M1-type macrophages but increased the proportion of M2-type macrophages （P＜0.01）. CONCLUSIONS ALO inhibits M1-type macrophage polarization and promotes M2-type polarization， ameliorates dyslipidemia and reduces arterial plaque formation in AS model mice， improve the structure of the aortic intima potentially through suppression of the NF-κB/STAT3 signaling pathway.

Objective To observe the clinical efficacy of modified Shoutai Pills in the treatment of polycystic ovary syndrome(PCOS)complicated with recurrent spontaneous abortion(RSA).Methods Ninety-six patients with PCOS complicated with RSA of kidney deficiency and blood stasis syndrome admitted to Lishui Hospital of Traditional Chinese Medicine from January 2021 to January 2022 were randomly divided into the observation group and the control group,with 48 cases in each group.The control group was treated with progesterone,aspirin and low molecular weight heparin,while the observation group was treated with modified Shoutai Pills on the basis of treatment for the control group.The course of treatment covered one month and then the follow-up lasted for one year.The changes of traditional Chinese medicine(TCM)syndrome scores,ovarian reserve function indicators of antral follicle count and mean ovarian volume,and coagulation and fibrinolysis indicators of fibrinogen(FIB),activated partial thromboplastin time(APTT),prothrombin time(PT),and D-dimer(D-D)level before and after the treatment in the two groups were observed.After treatment,the clinical efficacy,total incidence of adverse reactions and pregnancy outcome of the two groups of patients were compared.Results(1)After one month of treatment,the total effective rate of the observation group was 95.83%(46/48),and that of the control group was 72.92%(35/48);the comparison between the two groups showed that the overall efficacy(tested by Ridit test)and the total effective rate(tested by chi-square test)of the observation group were significantly superior to those of the control group(P<0.05).(2)After treatment,the scores of spontaneous abortion frequency and TCM symptoms such as pain in the lower abdomen,fatigue and weakness,and dizziness and tinnitus in the two groups were decreased compared with those before treatment(P<0.05),and the decrease of the scores in the observation group was significantly superior to that in the control group(P<0.05).(3)After treatment,ovarian reserve function indicators of antral follicle count and mean ovarian volume in the two groups were improved compared with those before treatment(P<0.05),and the improvement in the observation group was significantly superior to that in the control group(P<0.05).(4)After treatment,coagulation and fibrinolysis indicators such as FIB,APTT,PT,and D-D in the two groups were improved compared with those before treatment(P<0.05),and the improvement in the observation group was significantly superior to that in the control group(P<0.05).(5)The total incidence of adverse reactions in the observation group was 6.25%(3/48),while that in the control group was 10.42%(5/48),and the comparison between the two groups showed that the difference was not statistically significant(P>0.05).(6)The rate of full-term delivery in the observation group was 87.50%(42/48),higher than that in the control group[45.83%(22/48)];the preterm birth rate and abortion rate of the observation group were 8.33%(4/48)and 4.17%(2/48),respectively,lower than those of the control group[all being 27.08%(13/48)],with the differences being statistically significant(P<0.05 or P<0.01).Conclusion Modified Shoutai Pills can effectively improve the ovarian function of patients with PCOS complicated with RSA,correct the hypercoagulable state,relieve abdominal pain and other symptoms,reduce the rate of preterm birth and abortion,and no obvious adverse reactions occurred in the patients during treatment.

Objective To study the potential molecular biological mechanism of Wuzi decoction on polycystic ovary syndrome(PCOS)by using network pharmacology and molecular docking technology.Methods TCMSP database and literature survey were used to screen the active ingredients of Wuzi decoction and related target proteins,and the target protein names were translated into target gene names.Key genes of PCOS disease were queried in the database,cross analysis of genes and visual networks were generated.The interaction network between drugs and disease targets were establish,key target proteins were conducted by gene ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)analysis,and molecular docking validation of the proteins were encoded by the active components and the selected core target genes.Results According to the set conditions,81 active ingredients were found from the drug Wuzi decoction and a total of 221 targets genes were detected.A total of 151 TCM and disease interaction targets were obtained by using PCOS as the search term.The target genes were compared and analyzed,and the number of main core targets was 93.NPM1,HSPA5,YWHAZ,HNRNPA1,HNRNPK,MCM2,HSPA8,EEF1A1,VCP,and HSP90AB1 may be the main core targets for the treatment of PCOS.GO was used for analysis,and 376 enrichment results were obtained.A total of 102 related pathways were identified in the KEGG analysis.Corresponding active drug ingredient was docked with the core target protein molecule and shows good.Conclusion Wuzi decoction can play a role in the prevention and control of PCOS,and the mechanism of action involves multiple targets and signaling pathways.

Objective:To analyze the influencing factors for special interests in rheumatology diseases in residents after their completion of standardized residency training.Methods:A questionnaire survey was conducted among general practitioners who participated in residential training in the base from September 1, 2011 to June 30, 2024, and the possible influencing factors were collected and analyzed.Results:Eighty-six cases (63.2%) of general practitioners expressed interest in rheumatology. A higher proportion of physicians showed interest in rheumatology when they engaged in the following activities: taking rheumatology as a subspecialty in practice on rheumtic diseases [16.3% (14/86) vs. 0 (0/50), χ2=15.93, P<0.001], taking night shifts during rheumatology rotation [57.0%(49/86) vs. 20% (10/50), χ2=17.60, P<0.001], studying with mentors of rheumatogy[89.5%(77/86) vs. 54.0%(27/50), χ2=22.19, P<0.001], participating in research on rheamatic diseases[16.3% (14/86) vs. 2.0% (1/50), χ2=6.57, P=0.010], involved in rheumatology outpatient teaching sessions [33.7%(29/86) vs. 8.0% (4/50), χ2=11.38, P<0.001], and receiving career guidance on mentors of rheumatology[39.5%(34/86) vs. 18.0% (9/50), χ2=6.78, P=0.012]. Multivariate logistic analysis revealed that the following were independent promoting factors for developing interest in rheumatology: taking rheumatology as a subspecialty in practice [ OR(95% CI) =3.82 (1.5,9.7), P=0.005], taking night shifts during rheumatology rotation [ OR(95% CI) =3.41 (1.25,9.28), P=0.017], and studying with mentors of rheumatology[ OR(95% CI) =6.44 (2.18,19.08), P<0.001]. Conclusion:Most residents expressed interest in rheumatology. Taking rheumatology as a practice sub-specialty, taking night shifts and during rotation and learning from mentors have a positive impact on residents interest in rheumatology after their completion of residency.

Objective:To search, evaluate, and summarize the best evidence for difficult peripheral intravenous catheterization in children.Methods:Following the "6S" evidence pyramid model, literature related to the management of difficult peripheral veins in children was searched in both English and Chinese databases including UpToDate, BMJ Best Practice, National Guidelines Clearinghouse, the Joanna Briggs Institute Evidence-Based Health Care Database, PubMed, Medlive, SinoMed, CNKI, and Wanfang Database. The search period was from the establishment of the database to January 2023. Two researchers trained in systematic evidence-based nursing, independently evaluated the quality of included literature and extracted relevant evidence.Results:Five articles were included: two guidelines, two expert consensuses, and one systematic review. 19 best evidence were summarized, covering five aspects: difficult vein quality management, difficult vein assessment, difficult intravenous catheterization site and needle type selection, difficult intravenous catheterization auxiliary methods, and handling of failed difficult intravenous catheterization.Conclusions:This study summarizes the best evidence for difficult peripheral intravenous catheterization in children, demonstrating clinical nursing practicality. It provides evidence-based guidance for pediatric nursing staff performing difficult intravenous catheterization.

Background and purpose: Previous studies have confirmed that the expression of leucine-rich repeat-containing 3B (CLRRC3B) was significantly decreased in different human cancers, which was also associated with the migration and invasion of cancer cells. The aim of this study was to explore the potential mechanism of LRRC3B in the development of esophageal cancer. Methods: The LRRC3B expression was detected in 60 cancer tissues and 60 adjacent non-neoplastic tissues by immunohistochemistry. The mRNA and protein expression of LRRC3B in Eca109 and HEECs were detected using real-time fluorescence quantitative polymerase chain reaction (RTFQ-PCR) and Western blot, respectively. Eca109 cells with different treatments were divided into three groups:normal group, negative control group (transfected with pCMV6 plasmid), overexpression LRRC3B group (transfected with pCMV6-LRRC3B plasmid). Transwell assay was used to measure the migration and invasion of Eca109 cells in different groups. The protein levels of E-cadherin, N-cadherin, Vimentin and p-Akt were determined by Western blot. Results: The expression of LRRC3B in esophageal cancer tissues was lower than that of non-cancerous tissues, as well as the expression of LRRC3B in Eca109 was decreased compared with that of normal esophageal epithelial cell line HEEC. Overexpression of LRRC3B significantly inhibited Eca109 cells migration and invasion, upregulated the expression of E-cadherin and decreased the expression of N-cadherin and Vimentin. Moreover, overexpression of LRRC3B significantly inhibited the phosphorylation of Akt in Eca109 cells. Conclusion: The expression of LRRC3B was decreased in esophageal cancer. Overexpression of LRRC3B can efficiently inhibit the EMT progression in esophageal cancer cells by suppressing PI3K/Akt signaling pathway.

Aim To assay the possible targets of adriamycin (ADM), screening ADM resistance related proteins.Methods The drug sensitivity of the cells was analyzed by IC50 assay;RT-PCR assay was used to detect the expression of genes in the cells;CMPK1 protein expression was tested by Western blot assay;the expression of CMPK1 in the cells was decreased by siRNA of CMPK1.Results Data from IC50 assay showed the sensitivity of cells transfected with CMPK1 was increased most(IC50 HEK293-CMPK /IC50 HEK293-Control=0.15, P<0.01), and the expression of CMPK1 protein in ADM resistant breast cells (MCF7/ADM) was lower than that in parent MCF7 cells (P<0.05).When the expression level of CMPK1 was decreased by CMPK1 siRNA, the sensitivity of MCF7 cells to ADM decreased (IC50 MCF7-siCMPK1/IC50MCF7-Control=3.6, P< 0.01), and the sensitivity of MCF7 cells to paclitaxel and gemcitabine also decreased.Conclusions CMPK1 was related to the multidrug resistance of cells, and the expression of CMPK1 was positively related to the sensitivity to drugs, which provides the possibility of CMPK1 as a target in the treatment of multidrug resistance.

Objective To investigate the effects of CNTN-1 on the invasion and migration of human esophageal cancer EC9706 cells and the possible mechanism.Methods The expression of CNTN-1 in human esophageal cancer EC9706 cells was measured by qPCR and Western blot.After transfection with CNTN-1 siRNA or CNTN-1, the cells were divided into control group, scrambled siRNA group, CNTN-1 siRNA group, pcDNA3.1-vector group and pcDNA3.1-CNTN-1 group.Cell proliferation, invasion and migration were respectively analyzed by BrdU assay and Transwell test.The expression of MMP-2 and MMP-9 were detected by qPCR and Western blot.Results The mRNA and protein expression of CNTN-1 were significantly upregulated in EC9706 cells.Compared with control, cell proliferation, invasion and migration, as well as the expression of MMP-2 and MMP-9 were significantly decreased by CNTN-1 siRNA, while they were increased by CNTN-1 overexpression (P<0.05).ConclusionsCNTN-1 can influence the invasion and metastasis of esophageal cancer cells through the regulation of the expression of MMP-2 and MMP-9.