To address the problem of data silos in dental specialties caused by equipment heterogeneity, this study developed an Intelligent Internet of Things (IoT)-enabled dental chair platform (hereinafter referred to as the intelligent platform) based on the concept of medical-engineering integration. The platform adopts a three-tier chair-domain interconnection architecture: the bottom tier integrates multi-source sensors and standardized interfaces for automated data acquisition and linkage with hospital information systems; the middle tier provides clinic-level management and remote teaching collaboration; and the top tier employs a blockchain-based secure cloud database for resource allocation and data management. Clinical validation at The Affiliated Stomatological Hospital of Nanjing Medical University demonstrated that, compared with a control group from the same period in 2023, the trial group achieved a 38.0% increase in average daily patient visits (80.6±6.8 vs. 58.4±5.2, t=15.16, P<0.001), a 24.6% reduction in average treatment time [(36.1±6.3) min vs. (47.9±8.5) min, t=7.72, P<0.001], a 39.2% reduction in waiting time [23.3 (16.5, 30.1) min vs. 38.3 (28.3, 48.3) min, U=32.00, P<0.001], a 30.4% reduction in equipment idle rate [8.7% (5.1%, 12.3%) vs. 12.5% (7.4%, 17.6%), U=251.00, P=0.003], and an increase in patient satisfaction from 88.2% (1 519/1 723) to 94.3% (2 186/2 318) ( t=7.26, P<0.001). User research confirmed that the functions most favored by clinicians and patients were "dental chair parameter updating and clinical data integration" [74.7% (80/107)] and "chairside display of diagnostic images" [76.8% (119/155)], respectively. Looking forward, the intelligent platform has the potential to integrate artificial intelligence-assisted diagnosis and 5G-enabled multicenter collaboration to further expand its clinical applications and accelerate the digital transformation of dental healthcare.

AIM:This study aims to investigate distinct patterns in food reward behavior and neuroinflammato-ry responses within the ventral tegmental area(VTA)between obesity-prone(OP)and obesity-resistant(OR)rats,while elucidating their potential interplay.METHODS:Twenty-four male Sprague-Dawley rats(5-week-old)were adminis-tered a high-fat diet(HFD)for 8 weeks.Based on body weight tertiles,rats were stratified into OP(highest tertile,n=8)and OR(lowest tertile,n=8)groups.Food reward function was evaluated through conditioned place preference(CPP)test and operant food-seeking task(OFST).Serum lipid profiles were quantified via colorimetric microplate assays,with 24-hour energy expenditure monitored using CLAMS.Western blot and immunofluorescence assays quantified ionized cal-cium-binding adaptor molecule 1(Iba1)and tyrosine hydroxylase(TH)protein expression,while immunofluorescence lo-calized VTA-positive cell spatial distribution and density.RT-qPCR quantified mRNA expression of Iba1,TH,and proin-flammatory cytokines(TNF-α,IL-1β and IL-6).ELISA quantified proinflammatory cytokine protein concentrations.RE-SULTS:Following 8-week HFD exposure,OP rats exhibited elevated body weight,total food and calories,adiposity,Lee index,and levels of TG,LDL-C,TC,and NEFA,while HLD-C levels and 24-hour energy metabolism significantly decreased(P<0.05).OP rats demonstrated enhanced CPP preference for HFD-paired cues,elevated lever pressing fre-quency,and increased breakpoints versus OR counterparts(P<0.05),positively correlating with body weight(r=0.766,0.561 and 0.606;P<0.05).OP rats demonstrated elevated Iba1 positive cell density,protein and mRNA expression,and inflammatory mediators in VTA versus OR counterparts,contrasting with diminished TH positive neurons showing re-duced protein and mRNA levels(P<0.05).VTA neuroinflammatory mediators(Iba1,TNF-α,IL-1β and IL-6)exhibited inverse correlations with TH protein expression(r=-0.953,-0.866,-0.881 and-0.886;P<0.05).CONCLUSION:The OP rats exhibit attenuated reward sensitivity,elevated HFD preference,and increased palatable food-seeking behavior.These behavioral modifications correlate with VTA neuroinflammation suppressing dopaminergic(DA)biosynthesis.

To address the problem of data silos in dental specialties caused by equipment heterogeneity, this study developed an Intelligent Internet of Things (IoT)-enabled dental chair platform (hereinafter referred to as the intelligent platform) based on the concept of medical-engineering integration. The platform adopts a three-tier chair-domain interconnection architecture: the bottom tier integrates multi-source sensors and standardized interfaces for automated data acquisition and linkage with hospital information systems; the middle tier provides clinic-level management and remote teaching collaboration; and the top tier employs a blockchain-based secure cloud database for resource allocation and data management. Clinical validation at The Affiliated Stomatological Hospital of Nanjing Medical University demonstrated that, compared with a control group from the same period in 2023, the trial group achieved a 38.0% increase in average daily patient visits (80.6±6.8 vs. 58.4±5.2, t=15.16, P<0.001), a 24.6% reduction in average treatment time [(36.1±6.3) min vs. (47.9±8.5) min, t=7.72, P<0.001], a 39.2% reduction in waiting time [23.3 (16.5, 30.1) min vs. 38.3 (28.3, 48.3) min, U=32.00, P<0.001], a 30.4% reduction in equipment idle rate [8.7% (5.1%, 12.3%) vs. 12.5% (7.4%, 17.6%), U=251.00, P=0.003], and an increase in patient satisfaction from 88.2% (1 519/1 723) to 94.3% (2 186/2 318) ( t=7.26, P<0.001). User research confirmed that the functions most favored by clinicians and patients were "dental chair parameter updating and clinical data integration" [74.7% (80/107)] and "chairside display of diagnostic images" [76.8% (119/155)], respectively. Looking forward, the intelligent platform has the potential to integrate artificial intelligence-assisted diagnosis and 5G-enabled multicenter collaboration to further expand its clinical applications and accelerate the digital transformation of dental healthcare.

AIM:This study aims to investigate distinct patterns in food reward behavior and neuroinflammato-ry responses within the ventral tegmental area(VTA)between obesity-prone(OP)and obesity-resistant(OR)rats,while elucidating their potential interplay.METHODS:Twenty-four male Sprague-Dawley rats(5-week-old)were adminis-tered a high-fat diet(HFD)for 8 weeks.Based on body weight tertiles,rats were stratified into OP(highest tertile,n=8)and OR(lowest tertile,n=8)groups.Food reward function was evaluated through conditioned place preference(CPP)test and operant food-seeking task(OFST).Serum lipid profiles were quantified via colorimetric microplate assays,with 24-hour energy expenditure monitored using CLAMS.Western blot and immunofluorescence assays quantified ionized cal-cium-binding adaptor molecule 1(Iba1)and tyrosine hydroxylase(TH)protein expression,while immunofluorescence lo-calized VTA-positive cell spatial distribution and density.RT-qPCR quantified mRNA expression of Iba1,TH,and proin-flammatory cytokines(TNF-α,IL-1β and IL-6).ELISA quantified proinflammatory cytokine protein concentrations.RE-SULTS:Following 8-week HFD exposure,OP rats exhibited elevated body weight,total food and calories,adiposity,Lee index,and levels of TG,LDL-C,TC,and NEFA,while HLD-C levels and 24-hour energy metabolism significantly decreased(P<0.05).OP rats demonstrated enhanced CPP preference for HFD-paired cues,elevated lever pressing fre-quency,and increased breakpoints versus OR counterparts(P<0.05),positively correlating with body weight(r=0.766,0.561 and 0.606;P<0.05).OP rats demonstrated elevated Iba1 positive cell density,protein and mRNA expression,and inflammatory mediators in VTA versus OR counterparts,contrasting with diminished TH positive neurons showing re-duced protein and mRNA levels(P<0.05).VTA neuroinflammatory mediators(Iba1,TNF-α,IL-1β and IL-6)exhibited inverse correlations with TH protein expression(r=-0.953,-0.866,-0.881 and-0.886;P<0.05).CONCLUSION:The OP rats exhibit attenuated reward sensitivity,elevated HFD preference,and increased palatable food-seeking behavior.These behavioral modifications correlate with VTA neuroinflammation suppressing dopaminergic(DA)biosynthesis.

Objective:To explore the relationship between relapse tendency and childhood maltreatment in methamphetamine-dependent youths,and the role of impulsivity and quality of life in the relationship.Methods:To-tally 287 methamphetamine-dependent youths(160 females,127 males)were selected in compulsory drug rehabili-tation centers.The Relapse Tendency Questionnaire(RTQ),Childhood Trauma Questionnaire-Short Form(CTQ-SF),Barrett Impulsivity Scale(BIS-11)and Quality of Life for Drug Addicts(QOL-DA)for Drug Addicts were used to conduct the survey.SPSS macro program PROCESS was used to test the mediating role.Results:The BIS-11 total scores acted as a partial mediator between the total scores of CTQ-SF and RTQ,with an effect value of 0.03(95％CI:0.01-0.05),the QOL-DA total scores acted as a full mediator between the total scores of CTQ-SF and RTQ,with an effect value of 0.05(95％CI:0.02-0.08),and the scores of BIS-11 and QOL-DA acted as chain mediators between total scores of CTQ-SF and RTQ,with an effect value of 0.01(95％CI:0.00-0.03).Conclusion:Childhood maltreatment,impulsivity,and quality of life may be associated with relapse tendencies in methamphetamine-dependent youths.

Purpose/Significance To explore the attitudes,willingness and influencing factors of Chinese doctors towards medical ar-tificial intelligence(AI).Method/Process A cross-sectional survey is conducted by distributing closed-ended questionnaires via We-Chat to 327 doctors.The questionnaire content includes the doctors'background,their understanding of AI,their level of acceptance,and their willingness to use it.Descriptive statistics,inter-group comparison and logistic regression analysis are used.Result/Conclu-sion Most doctors have a positive attitude towards AI,and there are differences in the willingness to use AI based on factors such as gen-der and level of attention.

Background::Homoharringtonine (HHT) is an effective anti-inflammatory, anti-viral, and anti-tumor protein synthesis inhibitor that has been applied clinically. Here, we explored the therapeutic effects of HHT in a mouse heart transplant model.Methods::Healthy C57BL/6 mice were used to observe the toxicity of HHT in the liver, kidney, and hematology. A mouse heart transplantation model was constructed, and the potential mechanism of HHT prolonging allograft survival was evaluated using Kaplan–Meier analysis, immunostaining, and bulk RNA sequencing analysis. The HHT-T cell crosstalk was modeled ex vivo to further verify the molecular mechanism of HHT-induced regulatory T cells (Tregs) differentiation. Results::HHT inhibited the activation and proliferation of T cells and promoted their apoptosis ex vivo. Treatment of 0.5 mg/kg HHT for 10 days significantly prolonged the mean graft survival time of the allografts from 7 days to 48 days ( P <0.001) without non-immune toxicity. The allografts had long-term survival after continuous HHT treatment for 28 days. HHT significantly reduced lymphocyte infiltration in the graft, and interferon-γ-secreting CD4 + and CD8 + T cells in the spleen ( P <0.01). HHT significantly increased the number of peripheral Tregs (about 20%, P <0.001) and serum interleukin (IL)-10 levels. HHT downregulated the expression of T cell receptor (TCR) signaling pathway-related genes ( CD4, H2-Eb1, TRAT1, and CD74) and upregulated the expression of IL-10 and transforming growth factor (TGF) -β pathway-related genes and Treg signature genes ( CTLA4, Foxp3, CD74, and ICOS). HHT increased CD4 + Foxp3 + cells and Foxp3 expression ex vivo, and it enhanced the inhibitory function of inducible Tregs. Conclusions::HHT promotes Treg cell differentiation and enhances Treg suppressive function by attenuating the TCR signaling pathway and upregulating the expression of Treg signature genes and IL-10 levels, thereby promoting mouse heart allograft acceptance. These findings may have therapeutic implications for organ transplant recipients, particularly those with viral infections and malignancies, which require a more suitable anti-rejection medication.

Triggering receptor expressed on myeloid cells-1 (TREM-1) is a member of the immunoglobulin superfamily. As an amplifier of the inflammatory response, TREM-1 is mainly involved in the production of inflammatory mediators and the regulation of cell survival. TREM-1 has been studied in infectious diseases and more recently in non-infectious disorders. More and more studies have shown that TREM-1 plays an important pathogenic role in kidney diseases. There is evidence that TREM-1 can not only be used as a biomarker for diagnosis of disease but also as a potential therapeutic target to guide the development of novel therapeutic agents for kidney disease. This review summarized molecular biology of TREM-1 and its signaling pathways as well as immune response in the progress of acute kidney injury, renal fibrosis, diabetic nephropathy, immune nephropathy, and renal cell carcinoma.

Objective To investigate the antigen presentation characteristics of dendritic cells(DC)and B cells in cardiac grafts.Methods The heart of BALB/c mice was transplanted into the abdominal cavity of C57BL/6J mice.CD45+cells in the heart graft were extracted and sorted by flow cytometry at postoperative 5 d,and single cell RNA sequencing was performed.Taking DC and B cell subsets in cardiac grafts as the main study cells,the changing trend,antigen presenting ability and intercellular communication with T cells after heart transplantation were analyzed by bioinformatics analysis and flow cytometry.Gene ontology(GO)function enrichment difference analysis was adopted to prove the specific function and the reliability annotation of cell subsets.Results Germinal center-like B cell(GC-L B)was the B cell subset with the largest increase in quantity during the acute rejection phase,accounting for 87％.Classical DC(cDC)2 was the only DC subset with a significant increase in quantity during acute rejection of heart transplantation,accounting for 44％of DC subset,and it occupied the highest communication intensity with T cells after heart transplantation.Mononucleated DC(moDC)and memory B cell(MBC)were the main transmitters of T cell input signals in non-transplanted hearts,whereas transformed into cDC2 and GC-L B during the acute rejection phase.Among them,MBC and GC-L B were the main sources of T cell input signals in non-transplanted hearts and heart grafts.Conclusions Compared with DC,B cells occupy a higher number and weight in the intercellular communication with T cells in non-transplanted hearts and heart grafts,prompting that the antigen presenting activity of B cells is more active and stronger than DC in the early stage of acute rejection of heart transplantation.

Objective:To observe any effect of 12 weeks of moderate-intensity continuous training (MICT) and of high-intensity interval training (HIIT) on intestinal inflammation and the expression of α7 nicotinic acetylcholine receptor (α7nAChR) and nuclear factor kappa B p65 (NF-κΒp65) in rats fed a high-fat diet.Methods:Thirty-two healthy 5-week-old male Sprague-Dawley rats were divided at random into a normal diet and quiet group, a high-fat diet and quiet group, a high-fat diet MICT group, and a high-fat diet HIIT group, each of 8. The high-fat diet MICT group underwent continuous treadmill exercise at 70% of their maximum oxygen uptake (VO 2max), while the high-fat diet HIIT group did treadmill exercise at 40% to 45% of their VO 2max alternating with intervals at 95% to 99% of their VO 2max. The two quiet groups did no exercise. After 12 weeks, hematoxylin-eosin staining was used to observe the morphology of the rats′ intestinal tissue. Serum levels of low-density lipoprotein (LDL), high-density lipoprotein (HDL), triglycerides (TG) and free fatty acids (FFA) were determined, and immunofluorescence double labeling and western blotting were applied to detect the expression levels of α7nAChR, NF-κB p65 and tumor necrosis factor α (TNF-α) in the rats′ intestines. Results:Compared with the normal diet quiet group, the quiet group on a high fat diet had, on average, significantly heavier final body weights, lower total food intake, higher serum LDL, TG and FFA, lower HDL levels, and less protein expression of intestinal α 7nAChR. They showed higher average fluorescence intensity and expression of NF-κB p65 and TNF-α protein. Compared with the high-fat diet quiet group, the high-fat diet MICT and HIIT groups had significantly lighter final body weight, on average, lower total food intake, lower LDL and FFA levels and higher average fluorescence intensity. They showed significantly greater expression of α 7nAChR and NF-κB p65 protein, and lower expression of TNF-α protein. Compared with the high-fat diet MICT group, there was a significantly higher HDL content and lower average fluorescence intensity of NF-κ -Bp65 observed in the high-fat diet HIIT group. Moreover, reduced inflammatory infiltration, epithelial damage and mucosal crypt destruction were found in the colon tissue sections of both the high-fat diet MICT and HIIT groups.Conclusions:Twelve weeks of either MICT or HIIT can relieve intestinal inflammation resulting from a high-fat diet, at least in rats. The training increases the intestinal expression of α 7nAChR protein, and reduces the expression of NF-κBp65 and TNF-α. HIIT is superior to MICT in its effects.