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1.
Infect Drug Resist ; 17: 1763-1769, 2024.
Article in English | MEDLINE | ID: mdl-38736434

ABSTRACT

Background: Auxiliaries, a mixed chemicals, for printing and dyeing characterized by their diverse range and complex chemical compositions are commonly utilized in the textile industry. These chemicals can lead to environmental contamination and pose health risks to humans. Case Description: A 29-year-old man who worked in a printing and dyeing factory in Suzhou, China, reported having tightness in his chest and coughing. Despite seeking medical treatment at several hospitals, the initial diagnosis remained elusive. High-resolution chest CT scans showed multifocal lesions in both lungs. The patient had no significant medical history, and the respiratory symptoms only surfaced after exposure to dyeing auxiliaries. Physicians initially suspected chemical pneumonitis due to occupational exposure. However, a subsequent evaluation at a hospital specializing in occupational diseases led to a diagnosis of AIDS and pneumocystis pneumonia. Conclusion: This case underscores the importance of comprehensive clinical diagnosis to avoid biases and reduce the incidence of misdiagnosis.

2.
Discov Oncol ; 15(1): 65, 2024 Mar 06.
Article in English | MEDLINE | ID: mdl-38446257

ABSTRACT

BACKGROUND: The differential expression, biological function, and ceRNA regulatory mechanism of lncRNA XIST in bladder cancer (BC) were investigated, and its clinical values for the early diagnosis of bladder cancer patients were elucidated. METHODS: qRT-PCR was employed to detect the expression patterns of lncRNA XIST, miR-129-5p and TNFSF10. The biological functions were measured by CCK8 assay, wound healing assay and transwell assay. Bioinformatics analysis and Dual-Luciferase reporter assay were employed to evaluate the interactions between the lncRNA XIST, miR-129-5p and TNFSF10. RESULTS: LncRNA XIST and TNFSF10 were highly expressed and miR-129-5p was low expressed (P < 0.05) in bladder cancer cell line. The depletion of lncRNA XIST inhibited BC proliferation, migration and invasion. Mechanistically, lncRNA XIST could sponge miR-129-5p to regulate TNFSF10 expression in bladder cancer. Furthermore, compared with adjacent tissues, lncRNA XIST and miR-129-5p were lowly expressed (P < 0.01) in bladder cancer tissues, and TNFSF10 was highly expressed (P < 0.001). miR-129-5p and TNFSF10 were associated with the risk of bladder cancer (P < 0.05); the difference in AUC values for the diagnosis of bladder cancer by lncRNA XIST (AUC = 0.739), miR-129-5p (AUC = 0.850) and TNFSF10 (AUC = 0.753) was statistically significant (P < 0.01), and the three genes combined AUC was 0.900, 95%CI was 0.842-0.958 with a sensitivity of 83.3% and specificity of 86.7%. CONCLUSION: XIST, an elevated lncRNA in bladder cancer, inhibition of which could suppress the progression of BC. LncRNA XIST and miR-129-5p could form ceRNA to regulate the expression of TNFSF10.

3.
Sci Adv ; 10(5): eadj7813, 2024 Feb 02.
Article in English | MEDLINE | ID: mdl-38306420

ABSTRACT

Metabolic syndrome (MetS) is closely associated with an increased risk of dementia and cognitive impairment, and a complex interaction of genetic and environmental dietary factors may be implicated. Free fatty acid receptor 4 (Ffar4) may bridge the genetic and dietary aspects of MetS development. However, the role of Ffar4 in MetS-related cognitive dysfunction is unclear. In this study, we found that Ffar4 expression is down-regulated in MetS mice and MetS patients with cognitive impairment. Conventional and microglial conditional knockout of Ffar4 exacerbated high-fat diet (HFD)-induced cognitive dysfunction and anxiety, whereas microglial Ffar4 overexpression improved HFD-induced cognitive dysfunction and anxiety. Mechanistically, we found that microglial Ffar4 regulated microglial activation through type I interferon signaling. Microglial depletion and NF-κB inhibition partially reversed cognitive dysfunction and anxiety in microglia-specific Ffar4 knockout MetS mice. Together, these findings uncover a previously unappreciated role of Ffar4 in negatively regulating the NF-κB-IFN-ß signaling and provide an attractive therapeutic target for delaying MetS-associated cognitive decline.


Subject(s)
Cognitive Dysfunction , Metabolic Syndrome , Receptors, G-Protein-Coupled , Animals , Humans , Mice , Cognitive Dysfunction/genetics , Cognitive Dysfunction/complications , Metabolic Syndrome/complications , Metabolic Syndrome/genetics , Mice, Knockout , Microglia/metabolism , NF-kappa B/metabolism , Signal Transduction , Receptors, G-Protein-Coupled/metabolism
5.
Cell Commun Signal ; 21(1): 268, 2023 09 30.
Article in English | MEDLINE | ID: mdl-37777801

ABSTRACT

Due to the complexity and incomplete understanding of the crosstalk between liver and adipose tissue, especially the processes of hepatic lipogenesis and adipogenic differentiation, there are currently no effective drugs for the treatment of nonalcoholic fatty liver disease (NAFLD). Stearoyl-coenzyme A desaturase 1 (SCD1), which is abundantly expressed in liver and adipose tissue, may mediate the cross-talk between liver and adipose tissue. Thus, it is essential to develop specific SCD1 inhibitors that target the liver-adipose axis. Herein, we identified a novel SCD1 inhibitor, E6446, through a high-throughput virtual screen. E6646 significantly inhibited adipogenic differentiation and hepatic lipogenesis via SCD1-ATF3 signaling. The SPR results showed that E6446 had a strong interaction ability with SCD1 (KD:4.61 µM). Additionally, E6646 significantly decreased hepatic steatosis, hepatic lipid droplet accumulation and insulin resistance in high-fat diet (HFD)-fed mice. Taken together, our findings not only suggest that E6446 can serve as a new, safe and highly effective anti-NAFLD agent for future clinical use but also provide a molecular basis for the future development of SCD1 inhibitors that inhibit both adipogenic differentiation and hepatic lipogenesis. Video Abstract.


Subject(s)
Non-alcoholic Fatty Liver Disease , Mice , Animals , Non-alcoholic Fatty Liver Disease/drug therapy , Non-alcoholic Fatty Liver Disease/metabolism , Liver/metabolism , Obesity/metabolism , Lipogenesis , Diet, High-Fat , Mice, Inbred C57BL
6.
ACS Appl Mater Interfaces ; 14(21): 24415-24424, 2022 Jun 01.
Article in English | MEDLINE | ID: mdl-35593648

ABSTRACT

In this work, five vanadium oxide materials with a series of pre-intercalated cations A (AmV2O5), including Zn2+, Mg2+, NH4+, Li+, and Ag+, have been successfully prepared by a two-step method. All of them possess binary monoclinic and orthorhombic V2O5 phases with an open layered structure that allows the ionic storage and diffusion of hydrated cations. The interlayer space for the monoclinic V2O5 phase is strongly dependent on the radii of hydrated cations A, while the one for the orthorhombic V2O5 phase remains the same regardless of the radii of cations A. Among them, AmV2O5 with pre-intercalated Zn2+ (ZVO) has the best storage ability of Zn2+ with a reversible capacity close to 400 mAh g-1, and AmV2O5 with pre-intercalated Ag+ shows the highest rate capacity with a nearly 40% capacity retention at a current of 20 A g-1 (≈25 C). Kinetic studies have clearly shown that pseudocapacitive behavior dominates the electrochemical reaction on ZVO. During the Zn2+ (de)intercalation reaction, a highly reversible transformation of binary monoclinic or orthorhombic V2O5 phases into a single triclinic ZnxV2O5·nH2O phase is demonstrated on ZVO. Vanadium atoms are identified as the redox centers that undergo the mutual transition among the chemical states of V3+, V4+, and V5+. They together with oxygen atoms constitute reasonable V-O coordination polyhedra to generate a layered structure with a suitable interlayer space for the insertion or removal of zinc ions. Actually, the intrinsic coordination chemistry changes between VO5 square pyramids and VO6 octahedra account for the phase transformation during the Zn2+-(de)intercalation reaction.

7.
Nanotechnology ; 32(37)2021 Jun 25.
Article in English | MEDLINE | ID: mdl-34102626

ABSTRACT

In this work, an efficient and stable fluorescent probe for Al3+was established. The fluorescent probe based on the fluorescence 'turn-on' mode of zinc sulfide crystal composite zinc oxide quantum dots (ZnS/ZnO QDs). The ZnS/ZnO QDs were synthesized via two-step method using L-Cysteine (L-Cys) as a sulfur source and stabilizer. In the synthesis of ZnS/ZnO QDs, the fluorescence of zinc oxide quantum dots (ZnO QDs) decreased and its stability increased in aqueous solution after the addition of L-Cys. In addition, the as-synthesized ZnS/ZnO QDs shows fluorescent enhancement to Al3+. The ZnS/ZnO QDs based fluorescence 'turn-on' probe presented wide linear ranges (1 nM-8µM and 8-100µM). The availability of as-established sensing probe was also estimated by real water sample tests. Furthermore, the fluorescent enhancing mechanism was carried out by recording the fluorescent lifetime of samples, which might be related to the QDs dispersion and charge transfer weaken.

8.
Nanotechnology ; 32(37)2021 Jun 22.
Article in English | MEDLINE | ID: mdl-34062528

ABSTRACT

Effectively and quantificationally detecting hazardous gas n-butanol is very significant in daily life, which can bring about a safe living condition for humans. In this study, the one-dimensional In2O3nanorods were successfully synthesized via hydrothermal route and post-heat treatment. Noticeably, one-dimensional nanorods structures were obtained and the products presented a superior growth orientation along with (222) plane. Additionally, systematical gas-sensing measurements of the sensor made from In2O3nanorods towards hazardous n-butanol gas were conducted. Results exhibited that the fabricated sensor showed excellent n-butanol sensing properties, with aspects to a superior response value of 342.20 with concentration 100 ppm at 240 °C, remarkable selectivity, fast response/recovery times (77.5/34.2 s) and good stability. More interestingly, the detection limit of sensor as low as 500 ppb and a good linearity relationship between response values and n-butanol concentrations was presented. Gas-sensitive properties of this sensor are better than previously reported in n-butanol detection. All results demonstrate that one-dimensional In2O3nanorod is a promising sensor material to practical applications in effectively detecting n-butanol gas.

9.
Nanotechnology ; 32(40)2021 Jul 14.
Article in English | MEDLINE | ID: mdl-34186527

ABSTRACT

Due to the poor conductivity of Fe based, Cu based and Co based electrode materials commonly used in the electrochemical detection of glucose, and the uneven stirring and poor conductivity of the traditional preparation method based on glassy carbon electrode. In order to solve the above problems, in this work, CdIn2O4with high electrical conductivity was directly grown on three-dimensional (3D) Ni foam to prepare electrode materials for non-enzymatic glucose sensors. CdIn2O4nanoparticles is prepared from cadmium acetate and indium nitrate hydrate in benzyl alcohol by non-aqueous sol-gel method. The electrocatalytic oxidation performances of CdIn2O4electrode material for non-enzymatic glucose are studied. The results show that the proposed CdIn2O4electrode material has good electrochemical properties and sensing performance for glucose detection. The electrochemical response of CdIn2O4electrode material to glucose is recorded that calibration plot for glucose concentrations ranging from 1.0µM to 1.0 mM (R2 = 0.99), a limit detection of 0.08µM, an excellent sensitivity of 3.2925 mA.mM-1.cm-2, a rapid response time of 1.58 s, a good selectivity and a good long-term stability. These demonstrate the significant potential of CdIn2O4electrode material based on 3D Ni foam as non-enzymatic glucose sensors, which makes it possible to use it as a practical glucose detector. This work could introduce a new concept of nanoparticles modified electrode material grown directly on 3D Ni foam, thus a simple and reliable electrochemical glucose sensor platform is realized. This study was completed in 2019 in the school of materials and energy, Yunnan University.


Subject(s)
Electrochemical Techniques/methods , Glucose/analysis , Metals, Heavy/chemistry , Nanoparticles/chemistry , Oxides/chemistry , Electrodes , Humans , Limit of Detection , Linear Models
10.
Int J Occup Med Environ Health ; 28(2): 395-8, 2015.
Article in English | MEDLINE | ID: mdl-26182934

ABSTRACT

OBJECTIVES: The aim of this study has been to investigate serum activities of liver enzymes in workers exposed to sub-TLV levels of dimethylformamide (DMF). MATERIAL AND METHODS: Seventy-two workers and 72 healthy controls participated in the study. All subjects underwent complete physical examinations and abdominal ultrasound examination. Serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and c-glutamyl transpeptidase (c-GT) were determined by an auto-chemistry analyzer. The data of airborne concentrations of DMF was obtained from the local Center of Disease Control and Prevention. The level of urine N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC) was measured by means of high-performance liquid chromatography. RESULTS: Time weighted average (TWA) concentration of the DMF in workplace was 18.6 (range: 9.8-36.2) mg/m3. The concentration of the AMCC in workers' urine was 28.32 (range: 1.8-58.6) mg/l and 9 workers' AMCC exceeded the biological exposure index (40 mg/l). Thirty-one workers reported gastrointestinal symptoms (abdominal pain, nausea, anorexia) and 10 workers reported headache, dizziness and/or palpitation in the exposed group. Serum analysis revealed that both the mean of serum activities of liver enzymes (ALT, AST and c-GT) and the percentage of workers with abnormal liver function were significantly higher in the exposed group as compared to the controls. CONCLUSIONS: Dimethylformamide can cause liver damage even if air concentration is in the sub-threshold limit value (sub-TLV) level. The protection of skin contact against the exposure to the DMF might be a critical issue as far as the occupational health is concerned.


Subject(s)
Dimethylformamide/toxicity , Liver/drug effects , Occupational Exposure/adverse effects , Transferases/blood , Acetylcysteine/analogs & derivatives , Acetylcysteine/urine , Adult , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Case-Control Studies , Dimethylformamide/metabolism , Female , Humans , Liver Function Tests , Male , Occupational Exposure/analysis , Threshold Limit Values , gamma-Glutamyltransferase/blood
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