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1.
Sci Total Environ ; 930: 172510, 2024 Jun 20.
Article in English | MEDLINE | ID: mdl-38641119

ABSTRACT

Although complexation between dissolved organic matter (DOM) and ubiquitous Fe is known to have a major influence on electron transferring ability in redoximorphic soil, it was unclear whether and how this complexation affected nitrate reduction and N2O productivity. The nitrate reduction of paddy soil in the presence of crop residues returning under flooding conditions was explored in this study. The rate of nitrate reduction in control soil was 0.0677 d-1, while it improved 1.99 times in treatment soil with Chinese milk vetch (CMV) straw returning. During a 28-day incubation period, N2O productivity decreased 0.08-0.91 ppb in CMV soil and 0.43-0.50 ppb in rice straw soil compared with control. The presence of crop residue increased DOC content and Fe (III) reduction rate, which aided in the formation of Fe (II)-DOC complexation. Meanwhile, the addition of CMV increased the content of DOC by 5.14-78.77 mg/kg and HCl extractable Fe (II) by 35.12-1221.03 mg/kg. Crop residues returning to soil increased the relative abundance of iron reductive and electroactive genera, as well as denitrifying genera with more copies of denitrification genes (Archangiaceae, Gemmatimonadaceae, and Burkholderiaceae). The synergistic effect of Fe-DOC complexation, electroactive genera, and denitrifying genera contributed to up-regulated expression of napA and narG (5.84 × 106 and 3.39 × 107 copies increased in the CMV soil compared to the control) numbers and equally accelerated reduction of nitrate to nitrite, while further nitrite reduction was primarily attributed to the abiotic reaction by Fe (II). From a bio-electrochemical point of view, this work provided new insight into the nitrate reduction of paddy soil impacted by Fe-DOC complexation.


Subject(s)
Nitrates , Soil , Soil/chemistry , Oryza , Iron/chemistry , Agriculture/methods , Oxidation-Reduction , Crops, Agricultural , Soil Microbiology , Denitrification , Soil Pollutants
2.
Front Surg ; 9: 1040711, 2022.
Article in English | MEDLINE | ID: mdl-36406378

ABSTRACT

Background: The ectopic pancreas is a kind of congenital malformation formed during embryonic development, which has no anatomical relationship with the normal pancreas and is a rare solid disease. The ectopic pancreas in the adrenal glands is extremely rare. Case summary: A 32-year-old man was admitted to the hospital after experiencing elevated blood pressure for 2 years as well as dizziness and blurred vision for 2 weeks. He had an elevated blood pressure of 170/110 mmHg (1 mmHg = 0.133 kPa) on physical examination 2 years ago, without palpitations, chest pain, and chest tightness. Two weeks ago, he presented with dizziness and blurred vision. Blood renin and aldosterone levels were elevated. Plain CT and contrast-enhanced CT scan showed nodular thickening of the left adrenal and homogeneous enhancement, which was initially considered adrenal adenoma. The postoperative pathology supported the ectopic pancreas in the left adrenal. After 78 months of postoperative follow-up, no recurrence was observed, but his blood pressure remained persistently high. Conclusion: The ectopic pancreas occurring in the adrenal glands is extremely rare, has no specific clinical symptoms, and is mainly found for other reasons. It can easily be misdiagnosed as an adrenal adenoma. The final confirmation of the diagnosis still depends on the pathological biopsy. A great deal of reporting is still required for whether there is a correlation with elevated blood pressure.

3.
Sci Total Environ ; 838(Pt 4): 156632, 2022 Sep 10.
Article in English | MEDLINE | ID: mdl-35691358

ABSTRACT

BACKGROUND: The effect of high-altitude (HA) on venous thromboembolism (VTE) and its mechanism remains ambiguous. To clarify this, we aimed to conduct a meta-analysis and systematic review to evaluate the incidence of VTE at HA and comparatively low altitude (LA) and figure out the intrinsic risk factors such as susceptibility genes of patients with VTE at HA. METHODS: We selected studies that explored the risk factors for HA and VTE by searching PubMed, Embase, and Web of Science to analyze the impact of HA on VTE. All relevant studies before August 2021 were screened using the terms ([high altitude] OR [plateau] OR [mountain]) AND ([venous thromboembolism] OR [deep vein thrombosis] OR [pulmonary embolism]). Latest studies on the gene of HA-VTE patients were also summarized and analyzed. RESULTS: Fifteen studies were eventually assessed, and the overall numbers of subjects with and without VTE were 1475 and 286,926 respectively. The overall incidence of VTE, deep vein thrombosis (DVT) and pulmonary embolism (PE) in the HA group was significantly higher than that in the LA group (P < 0.01). The overall incidence of VTE, DVT and PE in the HA group was significantly higher than that in the LA group at 30 days post operation (P < 0.05, P < 0.05 and P < 0.01, respectively). At 90 days post operation, incidence of VTE and PE in the HA group was higher than that in the LA group (P < 0.01and P < 0.01, respectively), but there was no difference in the incidence of DVT (P = 0.07). Regarding endogenous factors, the analysis of genes in patients with HA-VTE revealed numerous targeted genes such as ANG, ACE, lncRNA-LINC00 659/UXT-AS1 and GP4. CONCLUSIONS: We observed a significant association between HA and the overall incidence of VTE and that at 30/90 days post operation, indicating that HA may be a risk factor for VTE.


Subject(s)
Pulmonary Embolism , Venous Thromboembolism , Venous Thrombosis , Humans , Altitude , Cell Cycle Proteins , Genetic Predisposition to Disease , Incidence , Molecular Chaperones , Pulmonary Embolism/epidemiology , Risk Factors , Venous Thromboembolism/epidemiology , Venous Thromboembolism/genetics , Venous Thrombosis/epidemiology
4.
J Interv Cardiol ; 2020: 3293587, 2020.
Article in English | MEDLINE | ID: mdl-33214774

ABSTRACT

PURPOSE: To evaluate the efficacy and safety of nicorandil for periprocedural myocardial injury in patients undergoing PCI through meta-analysis of randomized controlled trials. METHODS: We analyzed the clinical data of patients including the incidence of periprocedural myocardial injury (PMI) and major adverse cardiovascular events (MACE) from selected articles. RCTs were retrieved from medical literature databases. RR and 95% confidence intervals (CI) were calculated to compare the endpoints. RESULTS: In total, 15 articles (16 trial comparisons) were retrieved which contained 2221 patients. In general, 1130 patients (50.9%) were randomized to the experimental group, whereas 1091 patients (49.1%) were randomized to the control group. The result showed that nicorandil significantly reduced the incidence of PMI and MACE after PCI compared to the control group. CONCLUSIONS: Overall, early use of nicorandil in patients undergoing percutaneous coronary intervention (PCI) was associated with a significant reduction of PMI and MACE.


Subject(s)
Myocardial Ischemia , Nicorandil/pharmacology , Percutaneous Coronary Intervention/adverse effects , Humans , Intraoperative Complications/prevention & control , Myocardial Ischemia/etiology , Myocardial Ischemia/prevention & control , Risk Adjustment , Vasodilator Agents/pharmacology
8.
Ann Med ; 52(3-4): 145, 2020.
Article in English | MEDLINE | ID: mdl-32167392

Subject(s)
Neoplasms , Biomarkers , Humans
9.
Materials (Basel) ; 12(1)2018 Dec 29.
Article in English | MEDLINE | ID: mdl-30597990

ABSTRACT

Average grain size is usually used to describe a polycrystalline medium; however, many investigations demonstrate the grain-size distribution has a measurable effect on most of mechanical properties. This paper addresses the experimental quantification for the effects of grain-size distribution on attenuation in α-titanium alloy by laser ultrasonics. Microstructures with different mean grain sizes of 26⁻49 µm are obtained via annealing at 800 °C for different holding times, having an approximately log-normal distribution of grain sizes. Experimental measurements were examined by using two different theoretical models: (i) the classical Rokhlin's model considering a single mean grain size, and (ii) the improved Turner's model incorporating a log-normal distribution of grain sizes in the attenuation evaluation. Quantitative agreement between the experiment and the latter model was found in the Rayleigh and the Rayleigh-to-stochastic transition regions. A larger attenuation level was exhibited than the classical theoretical prediction considering a single mean grain size, and the frequency dependence of attenuation reduced from a classical fourth power to an approximately second power due to a greater probability of large grains than the assumed Poisson statistics. The provided results would help support the use of laser ultrasound technology for the non-destructive evaluation of grain size distribution in polycrystalline materials.

10.
Biomed Pharmacother ; 90: 147-152, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28351777

ABSTRACT

Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is a negative regulator of T cell activation, which competes with CD28 for B7.1/B7.2 binding with a greater affinity. Co-expression specific antigens and extracellular domain of CTLA4 represents a promising approach to increase the immunogenicity of DNA vaccines. In this study, we evaluated this interesting approach for its enhancement on G250/MN/CA IX (G250)-specific immune responses and its anti-tumor effects in renal carcinoma mice model. Consequently, we constructed a DNA vaccine containing the G250 and the CTLA-4 gene. Vaccination with the co-expression DNA not only induced much higher level of anti-CTLA4 and anti-G250 antibody, but also increased G250-specific T cell response in mice. To evaluate the anti-tumor efficacy of the plasmids, murine models with G250-expressing tumors were generated. After injection into the tumor-bearing mouse model, the plasmid carrying the co-expression gene of CTLA4 and G250 showed stronger inhibition of tumor growth than the plasmid expressing CTLA4 or G250 alone. These observations emphasize the potential of the CTLA4 and G250 co-expression DNA vaccine, which could represent a promising approach for tumor immunotherapy.


Subject(s)
Antigens, Neoplasm/immunology , CTLA-4 Antigen/immunology , T-Lymphocytes, Cytotoxic/immunology , Vaccines, DNA/immunology , Animals , Antigens, Neoplasm/genetics , CTLA-4 Antigen/genetics , Carcinoma, Renal Cell/genetics , Carcinoma, Renal Cell/immunology , Cell Line, Tumor , Cell Proliferation/genetics , Female , Gene Targeting/methods , Kidney Neoplasms/genetics , Kidney Neoplasms/immunology , Lymphocyte Activation/genetics , Lymphocyte Activation/immunology , Mice , Mice, Inbred BALB C , Plasmids/genetics , Plasmids/immunology , Vaccination/methods
11.
Bosn J Basic Med Sci ; 16(3): 201-8, 2016 Jul 02.
Article in English | MEDLINE | ID: mdl-27294569

ABSTRACT

This study aimed to identify the differential expression levels of androgen receptor (AR), estrogen receptors (ERα, ERß), and progesterone receptor (PGR) between normal prostate and benign prostatic hyperplasia (BPH). The combination of immunohistochemistry, quantitative real-time reverse transcription polymerase chain reaction, and Western blotting assay was used to identify the distribution and differential expression of these receptors at the immunoactive biomarker, transcriptional, and protein levels between 5 normal human prostate tissues and 40 BPH tissues. The results were then validated in a rat model of BPH induced by testosterone propionate and estradiol benzoate. In both human and rat prostate tissues, AR was localized mainly to epithelial and stromal cell nuclei; ERα was distributed mainly to stromal cells, but not exclusively; ERß was interspersed in the basal layer of epithelium, but sporadically in epithelial and stromal cells; PGR was expressed abundantly in cytoplasm of epithelial and stromal cells. There were decreased expression of ERα and increased expression of PGR, but no difference in the expression of ERß in the BPH compared to the normal prostate of both human and rat. Increased expression of AR in the BPH compared to the normal prostate of human was observed, however, the expression of AR in the rat prostate tissue was decreased. This study identified the activation of AR and PGR and repression of ERα in BPH, which indicate a promoting role of AR and PGR and an inhibitory role of ERα in the pathogenesis of BPH.


Subject(s)
Prostatic Hyperplasia/metabolism , Receptors, Androgen/biosynthesis , Receptors, Estrogen/biosynthesis , Receptors, Progesterone/biosynthesis , Adult , Aged , Aged, 80 and over , Animals , Cell Nucleus/metabolism , Cytoplasm/metabolism , Epithelial Cells/metabolism , Estradiol/analogs & derivatives , Estradiol/pharmacology , Humans , Male , Middle Aged , Prostate/drug effects , Prostate/metabolism , Rats , Rats, Sprague-Dawley , Reference Values , Stromal Cells/metabolism , Testosterone Propionate/pharmacology
12.
Nan Fang Yi Ke Da Xue Xue Bao ; 35(2): 295-300, 2015 Feb.
Article in Chinese | MEDLINE | ID: mdl-25736134

ABSTRACT

OBJECTIVE: To observe the effects of different loading doses of atorvastatin calcium on the outcomes of percutaneous coronary intervention (PCI) in elderly patients with coronary heart disease (CHD). METHODS: A total of 120 CHD patients aged over 80 years were randomly assigned into 3 equal groups to receive intensive pretreatment with statin at the doses of 20, 40, or 60 mg prior to PCI performed within 48 to 72 h after admission. The changes of postoperative cardiac biochemical markers including creatine kinase isoenzyme (CKMB), troponin I (cTNI) and high-sensitivity c-reactive protein (hs-CRP) were observed and the incidence of major adverse cardiac events (MACE, including cardiac death, myocardial infarction, and target vessel revascularization) were recorded within 30 days after PCI. RESULTS: Thirty-four patients in 20 mg statin group, 40 in 40 mg statin group, and 38 in 60 mg statin group completed this study. In all the 3 groups, hs-CRP level significantly increased at 12 and 24 h after PCI compared with the preoperative levels (P<0.05). The patients in 60 mg statin group showed significantly lower levels of CKMB, cTNI, and hs-CRP at 24 h after PCI than those in 20 mg statin group (P<0.05), and had also a significantly lower incidence of total MACE within 30 days after PCI (2.6% vs 26.5%, P=0.003) resulting primarily from significantly reduced myocardial infarction associated with PCI (2.6% vs 20.6%, P=0.016). The adverse drug reactions were comparable among the 3 groups (P>0.05). CONCLUSIONS: Intensive pretreatment with 60 mg/day atorvastatin calcium can significantly reduce myocardial infarction related to PCI with good safety in elderly patients with CHD.


Subject(s)
Coronary Disease/drug therapy , Heptanoic Acids/therapeutic use , Percutaneous Coronary Intervention , Pyrroles/therapeutic use , Aged, 80 and over , Atorvastatin , Biomarkers/metabolism , Coronary Disease/surgery , Dose-Response Relationship, Drug , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Myocardial Infarction/prevention & control
13.
Carbohydr Res ; 404: 87-92, 2015 Mar 02.
Article in English | MEDLINE | ID: mdl-25665784

ABSTRACT

A series of Pt nanoparticles supported on carbon nanotubes (CNTs) were synthesized using the incipient-wetness impregnation method. These catalysts were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscope (TEM) techniques. The characterization results indicate that the Pt nanoparticles were highly dispersed on the surface of the CNTs, and the mean size was less than 5 nm. These catalysts were utilized to convert cellulose to hexitol, ethylene glycerol (EG), and 1,2-propylene glycol (1,2-PG) under low H2 pressure. The total yields were as high as 71.4% for EG and 1,2-PG using 1Pt/CNTs as the catalyst in the hydrolytic hydrogenation of cellulose under mild reaction conditions.


Subject(s)
Cellulose/chemistry , Nanotubes/chemistry , Polymers/chemistry , Catalysis , Microscopy, Electron, Transmission , Particle Size , Spectrum Analysis, Raman , X-Ray Diffraction
14.
Cell Immunol ; 283(1-2): 31-7, 2013.
Article in English | MEDLINE | ID: mdl-23850961

ABSTRACT

OBJECTIVE: To investigate whether ESM-1 expression change reflects the impairment of endothelial cells and rejection after kidney transplantation, ESM-1 expression was detected under various immune states in this study. METHODS: Kidney transplantations were performed from BN to LEW rats. Syngenic LEW-LEW grafts were used as controls. The LEW recipient rats were divided into acute rejection (AR) group, ciclosporin A (CsA) group and control group. In each group, 10 rats were sacrificed at 1, 5, and 7d after operation, respectively, and blood and kidney samples were collected. In the rat model of kidney transplantation, ESM-1 mRNA and ESM-1 protein expression were detected in various immune states to verify if ESM-1 can reflect endothelial cell impairment sensitively. RESULTS: ESM-1 mRNA (1d vs. 3d, P<0.01;3d vs. 7d, P=0.018) and ESM-1 protein expression was upregulated significantly in the AR group (P<0.01, 5 and 7d), when compared to CsA group and control group. In CsA group, the cell apoptosis rate decreased when compared to AR group (P<0.01). Pathological impairment was more serious in AR group than in CsA group (P<0.01). CONCLUSIONS: Peripheral blood ESM-1 mRNA and ESM-1 protein expression in kidney grafts can reflect the severity of endothelial cell impairment. Thus, ESM-1 may be used as a new indicator for AR prediction and diagnosis. Nevertheless, further investigation is required to test if it meets the criteria for clinical utility.


Subject(s)
Graft Rejection/metabolism , Kidney Transplantation/physiology , Proteoglycans/metabolism , Animals , Blotting, Western , Enzyme-Linked Immunosorbent Assay , Fluorescent Antibody Technique , Graft Rejection/immunology , Rats , Rats, Inbred Lew , Real-Time Polymerase Chain Reaction , Transplantation, Homologous
15.
J Exp Clin Cancer Res ; 32: 10, 2013 Feb 26.
Article in English | MEDLINE | ID: mdl-23442927

ABSTRACT

BACKGROUND: Bladder transitional cell carcinoma greatly threatens human health all over the world. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) shows a strong apoptosis-inducing effect on a variety of cancer cells including bladder cancer. However, adenovirus-mediated TRAIL expression still showed cytotoxicity to normal cells mainly due to lack of tumor specificity. METHODS: To solve the problem, we applied miRNA response elements (MREs) of miR-1, miR-133 and miR-218 to confer TRAIL expression with specificity to bladder cancer cells. RESULTS: Expression of miR-1, miR-133 and miR-218 was greatly decreased in bladder cancer than normal bladder tissue. Luciferase assay showed that application of the 3 MREs was able to restrain exogenous gene expression to within bladder cancer cells. Subsequently, we constructed a recombinant adenovirus with TRAIL expression regulated by MREs of miR-1, miR-133 and miR-218, namely Ad-TRAIL-MRE-1-133-218. qPCR, immunoblotting and ELISA assays demonstrated that Ad-TRAIL-MRE-1-133-218 expressed in bladder cancer cells, rather than normal bladder cells. The differential TRAIL expression also led to selective apoptosis-inducing and growth-inhibiting effect of Ad-TRAIL-MRE-1-133-218 on bladder cancers. Finally, bladder cancer xenograft in mouse models further confirmed that Ad-TRAIL-MRE-1-133-218 effectively suppressed the growth of bladder cancers. CONCLUSIONS: Collectively, we demonstrated that MREs-based TRAIL delivery into bladder cancer cells was feasible and efficient for cancer gene therapy.


Subject(s)
Carcinoma, Transitional Cell/therapy , MicroRNAs/genetics , Response Elements , TNF-Related Apoptosis-Inducing Ligand/genetics , Urinary Bladder Neoplasms/therapy , Adenoviridae/genetics , Animals , Apoptosis/genetics , Carcinoma, Transitional Cell/genetics , Carcinoma, Transitional Cell/metabolism , Carcinoma, Transitional Cell/pathology , Cell Survival/genetics , Female , Genetic Therapy/methods , Humans , Mice , Mice, Inbred BALB C , Mice, Nude , MicroRNAs/biosynthesis , TNF-Related Apoptosis-Inducing Ligand/biosynthesis , Urinary Bladder Neoplasms/genetics , Urinary Bladder Neoplasms/metabolism , Urinary Bladder Neoplasms/pathology , Xenograft Model Antitumor Assays
16.
Mol Biol Rep ; 39(6): 6707-14, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22311018

ABSTRACT

The recent studies indicated that the epithelial cell adhesion molecule E-cadherin is a well-recognized molecule that is important in cell adhesion. To further investigate the molecular basis of this notion, we used small-interfering RNA to inhibit E-cadherin function and found that loss of E-cadherin promoted Colorectal cancer cell growth, invasion and drug resistance through induction of ß-catenin nuclear translocation and epithelial-to-mesenchymal transition. Further analysis of E-cadherin expression with clinicopathologic parameters showed that E-cadherin expression decreased in Colorectal cancer patients who developed liver metastasis (P = 0.043). These findings indicate that E-cadherin loss in tumors contributes to progression and metastatic dissemination. Thus, E-cadherin can act as a central modulator of the cell biological phenotypes and a potential prognostic marker in Colorectal cancer.


Subject(s)
Cadherins/genetics , Colorectal Neoplasms/pathology , Drug Resistance, Neoplasm , Liver Neoplasms/secondary , Active Transport, Cell Nucleus , Antimetabolites, Antineoplastic/pharmacology , Cadherins/metabolism , Cell Adhesion , Cell Movement , Cell Proliferation , Cell Survival/drug effects , Colorectal Neoplasms/metabolism , Epithelial-Mesenchymal Transition , Fluorouracil/pharmacology , Gene Knockdown Techniques , HCT116 Cells , HT29 Cells , Humans , Liver Neoplasms/metabolism , Methotrexate/pharmacology , Neoplasm Invasiveness , Transcription, Genetic , beta Catenin/metabolism
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