Synthesis, physico-chemical characterization and bacteriostatic study of Pt complexes with substituted amine ligands

Three complexes of general formula PtCl2R2 were synthesized, where R is the amine ligand with aromatic substituents. Coordination compounds [Pt(an)2Cl2] (1), [Pt(pa)2Cl2] (2) and [Pt(aph)2Cl2] (3), where an = 2-aminonaphthalene, pa = 2-aminopyrimidine, aph = 4-anilinophenol, were characterized by on-line coupled TG/DTA-MS, powder XRD and spectroscopic techniques (FTIR, ESI–MS and NMR), and tested against selected Gram(+) and Gram(–) bacteria. The thermal data show that all three compounds contain lattice or absorbed water, and the stability of the anhydrous compounds in nitrogen decreases in the order 2 > 1 > 3. Above 200 °C, the complexes loose characteristic fragments of their ligands. The spectroscopic data are in accordance with the thermal properties of the samples and prove their composition. The compounds are more effective inhibitors of Gram(+) than Gram(−) bacteria. © 2016 Akadémiai Kiadó, Budapest, Hungar

Novel copper complexes with glyoximes, amines, schiff bases, semi-and thiosemicarbazones ; synthesis and physico-chemical analysis

In our research project new copper(II) complexes were synthesized with -dioximes, amines, Schiff bases, semi- and thiosemicarbazones such as [Cu(DioxH)2L2], (DioxH2: methyl-butylglyoxime, ethyl-butyl-glyoxime, methyl-phenyl-glyoxime; L: diphenyl-amine, 2-methylimidazole, dibutyl-amine, 2-amino-4-methylpyridine, imidazole, 1-aminonaphthaline), [Cu(octan-2-one)2AL2], (A: hydrazine, phenylhydrazine, o-phenylene-diamine; L: 3-amino1H-1,2,4-triazole, 2-aminopyrimidine, 2-methylimidazole), [Cu(ketone-SC)2], [Cu(ketoneTSC)2], (ketone: propiophenone, butyrophenone; SC: semicarbazone; TSC: thiosemicarbazone), by the reaction of copper(II)-acetate in suitable solvent. After a short bibliographical survey, involving the classification and evolution of copper complexes with possible applications, we analyzed their physicochemical properties using FTIR, Raman, ESR, UV-VIS, powder X-ray diffraction (XRD), mass spectrometry, thermal analysis (TG, DTG, DTA) and SEM. The importance of this class of compounds lies in biochemistry as some of them are antibacterial agents and potential anti-tumour drugs

Ruptured Aortic Aneurysm and Dissection Related Death: an Autopsy Database Analysis

Acute aortic catastrophes (AAC), mainly ruptured aneurysms and dissections, lead all other vascular conditions in morbidity and mortality, even if intervention occurs. The aim of our study was to give a descriptive overview of the demographic and pathological characteristics of AAC. Between 1994 and 2013, 80,469 autopsies were performed at Semmelweis University hospitals in Budapest. After collecting the autopsy reports we were able to create the AAC database upon which we conducted our analysis. We found 567 cases of AAC. The cause of death in 120 of them was classified as a non-ruptured aorta with malperfusion or distal embolization. Of the remaining 447 cases, in 305 the cause of death was a ruptured aortic aneurysm (rAA), and in 142 it was a ruptured aortic dissection (rAD). The distribution of rAA cases was 34.4% thoracal, 4.3% thoracoabdominal, and 61.3% abdominal. We found female dominance where the rAA was thoracal. In rAD cases, 84% were Stanford A and 16% Stanford B type. In both groups we found different pathological distributions. In the prehospital group, the number of thoracal ruptures was considerable. 88% of the patients with Stanford A dissection died in the prehospital or perioperative period. The most progressive AACs were ruptures of intrapericardial aneurysms and Stanford A dissections., however survival rate can be elevated by using rapid imaging examination and immediate surgical intervention. We want to highlight that our study contains such gender differences, which are worth to be taken into consideration

Az új algoritmusok és kódolási eljárások alkalmazása a mobil hírközlésben és informatikában = Application of new algorithms and coding procedures in mobile communications and computing

A kutatási munka során az alábbi résztémákban értünk el eredményeket: - mobil IP, - all IP hálózatok, - útkeresési algoritmusok, - hívásátadási algoritmusok, - mobil technológiák együttműködése, - a szolgáltatás minősége (QoS), - a mobil és informatikai hálózatok és rendszerek biztonsági kérdései, - több-felhasználós vétel, - kódosztásos többszörös hozzáférés, - forgalmi modellezés, - kódkonstrukció kódosztásos technológiákhoz, - kvantum számítástechnikai eljárások, - gráfelmélet, - kombinatorikus optimalizálás. A fenti szakterületeken végzett kutatásaink eredményei közül azokat emeljük ki, amelyeket az alábbi témákban értünk el: - A heterogén mobil hálózatok együttműködési problémái, - A mobil Internet Protokoll alkalmazásával kapcsolatos vizsgálatok, - Többfelhasználós detekciós módszerek a kódosztásos többszörös hozzáféréses mobil rendszerekben, - A heterogén mobil hálózatok forgalmi modellezése, - A mobil informatikai és távközlési hálózatok, rendszerek és szolgáltatások - biztonsági kérdései, - Kvantum számítástechnika és mérnöki alkalmazásai, - Útkeresési és csatornakijelölési algoritmusok fejlesztése és vizsgálata mobil hálózatok számára, alkalmazott gráfelmélet. A kutatásban résztvevők az eredményeket három megvédett PhD disszertációban, egy benyújtás előtt álló akadémiai doktori értekezésben és több beadás előtt álló PhD értekezésben használták fel. A tudományos iskola publikációs listája 135 elemből áll. | The members of the Scientific School have got new results in the following scientific fields: - Mobile IP, all IP networks, - Routing algorithms, - Hand-over algorithms, - Interworking of heterogeneous mobile technologies, - Quality of services (QoS), - Security problems of mobile and information networks and systems, - Multi-user detection, - Code division multiple access, - Traffic modeling, - Code construction for code division technologies, - Quantum computing, - Graph theory, - Combinatorial optimization. On the above mentioned scientific field we have the most important results in the following areas: - Interoperability issues of heterogeneous mobile networks, - Investigations on the applicability of mobile Internet Protocol, - Multi-user detection methods in code division multiple access systems, - Traffic models of heterogeneous mobile networks, - Security issues of mobile information and telecommunication networks, systems and services, - Quantum computing and its engineering applications, - Development and research of routing and channel assigning algorithms for mobile networks, application of the graph theory. The participants of the research used their results in three defended PhD theses, in a dissertation for DSc title, and in some other PhD theses before the final process. The number of the publications of the Scientific School is 135

Oxidative/Nitrative Stress and Inflammation Drive Progression of Doxorubicin-Induced Renal Fibrosis in Rats as Revealed by Comparing a Normal and a Fibrosis-Resistant Rat Strain

Chronic renal fibrosis is the final common pathway of end stage renal disease caused by glomerular or tubular pathologies. Genetic background has a strong influence on the progression of chronic renal fibrosis. We recently found that Rowett black hooded rats were resistant to renal fibrosis. We aimed to investigate the role of sustained inflammation and oxidative/nitrative stress in renal fibrosis progression using this new model. Our previous data suggested the involvement of podocytes, thus we investigated renal fibrosis initiated by doxorubicin-induced (5 mg/kg) podocyte damage. Doxorubicin induced progressive glomerular sclerosis followed by increasing proteinuria and reduced bodyweight gain in fibrosis-sensitive, Charles Dawley rats during an 8-week long observation period. In comparison, the fibrosis-resistant, Rowett black hooded rats had longer survival, milder proteinuria and reduced tubular damage as assessed by neutrophil gelatinase-associated lipocalin (NGAL) excretion, reduced loss of the slit diaphragm protein, nephrin, less glomerulosclerosis, tubulointerstitial fibrosis and matrix deposition assessed by periodic acid-Schiff, Picro-Sirius-red staining and fibronectin immunostaining. Less fibrosis was associated with reduced profibrotic transforming growth factor-beta, (TGF-beta1) connective tissue growth factor (CTGF), and collagen type I alpha 1 (COL-1a1) mRNA levels. Milder inflammation demonstrated by histology was confirmed by less monocyte chemotactic protein 1 (MCP-1) mRNA. As a consequence of less inflammation, less oxidative and nitrative stress was obvious by less neutrophil cytosolic factor 1 (p47phox) and NADPH oxidase-2 (p91phox) mRNA. Reduced oxidative enzyme expression was accompanied by less lipid peroxidation as demonstrated by 4-hydroxynonenal (HNE) and less protein nitrosylation demonstrated by nitrotyrosine (NT) immunohistochemistry and quantified by Western blot. Our results demonstrate that mediators of fibrosis, inflammation and oxidative/nitrative stress were suppressed in doxorubicin nephropathy in fibrosis-resistant Rowett black hooded rats underlying the importance of these pathomechanisms in the progression of renal fibrosis initiated by glomerular podocyte damage

Activation of the miR-17 Family and miR-21 During Murine Kidney Ischemia-Reperfusion Injury.

Background: Ischemia-reperfusion (I/R) is the main cause of acute kidney injury (AKI) in patients. We investigated renal microRNA (miRNA) expression profiles and the time course of changes in selected miRNA expressions after renal I/R to characterize the miRNA network activated during development and recovery from AKI. Methods and Results: One day after lethal (30 minutes) and sublethal (20 minutes) renal ischemia, AKI was verified by renal histology (tubular necrosis, regeneration), blood urea nitrogen (BUN) level, renal mRNA expression, and plasma concentration of neutrophil gelatinase-associated lipocalin (NGAL) in C57BL/6J mice. On the first day after 30-minute, lethal I/R miR-21, miR-17-5p, and miR-106a were elevated out of the 21 miRNAs successfully profiled on the Luminex multiplex assay. After 20-minute, sublethal I/R, renal miR-17-5p and miR-106a expressions were elevated on the first and second days of reperfusion, while miR-21 expression increased later and lasted longer. Renal miR-17-5p and miR-21 expressions correlated with each other. Renal function returned to normal on the fourth day after sublethal I/R. Conclusions: Our results demonstrate that besides miR-21, miR-17-5p, and miR-106a are additionally activated during the maintenance and recovery phases of renal I/R injury. Furthermore, a correlation between renal miR-17-5p and miR-21 expressions warrants further investigation of how they may influence each other and the outcome of renal ischemia-reperfusion injury

Ezrin is down-regulated in diabetic kidney glomeruli and regulates actin reorganization and glucose uptake via GLUT1 in cultured podocytes

Diabetic nephropathy is a complication of diabetes and a major cause of end-stage renal disease. To characterize the early pathophysiological mechanisms leading to glomerular podocyte injury in diabetic nephropathy, we performed quantitative proteomic profiling of glomeruli isolated from rats with streptozotocin-induced diabetes and controls. Fluorescence-based two-dimensional difference gel electrophoresis, coupled with mass spectrometry, identified 29 differentially expressed spots, including actin-binding protein ezrin and its interaction partner, NHERF2, which were down-regulated in the streptozotocin group. Knockdown of ezrin by siRNA in cultured podocytes increased glucose uptake compared with control siRNA-transfected cells, apparently by increasing translocation of glucose transporter GLUT1 to the plasma membrane. Knockdown of ezrin also induced actin remodeling under basal conditions, but reduced insulin-stimulated actin reorganization. Ezrin-dependent actin remodeling involved cofilin-1 that is essential for the turnover and reorganization of actin filaments. Phosphorylated, inactive cofilin-1 was up-regulated in diabetic glomeruli, suggesting altered actin dynamics. Furthermore, IHC analysis revealed reduced expression of ezrin in the podocytes of patients with diabetes. Our findings suggest that ezrin may play a role in the development of the renal complication in diabetes by regulating transport of glucose and organization of the actin cytoskeleton in podocytes. Copyright © 2014 American Society for Investigative Pathology