TY - JOUR AU - Sántha, Petra AU - Veszelka, Szilvia AU - Hoyk, Zsófia AU - Mészáros, Mária AU - Walter, Fruzsina AU - Tóth, Andrea AU - Kiss, Lóránd AU - Kincses, András AU - Oláh, Zita AU - Seprényi, György AU - Rákhely, Gábor AU - Dér, András AU - Pákáski, Magdolna AU - Kálmán, János AU - Kittel, Ágnes AU - Deli, Mária Anna TI - Restraint stress-induced morphological changes at the blood-brain barrier in adult rats JF - FRONTIERS IN MOLECULAR NEUROSCIENCE J2 - FRONT MOL NEUROSCI VL - 8 PY - 2016 PG - 15 SN - 1662-5099 DO - 10.3389/fnmol.2015.00088 UR - https://m2.mtmt.hu/api/publication/2989762 ID - 2989762 N1 - These authors have contributed equally to this work: Ágnes Kittel6 and Mária A. Deli. This study was supported by the European Union and the State of Hungary (grant nos. TÁMOP-4.2.1/B-09/1/KONV-2010-0005, TÁMOP-4.2.2.A-11/1/KONV-2012-0052, “National Excellence Program” A/2-11-1-2012-0001) and the Hungarian Research Fund (OTKA 83667). LA - English DB - MTMT ER - TY - JOUR AU - Lénárt, Nikolett AU - Walter, Fruzsina AU - Bocsik, Alexandra AU - Sántha, Petra AU - Tóth, Erzsébet Melinda AU - Harazin, András AU - Tóth, Andrea AU - Vizler, Csaba AU - Török, Zsolt AU - Pilbat, Ana Maria AU - Vigh, László AU - Puskás, László AU - Sántha, Miklós AU - Deli, Mária Anna TI - Cultured cells of the blood-brain barrier from apolipoprotein B-100 transgenic mice: effects of oxidized low-density lipoprotein treatment JF - FLUIDS AND BARRIERS OF THE CNS J2 - FLUIDS BARRIERS CNS VL - 12 PY - 2015 PG - 16 SN - 2045-8118 DO - 10.1186/s12987-015-0013-y UR - https://m2.mtmt.hu/api/publication/2920970 ID - 2920970 LA - English DB - MTMT ER - TY - THES AU - Sántha, Petra TI - Stress-induced changes in gene transcriptions and translations related to Alzheimer’s disease PB - Szegedi Tudományegyetem (SZTE) PY - 2014 SP - 49 DO - 10.14232/phd.2358 UR - https://m2.mtmt.hu/api/publication/2781263 ID - 2781263 LA - English DB - MTMT ER - TY - JOUR AU - Sándor, Nikolett AU - Walter, Fruzsina AU - Bocsik, Alexandra AU - Sántha, Petra AU - Schilling-Tóth, Boglárka AU - Léner, Violetta AU - Varga, Zoltán AU - Kahán, Zsuzsanna AU - Deli, Mária Anna AU - Sáfrány, Géza AU - Hegyesi, Hargita TI - Low dose cranial irradiation-induced cerebrovascular damage is reversible in mice JF - PLOS ONE J2 - PLOS ONE VL - 9 PY - 2014 IS - 11 PG - 13 SN - 1932-6203 DO - 10.1371/journal.pone.0112397 UR - https://m2.mtmt.hu/api/publication/2773366 ID - 2773366 N1 - Contributed equally to this work with: Nikolett Sándor, Fruzsina R. Walter LA - English DB - MTMT ER - TY - JOUR AU - Tóth, Andrea AU - Walter, Fruzsina AU - Bocsik, Alexandra AU - Sántha, Petra AU - Veszelka, Szilvia AU - Nagy, Lajos István AU - Puskás, László AU - Couraud, PO AU - Takata, F AU - Dohgu, S AU - Kataoka, Y AU - Deli, Mária Anna TI - Edaravone protects against methylglyoxal-induced barrier damage in human brain endothelial cells JF - PLOS ONE J2 - PLOS ONE VL - 9 PY - 2014 IS - 7 PG - 14 SN - 1932-6203 DO - 10.1371/journal.pone.0100152 UR - https://m2.mtmt.hu/api/publication/2707330 ID - 2707330 N1 - Cited By :29 Export Date: 20 June 2022 CODEN: POLNC AB - BACKGROUND: Elevated level of reactive carbonyl species, such as methylglyoxal, triggers carbonyl stress and activates a series of inflammatory responses leading to accelerated vascular damage. Edaravone is the active substance of a Japanese medicine, which aids neurological recovery following acute brain ischemia and subsequent cerebral infarction. Our aim was to test whether edaravone can exert a protective effect on the barrier properties of human brain endothelial cells (hCMEC/D3 cell line) treated with methylglyoxal. METHODOLOGY: Cell viability was monitored in real-time by impedance-based cell electronic sensing. The barrier function of the monolayer was characterized by measurement of resistance and flux of permeability markers, and visualized by immunohistochemistry for claudin-5 and β-catenin. Cell morphology was also examined by holographic phase imaging. PRINCIPAL FINDINGS: Methylglyoxal exerted a time- and dose-dependent toxicity on cultured human brain endothelial cells: a concentration of 600 µM resulted in about 50% toxicity, significantly reduced the integrity and increased the permeability of the barrier. The cell morphology also changed dramatically: the area of cells decreased, their optical height significantly increased. Edaravone (3 mM) provided a complete protection against the toxic effect of methylglyoxal. Co-administration of edaravone restored cell viability, barrier integrity and functions of brain endothelial cells. Similar protection was obtained by the well-known antiglycating molecule, aminoguanidine, our reference compound. CONCLUSION: These results indicate for the first time that edaravone is protective in carbonyl stress induced barrier damage. Our data may contribute to the development of compounds to treat brain endothelial dysfunction in carbonyl stress related diseases. LA - English DB - MTMT ER - TY - CONF AU - Sántha, Petra AU - Veszelka, Szilvia AU - Kiss, Lóránd AU - Walter, Fruzsina AU - Oláh, Zita AU - Tóth, Andrea AU - Bocsik, Alexandra AU - Pákáski, Magdolna AU - Kálmán, János AU - Kittel, Ágnes AU - Deli, Mária TI - Stressz hatása a vér-agy-gátra: mikroszkópos vizsgálatok patkány agymetszeteken = [Effects of stress on the blood-brain-barrier: microscopic studies on rat brain sections] T2 - 14. Kolozsvári Biológus Napok : Kolozsvár, 2013. április 12-14. : kivonatfüzet = [14th Biology Days : Cluj-Napoca, 12-14 April 2013 : abstracts] PB - Kolozsvári Akadémiai Bizottság C1 - Kolozsvár PY - 2013 SP - 54 EP - 54 PG - 1 UR - https://m2.mtmt.hu/api/publication/2701829 ID - 2701829 LA - English DB - MTMT ER - TY - CONF AU - Fodor, Eszter AU - Pákáski, Magdolna AU - Sántha, Petra AU - Sántha, Miklós AU - Janka, Zoltán AU - Kálmán, János TI - Immobilizációs stressz hatása a β-aktin citoszkeletonra vad típusú és apoB transzgénikus egér agyban = [The effect of immobilization stress on the β-actin cytoskeleton in wild type and apoB transgenic mice brain] T2 - 14. Kolozsvári Biológus Napok : Kolozsvár, 2013. április 12-14. : kivonatfüzet = [14th Biology Days : Cluj-Napoca, 12-14 April 2013 : abstracts] PB - Kolozsvári Akadémiai Bizottság C1 - Kolozsvár PY - 2013 SP - 26 EP - 26 PG - 1 UR - https://m2.mtmt.hu/api/publication/2701821 ID - 2701821 LA - English DB - MTMT ER - TY - JOUR AU - Sántha, Petra TI - Életünk a stressz árnyékában JF - ÉLET ÉS TUDOMÁNY J2 - ÉLET ÉS TUDOMÁNY VL - 47 PY - 2013 SP - 1488 EP - 1489 PG - 2 SN - 0013-6077 UR - https://m2.mtmt.hu/api/publication/2500898 ID - 2500898 LA - Hungarian DB - MTMT ER - TY - JOUR AU - Sántha, Petra AU - Pákáski, Magdolna AU - Fodor, Eszter AU - Fazekas, OC AU - Kálmán, Sára AU - Kálmán, János (ifj.) AU - Janka, Zoltán AU - Szabó, Gyula AU - Kálmán, János TI - Cytoskeletal Protein Translation and Expression in the Rat Brain Are Stressor-Dependent and Region-Specific JF - PLOS ONE J2 - PLOS ONE VL - 8 PY - 2013 IS - 10 PG - 8 SN - 1932-6203 DO - 10.1371/journal.pone.0073504 UR - https://m2.mtmt.hu/api/publication/2437204 ID - 2437204 AB - Stress is an integral component of life that can sometimes cause a critical overload, depending on the qualitative and quantitative natures of the stressors. The involvement of actin, the predominant component of dendritic integrity, is a plausible candidate factor in stress-induced neuronal cytoskeletal changes. The major aim of this study was to compare the effects of three different stress conditions on the transcription and translation of actin-related cytoskeletal genes in the rat brain. Male Wistar rats were exposed to one or other of the frequently used models of physical stress, i.e. electric foot shock stress (EFSS), forced swimming stress (FSS), or psychosocial stress (PSS) for periods of 3, 7, 14, or 21 days. The relative mRNA and protein expressions of beta-actin, cofilin and mitogen-activated protein kinase 1 (MAPK-1) were determined by qRT- PCR and western blotting from hippocampus and frontal cortex samples. Stressor-specific alterations in both beta-actin and cofilin expression levels were seen after stress. These alterations were most pronounced in response to EFSS, and exhibited a U-shaped time course. FSS led to a significant beta-actin mRNA expression elevation in the hippocampus and the frontal cortex after 3 and 7 days, respectively, without any subsequent change. PSS did not cause any change in beta-actin or cofilin mRNA or protein expression in the examined brain regions. EFSS, FSS and PSS had no effect on the expression of MAPK-1 mRNA at any tested time point. These findings indicate a very delicate, stress type-dependent regulation of neuronal cytoskeletal components in the rat hippocampus and frontal cortex. LA - English DB - MTMT ER - TY - JOUR AU - Fodor, Eszter Klára AU - Sántha, Petra AU - Oláh, Zita AU - Sántha, Miklós AU - Pákáski, Magdolna AU - Janka, Zoltán AU - Kálmán, János TI - Immobilizációs stressz hatása a β-aktin citoszkeletonra apoB transzgénikus egér agyban JF - NEUROPSYCHOPHARMACOLOGIA HUNGARICA J2 - NEUROPSYCHOPHARM HUNG VL - 14 PY - 2012 IS - Suppl. 1 SP - 21 EP - 21 PG - 1 SN - 1419-8711 UR - https://m2.mtmt.hu/api/publication/2701705 ID - 2701705 LA - Hungarian DB - MTMT ER -