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16篇 您的检索式:作者名="IMRE V"
    题名 作者 年代 出处 被引量
1Aerylamide from Maillard reaction products显示文摘RICHARD H S IMRE B NATALIA V 2002Nature2002,419,:1
2Size-selective filtration and taxon-specific digestion of plankton algae by silver carp (Hypophthalmichthys molitrix Val.)显示文摘Lajos V?r?s Imre Oldal Mátyás Présing Katalin V.- Balogh Hydrobiologia0,,:1
3Controlled domain wall motion in micron-scale permalloy square rings 显示文摘Imre A Csaba G Metlushko V 2003PhysicaE2003,19,:1
4Calcium Distribution in the Vessel Wall and Intima-Media Thickness of the Human Carotid Arteries显示文摘Mária Tünde Magyar Zita Szikszai Zsófia Kertész Sándor Molnár Imre Uzonyi Gusztáv áron Szíki László Csiba 2007Ultrasound in Medicine & Biology2007,,8:1
5Histone deacetylase inhibitors suppress the inducibility of nuclear factor-kappaB by tumor necrosis factor-alpha receptor-1 down-regulation显示文摘IMRE G GEKELER V LEJA A 2006Cancer Res2006,66,10:1
6Reactome:a knowledge base of biologic pathways and processes显示文摘Imre V Peter D Esther S 2007Genome Biology2007,8,3:1
7Molecular phenotyping:a guide to improving detection of interstitial lung disease in patients with rheumatoid arthritis显示文摘Rekha V Denton CP Imre N 2015Am J Respirat Crit Care Med2015,191,12:1
8Novel method for the preparation of anionic surfactant - selective electrodes 显示文摘IMRE V RBERT M ZOLTN S 2005Lngmuir2005,21,:1
9UV-B induced free radical production in plant leaves and isolated thylakoid membranes显示文摘EVA H IMRE V 1996Plant Science1996,115,:1
10Histone deacetylase inhibitors suppress the inducibility of Nuclear Factor-κB by tumor Necrosis Factor-α Recepor-1 down-regulation显示文摘Imre G Gekeler V Leja A 2006Cancer Res2006,66,10:1
11Rafting MHC-II domains in the APC (presynaptic) plasma membrane and the thresholds for T-cell activation and immunological synapse formation显示文摘Imre G Cynthia D Gyrgy V 2004Immunology Letter2004,92,12:1
12Novel application of an in situ radiotracer method for the study of the formation of surface adlayers in the course of Cr(Ⅵ) reduction on a gold electrode显示文摘Kálmán V Imre S Lajos G 2002Journal of Electroanalytical Chemistry2002,,:1
13Influence of preharvest calcium applications, fruit injury, and storage atmospheres on postharvest brown rot of apple显示文摘IMRE J H BARBARAB B ALEX V 2012Postharvest Biology and Technology2012,67,:1
14Determination of trace elements in human liver biopsy samples by ICP-MS and TXRF: hepatic steatosis and nickel accumulation显示文摘IMRE V AGNES S NoRBET S 2005Anal Bioanal Chem2005,383,5:1
15In- vestigation of shape-dependent switching of coupled nanomag-nets显示文摘Imre A Csaba G Bernstein G H Porod W Metlushko V 2003Superlattices and Microsauctures2003,34,36:1
16A dual role of lysophosphatidic acid type 2 receptor(LPAR2)in nonsteroidal anti-inflammatory drug-induced mouse enteropathy显示文摘Lysophosphatidic acid(LPA)is a bioactive phospholipid mediator that has been found to ameliorate nonsteroidal anti-inflammatory drug(NSAID)-induced gastric injury by acting on lysophosphatidic acid type 2 receptor(LPAR2).In this study,we investigated whether LPAR2 signaling was implicated in the development of NSAID-induced small intestinal injury(enteropathy),another major complication of NSAID use.Wild-type(WT)and Lpar2 deficient(Lpar2^(^(^(−/−))))mice were treated with a single,large dose(20 or 30 mg/kg,i.g.)of indomethacin(IND).The mice were euthanized at 6 or 24 h after IND treatment.We showed that IND-induced mucosal enteropathy and neutrophil recruitment occurred much earlier(at 6 h after IND treatment)in Lpar2^(^(^(−/−)))mice compared to WT mice,but the tissue levels of inflammatory mediators(IL-1β,TNF-α,inducible COX-2,CAMP)remained at much lower levels.Administration of a selective LPAR2 agonist DBIBB(1,10 mg/kg,i.g.,twice at 24 h and 30 min before IND treatment)dose-dependently reduced mucosal injury and neutrophil activation in enteropathy,but it also enhanced IND-induced elevation of several proinflammatory chemokines and cytokines.By assessing caspase-3 activation,we found significantly increased intestinal apoptosis in IND-treated Lpar2^(^(^(−/−)))mice,but it was attenuated after DBIBB administration,especially in non-obese diabetic/severe combined immunodeficiency(NOD/SCID)mice.Finally,we showed that IND treatment reduced the plasma activity and expression of autotaxin(ATX),the main LPA-producing enzyme,and also reduced the intestinal expression of Lpar2 mRNA,which preceded the development of mucosal damage.We conclude that LPAR2 has a dual role in NSAID enteropathy,as it contributes to the maintenance of mucosal integrity after NSAID exposure,but also orchestrates the inflammatory responses associated with ulceration.Our study suggests that IND-induced inhibition of the ATX-LPAR2 axis is an early event in the pathogenesis of enteropathy.Barbara Hutka Anett Várallyay Szilvia B.László András S.Tóth Bálint Scheich Sándor Paku Imre Vörös Zoltán Pós Zoltán V.Varga Derek D.Norman Andrea Balogh Zoltán Benyó Gábor Tigyi Klára Gyires Zoltán S.Zádori 2024Acta Pharmacologica Sinica2024,45,2:0
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