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PLoS ONE, ISSN 1932-6203, 11/2014, Volume 9, Issue 11, p. e112394
Objective: In diabetes, vascular dysfunction is characterized by impaired endothelial function due to increased oxidative stress. Empagliflozin, as a selective... 
NADPH OXIDASE | GLYCEMIC CONTROL | ORGANIC NITRATES | ENDOTHELIAL DYSFUNCTION | OXIDANT STRESS | MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | MULTIDISCIPLINARY SCIENCES | NITRIC-OXIDE | BURST ACTIVITY | GLYCATION END-PRODUCTS | SGLT-2 INHIBITOR | Benzhydryl Compounds - administration & dosage | Male | Insulin - blood | Diabetes Mellitus, Experimental | Inflammation Mediators - metabolism | Streptozocin - adverse effects | Cytokines - genetics | Receptor for Advanced Glycation End Products | Diabetic Angiopathies - metabolism | Gene Expression | Glucosides - pharmacology | Cytokines - metabolism | Signal Transduction | Diabetes Complications - metabolism | RNA, Messenger - genetics | Rats | Diabetes Complications - drug therapy | Diabetic Angiopathies - drug therapy | Sodium-Glucose Transporter 2 - antagonists & inhibitors | Blood Glucose - drug effects | Insulin - metabolism | Animals | Glucosides - administration & dosage | Glucose - metabolism | Benzhydryl Compounds - pharmacology | Hemodynamics - drug effects | Oxidative Stress - drug effects | Receptors, Immunologic - metabolism | Type 2 diabetes | Oxidative stress | RNA | Streptozocin | Type 1 diabetes | Blood sugar | Fluorescence | Hypoglycemic agents | Health aspects | Enzyme-linked immunosorbent assay | Diabetes therapy | Drugs | Drinking water | Intravenous administration | Dehydrogenases | Staining | Diabetic neuropathy | Glucose | Blood | Isometric | Hyperglycemia | Rodents | Aorta | Oxidation | Pancreas | Cardiology | Age | Glucose transporter | Excretion | Advanced glycosylation end products | Diabetes mellitus | Blood vessels | Chemiluminescence | Inflammation | Glycosylation | Injection | Gene expression | Insulin | Studies | Polymerase chain reaction | Signaling | Inhibitors | Sodium | Islets of Langerhans | Diabetes | Laboratory animals | Transporter
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 06/2017, Volume 174, Issue 12, pp. 1620 - 1632
Background and Purpose Excessive inflammation in sepsis causes microvascular thrombosis and thrombocytopenia associated with organ dysfunction and high... 
CARDIAC-FUNCTION | DIPEPTIDYL PEPTIDASE-4 INHIBITOR | ADENOSINE-DEAMINASE | CONCISE GUIDE | PHARMACOLOGY | INFLAMMATION | INSULIN-SECRETION | CARDIOVASCULAR-DISEASE | PHARMACOLOGY & PHARMACY | SEPSIS | ATHEROSCLEROTIC LESION | Dipeptidyl Peptidase 4 - metabolism | Venous Thrombosis - chemically induced | Lipopolysaccharides - administration & dosage | Mice, Inbred C57BL | Venous Thrombosis - metabolism | Microvessels - metabolism | Endotoxemia - chemically induced | Microvessels - drug effects | Dipeptidyl Peptidase 4 - genetics | Male | Mice, Knockout | Glucagon-Like Peptide-1 Receptor - metabolism | Animals | Dipeptidyl Peptidase 4 - deficiency | Signal Transduction - drug effects | Mice | Platelet Activation - drug effects | Oxidative Stress - drug effects | Endotoxemia - metabolism | Glucagon-Like Peptide-1 Receptor - deficiency | Nitric Oxide - metabolism | Glucagon-Like Peptide-1 Receptor - agonists | Oxidative stress | Medical research | Glucagon | Mortality | Medicine, Experimental | Hemoglobin | Thrombosis | Blood clot | Protein kinase A | Fluorescence | Activation | Iron | Damage prevention | Lipopolysaccharides | Proteins | Clonal deletion | Deletion | Aorta | Inhibition | Supplementation | Thromboembolism | Thrombocytopenia | Peptidase | Incubation | Immunomodulation | Cyclic AMP | Inflammation | Injection | Survival | Nitric-oxide synthase | White blood cells | Monocytes | Medical prognosis | Sepsis | Microvasculature | Pulmonary circulation | Receptor mechanisms | Platelets | Themed Section | Research Paper
Journal Article
by Egea, Javier and Fabregat, Isabel and Frapart, Yves M and Ghezzi, Pietro and Görlach, Agnes and Kietzmann, Thomas and Kubaichuk, Kateryna and Knaus, Ulla G and Lopez, Manuela G and Olaso-Gonzalez, Gloria and Petry, Andreas and Schulz, Rainer and Vina, Jose and Winyard, Paul and Abbas, Kahina and Ademowo, Opeyemi S and Afonso, Catarina B and Andreadou, Ioanna and Antelmann, Haike and Antunes, Fernando and Aslan, Mutay and Bachschmid, Markus M and Barbosa, Rui M and Belousov, Vsevolod and Berndt, Carsten and Bernlohr, David and Bertrán, Esther and Bindoli, Alberto and Bottari, Serge P and Brito, Paula M and Carrara, Guia and Casas, Ana I and Chatzi, Afroditi and Chondrogianni, Niki and Conrad, Marcus and Cooke, Marcus S and Costa, João G and Cuadrado, Antonio and My-Chan Dang, Pham and De Smet, Barbara and Debelec–Butuner, Bilge and Dias, Irundika H.K and Dunn, Joe Dan and Edson, Amanda J and El Assar, Mariam and El-Benna, Jamel and Ferdinandy, Péter and Fernandes, Ana S and Fladmark, Kari E and Förstermann, Ulrich and Giniatullin, Rashid and Giricz, Zoltán and Görbe, Anikó and Griffiths, Helen and Hampl, Vaclav and Hanf, Alina and Herget, Jan and Hernansanz-Agustín, Pablo and Hillion, Melanie and Huang, Jingjing and Ilikay, Serap and Jansen-Dürr, Pidder and Jaquet, Vincent and Joles, Jaap A and Kalyanaraman, Balaraman and Kaminskyy, Danylo and Karbaschi, Mahsa and Kleanthous, Marina and Klotz, Lars-Oliver and Korac, Bato and Korkmaz, Kemal Sami and Koziel, Rafal and Kračun, Damir and Krause, Karl-Heinz and Křen, Vladimír and Krieg, Thomas and Laranjinha, João and Lazou, Antigone and Li, Huige and Martínez-Ruiz, Antonio and Matsui, Reiko and McBean, Gethin J and Meredith, Stuart P and Messens, Joris and Miguel, Verónica and Mikhed, Yuliya and Milisav, Irina and Milković, Lidija and Miranda-Vizuete, Antonio and Mojović, Miloš and Monsalve, María and Mouthuy, Pierre-Alexis and Mulvey, John and Münzel, Thomas and Muzykantov, Vladimir and Nguyen, Isabel T.N and Oelze, Matthias and Oliveira, Nuno G and Palmeira, Carlos M and Papaevgeniou, Nikoletta and ...
Redox Biology, ISSN 2213-2317, 10/2017, Volume 13, Issue C, pp. 94 - 162
Journal Article