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Artykuły w czasopismach na temat "Ouabain"
Fu, Yong, Dalian Ding, Lei Wei, Haiyan Jiang i Richard Salvi. "Ouabain-Induced Apoptosis in Cochlear Hair Cells and Spiral Ganglion NeuronsIn Vitro". BioMed Research International 2013 (2013): 1–16. http://dx.doi.org/10.1155/2013/628064.
Pełny tekst źródłaLewis, Lynley K., Timothy G. Yandle, Philip J. Hilton, Berit P. Jensen, Evan J. Begg i M. Gary Nicholls. "Endogenous Ouabain Is Not Ouabain". Hypertension 64, nr 4 (październik 2014): 680–83. http://dx.doi.org/10.1161/hypertensionaha.114.03919.
Pełny tekst źródłaTeixeira, Mariana Pires, Natalia Ferreira Haddad, Eliza Freitas Passos, Marcelle Novaes Andrade, Maria Luisa Arantes Campos, Joyle Moreira Carvalho da Silva, Camila Saggioro de Figueiredo i in. "Ouabain Effects on Human Anaplastic Thyroid Carcinoma 8505C Cells". Cancers 14, nr 24 (14.12.2022): 6168. http://dx.doi.org/10.3390/cancers14246168.
Pełny tekst źródłaCurras, M. C., i J. A. Boulant. "Effects of ouabain on neuronal thermosensitivity in hypothalamic tissue slices". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 257, nr 1 (1.07.1989): R21—R28. http://dx.doi.org/10.1152/ajpregu.1989.257.1.r21.
Pełny tekst źródłaBlanco, Gustavo, i Darren P. Wallace. "Novel role of ouabain as a cystogenic factor in autosomal dominant polycystic kidney disease". American Journal of Physiology-Renal Physiology 305, nr 6 (15.09.2013): F797—F812. http://dx.doi.org/10.1152/ajprenal.00248.2013.
Pełny tekst źródłaGomez-Sanchez, Elise P., Mark F. Foecking, Deborah Sellers, Mary S. Blankenship i Celso E. Gomez-Sanchez. "Is the Circulating Ouabain-like Compound Ouabain?" American Journal of Hypertension 7, nr 7_Pt_1 (lipiec 1994): 637–46. http://dx.doi.org/10.1093/ajh/7.7.637.
Pełny tekst źródłaGomez-Sanchez, Elise P., Mark F. Foecking, Sellers Deborah, Mary S. Blankenship i Celso E. Gomez-Sanchez. "Is the Circulating Ouabain-like Compound Ouabain?" American Journal of Hypertension 7, nr 7_Pt_1 (lipiec 1994): 647–50. http://dx.doi.org/10.1093/ajh/7.7.647.
Pełny tekst źródłaMurrell, Julie R., Jeffrey D. Randall, James Rosoff, Ji-liang Zhao, Roderick V. Jensen, Steven R. Gullans i Garner T. Haupert. "Endogenous Ouabain". Circulation 112, nr 9 (30.08.2005): 1301–8. http://dx.doi.org/10.1161/circulationaha.105.554071.
Pełny tekst źródłaHamlyn, John M., i Mordecai P. Blaustein. "Endogenous Ouabain". Hypertension 68, nr 3 (wrzesień 2016): 526–32. http://dx.doi.org/10.1161/hypertensionaha.116.06599.
Pełny tekst źródłaBlaustein, Mordecai P., i John M. Hamlyn. "Ouabain, endogenous ouabain and ouabain-like factors: The Na+ pump/ouabain receptor, its linkage to NCX, and its myriad functions". Cell Calcium 86 (marzec 2020): 102159. http://dx.doi.org/10.1016/j.ceca.2020.102159.
Pełny tekst źródłaRozprawy doktorskie na temat "Ouabain"
Cellnik, Torsten [Verfasser]. "Defunktionalisierung von Ouabain / Torsten Cellnik". Wuppertal : Universitätsbibliothek Wuppertal, 2019. http://d-nb.info/118842209X/34.
Pełny tekst źródłaMagnusson, Emma. "Ouabain Toxicity -Selectivity Towards Renal Cancer Cells". Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278574.
Pełny tekst źródłaOuabain och andra kardiotoniska steroider är kända för att inhibera Na + ,K + -ATPas (NKA),membranpumpen som är ansvarig för den aktiva jontransporten av natrium och kalium ochjongradienten över plasmamembranet. De har påvisat en selektiv toxicitet mot vissatumörceller i jämförelse med primära humana celler, men det är dock inte förstått hurmekanismen bakom denna företeelse fungerar. I denna studien undersökte vi ouabainstoxicitet i njurcancerceller (A-498) och papillomavirustransformerade proximala tubuliceller(hPTC) för att identifiera effektens nyckelkomponenter. Vid exponering av ouabain undersökte vi cellviabiliteten och -densiteten genom MTT- ochkristallviolett-analyser, samt cellmigrering genom scratch-analys. Den cytotoxiska effektenstuderades också under olika pH-förhållanden samt glukos- och kaliumkoncentrationer.Dessutom undersöktes det om apoptos orsakar celldöd genom TUNEL-analys, och omouabain dödar njurcancerceller genom aktivering av den volymreglerade anjonkanalen(VRAC) via NKA. Vi fann minskning av cellernas livskraft vid exponering av ≥ 10 nM ouabain, men effektentycktes dock inte se ut att vara selektiv gentemot cancerceller, inte heller på grund av apoptosoch aktivering av VRAC. Den cytotoxiska effekten var större vid lägre pH, men oberoendeav mediets glukoskoncentrationen. Intressant nog motverkades också effekten vid förhöjdkoncentration av kaliumjoner, och ouabain hämmade selektivt cancercellerna att migrera.Således finns det en viss potential för ouabain att kunna fungera som ett anticancermedel motnjurcancer och att hämma metastasutveckling.
Harwood, Steven Michael. "Development and application of an immunoassay for ouabain and a study of the nature of endogenous ouabain-like compound". Thesis, Queen Mary, University of London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325540.
Pełny tekst źródłaCarneiro, Luciana Teles. "Efeito modulador da ouabaína no sistema imunológico". Universidade Federal da Paraíba, 2011. http://tede.biblioteca.ufpb.br:8080/handle/tede/6866.
Pełny tekst źródłaCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES
Initially known as a cardiotonic steroid capable to inhibit the Na+/K+ATPase, ouabain was identified as an endogenous substance present in human plasma, produced by the adrenal, pituitary and hypothalamus and can interfere with various aspects of immune response. In this study, which aimed to study the modulating effect of ouabain on the immune system in vivo and in vitro using mouse models, we demonstrated that treatment for three consecutive days using 0,56 mg/kg ouabain was able to reduce cell migration induced by mitogen Concanavalian A (Con A) to the peritoneum, and this fact reflects a decrease in the number of polymorphonuclear leukocytes, mainly neutrophils. In this same model, ouabain was also able to increase the number of mononuclear leukocytes in the peritoneal cavity. Evaluating the effect of treatment on lymphocytes in peripheral organs, we found that, in lymphocytes from mesenteric lymph nodes, this substance induces a decrease of 20% of T CD3+ lymphocytes, concomitant with an increase in same percentage of B lymphocytes, without, however, modulating the proportion of CD4+ and CD8+ among themselves, as well as the number of regulatory T cells (CD4+/CD25+). In the thymus, the same treatment, does not affect the proportion of lymphocyte subpopulations studied. The analysis qualitative and quantitatively of peripheral blood leukocytes, biometrics and cellularity of spleen, thymus and lymph nodes showed no change in response to ouabain treatment. Comparative studies using treatment for one or two days, with the same dose of 0,56 mg/kg did not trigger modulation, in vivo, in populations of T lymphocytes, B lymphocytes and subpopulations of CD4+ and CD8+ cells in mesenteric lymph nodes. In addition, ouabain was able to inhibit mitochondrial activity of lymphocytes stimulated with Con A, using MTT assay.These findings indicate an immunomodulatory role of ouabain.
Inicialmente, conhecida como um esteróide cardiotônico e por sua propriedade de inibir a Na+/K+ATPase, a ouabaína foi identificada como uma substância endógena presente no plasma humano, produzida pela adrenal, hipófise e hipotálamo e capaz de interferir em vários aspectos da resposta imune. Neste trabalho, que teve como objetivo estudar o efeito modulador da ouabaína no sistema imunológico in vivo e in vitro por meio de modelos murinos, demonstrou-se que o tratamento por três dias consecutivos com ouabaína utilizando a dose de 0,56 mg/kg foi capaz de reduzir a migração celular induzida pelo mitógeno Concanavaliana A (Con A) para o peritôneo, sendo este fato reflexo da redução do número de leucócitos polimorfonucleares, principalmente, neutrófilos. Neste mesmo modelo, a ouabaína também foi capaz de aumentar o número de leucócitos mononucleares no lavado peritoneal. Avaliando-se o efeito desse tratamento no perfil linfocitário de órgãos periféricos, encontrou-se que, em linfócitos de linfonodos mesentéricos, esta substância induz a uma diminuição de 20% de linfócitos T CD3+, concomitante a um aumento de mesmo percentual de linfócitos B, sem, no entanto, modular a proporção de linfócitos TCD4+ e CD8+ entre si, bem como o número de células T regulatórias (CD4+CD25+). No timo, o mesmo tratamento com a ouabaína não interfere na proporção das subpopulações linfocitárias estudadas. As análises qualitativas e quantitativas de leucócitos do sangue periférico, da biometria e celularidade do baço, timo e linfonodos mesentéricos não apresentaram alteração em resposta ao tratamento com a ouabaína. Estudos comparativos utilizando tratamentos de um ou dois dias, com a mesma dose de 0,56 mg/Kg não desencadearam modulação, in vivo, nas populações de linfócitos T, linfócitos B e das subpopulações de linfócitos TCD4+ e CD8+ nos linfonodos mesentéricos. Adicionalmente, a ouabaína foi capaz de inibir a atividade mitocondrial de linfócitos estimulados com Con A, por meio do ensaio de MTT. Estes resultados indicam um papel imunomodulador da ouabaína.
Tennant, Brian Prichard. "Biosynthesis and physiological characteristics of endogenous ouabain-like substance". Thesis, King's College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.272367.
Pełny tekst źródłaSemra, Yemane Kurban. "Endogenous ouabain-like immunoreactive substance (OLIS) : characterisation and physiological studies". Thesis, King's College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313282.
Pełny tekst źródłaVasconcelos, Danielle Ingrid Bezerra de. "Análise do efeito imunomodulador da ouabaína na inflamação e nocicepção". Universidade Federal da Paraíba, 2011. http://tede.biblioteca.ufpb.br:8080/handle/tede/3640.
Pełny tekst źródłaCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES
Ouabain, known as a cardiotonic glycoside capable of inhibiting the Na+/K+ ATPase, was widely used for heart failure treatment. Identified as an endogenous substance, ouabain is capable of interfering with various physiological functions, including immune system modulation. Besides that, little is known about the involvement of this substance in nociceptive and inflammatory processes. The present study investigated the role of ouabain in acute peripheral inflammation induced by intraplantar administrartion of different phlogistic agents (carrageenan, compound 48/80, histamine, bradykinin, and PGE2) and in nociceptive processes (abdominal writhing induced by acetic acid and hot plate). Ouabain produced a significant reduction in the mouse paw edema induced by carrageenan and compound 48/80. This antiinflammatory effect of ouabain is associated to the inhibition of PGE2, bradykinin, and mast-cell degranulation, but not to histamine. Ouabain also presented a central and peripheral anti-nociceptive activity. This analgesic potential might be related to the inhibition of inflammatory mediators and to activation of opioid receptors, since it was reversed by naloxone, an opioid antagonist. Additionally, the analgesic effect of ouabain was not related to sedative effect or to motor function. Taken together, the present work demonstrated for the first time, in vivo, the antiinflammatory and analgesic potential of ouabain
A Ouabaína é um glicosídeo cardiotônico, inibidor da Na+/K+-ATPase, utilizada na clínica para o tratamento de insuficiência cardíaca. Atualmente, sabe-se que essa substância é endógena, e capaz de interferir em várias funções fisiológicas, inclusive em diversos aspectos do sistema imunológico. Apesar disso, pouco se sabe sobre seu envolvimento em processos inflamatórios e nociceptivos. Neste trabalho, foi avaliada a atividade da Ouabaína na inflamação aguda desencadeada pela administração de diversos agentes flogísticos (carragenina, composto 48/80, histamina, PGE2 e bradicinina) e em modelos nociceptivos (contorções abdominais induzidas por ácido acético e placa quente). A Ouabaína produziu uma redução no edema de pata produzido por carragenina e pelo composto 48/80. Esse potencial anti-inflamatório está relacionado ao bloqueio da degranulação de mastócitos, bem como pela inibição da via da PGE2 e da bradicinina, porém é independente da via da histamina. A Ouabaína também apresentou uma atividade anti-nociceptiva central e periférica. Esse efeito está vinculado à inibição da via dos mediadores inflamatórios e a mecanismos opióides, visto que foi revertido pela administração da naloxona, um inibidor dos receptores opióides. Adicionalmente, foi descrito que a inibição da dor pela Ouabaína não possui envolvimento com sedação ou diminuição da capacidade motora. O conjunto desses dados demonstra pela primeira vez, in vivo, a atividade anti-inflamatória e anti-nociceptiva da Ouabaína.
Gillingwater, Scott David. "Purification and characterisation of ouabain-like compound(s) from biological material". Thesis, King's College London (University of London), 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418070.
Pełny tekst źródłaHarris, Tanoya L. "Ouabain Regulates Caveolin-1 Vesicle Trafficking by a Src-Dependent Mechanism". University of Toledo Health Science Campus / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=mco1333732028.
Pełny tekst źródłaVeerasingham, Shereeni J. "Salt-induced hypertension, central regulation by ouabain-like compounds and angiotensin II". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ58297.pdf.
Pełny tekst źródłaKsiążki na temat "Ouabain"
Dare, Amos O. Ouabain potentiates kainate neurotoxicity: A new rat model of human temporal lobe epilepsy. [New Haven, Conn: s.n.], 1996.
Znajdź pełny tekst źródłaMorton, Sarah Wentworth. Ouabi; Or The Virtues Of Nature: An Indian Tale In Four Cantos. Kessinger Publishing, LLC, 2007.
Znajdź pełny tekst źródłaMorton, Sarah Wentworth. Ouabi; Or The Virtues Of Nature: An Indian Tale In Four Cantos. Kessinger Publishing, LLC, 2007.
Znajdź pełny tekst źródłaCzęści książek na temat "Ouabain"
Ezzaher, Abdellatif, Renaud Mougenot, Alain Gerbi, Nour el Houda Bouanani, Antoine Baggioni, Bertrand Crozatier i Jean-Michel Maixent. "Non Effectiveness of Ouabain and Decrease in Na+/K+ -ATPase Affinity for Ouabain in Failing Rabbit Heart". W The Sodium Pump, 828–31. Heidelberg: Steinkopff, 1994. http://dx.doi.org/10.1007/978-3-642-72511-1_151.
Pełny tekst źródłaHamlyn, J. M. "Discovery of Endogenous Ouabain — A New Mammalian Hormone". W The Sodium Pump, 722–31. Heidelberg: Steinkopff, 1994. http://dx.doi.org/10.1007/978-3-642-72511-1_132.
Pełny tekst źródłaNavaratnam, S., i J. C. Khatter. "Protective Effect of Nifedipine upon Ouabain-Induced Arrhythmias". W Developments in Cardiovascular Medicine, 59–73. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-2057-9_5.
Pełny tekst źródłaLingrel, Jerry B., James Van Huysse, William O’Brien, Elizabeth Jewell-Motz i Patrick Schultheis. "Amino Acid Residues Involved in Ouabain Sensitivity and Cation Binding". W Molecular and Cellular Mechanisms of H+ Transport, 173–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-79301-1_20.
Pełny tekst źródłaLee, Yee-Ki, Kwong-Man Ng, Wing-Hon Lai, Yau-Chi Chan, Yee-Man Lau, Hung-Fat Tse i Chung-Wah Siu. "Differentiation of Embryonic Stem Cells into Cardiomyocytes: Role of Ouabain". W Stem Cells and Cancer Stem Cells, Volume 6, 71–78. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-2993-3_7.
Pełny tekst źródłaRhee, Hee Min. "Parallelism Between Transport Inhibition and L1210 Cell Growth by Ouabain". W Oxygen Transport to Tissue X, 727–34. New York, NY: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-9510-6_89.
Pełny tekst źródłaStokke, E. S., J. Østensen i F. Kiil. "Effect of Ouabain and Acetazolamide on Proximal Tubular Transport in Dogs". W Diuretics: Basic, Pharmacological, and Clinical Aspects, 82–84. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-2067-8_17.
Pełny tekst źródłaGrupp, G., Ingrid L. Grupp, T. Hickerson, S. W. Lee i A. Schwartz. "Biphasic contractile response to ouabain: Species specific? Calcium dependent? Altered sensitivity?" W Cardiac Glycosides 1785–1985, 99–108. Heidelberg: Steinkopff, 1986. http://dx.doi.org/10.1007/978-3-662-11292-2_15.
Pełny tekst źródłaPetzinger, E., K. Fischer i H. Fasold. "Role of the bile acid transport system in hepatocellular ouabain uptake". W Cardiac Glycosides 1785–1985, 297–304. Heidelberg: Steinkopff, 1986. http://dx.doi.org/10.1007/978-3-662-11292-2_40.
Pełny tekst źródłade Lurdes Gonçalves, Maria. "Ouabain binding to erythrocytes from neonates, blood cord and pregnant women". W Cardiac Glycosides 1785–1985, 343–46. Heidelberg: Steinkopff, 1986. http://dx.doi.org/10.1007/978-3-662-11292-2_46.
Pełny tekst źródłaStreszczenia konferencji na temat "Ouabain"
Krivoi, Igor. "ENDOGENOUS OUABAIN AND SKELETAL MUSCLE". W XV International interdisciplinary congress "Neuroscience for Medicine and Psychology". LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m446.sudak.ns2019-15/245-246.
Pełny tekst źródłaBikmurzina, Anastasia, Arina Fedorova, Igor Krivoi i Alexander Markov. "CHANGES IN THE BLOOD-BRAIN BARRIER OF RATS WITH CHRONIC INJECTIONS OF OUABAIN". W XVI International interdisciplinary congress "Neuroscience for Medicine and Psychology". LLC MAKS Press, 2020. http://dx.doi.org/10.29003/m951.sudak.ns2020-16/100.
Pełny tekst źródłaWu, Jun, Mariele Mondala, Meng-Yin Hsieh, Eugene Roberts i Richard Ermel. "Abstract 4403: Antitumor properties of ouabain in lipid double emulsion integrated with tumor cell membrane fractions". W Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-4403.
Pełny tekst źródłaRhee, Chung-Ku, Sung Huyn Bae, So-Young Chang, Phil-Sang Chung i Jae-Yun Jung. "Effect of low level laser therapy (LLLT) on ouabain induced auditory neuropathy in gerbils (Conference Presentation)". W Optical Imaging, Therapeutics, and Advanced Technology in Head and Neck Surgery and Otolaryngology, redaktorzy Brian J. F. Wong i Justus F. Ilgner. SPIE, 2016. http://dx.doi.org/10.1117/12.2212553.
Pełny tekst źródłaWu, Jun, Meng-Yin Hsieh, Yan Wang, Eugene Roberts, Derek Vallejo, Abraham Lee i Richard Ermel. "Abstract 5412: Antitumor properties of ouabain in lipid double emulsion in orthotopic canine osteosarcoma xenografted mouse model". W Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-5412.
Pełny tekst źródłaHwang, Mihwa, Dong Wha Jun, Hyun Jung Kim, Soo Kyung Hwang, Chang-Hun Lee i Sunshin Kim. "Abstract 3335: Ouabain, a cardiac glycoside, inhibits the Fanconi Anemia-BRCA pathway activated by DNA crosslinking agents." W Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-3335.
Pełny tekst źródłaFurihata, Kenichi, Diane J. Nugent, Amy L. Bissonette, Elizabeth Vokac i Thomas J. Kunicki. "PRODUCTION OF HUMAN MONOCLONAL ANTIBODIESSPECIFIC FOR PLATELET MEMBRANE GLYCOPROTEIN IIIa". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643705.
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