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dc.contributor.authorSarapultsev, A.en
dc.contributor.authorChupakhin, O.en
dc.contributor.authorRantsev, M.en
dc.contributor.authorSarapultsev, P.en
dc.contributor.authorDanilova, I.en
dc.contributor.authorMedvedeva, S.en
dc.contributor.authorSidorova, L.en
dc.contributor.authorTseitler, T.en
dc.contributor.authorBrilliant, S.en
dc.contributor.authorTseĭlikman, V.en
dc.date.accessioned2020-09-29T09:47:10Z-
dc.date.available2020-09-29T09:47:10Z-
dc.date.issued2018-
dc.identifier.citationEffects of 1,3,4-thiadiazine compound with antidepressant properties in ligation model of acute pancreatitis / A. Sarapultsev, O. Chupakhin, M. Rantsev, P. Sarapultsev, et al. . — DOI 10.4149/gpb_2018012 // General Physiology and Biophysics. — 2018. — Vol. 5. — Iss. 37. — P. 549-562.en
dc.identifier.issn0231-5882-
dc.identifier.otherhttp://www.elis.sk/download_file.php?product_id=5846&session_id=ce556ltmkbe81jhvv3vbdt10o1pdf
dc.identifier.other1good_DOI
dc.identifier.otherc7397a53-a85a-45f4-9055-647356c922c6pure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85054728546m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/90385-
dc.description.abstractBased on hypotheses concerning the role of stress in acute pancreatitis development, the experimental approach for the decrease stress damage via the use the compound with proven antistress/neuroleptic action was conducted. The study was aimed to discover 2-morpholino-5-phenyl-6H-1,3,4-thiadiazine hydrobromide (compound L-17) therapeutic action in experimental acute pancreatitis. The experimental model used was the ligation model. The trial was carried out on 50 male Wistar rats with average body weight 180-240g. Histological picture of the pancreas was studied and biochemical and enzyme-immunoassays were carried out on the first and seventh days. The significant reduction in mortality on the background of L-17 compound administration was observed. While levels of all cytokines increased in induced experimental acute pancreatitis groups, the cytokine level rise was decreased when compound L-17 was administered. On the cellular level, the study revealed L-17’s ability to prevent granulocytosis and decrease granulocytes infiltration to inflammatory foci. The decrease in inflammatory reaction magnitude and prevention of abscess formation in experimental acute pancreatitis accompanied by sistemic inflamamtion was due to L-17’s ability to reduce neutrophilia and neutrophil entry into the injury zone. © 2018, Slovak Academy of Sciences. All rights reserved.en
dc.description.sponsorshipGovernment Council on Grants, Russian Federationen
dc.description.sponsorshipMinistry of Education and Science of the Russian Federation, Minobrnauka: 17.7255.2017/8.9en
dc.description.sponsorshipAAAA-A18-118020690020-1en
dc.description.sponsorshipFunding information. Partly the study was supported by the Act 211 of the Government of Russian Federation, contract No 02.A03.21.0006; Government contract of Russian Federation with Institute of Immunology and Physiology (AAAA-A18-118020690020-1) and the Ministry of Education and Science of the Russian Federation (# 17.7255.2017/8.9).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherSlovak Academy of Sciencesen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceGeneral Physiology and Biophysicsen
dc.subject1,3,4-THIADIAZINESen
dc.subjectACUTE PANCREATITISen
dc.subjectANTIPSYCHOTICSen
dc.subjectGRANULOCYTESen
dc.subjectNEUROLEPTICSen
dc.subjectSTRESSen
dc.subject1,3,4 THIADIAZINE DERIVATIVEen
dc.subject2 MORPHOLINO 5 PHENYL 6H 1,3,4 THIADIAZINE HYDROBROMIDEen
dc.subjectALANINE AMINOTRANSFERASEen
dc.subjectALPHA AMYLASE PANCREAS ISOENZYMEen
dc.subjectAMYLASEen
dc.subjectANTIDEPRESSANT AGENTen
dc.subjectASPARTATE AMINOTRANSFERASEen
dc.subjectBILIRUBINen
dc.subjectCREATININEen
dc.subjectHEMOGLOBINen
dc.subjectINTERLEUKIN 10en
dc.subjectINTERLEUKIN 1BETAen
dc.subjectUNCLASSIFIED DRUGen
dc.subjectANTIDEPRESSANT AGENTen
dc.subjectCYTOKINEen
dc.subjectTHIADIAZINE DERIVATIVEen
dc.subjectACUTE PANCREATITISen
dc.subjectALANINE AMINOTRANSFERASE BLOOD LEVELen
dc.subjectAMYLASE BLOOD LEVELen
dc.subjectANIMAL CELLen
dc.subjectANIMAL EXPERIMENTen
dc.subjectANIMAL MODELen
dc.subjectANIMAL TISSUEen
dc.subjectARTICLEen
dc.subjectASPARTATE AMINOTRANSFERASE BLOOD LEVELen
dc.subjectBILIRUBIN BLOOD LEVELen
dc.subjectBIOCHEMICAL ANALYSISen
dc.subjectCAUSE OF DEATHen
dc.subjectCELL COUNTen
dc.subjectCELL INFILTRATIONen
dc.subjectCOLLAGEN FIBERen
dc.subjectCONTROLLED STUDYen
dc.subjectCREATININE BLOOD LEVELen
dc.subjectCYTOKINE RESPONSEen
dc.subjectDRUG MECHANISMen
dc.subjectENZYME IMMUNOASSAYen
dc.subjectERYTHROCYTEen
dc.subjectEXOCRINE PANCREASen
dc.subjectFIBROBLASTen
dc.subjectGRANULOCYTEen
dc.subjectGRANULOCYTOSISen
dc.subjectHEMATOCRITen
dc.subjectIMMUNOHISTOCHEMISTRYen
dc.subjectLD50en
dc.subjectLYMPHOCYTEen
dc.subjectMALEen
dc.subjectMONOCYTEen
dc.subjectMORPHOMETRYen
dc.subjectMORTALITYen
dc.subjectMULTIPLE ORGAN FAILUREen
dc.subjectNONHUMANen
dc.subjectPANCREAS DUCT LIGATIONen
dc.subjectPANCREAS NECROSISen
dc.subjectPLASMA CELLen
dc.subjectRATen
dc.subjectTHROMBOCYTEen
dc.subjectACUTE DISEASEen
dc.subjectANIMALen
dc.subjectBLOODen
dc.subjectCYTOLOGYen
dc.subjectDISEASE MODELen
dc.subjectDRUG EFFECTen
dc.subjectIMMUNOLOGYen
dc.subjectLIGATIONen
dc.subjectPANCREATITISen
dc.subjectPSYCHOLOGYen
dc.subjectWISTAR RATen
dc.subjectACUTE DISEASEen
dc.subjectANIMALSen
dc.subjectANTIDEPRESSIVE AGENTSen
dc.subjectCELL COUNTen
dc.subjectCYTOKINESen
dc.subjectDISEASE MODELS, ANIMALen
dc.subjectGRANULOCYTESen
dc.subjectLIGATIONen
dc.subjectMALEen
dc.subjectMONOCYTESen
dc.subjectPANCREATITISen
dc.subjectRATSen
dc.subjectRATS, WISTARen
dc.subjectTHIADIAZINESen
dc.titleEffects of 1,3,4-thiadiazine compound with antidepressant properties in ligation model of acute pancreatitisen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi35651595-
dc.identifier.doi10.4149/gpb_2018012-
dc.identifier.scopus85054728546-
local.affiliationUral Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federationen
local.affiliationInstitute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationen
local.affiliationThe IJ Postovsky Institute of Organic Synthesis of the Ural Branch of the RAS, Ekaterinburg, Russian Federationen
local.affiliationSouth Ural State University, Chelyabinsk, Russian Federationen
local.contributor.employeeSarapultsev, A., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeChupakhin, O., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, The IJ Postovsky Institute of Organic Synthesis of the Ural Branch of the RAS, Ekaterinburg, Russian Federationru
local.contributor.employeeRantsev, M., Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeSarapultsev, P., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeDanilova, I., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeMedvedeva, S., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeSidorova, L., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federationru
local.contributor.employeeTseitler, T., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federationru
local.contributor.employeeBrilliant, S., Ural Federal University Named After the First Pres. Of Russ. B.N. Yeltsin, Ekaterinburg, Russian Federation, Institute of Immunology and Physiology of the Ural Branch of the RAS, 106 Pervomayskaya street, Ekaterinburg, 620002, Russian Federationru
local.contributor.employeeTseĭlikman, V., South Ural State University, Chelyabinsk, Russian Federationru
local.description.firstpage549-
local.description.lastpage562-
local.issue37-
local.volume5-
dc.identifier.wos000448096800006-
local.identifier.pure8177112-
local.identifier.eid2-s2.0-85054728546-
local.identifier.wosWOS:000448096800006-
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