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Relative effects of furosemide and ethacrynic acid on ion transport and energy metabolism in slices of rat kidney-cortex

dc.contributor.authorRusso, M. A.en_US
dc.contributor.authorRossum, George D. V.en_US
dc.contributor.authorErnst, Stephen A.en_US
dc.date.accessioned2006-09-11T17:37:23Z
dc.date.available2006-09-11T17:37:23Z
dc.date.issued1981-08en_US
dc.identifier.citationRossum, G. D. V.; Ernst, S. A.; Russo, M. A.; (1981). "Relative effects of furosemide and ethacrynic acid on ion transport and energy metabolism in slices of rat kidney-cortex." Naunyn-Schmiedeberg's Archives of Pharmacology 317(1): 90-96. <http://hdl.handle.net/2027.42/46309>en_US
dc.identifier.issn1432-1912en_US
dc.identifier.issn0028-1298en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46309
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7279013&dopt=citationen_US
dc.description.abstractThe effects of furosemide and ethacrynic acid have been studied using slices of rat kidney cortex incubated in a Ringer medium. At concentrations from 0.2–2.0 mM, furosemide had no significant effect on the tissue ATP content or on the metabolism-dependent net movements of intracellular Na + , K + and Ca 2+ . It did, however, induce an increase in the net, outward movement of Cl − ; we suggest that this may have srisen from inhibition of a Cl − accumulating mechanism. In contrast, ethacrynic acid in the same concentration range caused marked reduction of cell respiration and ATP content and virtually total inhibitition of several processes of ion transport (Na + , Cl − and Ca 2+ loss, and K + uptake). Concentrations of furosemide greater than 5 mM caused marked inhibition of energy metabolism and transport of ions, and 10 mM furosemide had quantitatively similar effects to 2 mM ethacrynic acid. Electron micrographs of kidney-cortex slices treated with the diuretics at 2 mM show that the ultrastructure was well maintained in the presence of furosemide but that ethacrynic acid caused severe structural disorganisation and necrosis. The mitochondria were generally in the orthodox configuration in the presence of furosemide, but swollen in ethacrynic acid in accord with the marked effects of 2 mM ethacrynate on mitochondrial energy metabolism. Of the effects we have detected, that of low concentrations of furosemide on Cl − movement appears to be rather specific. Higher concentrations of this agent (5 mM and above), and all concentrations of ethacrynic acid studied (0.1–5.0 mM), have several inhibitory effects which seem to result from primary inhibition of mitochondrial activities and are presumably manifestations of toxicity.en_US
dc.format.extent2384777 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherCl − Transporten_US
dc.subject.otherEnergy Metabolismen_US
dc.subject.otherFurosemideen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherKidney Cortexen_US
dc.subject.otherNeurosciencesen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherEthacrynic Aciden_US
dc.subject.otherCation Transporten_US
dc.titleRelative effects of furosemide and ethacrynic acid on ion transport and energy metabolism in slices of rat kidney-cortexen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Anatomy, University of Michigan School of Medicine, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Pharmacology, Temple University School of Medicine, 19140, Philadelphia, Pennsylvania, USA; Istituto di Patologia Generale, Università degli Studi, Viale Regina Elena, 324, 00161, Roma, Italyen_US
dc.contributor.affiliationotherDepartment of Pharmacology, Temple University School of Medicine, 19140, Philadelphia, Pennsylvania, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid7279013en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46309/1/210_2004_Article_BF00506264.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00506264en_US
dc.identifier.sourceNaunyn-Schmiedeberg's Archives of Pharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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