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dc.contributor.authorPetrou, Steven
dc.contributor.authorOrdway, Richard W.
dc.contributor.authorKirber, Michael T.
dc.contributor.authorDopico, Alejandro M.
dc.contributor.authorHamilton, James A.
dc.contributor.authorWalsh, John V.
dc.contributor.authorSinger, Joshua J.
dc.date2022-08-11T08:09:02.000
dc.date.accessioned2022-08-23T16:16:27Z
dc.date.available2022-08-23T16:16:27Z
dc.date.issued1995-02-01
dc.date.submitted2008-11-25
dc.identifier.citationProstaglandins Leukot Essent Fatty Acids. 1995 Feb-Mar;52(2-3):173-8.
dc.identifier.issn0952-3278 (Print)
dc.identifier.pmid7784455
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34336
dc.description.abstractA variety of fatty acids increase the activity of certain types of K+ channels. This effect is not dependent on the three enzymatic pathways that convert arachidonic acid to various bioactive oxygenated metabolites. One type of K+ channel in toad stomach smooth muscle cell membranes in activated by fatty acids and other single chain lipids which possess both a negatively charged head group and a sufficiently hydrophobic acyl chain. Neutral lipids have no effect on K+ channel activity, while positively charged lipids with a sufficiently hydrophobic acyl chain suppress channel activity. Acyl Coenzyme A's, which do not flip across the bilayer, act only from the cytosolic surface of the membrane, suggesting that the binding site for channel activation is also located there. This fatty acid-activated channel is also activated by membrane stretch. Moreover, this mechanical response is either mediated or modulated by fatty acids. Thus, fatty acids and other charged single chain lipids may comprise another class of first or second messenger molecules that target ion channels.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7784455&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/0952-3278(95)90018-7
dc.subjectAcyl Coenzyme A; Animals; Bufo marinus; Fatty Acids; Models, Biological; Muscle, Smooth; Patch-Clamp Techniques; Physical Stimulation; Potassium Channels; Stimulation, Chemical; Stomach
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleDirect effects of fatty acids and other charged lipids on ion channel activity in smooth muscle cells
dc.typeJournal Article
dc.source.journaltitleProstaglandins, leukotrienes, and essential fatty acids
dc.source.volume52
dc.source.issue2-3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/984
dc.identifier.contextkey672512
html.description.abstract<p>A variety of fatty acids increase the activity of certain types of K+ channels. This effect is not dependent on the three enzymatic pathways that convert arachidonic acid to various bioactive oxygenated metabolites. One type of K+ channel in toad stomach smooth muscle cell membranes in activated by fatty acids and other single chain lipids which possess both a negatively charged head group and a sufficiently hydrophobic acyl chain. Neutral lipids have no effect on K+ channel activity, while positively charged lipids with a sufficiently hydrophobic acyl chain suppress channel activity. Acyl Coenzyme A's, which do not flip across the bilayer, act only from the cytosolic surface of the membrane, suggesting that the binding site for channel activation is also located there. This fatty acid-activated channel is also activated by membrane stretch. Moreover, this mechanical response is either mediated or modulated by fatty acids. Thus, fatty acids and other charged single chain lipids may comprise another class of first or second messenger molecules that target ion channels.</p>
dc.identifier.submissionpathgsbs_sp/984
dc.contributor.departmentDepartment of Physiology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages173-8


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