Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid
dc.contributor.author | Culp, Brenda R. | en_US |
dc.contributor.author | Titus, Bradley G. | en_US |
dc.contributor.author | Lands, William E. M. | en_US |
dc.date.accessioned | 2006-04-07T17:31:36Z | |
dc.date.available | 2006-04-07T17:31:36Z | |
dc.date.issued | 1979-11 | en_US |
dc.identifier.citation | Culp, Brenda R., Titus, Bradley G., Lands, William E. M. (1979/11)."Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid." Prostaglandines and Medicine 3(5): 269-278. <http://hdl.handle.net/2027.42/23460> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B7GHB-4C3C8RN-64/2/a9decc4cac722f28312eff42e40f1f26 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/23460 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=121610&dopt=citation | en_US |
dc.description.abstract | Eicosapentaenoic acid [20:5(n-3)] is not oxidized by the purified cyclooxygenase from sheep vesicular glands in the conditions of low peroxide tone in which arachidonate [20:4(n-6)] is rapidly oxygenated. When the level of peroxide in incubation mixtures is allowed to rise, there is a dramatic change in reactivity of the cyclooxygenase to react with 20:5(n-3) at one-half the rate and one-third the extent observed with 20:4(n-6). Overall, the low peroxide levels expected in vivo would most probably cause the (n-3) type of fatty acid to be a general inhibitor of prostaglandin formation, through both reversible and irreversible actions at the enzyme site. | en_US |
dc.format.extent | 655133 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Chemistry | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Departments of Internal Medicine (Cardiology Division) and Biological Chemistry, The University of Michigan, Ann Arbor, MI 48109, USA | en_US |
dc.contributor.affiliationum | Departments of Internal Medicine (Cardiology Division) and Biological Chemistry, The University of Michigan, Ann Arbor, MI 48109, USA | en_US |
dc.contributor.affiliationum | Departments of Internal Medicine (Cardiology Division) and Biological Chemistry, The University of Michigan, Ann Arbor, MI 48109, USA | en_US |
dc.identifier.pmid | 121610 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/23460/1/0000412.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0161-4630(79)90068-5 | en_US |
dc.identifier.source | Prostaglandines and Medicine | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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