O Loreau
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Explore the profile of O Loreau including associated specialties, affiliations and a list of published articles.
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13
Citations
56
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Recent Articles
1.
Aigbirhio F, Allwein S, Anwar A, Atzrodt J, Audisio D, Badman G, et al.
J Labelled Comp Radiopharm
. 2016 Mar;
59(4):175-86.
PMID: 26991121
The 24th annual symposium of the International Isotope Society's United Kingdom Group took place at the Møller Centre, Churchill College, Cambridge, UK on Friday 6th November 2015. The meeting was...
2.
Gruffat D, Remond C, Durand D, Loreau O, Bauchart D
Animal
. 2012 Mar;
2(4):645-52.
PMID: 22443582
Although endogenous synthesis of conjugated linoleic acid (CLA) in the mammary gland of lactating cows has been already well documented, no study has determined so far as to which tissue...
3.
Chardigny J, Masson E, Sergiel J, DARBOIS M, Loreau O, Noel J, et al.
J Nutr
. 2003 Dec;
133(12):4212-4.
PMID: 14652374
The metabolic fate of rumenic acid (9cis,11trans-octadecenoic acid) related to its position on the glycerol moiety has not yet been studied. In the present work, synthetic triacylglycerols (TAG) esterified with...
4.
Loreau O, Chardigny J, Sebedio J, Noel J
Chem Phys Lipids
. 2003 Jun;
124(2):135-45.
PMID: 12818739
To study the metabolic fate of conjugated linoleic acid isomers, we synthesized, in seven steps, from 1-heptyne, (6Z,10E,12Z)-octadeca-6,10,12-trienoic acid, (8Z,12E,14Z)-eicosa-8,12,14-trienoic acid, and their [1-(14)C]-analogs. In the case of (6Z,10E,12Z)-octadecatrienoic acid,...
5.
Berdeaux O, Gnadig S, Chardigny J, Loreau O, Noel J, Sebedio J
Lipids
. 2003 Feb;
37(11):1039-45.
PMID: 12558053
Various nutritional studies on CLA, a mixture of isomers of linoleic acid, have reported the occurrence of conjugated long-chain PUFA after feeding experimental animals with rumenic acid, 9c,11t-18:2, the major...
6.
Joffre F, Genty M, Demaison L, Loreau O
J Nutr Biochem
. 2002 May;
12(10):554-558.
PMID: 12031260
Cyclic fatty acid monomers (CFAM) occur from linoleic (CFAM-18:2) or linolenic (CFAM-18:3) acids present in some edible oils as a result of domestic frying or industrial refining. They present adverse...
7.
Sergiel J, Chardigny J, Sebedio J, Berdeaux O, Juaneda P, Loreau O, et al.
Lipids
. 2002 Feb;
36(12):1327-9.
PMID: 11834084
To assess the oxidative metabolism of conjugated linoleic acid (CLA) isomers, rats were force-fed 1.5-2.6 MBq of [1-14C]-linoleic acid (9c,12c-18:2), -rumenic acid (9c,11t-18:2), or-10trans,12cis-18:2 (10t,12c-18:2), and 14CO2 production was monitored...
8.
Gnadig S, Berdeaux O, Loreau O, Noel J, Sebedio J
Chem Phys Lipids
. 2001 Sep;
112(2):121-35.
PMID: 11551536
In order to study the metabolic pathway and the physiological effects of 9c,11t-18:2 (major isomer of conjugated linoleic acid) and its C(18:3) and C(20:3) metabolites, 6c,9c,11t-18:3 and 8c,11c,13t-20:3 and their...
9.
Bretillon L, Chardigny J, Sebedio J, Noel J, Scrimgeour C, Fernie C, et al.
J Lipid Res
. 2001 May;
42(6):995-7.
PMID: 11369808
Human lipid intake contains various amounts of trans fatty acids. Refined vegetable and frying oils, rich in linoleic acid and/or alpha-linolenic acid, are the main dietary sources of trans-18:2 and...
10.
Loreau O, Maret A, Chardigny J, Sebedio J, Noel J
Chem Phys Lipids
. 2001 Mar;
110(1):57-67.
PMID: 11245835
Conjugated linoleic acid (CLA) isomers are present in human foods derived from milk or ruminant meat. To study their metabolism, (9Z,11E)-, (10E,12Z)- and (10Z,12Z)-[1-(14)C]-octadecadienoic acids with high radiochemical and isomeric...