1997
DOI: 10.1016/s0005-2760(97)00015-5
|View full text |Cite
|
Sign up to set email alerts
|

Metabolites of conjugated isomers of linoleic acid (CLA) in the rat

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

6
103
2
8

Year Published

1999
1999
2020
2020

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 167 publications
(119 citation statements)
references
References 23 publications
6
103
2
8
Order By: Relevance
“…This may relate to the isomer being metabolized, via desaturation and elongation pathways (Sebedio et al, 1997), or being more easily oxidized due to its structure (Martin et al, 2000). However, irrespective of the reasons for the lack of incorporation into plasma lipids, a low exposure of bone cells to circulating trans-10,cis-12 isomer of CLA (potentially the more bone-active isomer of CLA) might be one explanation of the lack of effect of CLA supplementation on bone metabolism in the present study.…”
Section: Conjugated Linoleic Acid and Bone Metabolism L Doyle Et Almentioning
confidence: 99%
“…This may relate to the isomer being metabolized, via desaturation and elongation pathways (Sebedio et al, 1997), or being more easily oxidized due to its structure (Martin et al, 2000). However, irrespective of the reasons for the lack of incorporation into plasma lipids, a low exposure of bone cells to circulating trans-10,cis-12 isomer of CLA (potentially the more bone-active isomer of CLA) might be one explanation of the lack of effect of CLA supplementation on bone metabolism in the present study.…”
Section: Conjugated Linoleic Acid and Bone Metabolism L Doyle Et Almentioning
confidence: 99%
“…The presence of these derivatives has been mentioned in the liver of different species such as the rat [16][17][18]21], lamb [19] and mouse [20]. Moreover, it has been recently demonstrated in the rat that the liver is able to convert rumenic acid into a conjugated derivative identified on the basis of its retention time as the cis-6, cis-9, trans-11 C18:3 [21].…”
Section: Discussionmentioning
confidence: 99%
“…FA methyl esters (FAME) were prepared from total lipids at room temperature by using sodium methylate (1 M) followed by boron trifluoride in methanol (14% v/v) as previously described by Sébédio et al [17]. FAME containing [1-14 C] FAME were then analysed by gas-liquid chromatography using a Hewlett-Packard 5890 series II gas chromatograph (Palo Alto, CA) equipped with a splitless injector and fused Stabilwax wide-bore silica column (60 m × 0.53 mm i.d., film thickness: 0.50 µM, Restek, Evry, France).…”
Section: Determination Of Fa Bioconversionmentioning
confidence: 99%
See 1 more Smart Citation
“…By the same deduction, the low content of c/t CLA isomers in the liver PL could be due to rapid metabolism, oxidation and poor geometrical configuration. In this regard, Sebedio et al (1997) analysed the conjugated 20 : 3 and 20 : 4 isomers in rats fed a diet containing 180 mg CLA/d and suggested that some c/t CLA isomers were preferentially metabolised to form longer-chain products via desaturation and elongation pathways, thus leading tissue to accumulate more t/t but fewer c/t isomers. The distribution of CLA and its metabolites into rat liver lipid classes has also been reported by Banni et al (2001).…”
Section: Discussionmentioning
confidence: 99%