2004
DOI: 10.1271/bbb.68.2643
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The 9cis,11trans,13cisIsomer of Conjugated Linolenic Acid Reduces Apolipoprotein B100 Secretion and Triacylglycerol Synthesis in HepG2 Cells

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Cited by 55 publications
(53 citation statements)
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References 21 publications
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“…Current data on the effect of PSO on lipid concentration and metabolism are controversial (8,9,17) . Similar to our findings, the liver accumulation of TAG was reduced by PSO administration (8,18) ; a plausible mechanism, demonstrated in an in vitro study, that 9-cis, 11-trans, 13-cis CLN suppressed cellular synthesis of TAG in HepG2 cells (19) .…”
Section: Discussionsupporting
confidence: 90%
“…Current data on the effect of PSO on lipid concentration and metabolism are controversial (8,9,17) . Similar to our findings, the liver accumulation of TAG was reduced by PSO administration (8,18) ; a plausible mechanism, demonstrated in an in vitro study, that 9-cis, 11-trans, 13-cis CLN suppressed cellular synthesis of TAG in HepG2 cells (19) .…”
Section: Discussionsupporting
confidence: 90%
“…LA treatments tended to increase [1-14 C] oleate incorporation into cellular TG, which meant enhanced TG synthesis, but the increase was significantly reduced by LAME as compared with control medium. This result is consistent with our previous report showing that conjugated fatty acids reduced apo B100 secretion through the suppression of TG synthesis in HepG2 cells 26,27) . Hence we consider that the reduction of apo B100 secretion by LAME is at least in part attributable to the suppression of cellular TG synthesis in HepG2 cells.…”
Section: Discussionsupporting
confidence: 94%
“…The three double bonds present in CLNAs are primarily in positions Δ9,11,13 and Δ8,10,12 and exist in both cis and trans geometrical isomer forms (SASSANO et al, 2009). CLNAs have been reported to occur in terrestrial plant lipids, especially seed oils (KINAMI et al, 2007), present in high amounts accounting for 40-80% of total fatty acids (YANG et al, 2005;ARAO et al, 2004b). Five CLNA isomers occur as components of major seed oils of several plants: α-eleostearic acid cis9,trans11,, punicic acid (PA,cis9,trans11,calendic acid (trans8,trans10,jacaric acid (cis8,trans10,, and catalpic acid (trans9, trans11, cis13-18:3) (IWABUCHI; KOHNO-MURASE; IMAMURA, 2003; further studies are needed to provide a clearer understanding of this mechanism of CLNAs metabolism (YUAN, G. F.; YUAN, J. Q.; LI, 2009).…”
Section: Structure Isomers and Sourcesmentioning
confidence: 99%