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Rapid alternative absorption of dietary long-chain fatty acids with upregulation of intestinal glycosylated CD36 in liver cirrhosis.

Authors :
Yamamoto, Yasunori
Hiasa, Yoichi
Murakami, Hidehiro
Ikeda, Yoshio
Yamanishi, Hirofiimi
Abe, Masanori
Matsuura, Bunzo
Onji, Morikazu
Source :
American Journal of Clinical Nutrition; Jul2012, Vol. 96 Issue 1, p90-101, 12p, 16 Color Photographs, 2 Diagrams, 3 Charts, 4 Graphs
Publication Year :
2012

Abstract

Background: Dietary long-chain fatty acid (LCFA) intake is an important risk factor for hepatic inflammation and hepatocarcino- genesis. An alternate route of dietary LCFA absorption has been suggested in patients with liver cirrhosis (LC). Objective: We aimed to determine this alternate route and to identify its mechanism. Design: Twenty healthy control subjects and 47 patients with LC- n = 23 with portal hypertension [PH(+)LC] and 24 without portal hypertension [PH(-)LC)]-were enrolled. [<superscript>13</superscript>C]Palmitate (an LCFA) and octanoate (a medium-chain fatty acid [MCFA]) were administered by using gastrointestinal endoscopy. Breath <superscript>13</superscript>CO<subscript>2</subscript> was measured to quantify metabolized fatty acids. We also examined intestinal specimens of patients in these groups. Results: A more rapid increase in metabolized palmitate, which showed a pattern similar to that of octanoate metabolism, was observed in patients with LC than in healthy control subjects. The increase in the PH(-)LC group was higher than that in the PH(+)LC group. However, the concentration of metabolized palmitate increased with treatment of the PH(+)LC group with a portal-systemic shunt. Morphologic changes such as expanded lymph and blood vessels were present, and glycosylated CD36 increased in the jejunum of the PH(+)LC group. This group had high serum concentrations of glucagon-like peptide-2. These data suggest that dietary LCFAs, similar to MCFAs, are absorbed via blood vessels in patients with LC. Conclusions: Rapid absorption of LCFAs by an alternative method occurred in patients with LC. This altered LCFA processing is likely related to upregulation of intestinal glycosylated CD36 and could contribute to pathogenesis in patients with LC. This trial was registered at http://www.umin.ac.jp/ctr/index.htm as UMIN000006637 and UMIN000006638. Am J Clin Nutr 2012;96:90-101. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029165
Volume :
96
Issue :
1
Database :
Complementary Index
Journal :
American Journal of Clinical Nutrition
Publication Type :
Academic Journal
Accession number :
77342073
Full Text :
https://doi.org/10.3945/ajcn.111.033084