Literature DB >> 15522828

Differential effects of dietary fatty acids on rat liver alpha-amino-beta-carboxymuconate-epsilon-semialdehyde decarboxylase activity and gene expression.

Yukari Egashira1, Gen Murotani, Atsushi Tanabe, Kuniaki Saito, Koich Uehara, Akiko Morise, Mayuki Sato, Hiroo Sanada.   

Abstract

Hepatic alpha-amino-beta-carboxymuconate-epsilon-semialdehyde decarboxylase (ACMSD; formerly termed picolinic carboxylase) [EC4.1.1.45] plays a key role in regulating NAD biosynthesis and the generation of quinolinate (quinolinic acid) from tryptophan. Quinolinate is a potent endogenous excitotoxin of neuronal cells. We previously reported that ingestion of fatty acids by rats leads to a decrease in their hepatic ACMSD activity. However, the mechanism of this phenomenon is not clarified. We previously purified ACMSD and cloned cDNA encoding rat ACMSD. Therefore, in this study, we examined the differential effect of fatty acids on ACMSD mRNA expression by Northern blot. Moreover, we measured quinolinic acid concentration in rats fed on fatty acid. When diets containing 2% level of fatty acid were given to male Sprague-Dawley rats (4 weeks old) for 8 days, long-chain saturated fatty acids and oleic acid did not affect ACMSD mRNA expression in the liver. Eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) strongly suppressed the liver ACMSD mRNA expression. In rats fed with high linoleic acid diet for 8 days, serum quinolinic acid was significantly increased as compared with the rats fed on a fatty acid-free diet under the condition of the approximately same calorie ingestion. These results suggest that the transcription level of ACMSD is modulated by polyunsaturated fatty acids, and suppressive potency of ACMSD mRNA is n-3 fatty acid family>linoleic acid (n-6 fatty acid)>saturated fatty acid. Moreover, this study provides the information that a high polyunsaturated fatty acid diet affects the production of quinolinic acid in serum by suppressing the ACMSD activity.

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Year:  2004        PMID: 15522828     DOI: 10.1016/j.bbalip.2004.04.010

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  6 in total

1.  Regulation of rat hepatic α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase, a key enzyme in the tryptophan- NAD pathway, by dietary cholesterol and sterol regulatory element-binding protein-2.

Authors:  Hiroko Matsuda; Mayumi Sato; Mako Yakushiji; Manami Koshiguchi; Shizuka Hirai; Yukari Egashira
Journal:  Eur J Nutr       Date:  2014       Impact factor: 5.614

2.  Down-regulation of alpha-amino-beta-carboxymuconate-epsilon-semialdehyde decarboxylase by polyunsaturated fatty acids in hepatocytes is not mediated by PPARalpha.

Authors:  Naho Sasaki; Yukari Egashira; Hiroo Sanada
Journal:  Eur J Nutr       Date:  2008-03-04       Impact factor: 5.614

3.  Production of L-tryptophan-derived catabolites in hepatocytes from streptozotocin-induced diabetic rats.

Authors:  Naho Sasaki; Yukari Egashira; Hiroo Sanada
Journal:  Eur J Nutr       Date:  2009-01-23       Impact factor: 5.614

4.  The physiological action of picolinic Acid in the human brain.

Authors:  R S Grant; S E Coggan; G A Smythe
Journal:  Int J Tryptophan Res       Date:  2009-04-28

5.  An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation.

Authors:  L Brundin; C M Sellgren; C K Lim; J Grit; E Pålsson; M Landén; M Samuelsson; K Lundgren; P Brundin; D Fuchs; T T Postolache; L Traskman-Bendz; G J Guillemin; S Erhardt
Journal:  Transl Psychiatry       Date:  2016-08-02       Impact factor: 6.222

6.  Nutritional aspect of tryptophan metabolism.

Authors:  Tsutomu Fukuwatari; Katsumi Shibata
Journal:  Int J Tryptophan Res       Date:  2013-07-21
  6 in total

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