Literature DB >> 3119935

The role of peroxisomes in mammalian cellular metabolism.

P B Lazarow1.   

Abstract

Peroxisomes, which are widely distributed in mammalian tissues, carry out several important functions in cellular metabolism. Production of alkylglycerol-3-phosphate, a key intermediate in the synthesis of plasmalogens and other ether lipids, occurs in the peroxisome. A fatty acid beta-oxidation system with significant differences from mitochondrial beta-oxidation is also found in the peroxisomes; the acetyl-CoA produced is used for synthetic reactions. This pathway has a particularly important physiological role in the oxidation of very long chain fatty acids and the side chain of cholesterol. Peroxisomes also possess a number of oxidases that produce H2O2 which is decomposed by peroxisomal catalase. The function of this peroxisomal respiratory pathway is disposal of excess reducing equivalents, protection of the cell against H2O2 and possibly a role in thermogenesis in brown adipose tissue. Other peroxisomal functions include a role in gluconeogenesis and in purine and polyamine catabolism. Some enzymes of peroxisomes can be induced by dietary, hormonal and other physiological changes. The entire organelle proliferates under certain of these conditions.

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Year:  1987        PMID: 3119935     DOI: 10.1007/bf01812843

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  63 in total

1.  The role of H 2 O 2 generation in perfused rat liver and the reaction of catalase compound I and hydrogen donors.

Authors:  N Oshino; B Chance; H Sies; T Bücher
Journal:  Arch Biochem Biophys       Date:  1973-01       Impact factor: 4.013

2.  Identity of long-chain acyl-coenzyme A synthetase of microsomes, mitochondria, and peroxisomes in rat liver.

Authors:  S Miyazawa; T Hashimoto; S Yokota
Journal:  J Biochem       Date:  1985-09       Impact factor: 3.387

3.  Palmityl-CoA oxidase: detection in several guinea pig tissues and peroxisomal localisation in mucosa, of small intestine.

Authors:  G M Small; D Brolly; M J Connock
Journal:  Life Sci       Date:  1980-11-10       Impact factor: 5.037

4.  Individual peroxisomal beta-oxidation enzymes.

Authors:  T Hashimoto
Journal:  Ann N Y Acad Sci       Date:  1982       Impact factor: 5.691

5.  Peroxisomal localization of serine:pyruvate aminotransferase in human liver.

Authors:  T Noguchi; Y Takada
Journal:  J Biol Chem       Date:  1978-11-10       Impact factor: 5.157

6.  Oxidation of spermidine and spermine in rat liver: purification and properties of polyamine oxidase.

Authors:  E Hölttä
Journal:  Biochemistry       Date:  1977-01-11       Impact factor: 3.162

7.  Cyanide-insensitive and clofibrate enhanced beta-oxidation of dodecanedioic acid in rat liver. An indication of peroxisomal beta-oxidation of N-dicarboxylic acids.

Authors:  P B Mortensen; S Kølvraa; N Gregersen; K Rasmussen
Journal:  Biochim Biophys Acta       Date:  1982-11-12

8.  Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.

Authors:  I Singh; A E Moser; S Goldfischer; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

9.  Cold adaptation in the rat: increased brown fat peroxisomal beta-oxidation relative to maximal mitochondrial oxidative capacity.

Authors:  J Nedergaard; S Alexson; B Cannon
Journal:  Am J Physiol       Date:  1980-11

10.  3-Hydroxy-3-methylglutaryl-coenzyme A reductase is present in peroxisomes in normal rat liver cells.

Authors:  G A Keller; M C Barton; D J Shapiro; S J Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

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  15 in total

Review 1.  Metabolic pigmentary retinopathies: diagnosis and therapeutic attempts.

Authors:  B T Poll-The; T Billette de Villemeur; M Abitbol; J L Dufier; J M Saudubray
Journal:  Eur J Pediatr       Date:  1992-01       Impact factor: 3.183

Review 2.  Dysmorphic syndromes with demonstrable biochemical abnormalities.

Authors:  P T Clayton; E Thompson
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

Review 3.  Lipid-lowering drugs.

Authors:  K Pahan
Journal:  Cell Mol Life Sci       Date:  2006-05       Impact factor: 9.261

4.  Protein kinase C activity, phosphate uptake and endogenous substrate phosphorylation are altered in Zellweger syndrome.

Authors:  A Boneh
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

5.  IDH1 deficiency attenuates gluconeogenesis in mouse liver by impairing amino acid utilization.

Authors:  Jing Ye; Yu Gu; Feng Zhang; Yuanlin Zhao; Yuan Yuan; Zhenyue Hao; Yi Sheng; Wanda Y Li; Andrew Wakeham; Rob A Cairns; Tak W Mak
Journal:  Proc Natl Acad Sci U S A       Date:  2016-12-23       Impact factor: 11.205

6.  The MR spectrum of peroxisomal disorders.

Authors:  M S van der Knaap; J Valk
Journal:  Neuroradiology       Date:  1991       Impact factor: 2.804

Review 7.  Very long chain fatty acids in higher animals--a review.

Authors:  A Poulos
Journal:  Lipids       Date:  1995-01       Impact factor: 1.880

8.  Peroxisome induction potential and lipid-regulating activity in rats. Quantitative microscopy and chemical structure-activity relationships.

Authors:  E J McGuire; J A Lucas; R H Gray; F A de la Iglesia
Journal:  Am J Pathol       Date:  1991-07       Impact factor: 4.307

9.  IDH1 regulates phospholipid metabolism in developing astrocytes.

Authors:  Elena Bogdanovic; Ali-Reza Sadri; Michael Catapano; Jean E Vance; Marc G Jeschke
Journal:  Neurosci Lett       Date:  2014-09-16       Impact factor: 3.046

Review 10.  Roles of Phase Separation for Cellular Redox Maintenance.

Authors:  Yuichi Saito; Wataru Kimura
Journal:  Front Genet       Date:  2021-07-09       Impact factor: 4.599

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