메뉴 건너뛰기




Volumn 51, Issue 1, 1998, Pages 26-32

MRI evidence that docosahexaenoic acid ethyl ester improves myelination in generalized peroxisomal disorders

Author keywords

[No Author keywords available]

Indexed keywords

DOCOSAHEXAENOIC ACID; MYELIN; PLASMALOGEN; VERY LONG CHAIN FATTY ACID;

EID: 0031869030     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.1.26     Document Type: Article
Times cited : (108)

References (34)
  • 1
    • 0015848845 scopus 로고
    • Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome
    • Goldfischer S, Moore CL, Johnson AB, et al. Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science 1973;182:62-64.
    • (1973) Science , vol.182 , pp. 62-64
    • Goldfischer, S.1    Moore, C.L.2    Johnson, A.B.3
  • 4
    • 0019963317 scopus 로고
    • Neonatal adrenoleukodystrophy: Clinical, pathological, and biochemical delineation of a syndrome affecting both males and females
    • Jaffe R, Crumrine P, Hashida Y, Moser HW. Neonatal adrenoleukodystrophy: clinical, pathological, and biochemical delineation of a syndrome affecting both males and females. Am J Pathol 1982;108:100-111.
    • (1982) Am J Pathol , vol.108 , pp. 100-111
    • Jaffe, R.1    Crumrine, P.2    Hashida, Y.3    Moser, H.W.4
  • 5
    • 0022610977 scopus 로고
    • Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction
    • Poll-The BT, Saudubray JM, Ogier H, et al. Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction. J Inherit Metab Dis 1986;9:169-174.
    • (1986) J Inherit Metab Dis , vol.9 , pp. 169-174
    • Poll-The, B.T.1    Saudubray, J.M.2    Ogier, H.3
  • 6
    • 0020002346 scopus 로고
    • Glycerolipid biosynthesis in peroxisomes via de acyl dihydroxyacetone phosphate pathway
    • Hajra AK, Bishop JE. Glycerolipid biosynthesis in peroxisomes via de acyl dihydroxyacetone phosphate pathway. Am NY Acad Sci 1982;386:170-182.
    • (1982) Am NY Acad Sci , vol.386 , pp. 170-182
    • Hajra, A.K.1    Bishop, J.E.2
  • 7
    • 0021961770 scopus 로고
    • 3-Hydroxy-3-methylglutaryl coenzyme A reductase is present in peroxisomes in normal rat liver cells
    • Keller GA, Barton MC, Shapiro DJ, Singer SJ. 3-Hydroxy-3-methylglutaryl coenzyme A reductase is present in peroxisomes in normal rat liver cells. Proc Natl Acad Sci USA 1985; 82:770-774.
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 770-774
    • Keller, G.A.1    Barton, M.C.2    Shapiro, D.J.3    Singer, S.J.4
  • 9
    • 0029017096 scopus 로고
    • Phytanic acid oxidation: Topographical localization of phytanoyl-CoA ligase and transport of phytanic acid into human peroxisomes
    • Pahan K, Singh I. Phytanic acid oxidation: topographical localization of phytanoyl-CoA ligase and transport of phytanic acid into human peroxisomes. J Lipid Res 1995;36:986-997.
    • (1995) J Lipid Res , vol.36 , pp. 986-997
    • Pahan, K.1    Singh, I.2
  • 10
    • 0344803532 scopus 로고
    • Lignoceric acid is oxidized in the peroxisome: Implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy
    • Singh I, Moser AB, Goldfischer S, Moser HW. Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy. Proc Natl Acad Sci USA 1984;81:4203-4207.
    • (1984) Proc Natl Acad Sci USA , vol.81 , pp. 4203-4207
    • Singh, I.1    Moser, A.B.2    Goldfischer, S.3    Moser, H.W.4
  • 11
    • 0020345656 scopus 로고
    • Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: Similarities in phenotype and accumulation of very long chain fatty acids
    • Brown FR, McAdams AJ, Cumins JW, et al. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids. Johns Hopkins Med J 1982;151: 344-361.
    • (1982) Johns Hopkins Med J , vol.151 , pp. 344-361
    • Brown, F.R.1    McAdams, A.J.2    Cumins, J.W.3
  • 12
    • 0020574070 scopus 로고
    • Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)
    • Heymans HSA, Schutgens RBH, Tan R, van den Bosch H, Borst P. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome). Nature 1983;306: 69-70.
    • (1983) Nature , vol.306 , pp. 69-70
    • Heymans, H.S.A.1    Schutgens, R.B.H.2    Tan, R.3    Van Den Bosch, H.4    Borst, P.5
  • 13
    • 0021132819 scopus 로고
    • Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome
    • Datta NS, Wilson GN, Hajra AK. Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. N Engl J Med 1984;311:1080-1083.
    • (1984) N Engl J Med , vol.311 , pp. 1080-1083
    • Datta, N.S.1    Wilson, G.N.2    Hajra, A.K.3
  • 14
    • 0021858767 scopus 로고
    • Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy and Refsum's disease: Plasma changes and skin fibroblast phytanic acid oxidase
    • Poulos A, Sharp P, Fellenberg AJ, Danks DM. Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase. Hum Genet 1985;70:172-177.
    • (1985) Hum Genet , vol.70 , pp. 172-177
    • Poulos, A.1    Sharp, P.2    Fellenberg, A.J.3    Danks, D.M.4
  • 16
    • 0024507789 scopus 로고
    • Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome
    • Martinez M. Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome. Lipids 1989;24: 261-265.
    • (1989) Lipids , vol.24 , pp. 261-265
    • Martinez, M.1
  • 17
    • 0025039469 scopus 로고
    • Severe deficiency of docosahexaenoic acid in peroxisomal disorders: A defect of D4 desaturation?
    • Martinez M. Severe deficiency of docosahexaenoic acid in peroxisomal disorders: a defect of D4 desaturation? Neurology 1990;40:1292-1298.
    • (1990) Neurology , vol.40 , pp. 1292-1298
    • Martinez, M.1
  • 18
    • 0026715768 scopus 로고
    • Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders
    • Martinez M. Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders. Brain Res 1992;583:171-182.
    • (1992) Brain Res , vol.583 , pp. 171-182
    • Martinez, M.1
  • 19
    • 0028293574 scopus 로고
    • Blood polyunsaturated fatty acids in patients with peroxisomal disorders. A multicenter study
    • Martinez M, Mougan I, Roig M, Ballabriga A. Blood polyunsaturated fatty acids in patients with peroxisomal disorders. A multicenter study. Lipids 1994;29:273-280.
    • (1994) Lipids , vol.29 , pp. 273-280
    • Martinez, M.1    Mougan, I.2    Roig, M.3    Ballabriga, A.4
  • 20
    • 0029205479 scopus 로고
    • The nervous system has an absolute molecular species requirement for proper function
    • Salem N Jr., Niebylski CD. The nervous system has an absolute molecular species requirement for proper function. Mol Membr Biol 1995;12:131-134.
    • (1995) Mol Membr Biol , vol.12 , pp. 131-134
    • Salem N., Jr.1    Niebylski, C.D.2
  • 21
    • 0022445141 scopus 로고
    • Biochemical and functional effects of prenatal and postnatal omega-3 fatty acid deficiency on retina and brain in rhesus monkeys
    • Neuringer M, Connor WE, Lin DS, Barstad L, Luck S. Biochemical and functional effects of prenatal and postnatal omega-3 fatty acid deficiency on retina and brain in rhesus monkeys. Proc Natl Acad Sci USA 1986;83:4021-4025.
    • (1986) Proc Natl Acad Sci USA , vol.83 , pp. 4021-4025
    • Neuringer, M.1    Connor, W.E.2    Lin, D.S.3    Barstad, L.4    Luck, S.5
  • 22
    • 0027319874 scopus 로고
    • Docosahexaenoic acid - A new therapeutic approach to peroxisomal-disorder patients: Experience with two cases
    • Martinez M, Pineda M, Vidai R, Conill J, and Martin B. Docosahexaenoic acid - a new therapeutic approach to peroxisomal-disorder patients: experience with two cases. Neurology 1993;43:1389-1397.
    • (1993) Neurology , vol.43 , pp. 1389-1397
    • Martinez, M.1    Pineda, M.2    Vidai, R.3    Conill, J.4    Martin, B.5
  • 23
    • 0029584553 scopus 로고
    • Polyunsaturated fatty acids in the developing human brain, erythrocytes and plasma in peroxisomal disease: Therapeutic implications
    • Martinez M. Polyunsaturated fatty acids in the developing human brain, erythrocytes and plasma in peroxisomal disease: therapeutic implications. J Inherit Metab Dis 1995; 18(suppl 1):61-75.
    • (1995) J Inherit Metab Dis , vol.18 , Issue.1 SUPPL. , pp. 61-75
    • Martinez, M.1
  • 24
    • 0029912369 scopus 로고    scopus 로고
    • Docosahexaenoic acid therapy in DHA-deficient patients with disorders of peroxisomal biogenesis
    • Martinez M. Docosahexaenoic acid therapy in DHA-deficient patients with disorders of peroxisomal biogenesis. Lipids 1996;31:S145-152.
    • (1996) Lipids , vol.31
    • Martinez, M.1
  • 25
    • 0022803343 scopus 로고
    • A comparison of pyrrolidide and picolinyl ester derivatives for the identification of fatty acids in natural samples by gas chromatography-mass spectrometry
    • Christie WW, Brechany EY, Johnson SB, and Holman RT. A comparison of pyrrolidide and picolinyl ester derivatives for the identification of fatty acids in natural samples by gas chromatography-mass spectrometry. Lipids 1986;21:657-661.
    • (1986) Lipids , vol.21 , pp. 657-661
    • Christie, W.W.1    Brechany, E.Y.2    Johnson, S.B.3    Holman, R.T.4
  • 26
    • 0026511868 scopus 로고
    • Formation, maturation and disorders of white matter
    • Barkovich AJ, Lyonn G, Evrard P. Formation, maturation and disorders of white matter. Am J Neuroradiol 1992;13:447-460.
    • (1992) Am J Neuroradiol , vol.13 , pp. 447-460
    • Barkovich, A.J.1    Lyonn, G.2    Evrard, P.3
  • 29
    • 0013804809 scopus 로고
    • Fatty acid and fatty aldehyde composition of the major lipids in normal human grey matter, white matter and myelin
    • O'Brien JS, Sampson EI. Fatty acid and fatty aldehyde composition of the major lipids in normal human grey matter, white matter and myelin. J Lipid Res 1965;6:545-551.
    • (1965) J Lipid Res , vol.6 , pp. 545-551
    • O'Brien, J.S.1    Sampson, E.I.2
  • 30
    • 0016639611 scopus 로고
    • The isolation and characterization of a plasma membrane and a myelin fraction derived from oligodendoglia of calf brain
    • Poduslo SE. The isolation and characterization of a plasma membrane and a myelin fraction derived from oligodendoglia of calf brain. J Neurochem 1975;647-654.
    • (1975) J Neurochem , pp. 647-654
    • Poduslo, S.E.1
  • 31
    • 0021238259 scopus 로고
    • Alterations in the fatty acid composition of rat brain cells (neurons, astrocytes, and oligodendrocytes) and of subcellular fractions (myelin and synaptosomes) induced by a diet devoid of n-3 fatty acids
    • Bourre JM, Pascal G, Durand G, Masson M, Sumont O, Piciotti M. Alterations in the fatty acid composition of rat brain cells (neurons, astrocytes, and oligodendrocytes) and of subcellular fractions (myelin and synaptosomes) induced by a diet devoid of n-3 fatty acids. J Neurochem 1984;43:342-348.
    • (1984) J Neurochem , vol.43 , pp. 342-348
    • Bourre, J.M.1    Pascal, G.2    Durand, G.3    Masson, M.4    Sumont, O.5    Piciotti, M.6
  • 32
    • 0025841905 scopus 로고
    • The metabolism of 7,10,13,16,19-docosapentaenoic acid to 4,7,10,13,16,19-docosahexaenoic acid in rat liver is independent of a 4-desaturase
    • Voss A, Reinhart M, Sankarappa S, Sprecher H. The metabolism of 7,10,13,16,19-docosapentaenoic acid to 4,7,10,13,16,19-docosahexaenoic acid in rat liver is independent of a 4-desaturase. J Biol Chem 1991;266:19995-20000.
    • (1991) J Biol Chem , vol.266 , pp. 19995-20000
    • Voss, A.1    Reinhart, M.2    Sankarappa, S.3    Sprecher, H.4
  • 33
    • 0028868819 scopus 로고
    • Docosa-hexaenoic acid synthesis in human skin fibroblasts involves peroxisomal retroconversion of tetracosahexaenoic acid
    • Moore SA, Hurt E, Yoder E, Sprecher H, Spector AA. Docosa-hexaenoic acid synthesis in human skin fibroblasts involves peroxisomal retroconversion of tetracosahexaenoic acid. J Lipid Res 1995;36:2433-2443.
    • (1995) J Lipid Res , vol.36 , pp. 2433-2443
    • Moore, S.A.1    Hurt, E.2    Yoder, E.3    Sprecher, H.4    Spector, A.A.5
  • 34
    • 0031041126 scopus 로고    scopus 로고
    • On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders
    • Infante JP, Huszagh VA. On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders. Mol Cell Biochem 1997;168:101-115.
    • (1997) Mol Cell Biochem , vol.168 , pp. 101-115
    • Infante, J.P.1    Huszagh, V.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.