Lipid abnormalities in succinate semialdehyde dehydrogenase (Aldh5a1-/-) deficient mouse brain provide additional evidence for myelin alterations

被引:16
作者
Barcelo-Coblijn, G.
Murphy, E. J.
Mills, K.
Winchester, B.
Jakobs, C.
Snead, O. C., III
Gibson, K. M.
机构
[1] Childrens Hosp Pittsburgh, Div Med Genet, Dept Pediat, Pittsburgh, PA 15213 USA
[2] Childrens Hosp Pittsburgh, Div Med Genet, Dept Pathol, Pittsburgh, PA 15213 USA
[3] Childrens Hosp Pittsburgh, Div Med Genet, Dept Human Genet, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15213 USA
[5] Univ N Dakota, Sch Med & Hlth Sci, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58203 USA
[6] UCL, Biochem Endocrinol & Metab Unit, Inst Child Hlth, Great Ormond St Hosp, London, England
[7] Vrije Univ Amsterdam, Med Ctr, Amsterdam, Netherlands
[8] Univ Toronto, Toronto, ON, Canada
[9] Hosp Sick Children, Brain & Behav Program, Div Neurol, Toronto, ON, Canada
[10] Hosp Sick Children, Dept Pediat, Fac Med, Toronto, ON, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2007年 / 1772卷 / 05期
关键词
succinate semialdehyde dehydrogenase (SSADH); aldehyde dehydrogenase 5al (Aldh5a1); gamma-hydroxybutyric acid; gamma-aminobutyric acid (GABA); myelin; phospholipids; ethanolamine glycerophospholipid; ethanolamine plasmalogen; galactosylceramide; docosohexaenoic acid (DHA);
D O I
10.1016/j.bbadis.2006.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Earlier work from our laboratory provided evidence for myelin abnormalities (decreased quantities of proteins associated with myelin compaction, decreased sheath thickness) in cortex and hippocampus of Aldh5al(-/-) mice, which have a complete ablation of the succinate semialdehyde dehydrogenase protein [E.A. Donarum, D.A. Stephan, K. Larkin, E.J. Murphy, M. Gupta, H. Senephansiri, R.C. Switzer, P.L. Pearl, O.C. Snead, C. Jakobs, K.M. Gibson, Expression profiling reveals multiple myelin alterations in murine succinate semialdehyde dehydrogenase deficiency, J. Inher. Metab. Dis. 29 (2006) 143-156]. In the current report, we have extended these findings via comprehensive analysis of brain phospholipid fractions, including quantitation of fatty acids in individual phospholipid subclasses and estimation of hexose-ceramide in Aldh5al(-/-) brain. In comparison to wild-type littermates (Aldh5a(+/+)), we detected a 20% reduction in the ethanolamine glycerophospholipid content of Aldh5al(-/-) mice, while other brain phospholipids (choline glycerophospholipid, phosphatidylserine and phosphatidylinositol) were within normal limits. Analysis of individual fatty acids in each of these fractions revealed consistent alterations in n-3 fatty acids, primarily increased 22:6n-3 levels (docosahexaenoic acid; DHA). In the phosphatidyl serine fraction there were marked increases in the proportions of polyunsaturated fatty acids with corresponding decreases of monounsaturated fatty acids. Interestingly, the levels of hexose-ceramide (glucosyl- and galactosylceramide, principal myelin cerebrosides) were decreased in Aldh5al(-/-) brain tissue (one-tailed t test, p=0.0449). The current results suggest that lipid and myelin abnormalities in this animal may contribute to the pathophysiology. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:556 / 562
页数:7
相关论文
共 44 条
[31]   Sulfatide is essential for the maintenance of CNS myelin and axon structure [J].
Marcus, J ;
Honigbaum, S ;
Shroff, S ;
Honke, K ;
Rosenbluth, J ;
Dupree, JL .
GLIA, 2006, 53 (04) :372-381
[32]   Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry disease [J].
Mills, K ;
Morris, P ;
Lee, P ;
Vellodi, A ;
Waldek, S ;
Young, E ;
Winchester, B .
JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 (01) :35-48
[33]   Monitoring the clinical and biochemical response to enzyme replacement therapy in three children with Fabry disease [J].
Mills, K ;
Vellodi, A ;
Morris, P ;
Cooper, D ;
Morris, M ;
Young, E ;
Winchester, B .
EUROPEAN JOURNAL OF PEDIATRICS, 2004, 163 (10) :595-603
[34]   Synthesis of novel internal standards for the quantitative determination of plasma ceramide trihexoside in Fabry disease by tandem mass spectrometry [J].
Mills, K ;
Johnson, A ;
Winchester, B .
FEBS LETTERS, 2002, 515 (1-3) :171-176
[35]   Inherited disorders of neurotransmitters in children and adults [J].
Pearl, PL ;
Capp, PK ;
Novotny, EJ ;
Gibson, KM .
CLINICAL BIOCHEMISTRY, 2005, 38 (12) :1051-1058
[36]   QUANTITATIVE ANALYSIS OF PHOSPHOLIPIDS BY THIN-LAYER CHROMATOGRAPHY AND PHOSPHORUS ANALYSIS OF SPOTS [J].
ROUSER, G ;
SIAKOTOS, AN ;
FLEISCHER, S .
LIPIDS, 1966, 1 (01) :85-+
[37]  
SGARAVATTI AM, IN PRESS NEUROCHEM I
[38]   Metabolism of γ-hydroxybutyrate to D-2-hydroxyglutarate in mammals:: further evidence for D-2-hydroxyglutarate transhydrogenase [J].
Struys, EA ;
Verhoeven, NM ;
Jansen, EEW ;
ten Brink, HJ ;
Gupta, M ;
Burlingame, TG ;
Quang, LS ;
Maher, T ;
Rinaldo, P ;
Snead, OC ;
Goodwin, AK ;
Weerts, EM ;
Brown, PR ;
Murphy, TC ;
Picklo, MJ ;
Jakobs, C ;
Gibson, KM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2006, 55 (03) :353-358
[39]   EFFECTS OF CHRONIC ETHANOL ADMINISTRATION ON RAT-BRAIN PHOSPHOLIPID-METABOLISM [J].
SUN, GY ;
HUANG, HM ;
CHANDRASEKHAR, R ;
LEE, DZ ;
SUN, AY .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (03) :974-980
[40]   IMMUNOLOGICAL DETERMINATION OF GALACTOSYLCERAMIDE LEVEL IN BLOOD AS A SERUM INDEX OF ACTIVE DEMYELINATION [J].
THUILLIER, Y ;
LUBETZKI, C ;
GOUJETZALC, C ;
GALLI, A ;
LHERMITTE, F ;
ZALC, B .
JOURNAL OF NEUROCHEMISTRY, 1988, 51 (02) :380-384