Brain regional development of the activity of α-ketoglutarate dehydrogenase complex in the rat

被引:18
作者
Buerstatte, CR
Behar, KL
Novotny, EJ
Lai, JCK
机构
[1] Idaho State Univ, Coll Pharm, Dept Pharmaceut Sci, Pocatello, ID 83209 USA
[2] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Magnet Resonance Ctr, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06520 USA
来源
DEVELOPMENTAL BRAIN RESEARCH | 2000年 / 125卷 / 1-2期
关键词
brain development; alpha-ketoglutarate dehydrogenase complex; glucose oxidative metabolism; tricarboxylic acid cycle; thiamine-dependent enzyme;
D O I
10.1016/S0165-3806(00)00134-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study was initiated to test the hypothesis that the development of alpha -ketoglutarate dehydrogenase complex (KGDHC) activity, like that of pyruvate dehydrogenase complex, is one of the late developers of tricarboxylic acid (TCA) cycle enzymes. The postnatal development of KGDHC in rat brain exhibits four distinct region-specific patterns. The age-dependent increases in olfactory bulb (OB) and hypothalamus (HYP) form one pattern: low in postnatal days (P) 2 and 4, KGDHC activity rose linearly to attain adult level at P30. The increases in mid-brain (MB) and striatum (ST) constitute a second pattern: being < 40% of adult level at P2 and P4, KGDHC activity rose steeply between P10 and P17 and attained adult level by P30. The increases in cerebellum (CB), cerebral cortex (CC), and hippocampus (HIP) form a third pattern: being 25-30% of adult level at P2 and P4, KGDHC activity doubled between P10 and P17 and rose to adult level by P30. KGDHC activity development is unique in pens and medulla (PM): being > 60% of the adult level at P2, it rose rapidly to adult level by PIG. Thus, KGDHC activity develops earlier in phylogenetically older regions (PM) than in phylogenetically younger regions (CB, CC, HIP). Being lowest in activity among all TCA cycle enzymes, KGDHC activity in any region at any age will exert a limit on the maximum TCA cycle flux therein. The results may have functional and pathophysiological implications in control of brain glucose oxidative metabolism, energy metabolism, and neurotransmitter syntheses. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 145
页数:7
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