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首页> 外文期刊>Brain research. Developmental brain research >Brain regional development of the activity of alpha-ketoglutarate dehydrogenase complex in the rat.
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Brain regional development of the activity of alpha-ketoglutarate dehydrogenase complex in the rat.

机译:大鼠大脑中α-酮戊二酸脱氢酶复合物活性的大脑区域发展。

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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 pons and medulla (PM): being >60% of the adult level at P2, it rose rapidly to adult level by P10. 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.
机译:这项研究的开始是为了检验以下假设:α-酮戊二酸脱氢酶复合物(KGDHC)活性的发展,与丙酮酸脱氢酶复合物的发展一样,是三羧酸(TCA)循环酶的最新开发者之一。大鼠脑中KGDHC的出生后发育表现出四种不同的区域特异性模式。嗅球(OB)和下丘脑(HYP)的年龄依赖性增加形成一种模式:出生后(P)2和4天低,KGDHC活性线性上升,达到P30的成人水平。中脑(MB)和纹状体(ST)的增加构成第二种模式:在P2和P4时,KGDHC活性<成人的40%,在P10和P17之间急剧上升,到P30达到成人水平。小脑(CB),大脑皮层(CC)和海马(HIP)的增加形成了第三种模式:在P2和P4时,成年人的KGDHC活性增加了25%至30%,在P10和P17之间,KGDHC的活性增加了一倍,并在成人时上升到成年人的水平P30。 KGDHC活性的发育在脑桥和延髓(PM)中是独特的:在P2时超过成人水平的60%,到P10时迅速上升到成人水平。因此,与系统发育较年轻的区域(CB,CC,HIP)相比,系统发育较老的区域(PM)的KGDHC活性更早形成。在所有TCA循环酶中活性最低,在任何年龄的任何区域的KGDHC活性都会限制其中最大的TCA循环通量。结果可能在控制脑葡萄糖氧化代谢,能量代谢和神经递质合成方面具有功能和病理生理意义。

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