Inhibition of brain energy metabolism by the branched-chain amino acids accumulating in maple syrup urine disease

被引:55
|
作者
Ribeiro, Cesar A.
Sgaravatti, Angela M.
Rosa, Rafael B.
Schuck, Patricia F.
Grando, Vanessa
Schmidt, Anna L.
Ferreira, Gustavo C.
Perry, Marcos L. S.
Dutra-Filho, Carlos S.
Wajner, Moacir
机构
[1] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Bioquim, BR-90035003 Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Serv Genet Med, Porto Alegre, RS, Brazil
[3] Univ Luterana Brazil, Canoas, RS, Brazil
关键词
maple syrup urine disease; leucine; valine; isoleucine; energy metabolism;
D O I
10.1007/s11064-007-9423-9
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
In the present work we investigated the in vitro effect of the branched-chain amino acids (BCAA) accumulating in maple syrup urine disease (MSUD) on some parameters of energy metabolism in cerebral cortex of rats. (CO2)-C-14 production from [1-C-14]acetate, [1-5-C-14]citrate and [U-C-14]glucose, as well as glucose uptake by the brain were evaluated by incubating cortical prisms from 30-day-old rats in the absence (controls) or presence of leucine (Leu), valine (Val) or isoleucine (Ile). All amino acids significantly reduced (CO2)-C-14 production by around 20-55%, in contrast to glucose utilization, which was significantly increased by up to 90%. Furthermore, Leu significantly inhibited the activity of the respiratory chain complex IV, whereas Val and Ile markedly inhibited complexes II-III, III and IV by up to 40%. We also observed that trolox (alpha-tocopherol) and creatine totally prevented the inhibitory effects provoked by the BCAA on the respiratory chain complex activities, suggesting that free radicals were involved in these effects. The results indicate that the major metabolites accumulating in MSUD disturb brain aerobic metabolism by compromising the citric acid cycle and the electron flow through the respiratory chain. We presume that these findings may be of relevance to the understanding of the pathophysiology of the neurological dysfunction of MSUD patients.
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页码:114 / 124
页数:11
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