Drug uptake by brain. II. Barbiturate uptake alters the transport of amino acids in vitro(1).

Voprosy biokhimii mozga Pub Date : 1974-01-01
D N Teller, T De Guzman, A Lajtha
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Abstract

1. Valine and leucine uptake into mouse brain slices was stimulated by 1 to 4 mM phenobarbital and pentobarbital. Greater concentrations of these two barbiturates inhibited the transport of these amino acids. Barbital, isobarbituric acid, and 5-nitrobarbituric acid had no effect, while amobarbital and secobarbital produced only inhibition of uptake. 2. Transport of glutamate and aspartate was unaffected by phenobarbital concentrations that inhibited uptake of lysine and alpha-aminoisobutyric acid. 3. Changes in the Na+ and K+ content of the slices were not related to stimulation of valine or leucine uptake. 4. There was no concentrative uptake of phenobarbital by brain slices. The partially saturable uptake of pentobarbital was not by active transport, because the uptake increased after heating brain, liver, or kidney slices to 95 degrees for 10 min. 5. This study shows that individual members of a pharmacologically related group may have specific effects on a composite physiological function (amino acid transport) of brain tissue.

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大脑对药物的吸收。2巴比妥酸盐的摄取改变了体外氨基酸的转运(1)。
1. 用1 ~ 4mm苯巴比妥和戊巴比妥刺激缬氨酸和亮氨酸进入小鼠脑切片。较高浓度的这两种巴比妥酸盐抑制了这些氨基酸的运输。巴比妥、异巴比妥酸和5-硝基巴比妥酸没有作用,而阿莫巴比妥和西巴比妥只产生摄取抑制作用。2. 抑制赖氨酸和α -氨基异丁酸摄取的苯巴比妥浓度不影响谷氨酸和天冬氨酸的转运。3.Na+和K+含量的变化与缬氨酸和亮氨酸摄取的刺激无关。4. 脑切片未见苯巴比妥的集中摄取。戊巴比妥的部分饱和摄取不是通过主动运输,因为将脑、肝或肾片加热至95度10分钟后摄取增加。该研究表明,药理学相关群体的个体成员可能对脑组织的复合生理功能(氨基酸运输)有特定的影响。
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[Heterogeneity and regulation of glutamate dehydrogenase activity in mammalian brain and liver]. [Certain neurochemical aspects of the metabolism of hormones and mediators (development of a single concept]. GABA and central monoamine release. [Breakdown of luliberin, somatostatin and substance P as an effect of hypothalamic endopeptidases]. [Participation of phosphopeptides in oxidative amino acid exchange in brain tissue].
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