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一种将L-精氨酸和L-赖氨酸转运到活体大鼠大脑中的共享机制的饱和。

Saturation of a shared mechanism which transports L-arginine and L-lysine into the brain of the living rat.

作者信息

Baños G, Daniel P M, Pratt O E

出版信息

J Physiol. 1974 Jan;236(1):29-41. doi: 10.1113/jphysiol.1974.sp010420.

Abstract
  1. The rate of entry of L-arginine and L-lysine into the brain of the rat was measured in vivo by a direct method in which the amino acid concentration was at a constant level in the blood plasma over the period of the experiment.2. Both L-arginine and L-lysine enter the brain by a transport mechanism which can be saturated by a high concentration of the same amino acid in the bloodstream. The rate of entry can be explained by Michaelis-Menten kinetics.3. The entry into the brain of L-arginine can be inhibited by raised plasma concentrations of L-lysine or L-ornithine and the entry of L-lysine by raised concentrations of L-arginine.4. The inhibition of entry of an amino acid is most severe when its own concentration in the blood plasma is low and that of the inhibitor is high. The inhibition appears to be basically competitive in type, suggesting that common transport systems are shared by three dibasic amino acids.5. It is suggested that the raised levels of amino acids found in various disorders of amino acid metabolism are likely to reduce the rate of entry into the brain of other amino acids and a way is suggested in which the dietary treatment of hyperlysinaemia may be made more effective.
摘要
  1. 通过一种直接方法在体内测量了L-精氨酸和L-赖氨酸进入大鼠脑内的速率,该方法能使实验期间血浆中的氨基酸浓度保持恒定。

  2. L-精氨酸和L-赖氨酸均通过一种转运机制进入脑内,该机制可被血液中高浓度的同一种氨基酸饱和。进入速率可用米氏动力学来解释。

  3. 血浆中L-赖氨酸或L-鸟氨酸浓度升高可抑制L-精氨酸进入脑内,而L-精氨酸浓度升高则可抑制L-赖氨酸进入脑内。

  4. 当血浆中某氨基酸自身浓度较低而抑制剂浓度较高时,该氨基酸进入脑内的抑制作用最为明显。这种抑制作用在类型上似乎基本属于竞争性抑制,这表明三种二碱基氨基酸共用共同的转运系统。

  5. 有人提出,在各种氨基酸代谢紊乱中发现的氨基酸水平升高可能会降低其他氨基酸进入脑内的速率,并提出了一种可提高高赖氨酸血症饮食治疗效果的方法。

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引用本文的文献

5
The requirements of the brain for some amino acids.大脑对某些氨基酸的需求。
J Physiol. 1975 Apr;246(3):539-48. doi: 10.1113/jphysiol.1975.sp010903.

本文引用的文献

2
HYPERLYSINEMIA.高赖氨酸血症
Am J Dis Child. 1964 Nov;108:543-53. doi: 10.1001/archpedi.1964.02090010545015.

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