Jonung T, Rigotti P, Jeppsson B, James J H, Peters J C, Fischer J E
J Surg Res. 1984 Apr;36(4):349-53. doi: 10.1016/0022-4804(84)90110-0.
Accumulation of neutral amino acids in the brain due to altered transport across the blood-brain barrier appears to be a consequence of portal-systemic shunting and hyperammonemia. It has been suggested that high brain concentrations of glutamine, a product of cerebral ammonia detoxification, accelerates the transport of other neutral amino acids from blood to brain. To test this hypothesis, normal rats were infused with ammonium salts with or without pretreatment with L-methionine-dl-sulfoximine (MSO), an inhibitor of glutamine synthesis. Pretreatment with MSO prevented most ammonium salt-induced changes in the concentrations of the neutral amino acids in brain, suggesting that hyperammonemia alters the transport of neutral amino acids across the blood-brain barrier by causing the brain glutamine level to rise.
由于跨血脑屏障转运改变导致大脑中中性氨基酸的蓄积似乎是门体分流和高氨血症的结果。有人提出,大脑中高浓度的谷氨酰胺(脑内氨解毒的产物)会加速其他中性氨基酸从血液到大脑的转运。为了验证这一假设,给正常大鼠输注铵盐,部分大鼠在输注前用谷氨酰胺合成抑制剂L-蛋氨酸-dl-磺胺肟(MSO)进行预处理。MSO预处理可防止大多数铵盐诱导的大脑中中性氨基酸浓度变化,这表明高氨血症通过使脑内谷氨酰胺水平升高来改变中性氨基酸跨血脑屏障的转运。