Meijer A J, Lof C, Ramos I C, Verhoeven A J
Eur J Biochem. 1985 Apr 1;148(1):189-96. doi: 10.1111/j.1432-1033.1985.tb08824.x.
Control of urea synthesis was studied in rat hepatocytes incubated with physiological mixtures of amino acids in which arginine was replaced by equimolar amounts of ornithine. The following observations were made. Intramitochondrial carbamoyl phosphate was always below 0.1 mM. Only when ornithine was absent and when, in addition, the concentration of amino acids was higher than four times their plasma concentration, intramitochondrial carbamoyl phosphate rose up to about 3 mM; under these conditions ammonia accumulated in the medium. The relationship between ornithine-cycle flux and the concentration of the cycle intermediates at varying amino acid concentration indicated that under near-physiological conditions the ornithine-cycle enzymes are far from being saturated with their subsidiaries. Moderate concentrations of norvaline had no effect on the rate of urea synthesis unless the cells were severely depleted of ornithine. Activation of carbamoyl-phosphate synthetase (ammonia) by addition of N-carbamoylglutamate only slightly stimulated urea production at all amino acid concentrations. However, in the presence of the activator the curve relating ornithine-cycle flux to the steady-state ammonia concentration was shifted to lower concentrations of ammonia. The intramitochondrial concentration of carbamoyl phosphate in rat liver in vivo was below 0.1 mM. This value is far below the concentration required for substantial inhibition of carbamoyl-phosphate synthetase. It is concluded that in vivo the function of activity changes in carbamoyl-phosphate synthetase, via the well-documented alterations in the intramitochondrial concentration of N-acetylglutamate, is to buffer the intrahepatic ammonia concentration rather than to affect urea production per se. At constant concentration of ammonia the rate of urea production is entirely controlled by the activity of carbamoyl-phosphate synthetase.
在大鼠肝细胞中,用氨基酸的生理混合物进行孵育,其中精氨酸被等摩尔量的鸟氨酸替代,以此来研究尿素合成的调控。得到了以下观察结果。线粒体内的氨甲酰磷酸始终低于0.1 mM。只有当鸟氨酸缺失,并且氨基酸浓度高于其血浆浓度四倍时,线粒体内的氨甲酰磷酸才会升至约3 mM;在这些条件下,氨会在培养基中积累。在不同氨基酸浓度下,鸟氨酸循环通量与循环中间产物浓度之间的关系表明,在接近生理条件下,鸟氨酸循环酶远未被其底物饱和。中等浓度的正缬氨酸对尿素合成速率没有影响,除非细胞严重缺乏鸟氨酸。添加N - 氨甲酰谷氨酸激活氨甲酰磷酸合成酶(氨),在所有氨基酸浓度下仅略微刺激尿素生成。然而,在有激活剂存在的情况下,将鸟氨酸循环通量与稳态氨浓度相关的曲线向较低氨浓度方向移动。大鼠肝脏体内线粒体内氨甲酰磷酸的浓度低于0.1 mM。该值远低于对氨甲酰磷酸合成酶产生显著抑制所需的浓度。结论是,在体内,通过线粒体中N - 乙酰谷氨酸浓度的充分记录的变化,氨甲酰磷酸合成酶活性变化的功能是缓冲肝内氨浓度,而不是影响尿素生成本身。在氨浓度恒定的情况下,尿素生成速率完全由氨甲酰磷酸合成酶的活性控制。