Young S N, Sourkes T L
J Biol Chem. 1975 Jul 10;250(13):5009-14.
We investigated how changes in tryptophan pyrrolase activity and tryptophan loads affect the breakdown of tryptophan was estimated by injecting rats with [ring-2-14-C]tryptophan and measuring respiratory 14-CO2. We concluded, contrary to previous reports, that induction of tryptophan pyrrolase definitely will increase the rate of tryptophan breakdown. Tryptophan loads also increase tryptophan breakdown even in circumstances where there is no increase in tryptophan pyrrolase activity, presumably by increasing the saturation of the enzyme. After a tryptophan load (50 mg per kg) the increase in liver tryptophan concentration lasts only 30 min. The rapid return of liver tryptophan to normal may be due partly to the high turnover rate of liver tryptophan. We estimate that tryptophan pyrrolase degrades tryptophan in vivo at a rate that is equivalent to the whole liver tryptophan concentration in 7.5 min or less.
我们通过给大鼠注射[环-2-¹⁴C]色氨酸并测量呼出的¹⁴CO₂来估计色氨酸分解代谢,从而研究色氨酸吡咯酶活性变化和色氨酸负荷如何影响色氨酸的分解。与之前的报道相反,我们得出结论,色氨酸吡咯酶的诱导肯定会提高色氨酸的分解速率。即使在色氨酸吡咯酶活性没有增加的情况下,色氨酸负荷也会增加色氨酸的分解,推测这是通过增加酶的饱和度来实现的。在给予色氨酸负荷(每千克50毫克)后,肝脏色氨酸浓度的升高仅持续30分钟。肝脏色氨酸迅速恢复正常可能部分归因于肝脏色氨酸的高周转率。我们估计,色氨酸吡咯酶在体内降解色氨酸的速率相当于整个肝脏色氨酸浓度在7.5分钟或更短时间内的变化。