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The regulation of phenylalanine hydroxylase in rat tissues in vivo. Substrate- and cortisol-induced elevations in phenylalanine hydroxylase activity

机译:体内大鼠组织中苯丙氨酸羟化酶的调节。底物和皮质醇诱导的苯丙氨酸羟化酶活性升高

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pInjections of phenylalanine increased a 2.5-fold in 9 h the hepatic phenylalanine hydroxylase activity of 6-day-old or adult rats that had been pretreated (24h earlier) with p-chlorophenylalanine; without such pretreatment, phenylalanine did not raise the enzyme concentration. This difference is paralleled by the much greater extent to which the injected phenylalanine accumulated in livers of the pretreated compared with the normal animals. The hormonal induction of hepatic phenylalanine hydroxylase activity obeyed different rules: an injection of cortisol was without effect on adult livers but caused a threefold rise in phenylalanine hydroxylase activity of immature ones, both without and after pretreatment with p-chlorophenylalanine. In the latter instance, the effects of cortisol, and of phenylalanine were additive. Actinomycin inhibited the cortisol- but not the substrate-induced increase of phenylalanine hydroxylase, whereas puromycin inhibited both. The results indicate that substrate and hormone, two potential positive regulators of the amount of the hepatic (but not the renal) phenylalanine hydroxylase, act independently by two different mechanisms. The negative effector, p-chlorophenylalanine, also appears to interact with the synthetic (or degradative) machinery rather than with the existing phenylalanine hydroxylase molecules: 24h were required in vivo for an 85% decrease to ensue, and no inhibition occurred in vitro when incubating the enzyme with p-chlorophenylalanine or with liver extracts from p-chlorophenylalanine-treated rats./p
机译:>注射苯丙氨酸在9小时内使对-氯苯丙氨酸预处理(24小时之前)的6日龄或成年大鼠的肝脏苯丙氨酸羟化酶活性增加了2.5倍;没有这种预处理,苯丙氨酸不会提高酶的浓度。与正常动物相比,这种差异与所预处理的肝脏中注射的苯丙氨酸积累的程度更大有关。激素对肝中苯丙氨酸羟化酶活性的诱导遵循不同的规则:皮质醇注射对成年肝脏无影响,但未成熟和未用对氯苯丙氨酸预处理后,未成熟肝脏的苯丙氨酸羟化酶活性增加了三倍。在后一种情况下,皮质醇和苯丙氨酸的作用是累加的。放线菌素抑制皮质醇,但不抑制底物诱导的苯丙氨酸羟化酶的增加,而嘌呤霉素抑制两者。结果表明,底物和激素是肝(而非肾脏)苯丙氨酸羟化酶量的两个潜在的正调节剂,它们通过两种不同的机制独立发挥作用。负效应物对氯苯丙氨酸也似乎与合成(或降解)机制相互作用,而不是与现有的苯丙氨酸羟化酶分子相互作用:体内需要24小时才能减少85%,并且在孵育时体外没有抑制作用对氯苯丙氨酸或经对氯苯丙氨酸处理的大鼠肝脏提取物中的酶。

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