Kunjara S, Sochor M, Adeoya A, McLean P, Greenbaum A L
Biochem J. 1986 Mar 15;234(3):579-85. doi: 10.1042/bj2340579.
The effect of developmental growth on the kidney content of phosphoribosyl pyrophosphate PPRibP was studied in rats at ages between the foetal animal and up to 100 days of age. In addition, the effect of short-term diabetes (up to 14 days) on the renal content of PPRibP was studied in immature rats and in adults aged approx. 60 days. The developmental pattern of PPRibP is such that the PPRibP content is lowest in the young rat and increases as the rate of kidney growth slows. In the adult rat, the early kidney hypertrophy of diabetes is accompanied by a fall in PPRibP content and, again, the PPRibP content returns to normal as the rate of kidney hypertrophy diminishes. Induction of diabetes in the immature rat causes a lesser degree of kidney hypertrophy and also a smaller depression of renal PPRibP content. The activity of PPRibP synthetase (EC 2.7.6.1) is not significantly affected by age or diabetes. The changes in PPRibP content are discussed in relation to the generation of ribose 5-phosphate by the pentose phosphate pathway and the utilization of PPRibP for nucleotide synthesis via the 'de novo' and salvage pathways.
研究了从胎鼠到100日龄大鼠发育生长对肾脏磷酸核糖焦磷酸(PPRibP)含量的影响。此外,还研究了短期糖尿病(长达14天)对未成熟大鼠和大约60日龄成年大鼠肾脏PPRibP含量的影响。PPRibP的发育模式是,幼鼠的PPRibP含量最低,随着肾脏生长速率减缓而增加。在成年大鼠中,糖尿病早期的肾脏肥大伴随着PPRibP含量下降,并且随着肾脏肥大速率降低,PPRibP含量又恢复正常。未成熟大鼠诱导糖尿病会导致较轻程度的肾脏肥大,同时肾脏PPRibP含量的降低幅度也较小。PPRibP合成酶(EC 2.7.6.1)的活性不受年龄或糖尿病的显著影响。结合磷酸戊糖途径生成5-磷酸核糖以及PPRibP通过“从头合成”和补救途径用于核苷酸合成的情况,对PPRibP含量的变化进行了讨论。