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大鼠小肠黏膜制剂中外源性尿苷二磷酸葡萄糖醛酸的分解。其他核苷酸的作用。

Exogenous uridine diphosphoglucuronic acid breakdown in rat small intestinal mucosa preparations. Effect of other nucleotides.

作者信息

Mottino A D, Denoya O, Rodríguez Garay E A

出版信息

Res Commun Chem Pathol Pharmacol. 1985 Sep;49(3):455-8.

PMID:4059659
Abstract

Breakdown of UDPGA incorporated in a mixture containing rat liver or small intestinal mucosa preparations was investigated in the absence of exogenous sugar acceptor. A rapid UDPGA breakdown was seen with intestinal mucosa preparations in such a way that UDPGA decreased to about 1% or less of the initial value after 15 min of incubation. It was estimated that 60 to 70% of total products derived from UDPGA at the end of the incubation with intestinal tissue was in the form of uridine (90%) and uracil (10%). The addition of UDPG, ATP or UDP-N-acetylglucosamine protected UDPGA against degradation by tissue. The results indicated that care must be taken during the incubation of exogenous UDPGA for glucuronyltransferase assay in the intestinal mucosa due to the predominance in this tissue of enzyme systems involved in UDPGA breakdown.

摘要

在没有外源性糖受体的情况下,研究了掺入含有大鼠肝脏或小肠粘膜制剂的混合物中的尿苷二磷酸葡萄糖醛酸(UDPGA)的分解情况。在小肠粘膜制剂中观察到UDPGA迅速分解,孵育15分钟后,UDPGA降至初始值的约1%或更低。据估计,在与肠道组织孵育结束时,来自UDPGA的总产物的60%至70%是以尿苷(90%)和尿嘧啶(10%)的形式存在。添加UDPG、ATP或UDP-N-乙酰葡糖胺可保护UDPGA不被组织降解。结果表明,由于该组织中参与UDPGA分解的酶系统占主导地位,因此在小肠粘膜中进行葡糖醛酸转移酶测定而孵育外源性UDPGA时必须小心。

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