首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >IN VIVO SUPPRESSION OF THE RENAL NA+/P-I COTRANSPORTER BY ANTISENSE OLIGONUCLEOTIDES
【24h】

IN VIVO SUPPRESSION OF THE RENAL NA+/P-I COTRANSPORTER BY ANTISENSE OLIGONUCLEOTIDES

机译:反义寡核苷酸体内抑制肾脏NA + / P-I转运蛋白

获取原文
获取原文并翻译 | 示例
       

摘要

A 20-mer phosphorothioate oligonucleotide (AS1) aas designed to hybridize to the message for the rat kidney sodium phosphate cotransporter NaPi-2 close to the translation initiation site. Single intravenous doses of this oligonucleotide were given to rats maintained on a low phosphorus diet to increase NaPi-2 expression. At 3 days after oligonucleotide infusion, rats receiving 2.5 mu mol of AS1 exhibited a reduction in renal NaPi-2 to cyclophilin mRNA ratio by 40% +/- 17%, and rats receiving 7.5 mu mol of AS1 exhibited a reduction in NaPi-2 to cyclophilin mRNA ratio by 46% +/- 21%. Reversed-sequence ASI was without effect. The higher dose of 7.5 mu mol of AS1 also reduced the rate of phosphate uptake into renal brush border membrane vesicles and the expression of NaPi-2 protein detected by Western blotting in these resides. Reversed sequence ASI was again without effect on these parameters. These results suggest that systemically infused oligonucleotides can exert antisense effects in the renal proximal tubule. [References: 29]
机译:一种20聚硫代磷酸酯寡核苷酸(AS1)aas设计用于与大鼠肾磷酸钠共转运蛋白NaPi-2靠近翻译起始位点的信息杂交。将这种寡核苷酸的单次静脉内剂量给予维持低磷饮食以增加NaPi-2表达的大鼠。注入寡核苷酸后3天,接受2.5μmol AS1的大鼠肾NaPi-2与亲环素mRNA比例降低40%+/- 17%,接受7.5μmol AS1的大鼠NaNa-2降低与亲环蛋白mRNA的比率为46%+ /-21%。反向序列ASI无效。较高剂量的7.5μmol的AS1也降低了磷酸盐吸收到肾刷缘膜囊泡中的速率,并且通过Western印迹检测到了这些残留物中NaPi-2蛋白的表达。反向序列ASI再次对这些参数没有影响。这些结果表明,全身注入的寡核苷酸可以在肾近端小管中发挥反义作用。 [参考:29]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号