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新型三唑衍生物JTP-59557对体外和体内肠道磷酸盐转运的抑制作用。

Inhibitory effect of JTP-59557, a new triazole derivative, on intestinal phosphate transport in vitro and in vivo.

作者信息

Matsuo Akira, Negoro Tamotsu, Seo Tomohisa, Kitao Yuki, Shindo Masanori, Segawa Hiroko, Miyamoto Ken-Ichi

机构信息

Central Pharmaceutical Research Institute, Japan Tobacco Inc., 1-1 Murasaki-Cho, Takatsuki, Osaka 569-1125, Osaka, Japan.

出版信息

Eur J Pharmacol. 2005 Jul 4;517(1-2):111-9. doi: 10.1016/j.ejphar.2005.05.003.

Abstract

JTP-59557 [(-)-4-(2-tert-Butyl-4,5-dichlorophenyl)-5-(5-trifluoromethylpyridin-2-ylsulfanyl)-4H-[1,2,4]triazol-3-ol] showed an inhibitory effect on Na(+)-dependent inorganic phosphate (Pi) transport in intestinal brush border membrane vesicles with an IC(50) value of 0.40 microM in rabbit and with an IC(50) of 0.19 microM in rat, without affecting Na(+)-independent Pi and Na(+)-dependent d-glucose transport activities. In Chinese hamster ovary (CHO) cells expressing human type IIb Na/Pi cotransporter (type IIb), JTP-59557 decreased human type IIb-mediated Pi uptake with an IC(50) of 0.12 microM. In rabbit intestinal brush border membrane vesicles, JTP-59557 behaved as a noncompetitive inhibitor with respect to Pi. In an in vivo study, single administration of JTP-59557 significantly decreased the intestinal Pi absorption rate, when either Pi solution or laboratory chow was given to rats. In this report, we show that JTP-59557 is a potent, selective, stereospecific, noncompetitive inhibitor of intestinal Na/Pi cotransporters including type IIb, and it may represent a new class of intestinal Pi absorption inhibitor.

摘要

JTP-59557 [(-)-4-(2-叔丁基-4,5-二氯苯基)-5-(5-三氟甲基吡啶-2-基硫烷基)-4H-[1,2,4]三唑-3-醇] 对兔小肠刷状缘膜囊泡中依赖钠离子的无机磷酸盐(Pi)转运具有抑制作用,在兔中的半数抑制浓度(IC50)值为0.40微摩尔,在大鼠中为0.19微摩尔,且不影响不依赖钠离子的Pi转运以及依赖钠离子的d-葡萄糖转运活性。在表达人IIb型钠/磷共转运体(IIb型)的中国仓鼠卵巢(CHO)细胞中,JTP-59557降低了人IIb型介导的Pi摄取,IC50为0.12微摩尔。在兔小肠刷状缘膜囊泡中,JTP-59557对Pi表现为非竞争性抑制剂。在一项体内研究中,当给大鼠给予Pi溶液或实验室饲料时,单次给予JTP-59557可显著降低小肠Pi吸收率。在本报告中,我们表明JTP-59557是一种强效、选择性、立体特异性、非竞争性的肠道钠/磷共转运体抑制剂,包括IIb型,它可能代表一类新型的肠道Pi吸收抑制剂。

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