Suppr超能文献

甜菊醇对离体灌注兔肾近端小管对氨基马尿酸转运的影响。

Effect of steviol on para-aminohippurate transport by isolated perfused rabbit renal proximal tubule.

作者信息

Chatsudthipong V, Jutabha P

机构信息

Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

出版信息

J Pharmacol Exp Ther. 2001 Sep;298(3):1120-7.

Abstract

An inhibitory effect of steviol, metabolite of the natural sweetener stevioside, on transepithelial transport of p-aminohippurate (J(PAH)) was observed in isolated S(2) segments of rabbit renal proximal tubules using in vitro microperfusion. Addition of steviol (0.01--0.25 mM) to the bathing medium significantly depressed J(PAH) (approximately 50--90%). This inhibitory effect was dose-dependent and was maximum at a concentration of 0.05 mM. To further examine this effect, a steviol concentration (0.01 mM) that produced approximately 50% inhibition of J(PAH), was chosen. Addition of 0.01 mM steviol to the bathing medium significantly depressed J(PAH) by about 50 to 60%. Steviol at the same concentration (0.01 mM), when present in the tubule lumen, had no significant effect on J(PAH). Addition of 0.01 mM steviol to lumen and bath simultaneously, produced a slightly greater inhibitory effect compared with addition to bath alone (60 versus 70%). A higher concentration of steviol, 0.05 mM (which maximally inhibited J(PAH) when on the basolateral side), was required on the luminal side than on the basolateral side before an inhibitory effect was observed. To further examine the mechanism by which steviol inhibited J(PAH), its effect on Na(+)-K(+) ATPase activity and ATP content was determined. Steviol at concentrations of 0.01 and 0.05 mM had no effect on Na(+)-K(+) ATPase activity or cell ATP content. Kinetic analyses indicated that steviol can competitively inhibit PAH transport at the basolateral membrane. The present study clearly showed that steviol can have a direct inhibitory effect on renal tubular transport by competitive binding with organic anion transporter.

摘要

利用体外微灌注技术,在兔肾近端小管分离的S(2)节段中观察到天然甜味剂甜菊糖苷的代谢产物甜菊醇对对氨基马尿酸跨上皮转运(J(PAH))具有抑制作用。向灌流液中添加甜菊醇(0.01--0.25 mM)可显著降低J(PAH)(约50--90%)。这种抑制作用呈剂量依赖性,在浓度为0.05 mM时达到最大。为进一步研究这种作用,选择了产生约50% J(PAH)抑制作用的甜菊醇浓度(0.01 mM)。向灌流液中添加0.01 mM甜菊醇可使J(PAH)显著降低约50%至60%。当甜菊醇以相同浓度(0.01 mM)存在于肾小管管腔中时,对J(PAH)无显著影响。同时向管腔和灌流液中添加0.01 mM甜菊醇,与仅添加到灌流液中相比,产生的抑制作用略大(分别为60%和70%)。在管腔侧需要比基底外侧侧更高浓度的甜菊醇(0.05 mM,当在基底外侧侧时对J(PAH)具有最大抑制作用)才能观察到抑制作用。为进一步研究甜菊醇抑制J(PAH) 的机制,测定了其对Na(+)-K(+) ATP酶活性和ATP含量的影响。浓度为0.01和0.05 mM的甜菊醇对Na(+)-K(+) ATP酶活性或细胞ATP含量无影响。动力学分析表明,甜菊醇可在基底外侧膜竞争性抑制PAH转运。本研究清楚地表明,甜菊醇可通过与有机阴离子转运体竞争性结合而对肾小管转运产生直接抑制作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验