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首页> 外文期刊>Pharmaceutical research >Influence of fed-fasted state on intestinal PEPT1 expression and in vivo pharmacokinetics of glycylsarcosine in wild-type and Pept1 knockout mice.
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Influence of fed-fasted state on intestinal PEPT1 expression and in vivo pharmacokinetics of glycylsarcosine in wild-type and Pept1 knockout mice.

机译:禁食状态对野生型和Pept1基因敲除小鼠肠道PEPT1表达和甘氨酰肌氨酸的体内药代动力学的影响。

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摘要

To determine if fasting would affect the intestinal expression and in vivo functional activity of PEPT1 as determined after oral dosing of the dipeptide glycylsarcosine (GlySar).Systemic exposure and tissue distribution studies were performed in wild-type and Pept1 knockout mice, under fed and fasted conditions, following both intravenous and oral doses of [(14)C]GlySar at 5?nmol/g body weight. Intestinal PEPT1 expression was evaluated by real-time PCR and immunoblot analyses.We found that expression of PEPT1 protein in the small intestine was increased ~2-fold in wild-type mice during fasted as compared to fed conditions. In agreement, systemic exposure and peak plasma concentrations of orally administered GlySar were 40 and 65% greater, respectively, in wild-type mice during fasted vs. fed state. No significant differences were observed between fed and fasted animals during PEPT1 ablation. Tissue distribution of GlySar was unchanged after oral dosing for all four treatment groups.As little as 16?h of fasting can cause significant upregulation of PEPT1 protein expression in the small intestine, which then translates into a significant increase in in vivo oral absorption of GlySar.
机译:为了确定禁食是否会影响口服口服二肽糖基肌氨酸(GlySar)后确定的PEPT1的肠道表达和体内功能活性。在野生型和Pept1基因敲除小鼠中,在进食和禁食下进行了全身暴露和组织分布研究静脉和口服[[14] C] GlySar的剂量为5?nmol / g体重。通过实时PCR和免疫印迹分析评估肠道PEPT1的表达。我们发现,禁食期间野生型小鼠的小肠中PEPT1蛋白的表达与进食条件相比增加了约2倍。一致的是,在禁食与进食状态下,野生型小鼠口服GlySar的全身暴露和血浆峰值浓度分别高40%和65%。在PEPT1消融期间,在喂食和禁食的动物之间未观察到显着差异。四个给药组口服给药后GlySar的组织分布均未改变。禁食16小时可导致小肠PEPT1蛋白表达显着上调,然后转化为GlySar的体内口服吸收显着增加。

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