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Vitamin D-restricted high-fat diet down-regulates expression of intestinal alkaline phosphatase isozymes in ovariectomized rats

机译:维生素D型限制性高脂饮食下调卵巢切除大鼠肠碱性磷酸酶同工酶的表达

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Intestinal alkaline phosphatase (IAP) is expressed at a high concentration in the brush border membrane of intestinal epithelial cells. Intestinal alkaline phosphatase controls bacterial endotoxin-induced inflammation by dephosphorylating lipopolysaccharide and is a gut mucosal defense factor. Previously, we reported that IAP activity in the duodenum was significantly decreased in male rats receiving a high-fat diet with vitamin D restriction. Here, we tested the hypothesis that IAP is also regulated by a vitamin D-restricted high-fat diet in an animal model of menopause. Twenty-four female rats were ovariectomized (OVX), and another 6 female rats were sham operated. The OVX rats were divided into 4 groups and fed experimental diets: a basic control diet, a basic control diet with vitamin D restriction, a high-fat diet, and a high-fat diet with vitamin D restriction. After 28 days of the experimental diets, the vitamin D-restricted high-fat diet decreased alkaline phosphatase activity in the duodenum of the OVX groups. The vitamin D-restricted high fat diet down-regulated mRNA expressions of IAP isozymes in the duodenum of the OVX groups. These findings support the hypothesis that the expression of IAP is suppressed by a vitamin D-restricted high-fat diet in OVX rats. An adequate vitamin D intake and prevention of low vitamin D levels may be important for IAP expression in gut homeostasis. (C) 2018 Elsevier Inc. All rights reserved.
机译:肠碱性磷酸酶(IAP)以高浓度的肠道上皮细胞的刷边膜中的高浓度表达。肠道碱性磷酸酶通过去磷酸化脂多糖对抗细菌内毒素诱导的炎症,是肠道防御因子。以前,我们报道,在患有维生素D限制的高脂饮食接受高脂饮食的雄性大鼠中,十二指肠中的IAP活性显着降低。在这里,我们测试了IAP的假设,即在更年期的动物模型中,IAP也受到维生素D限制的高脂饮食。二十四只雌性大鼠卵巢切除(OVX),另外6只雌性大鼠都是假的。将OVX大鼠分为4组,喂养实验饮食:基本控制饮食,具有维生素D限制的基本控制饮食,高脂饮食和维生素D限制的高脂饮食。在实验饮食28天后,维生素D型限制的高脂饮食在OVX组的十二指肠中降低了碱性磷酸酶活性。维生素D型限制高脂肪饮食下调IAP同工酶在OVX组的十二指肠中的mRNA表达。这些调查结果支持假设IAP的表达被维生素D型限制的高脂饮食在OVX大鼠中受到抑制。足够的维生素D摄入和预防低维生素D水平对于肠道稳态中的IAP表达可能是重要的。 (c)2018年Elsevier Inc.保留所有权利。

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