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首页> 外文期刊>American Journal of Physiology >Chylomicron components mediate intestinal lipid-induced inhibition of gastric motor function.
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Chylomicron components mediate intestinal lipid-induced inhibition of gastric motor function.

机译:乳糜微粒组分介导肠脂质诱导的胃运动功能抑制。

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摘要

Lipid, particularly long-chain triglyceride, initiates feedback regulation of gastrointestinal function. To determine whether the site of action of lipid is pre- or postabsorptive, we investigated the ability of mesenteric lipid-fed lymph to inhibit gastric motor function. Lymph was collected from awake lymph-fistula rats during intestinal infusion with either a glucose-saline maintenance solution or lipid. Intra-arterial injection of lymph collected during intestinal lipid infusion significantly inhibited gastric motility in anesthetized recipient rats compared with injection of equivalent amounts of triglyceride or lymph collected during intestinal infusion of maintenance solution. Lymph collected from rats during lipid infusion with Pluronic L-81 [an inhibitor of chylomicron formation and apolipoprotein (apo) A-IV secretion] compared with lymph injection from donor animals treated with Pluronic L-63 (a noninhibitory control for Pluronic L-81) was significantly less potent. Injection of purified recombinant apo A-IV significantly inhibited gastric motility. Products of lipid digestion and absorption, other than fatty acids or triglyceride, released by the intestine during lipid digestion likely serve as signals to initiate intestinal feedback regulation of gastrointestinal function. Most likely, apo A-IV is one of the signals involved.
机译:脂质,特别是长链甘油三酸酯,启动胃肠功能的反馈调节。为了确定脂质的作用部位是吸收前还是吸收后,我们研究了肠系膜脂质喂养的淋巴液抑制胃运动功能的能力。在肠道输注葡萄糖-盐水维持溶液或脂质的过程中,从清醒的淋巴瘘大鼠中收集淋巴液。与注射保持液肠内注射等量的甘油三酸酯或淋巴液注射相比,动脉内注射肠内脂质输注期间收集的淋巴液显着抑制了麻醉受体大鼠的胃动力。与使用Pluronic L-63治疗的供体动物的淋巴注射相比,在使用Pluronic L-81 [乳糜微粒形成和载脂蛋白(apo)A-IV分泌抑制剂]脂质输注期间从大鼠收集的淋巴液)的效力明显降低。注射纯化的重组载脂蛋白A-IV可显着抑制胃动力。除脂肪酸或甘油三酸酯外,在脂质消化过程中,由肠释放的脂质消化和吸收产物可能是启动胃肠功能肠道反馈调节的信号。载脂蛋白A-IV最有可能是所涉及的信号之一。

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