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Salt Appetite Is Reduced by a Single Experience of Drinking Hypertonic Saline in the Adult Rat

机译:在成年大鼠中喝高渗盐水的单一经验会降低食欲

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摘要

Salt appetite, the primordial instinct to favorably ingest salty substances, represents a vital evolutionary important drive to successfully maintain body fluid and electrolyte homeostasis. This innate instinct was shown here in Sprague-Dawley rats by increased ingestion of isotonic saline (IS) over water in fluid intake tests. However, this appetitive stimulus was fundamentally transformed into a powerfully aversive one by increasing the salt content of drinking fluid from IS to hypertonic saline (2% w/v NaCl, HS) in intake tests. Rats ingested HS similar to IS when given no choice in one-bottle tests and previous studies have indicated that this may modify salt appetite. We thus investigated if a single 24 h experience of ingesting IS or HS, dehydration (DH) or 4% high salt food (HSD) altered salt preference. Here we show that 24 h of ingesting IS and HS solutions, but not DH or HSD, robustly transformed salt appetite in rats when tested 7 days and 35 days later. Using two-bottle tests rats previously exposed to IS preferred neither IS or water, whereas rats exposed to HS showed aversion to IS. Responses to sweet solutions (1% sucrose) were not different in two-bottle tests with water, suggesting that salt was the primary aversive taste pathway recruited in this model. Inducing thirst by subcutaneous administration of angiotensin II did not overcome this salt aversion. We hypothesised that this behavior results from altered gene expression in brain structures important in thirst and salt appetite. Thus we also report here lasting changes in mRNAs for markers of neuronal activity, peptide hormones and neuronal plasticity in supraoptic and paraventricular nuclei of the hypothalamus following rehydration after both DH and HS. These results indicate that a single experience of drinking HS is a memorable one, with long-term changes in gene expression accompanying this aversion to salty solutions.
机译:食欲是食盐类食物的本能,它是成功维持体液和电解质稳态的重要进化动力。在先天性本能在Sprague-Dawley大鼠中通过在液体摄入试验中等渗盐水(IS)的摄入量较水增加了。但是,通过在摄入测试中增加从IS到高渗盐水(2%w / v NaCl,HS)的饮用液中的盐含量,可以将这种刺激性刺激从根本上转变为一种强烈的厌恶刺激。在单瓶试验中没有选择的情况下,大鼠摄入类似于IS的HS,先前的研究表明这可能会改变食盐的食欲。因此,我们调查了摄入IS或HS,脱水(DH)或4%高盐食物(HSD)的单次24小时经历是否改变了盐的偏爱。在这里,我们显示当在7天和35天后进行测试时,摄入IS和HS溶液而不是DH或HSD的24 h能够强烈地转化大鼠的食欲。使用两瓶试验,先前暴露于IS的大鼠既不喜欢IS也不喜欢水,而暴露于HS的大鼠则表现出对IS的厌恶。用水进行两瓶测试时,对甜味溶液(1%蔗糖)的反应没有差异,这表明盐是该模型中招募的主要厌恶味道途径。皮下注射血管紧张素II引起的口渴不能克服这种食盐厌恶。我们假设这种行为是由于口渴和食盐重要的大脑结构中基因表达的改变引起的。因此,我们还报告了DH和HS复水后下丘脑上视和室旁核中神经元活性,肽激素和神经元可塑性标记的mRNA的持久变化。这些结果表明,一次饮用HS的经历令人难忘,伴随对盐溶液的厌恶,基因表达会发生长期变化。

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