首页> 外文期刊>American Journal of Physiology >The influence of dehydroepiandrosterone and 8-OH-DPAT on the caloric intake and hypothalamic neurotransmitters of lean and obese Zucker rats.
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The influence of dehydroepiandrosterone and 8-OH-DPAT on the caloric intake and hypothalamic neurotransmitters of lean and obese Zucker rats.

机译:脱氢表雄酮和8-OH-DPAT对瘦和肥胖Zucker大鼠的热量摄入和下丘脑神经递质的影响。

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摘要

The 5 HT(1A) receptor agonist 8-hydroxy-2-(di-n-propylamino)-tetraline (8-OH-DPAT) increases the food intake of satiated Zucker rats, both lean and obese. Associated with this increased intake are changes in the hypothalamic content of serotonin and its metabolite, 5-HIAA (5-hydroxyindole-3-acetic acid); serotonin is increased while the level of 5-HIAA is decreased. Analysis of individual 5-HIAA/5-hydroxytryptamine (5-HT) ratios, a measure of serotonin turnover indicate that 8-OH DPAT affected serotonin turnover equally and dramatically in both phenotypes. This would be an expected physiological action of an autofeedback mechanism by a 5-HT(1A) receptor agonist. Dehydroepiandrosterone (DHEA) at doses as low as 10 mg/kg blocks the 8-OH-DPAT-induced increase in food intake but does not alter food intake of control satiated Zucker rats. The mechanism of DHEA's action was investigated by monitoring the steroid's effect on hypothalamic neurotransmitters in this satiated model. DHEA by itself induced some change in 5-HIAA in the obese satiated model but not the lean. 8-OH-DPAT, by itself, dramatically decreased serotonin turnover in either lean or obese rats, and DHEA combined with 8-OH-DPAT did not further change serotonin turnover, suggesting DHEA may work through mechanisms other than monoamines to cause its inhibition of 8-OH-DPAT-induced behavioral effects at such low doses.
机译:5 HT(1A)受体激动剂8-羟基-2-(二-正丙基氨基)-四氢呋喃(8-OH-DPAT)增加了饱足的Zucker大鼠的饮食,无论是瘦的还是肥胖的。与摄入量增加有关的是5-羟色胺及其代谢产物5-HIAA(5-羟基吲哚-3-乙酸)的下丘脑含量的变化;血清素升高,而5-HIAA降低。对5-羟色胺5-羟色胺(5-HT)比率(5-羟色胺更新率的一种测量)的分析表明,在两种表型中,8-OH DPAT均会同时显着地影响5-羟色胺的转化率。这将是5-HT(1A)受体激动剂自动反馈机制的预期生理作用。剂量低至10 mg / kg的脱氢表雄酮(DHEA)可以阻止8-OH-DPAT诱导的食物摄入增加,但不会改变对照组饱足的Zucker大鼠的食物摄入。通过监测类固醇对饱足模型中下丘脑神经递质的作用,研究了脱氢表雄酮(DHEA)作用的机制。 DHEA本身在肥胖饱足模型中诱导了5-HIAA的变化,但没有引起瘦肉。 8-OH-DPAT本身可显着降低瘦或肥胖大鼠的5-羟色胺转化率,DHEA与8-OH-DPAT的结合不会进一步改变5-羟色胺的转化率,这表明DHEA可能通过单胺以外的其他机制起作用,从而导致其抑制低剂量的8-OH-DPAT诱导的行为效应。

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