首页> 外文期刊>Appetite >Exaggerated feedback control decreases brain serotonin concentration and elicits hyperactivity in a rat model of diet-restriction-induced anorexia nervosa.
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Exaggerated feedback control decreases brain serotonin concentration and elicits hyperactivity in a rat model of diet-restriction-induced anorexia nervosa.

机译:在饮食限制引起的神经性厌食症的大鼠模型中,夸大的反馈控制降低了脑5-羟色胺的浓度,并引起机能亢进。

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摘要

5-Hydroxytryptamine (5-HT; serotonin) system is the major neurotransmitter system of interest in research on anorexia nervosa (AN). The AN patients show extreme dieting weight loss, hyperactivity and low basal levels of 5-hydroxyindoleacetic acid (5-HIAA), a major metabolite of 5-HT in the cerebrospinal fluid (CSF). Studies on animal models show that diet restriction (DR) decreases 5-HT metabolism in the brain and hypothalamus which is not necessarily associated with a decrease in the availability of essential amino acid tryptophan (TRP) the precursor of serotonin. To further investigate the mechanism involved in DR-induced decreases of 5-HT the present study uses 8-hydroxy-(2-di-n-propylamino) tetralin (8-OH-DPAT), a selective 5-HT-1A agonist, as a probe to monitor the responsiveness of negative feedback control over 5-HT metabolism. Effects of DR and of 8-OHDPAT on TRP, 5-HT and 5-HIAA concentrations are determined in the hypothalamus, a region of the brain known to role in the regulation of appetite. Animals of DR group given access to food 2h daily for 6 days exhibited 21.6% decrease in the body weight compared to freely feeding (FF) controls. The levels of TRP in the plasma and of 5-HT in the hypothalamus decreased. No effect was found on the levels of TRP in the hypothalamus. 8-OH-DPAT-induced decreases of 5-HT and 5-HIAA were greater in DR than FF group. 8-OH-DPAT-induced hyperactivity was also greater in DR than FF group. The results show that DR-induced decreases of 5-HT are due to an increase in the responsiveness of negative feedback control over 5-HT and not due to smaller availability of TRP. DR-induced increase in activity and 8-OH-DPAT-induced greater hyperactivity in DR than FF group may also be due to exaggerated negative feedback control over 5-HT. It is suggested that drugs decreasing the responsiveness of negative feedback control over 5-HT may be of use for the treatment and prevention of AN in under weight patients on restricted diet.
机译:5-羟色胺(5-HT; 5-羟色胺)系统是神经性厌食症(AN)研究中关注的主要神经递质系统。 AN患者表现出极端节食的减肥,活动过度和低水平的5-羟吲哚乙酸(5-HIAA),这是脑脊液(CSF)中5-HT的主要代谢产物。动物模型研究表明,饮食限制(DR)会降低大脑和下丘脑中的5-HT代谢,这不一定与5-羟色胺前体必需氨基酸色氨酸(TRP)的利用率降低有关。为了进一步研究DR诱导的5-HT降低的机制,本研究使用了选择性5-HT-1A激动剂8-羟基-(2-二-正丙基氨基)四氢萘(8-OH-DPAT),作为监测5-HT代谢负反馈控制反应的探针。在下丘脑中确定了DR和8-OHDPAT对TRP,5-HT和5-HIAA浓度的影响,下丘脑是已知的调节食欲的大脑区域。与自由喂养(FF)对照相比,每天2h连续6天进食的DR组动物的体重下降21.6%。血浆中的TRP水平和下丘脑中的5-HT水平下降。在下丘脑中未发现对TRP水平的影响。与FF组相比,DR的8-OH-DPAT诱导的5-HT和5-HIAA降低更大。在DR中,由8-OH-DPAT诱导的机能亢进也大于FF组。结果表明,DR诱导的5-HT降低是由于负反馈控制对5-HT的响应能力增强,而不是由于TRP的可用性较小。与FF组相比,DR导致DR引起的活动增加和8-OH-DPAT引起的DR过度活跃可能也归因于对5-HT的过度负反馈控制。建议降低对5-HT负反馈控制的反应性的药物可能用于治疗和预防体重受限的体重不足患者的AN。

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