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血清素、饮食行为与脂肪摄入。

Serotonin, eating behavior, and fat intake.

作者信息

Blundell J E, Lawton C L, Halford J C

机构信息

Psychology Department, University of Leeds, UK.

出版信息

Obes Res. 1995 Nov;3 Suppl 4:471S-476S. doi: 10.1002/j.1550-8528.1995.tb00214.x.

Abstract

There is an intimate relationship between nutritional intake (eating) and serotonin activity. Experimental manipulations (mainly neuropharmacological) of serotonin influence the pattern of eating behavior, subjective feelings of appetite motivation, and the response to nutritional challenges. Similarly, nutritional manipulations (food restriction, dieting, or altered nutrient supply) change the sensitivity of the serotonin network. Traditionally, serotonin has been linked to the macronutrient carbohydrate via the intermediary step of plasma amino acid ratios. However, it has also been demonstrated that 5-HT drugs will reduce energy intake and reverse body weight gain in rats exposed to weight increasing high fat diets. 5-HT drugs can also reduce food intake and block weight gain of rats on a high fat cafeteria diet. Some diet selection studies in rats indicate that the most prominent reduction of macronutrient intake is for fat. These data indicate that 5-HT activity can bring about a reduction in fat consumption. In turn, different types of dietary fat can alter brain 5-HT activity. In human studies the methodology of food choice experiments has often precluded the detection of an effect of 5-HT manipulation on fat intake. However, there is evidence that in obese and lean subjects some 5-HT drugs can readily reduce the intake of high fat foods. Data also suggest that 5-HT activation can lead to a selective avoidance of fat in the diet. These effects of 5-HT on the intake of dietary fat may involve a pre-absorptive mechanism and there is evidence that 5-HT is linked to cholecystokinin and enterostatin. These proposals have theoretical and practical implications and suggest possible strategies to intensify or advance fat-induced satiety signals.

摘要

营养摄入(饮食)与血清素活性之间存在密切关系。对血清素进行实验性操作(主要是神经药理学方面)会影响饮食行为模式、食欲动机的主观感受以及对营养挑战的反应。同样,营养操作(食物限制、节食或改变营养供应)会改变血清素网络的敏感性。传统上,血清素通过血浆氨基酸比例的中间步骤与常量营养素碳水化合物相关联。然而,也已证明,5-羟色胺药物会减少暴露于导致体重增加的高脂肪饮食的大鼠的能量摄入并逆转体重增加。5-羟色胺药物还可以减少大鼠在高脂自助餐厅饮食中的食物摄入量并阻止体重增加。一些对大鼠的饮食选择研究表明,常量营养素摄入量减少最显著的是脂肪。这些数据表明,5-羟色胺活性可导致脂肪消耗减少。反过来,不同类型的膳食脂肪会改变大脑5-羟色胺活性。在人体研究中,食物选择实验的方法常常排除了检测5-羟色胺操作对脂肪摄入影响的可能性。然而,有证据表明,在肥胖和瘦的受试者中,一些5-羟色胺药物可以很容易地减少高脂肪食物的摄入量。数据还表明,5-羟色胺激活可导致在饮食中选择性地避免脂肪。5-羟色胺对膳食脂肪摄入的这些影响可能涉及一种吸收前机制,并且有证据表明5-羟色胺与胆囊收缩素和肠抑胃素有关。这些观点具有理论和实际意义,并提出了增强或促进脂肪诱导的饱腹感信号的可能策略。

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