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血清素和去甲肾上腺素再摄取抑制与进食行为。

Serotonin and norepinephrine reuptake inhibition and eating behavior.

作者信息

Hainer Vojtech, Kabrnova Karolina, Aldhoon Bashar, Kunesova Marie, Wagenknecht Martin

机构信息

Institute of Endocrinology, Narodni 8, 116 94 Prague 1, Czech Republic.

出版信息

Ann N Y Acad Sci. 2006 Nov;1083:252-69. doi: 10.1196/annals.1367.017.

Abstract

Brain neurotransmitters, serotonin and norepinephrine, play an important role in the central nervous control of energy balance and are involved in symptomatology related to both obesity and depression. Therefore both serotonin and norepinephrine neural pathways have been paid a special attention as targets for the antiobesity drugs, antidepressants, and drugs used in the treatment of eating disorders. Selective serotonin reuptake inhibitors (SSRI) have been used in the treatment of depression and eating disorders but have failed to achieve sustained weight loss in the treatment of obesity. Sibutramine, a serotonin and norepinephrine reuptake inhibitor, which induces satiety and prevents decline in metabolic rate associated with a hypocaloric diet, is currently the sole centrally acting drug indicated for the long-term treatment of obesity. Depression, dietary disinhibition (evaluated by the Eating Inventory [EI]), and stress are associated with the accumulation of abdominal fat and the development of metabolic syndrome and related diseases. Subjects with abdominal obesity demonstrate neuroendocrine abnormalities which result in disturbances in hypothalamo-pituitary-adrenal (HPA) function. Treatment with SSRI might interrupt the vicious circle which leads to endocrine abnormalities and the accumulation of abdominal fat. Obesity treatment with sibutramine results, not only in significant weight loss, but also in reduction of abdominal fat and in the improvement of health risks associated with metabolic syndrome (lipid profile, blood glucose, insulin, HbA1c, and uric acid), as well as in the decline in disinhibition score of the EI. In a 1-year sibutramine trial, only a decrease in the disinhibition score remained a significant correlate of weight loss among the psychobehavioral and nutritional factors which were taken into account.

摘要

脑内神经递质5-羟色胺和去甲肾上腺素在能量平衡的中枢神经控制中发挥重要作用,且与肥胖症和抑郁症相关症状有关。因此,5-羟色胺和去甲肾上腺素神经通路作为抗肥胖药物、抗抑郁药物以及用于治疗饮食失调药物的靶点受到了特别关注。选择性5-羟色胺再摄取抑制剂(SSRI)已用于治疗抑郁症和饮食失调,但在肥胖症治疗中未能实现持续减重。西布曲明是一种5-羟色胺和去甲肾上腺素再摄取抑制剂,可诱导饱腹感并防止与低热量饮食相关的代谢率下降,是目前唯一被批准用于肥胖症长期治疗的中枢作用药物。抑郁症、饮食抑制(通过饮食量表[EI]评估)和压力与腹部脂肪堆积、代谢综合征及相关疾病的发生有关。腹部肥胖的受试者表现出神经内分泌异常,导致下丘脑-垂体-肾上腺(HPA)功能紊乱。使用SSRI进行治疗可能会中断导致内分泌异常和腹部脂肪堆积的恶性循环。用西布曲明治疗肥胖症不仅能显著减重,还能减少腹部脂肪,改善与代谢综合征相关的健康风险(血脂、血糖、胰岛素、糖化血红蛋白和尿酸),同时降低EI的抑制评分。在一项为期1年的西布曲明试验中,在考虑到的心理行为和营养因素中,只有抑制评分的降低仍然是体重减轻的显著相关因素。

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