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地塞米松和体重减轻对肥胖个体血清瘦素水平调节的影响。

Influence of dexamethasone and weight loss on the regulation of serum leptin levels in obese individuals.

作者信息

Lerario D D, Ferreira S R, Miranda W L, Chacra A R

机构信息

Disciplina de Endocrinologia, Departamento de Medicina, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 910, 04039-000 São Paulo, SP, Brazil.

出版信息

Braz J Med Biol Res. 2001 Apr;34(4):479-87. doi: 10.1590/s0100-879x2001000400007.

Abstract

The adipocyte hormone leptin is thought to serve as a signal to the central nervous system reflecting the status of fat stores. Serum leptin levels and adipocyte leptin messenger RNA levels are clearly increased in obesity. Nevertheless, the factors regulating leptin production are not fully understood. The aim of this study was to determine the effects of in vivo administration of the synthetic glucocorticoid dexamethasone and weight loss on serum leptin levels in two independent protocols. Twenty-five obese subjects were studied (18 women and 7 men, mean age 26.6 +/- 6 years, BMI 31.1 +/- 2.5 kg/m(2), %fat 40.3 +/- 8.3) and compared at baseline to 22 healthy individuals. Serum levels of leptin, insulin, proinsulin and glucose were assessed at baseline and after ingestion of dexamethasone, 4 mg per day (2 mg, twice daily) for two consecutive days. To study the effects of weight loss on serum leptin, 17 of the obese subjects were submitted to a low-calorie dietary intervention trial for 8 weeks and again blood samples were collected. Serum leptin levels were significantly higher in the obese group compared to the control group and a high positive correlation between leptinemia and the magnitude of fat mass was found (r = 0.88, P<0.0001). After dexamethasone, there was a significant increase in serum leptin levels (22.9 +/- 12.3 vs 51.4 +/- 23.3 ng/ml, P<0.05). Weight loss (86.1 +/- 15.1 vs 80.6 +/- 14.2 kg, P<0.05) led to a reduction in leptin levels (25.13 +/- 12.8 vs 15.9 +/- 9.1 ng/ml, P<0.05). We conclude that serum leptin levels are primordially dependent on fat mass magnitude. Glucocorticoids at supraphysiologic levels are potent secretagogues of leptin in obese subjects and a mild fat mass reduction leads to a disproportionate decrease in serum leptin levels. This suggests that, in addition to the changes in fat mass, complex nutritional and hormonal interactions may also play an important role in the regulation of leptin levels.

摘要

脂肪细胞激素瘦素被认为是向中枢神经系统传递反映脂肪储备状况信号的物质。在肥胖状态下,血清瘦素水平和脂肪细胞瘦素信使核糖核酸水平明显升高。然而,调节瘦素产生的因素尚未完全明确。本研究的目的是通过两个独立的方案,确定体内给予合成糖皮质激素地塞米松和体重减轻对血清瘦素水平的影响。对25名肥胖受试者(18名女性和7名男性,平均年龄26.6±6岁,体重指数31.1±2.5kg/m²,体脂率40.3±8.3)进行了研究,并在基线时与22名健康个体进行比较。在基线以及连续两天每天摄入4mg地塞米松(2mg,每日两次)后,评估血清瘦素、胰岛素、胰岛素原和葡萄糖水平。为研究体重减轻对血清瘦素的影响,17名肥胖受试者接受了为期8周的低热量饮食干预试验,并再次采集血样。肥胖组血清瘦素水平显著高于对照组,且发现瘦素血症与脂肪量大小之间存在高度正相关(r = 0.88,P<0.0001)。给予地塞米松后,血清瘦素水平显著升高(22.9±12.3对51.4±23.3ng/ml,P<0.05)。体重减轻(86.1±15.1对80.6±14.2kg,P<0.05)导致瘦素水平降低(25.13±12.8对15.9±9.1ng/ml,P<0.05)。我们得出结论,血清瘦素水平主要取决于脂肪量大小。超生理水平的糖皮质激素是肥胖受试者瘦素的有效促分泌剂,轻度的脂肪量减少会导致血清瘦素水平不成比例地下降。这表明,除了脂肪量的变化外,复杂的营养和激素相互作用可能在瘦素水平的调节中也起重要作用。

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