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Efficacy of metreleptin in obese patients with type 2 diabetes: cellular and molecular pathways underlying leptin tolerance.肥胖 2 型糖尿病患者 metreleptin 的疗效:瘦素耐受的细胞和分子途径。
Diabetes. 2011 Jun;60(6):1647-56. doi: 10.2337/db10-1791.
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Leptin in human physiology and therapeutics.瘦素在人类生理学和治疗学中的作用。
Front Neuroendocrinol. 2010 Jul;31(3):377-93. doi: 10.1016/j.yfrne.2010.06.002. Epub 2010 Jun 17.
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Resistance to leptin-replacement therapy in Berardinelli-Seip congenital lipodystrophy: an immunological origin.Berardinelli-Seip 先天性脂肪营养不良症对瘦素替代治疗的抵抗:免疫学起源。
Eur J Endocrinol. 2010 Jun;162(6):1083-91. doi: 10.1530/EJE-09-1027. Epub 2010 Mar 17.
4
Moderate energy restriction-induced weight loss affects circulating IGF levels independent of dietary composition.适度能量限制引起的体重减轻与饮食组成无关,会影响循环 IGF 水平。
Eur J Endocrinol. 2010 Jun;162(6):1075-82. doi: 10.1530/EJE-10-0062. Epub 2010 Mar 8.
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Weight-loss outcomes: a systematic review and meta-analysis of weight-loss clinical trials with a minimum 1-year follow-up.减肥效果:对至少随访1年的减肥临床试验进行的系统评价和荟萃分析。
J Am Diet Assoc. 2007 Oct;107(10):1755-67. doi: 10.1016/j.jada.2007.07.017.
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Soluble receptor inhibits leptin transport.可溶性受体抑制瘦素转运。
J Cell Physiol. 2008 Feb;214(2):301-5. doi: 10.1002/jcp.21195.
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Efficacy and safety of leptin-replacement therapy and possible mechanisms of leptin actions in patients with generalized lipodystrophy.瘦素替代疗法在泛发性脂肪营养不良患者中的疗效与安全性以及瘦素作用的可能机制
J Clin Endocrinol Metab. 2007 Feb;92(2):532-41. doi: 10.1210/jc.2006-1546. Epub 2006 Nov 21.
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Differential regulation of metabolic, neuroendocrine, and immune function by leptin in humans.瘦素对人类代谢、神经内分泌和免疫功能的差异性调节。
Proc Natl Acad Sci U S A. 2006 May 30;103(22):8481-6. doi: 10.1073/pnas.0505429103. Epub 2006 May 19.
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Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight.低剂量瘦素可逆转骨骼肌、自主神经及神经内分泌对维持体重减轻的适应性变化。
J Clin Invest. 2005 Dec;115(12):3579-86. doi: 10.1172/JCI25977.
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Long-term efficacy of leptin replacement in patients with generalized lipodystrophy.瘦素替代疗法对泛发性脂肪营养不良患者的长期疗效。
Diabetes. 2005 Jul;54(7):1994-2002. doi: 10.2337/diabetes.54.7.1994.

给予超重和肥胖受试者 6 个月的瘦素治疗会增加游离瘦素浓度,但在低卡路里饮食诱导的体重减轻期间不会改变甲状腺和 IGF 轴的循环激素。

Leptin administration to overweight and obese subjects for 6 months increases free leptin concentrations but does not alter circulating hormones of the thyroid and IGF axes during weight loss induced by a mild hypocaloric diet.

机构信息

Division of Endocrinology, Diabetes and Metabolism, Harvard Medical School and Harvard School of Public Health, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215, USA.

出版信息

Eur J Endocrinol. 2011 Aug;165(2):249-54. doi: 10.1530/EJE-11-0252. Epub 2011 May 20.

DOI:10.1530/EJE-11-0252
PMID:21602313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3159386/
Abstract

OBJECTIVE

Short-term energy deprivation reduces leptin concentrations and alters the levels of circulating hormones of the hypothalamic-pituitary-peripheral axis in lean subjects. Whether the reduction in leptin concentration during long-term weight loss in obese individuals is linked to the same neuroendocrine changes seen in lean, leptin-sensitive subjects remains to be fully clarified.

METHODS

In this study, 24 overweight and obese adults (16 women and eight men; body mass index (BMI): 27.5-38.0 kg/m(2)) were prescribed a hypocaloric diet (-500 kcal/day) and were randomized to receive recombinant methionyl leptin (n=18, metreleptin, 10 mg/day self-injected s.c.) or placebo (n=6, same volume and time as metreleptin) for 6 months.

RESULTS

Metreleptin administration did not affect weight loss beyond that induced by hypocaloric diet alone (P for interaction=0.341) but increased the serum concentrations of total leptin by six- to eight-fold (P<0.001) and led to the generation of anti-leptin antibodies. Despite free leptin concentration (P for interaction=0.041) increasing from 9±1 ng/ml at baseline to 43±15 and 36±12 ng/ml at 3 and 6 months, respectively, changes in circulating hormones of the thyroid and IGF axes at 3 and 6 months were not significantly different in the placebo- and metreleptin-treated groups.

CONCLUSIONS

Leptin does not likely mediate changes in neuroendocrine function in response to weight loss induced by a mild hypocaloric diet in overweight and obese subjects.

摘要

目的

短期能量剥夺可降低瘦素浓度,并改变瘦素敏感受试者下丘脑-垂体-外周轴中环流激素的水平。肥胖个体长期减肥过程中瘦素浓度的降低是否与瘦素敏感受试者中所见的相同神经内分泌变化有关,仍有待充分阐明。

方法

本研究纳入 24 名超重和肥胖成年人(16 名女性和 8 名男性;体重指数(BMI):27.5-38.0kg/m²),给予低热量饮食(-500kcal/天),并随机分为接受重组甲硫氨酸瘦素(n=18,metreleptin,10mg/天皮下注射)或安慰剂(n=6,与 metreleptin 相同的体积和时间)治疗 6 个月。

结果

metreleptin 治疗并未增加低热量饮食单独诱导的体重减轻(交互作用 P=0.341),但使总瘦素血清浓度增加 6-8 倍(P<0.001),并导致抗瘦素抗体的产生。尽管游离瘦素浓度(交互作用 P=0.041)从基线时的 9±1ng/ml 分别增加至 3 个月时的 43±15ng/ml 和 6 个月时的 36±12ng/ml,但在安慰剂和 metreleptin 治疗组中,甲状腺和 IGF 轴中环流激素的变化在 3 个月和 6 个月时并无显著差异。

结论

在超重和肥胖个体中,瘦素不太可能介导轻度低热量饮食诱导的体重减轻对神经内分泌功能的变化。