Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight

被引:419
作者
Rosenbaum, M [1 ]
Goldsmith, R [1 ]
Bloomfield, D [1 ]
Magnano, A [1 ]
Weimer, L [1 ]
Heymsfield, S [1 ]
Gallagher, D [1 ]
Mayer, L [1 ]
Murphy, E [1 ]
Leibel, RL [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
关键词
D O I
10.1172/JCI25977
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Maintenance of a reduced body weight is accompanied by decreased energy expenditure that is due largely to increased skeletal muscle work efficiency. In addition, decreased sympathetic nervous system tone and circulating concentrations of leptin, thyroxine, and triiodothyronine act coordinately to favor weight regain. These "weight-reduced" phenotypes are similar to those of leptin-deficient humans and rodents. We examined metabolic, autonomic, and neuroendocrine phenotypes in 10 inpatient subjects (5 males, 5 females [3 never-obese, 7 obese]) under 3 sets of experimental conditions: (a) maintaining usual weight by ingesting a liquid formula diet; (b) maintaining a 10% reduced weight by ingesting a liquid formula diet; and (c) receiving twice-daily subcutaneous doses of leptin sufficient to restore 8 am circulating leptin concentrations to pre-weight-loss levels and remaining on the same liquid formula diet required to maintain a 10% reduced weight. During leptin administration, energy expenditure, skeletal muscle work efficiency, sympathetic nervous system tone, and circulating concentrations of thyroxine and triiodothyronine returned to pre-weight-loss levels. These responses suggest that the weight-reduced state may be regarded as a condition of relative leptin insufficiency. Prevention of weight regain might be achievable by strategies relevant to reversing this leptin-insufficient state.
引用
收藏
页码:3579 / 3586
页数:8
相关论文
共 86 条
  • [1] Distinct physiologic and neuronal responses to decreased leptin and mild hyperleptinemia
    Ahima, RS
    Kelly, J
    Elmquist, JK
    Flier, JS
    [J]. ENDOCRINOLOGY, 1999, 140 (11) : 4923 - 4931
  • [2] Role of leptin in the neuroendocrine response to fasting
    Ahima, RS
    Prabakaran, D
    Mantzoros, C
    Qu, DQ
    Lowell, B
    MaratosFlier, E
    Flier, JS
    [J]. NATURE, 1996, 382 (6588) : 250 - 252
  • [3] *AM PHYS SOC, 2002, AM J PHYSIOL-REG I, V283, pR281, DOI DOI 10.1152/AJPREGU.00279.2002
  • [4] AUTONOMIC NERVOUS-SYSTEM ACTIVITY IN WEIGHT-GAIN AND WEIGHT-LOSS
    ARONNE, LJ
    MACKINTOSH, R
    ROSENBAUM, M
    LEIBEL, RL
    HIRSCH, J
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1995, 269 (01) : R222 - R225
  • [5] Insulin and leptin as adiposity signals
    Benoit, SC
    Clegg, DJ
    Seeley, RJ
    Woods, SC
    [J]. RECENT PROGRESS IN HORMONE RESEARCH, VOL 59: CARDIOVASCULAR ENDOCRINOLOGY & OBESITY, 2004, 59 : 267 - 285
  • [6] Leptin stimulates glucose uptake in C2C12 muscle cells by activation of ERK2
    Berti, L
    Gammeltoft, S
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 157 (1-2) : 121 - 130
  • [7] BOUGET S, 2004, SCIENCE, V304, P108
  • [8] Effect of leptin deficiency on metabolic rate in ob/ob mice
    Breslow, MJ
    Min-Lee, K
    Brown, DR
    Chacko, VP
    Palmer, D
    Berkowitz, DE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 276 (03): : E443 - E449
  • [9] Novel transitions in MHC isoforms: separate and combined effects of thyroid hormone and mechanical unloading
    Caiozzo, VJ
    Baker, MJ
    Baldwin, KM
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1998, 85 (06) : 2237 - 2248
  • [10] RECOMBINANT MOUSE OB PROTEIN - EVIDENCE FOR A PERIPHERAL SIGNAL LINKING ADIPOSITY AND CENTRAL NEURAL NETWORKS
    CAMPFIELD, LA
    SMITH, FJ
    GUISEZ, Y
    DEVOS, R
    BURN, P
    [J]. SCIENCE, 1995, 269 (5223) : 546 - 549