Role of leptin in the neuroendocrine response to fasting

瘦素在禁食神经内分泌反应中的作用

• 批准号: 8037912
• 负责人: CHRISTOS S MANTZOROS
• 金额: $ 10.21万
• 依托单位: BETH ISRAEL DEACONESS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-05 至 2011-04-04
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8037912
• 关键词: Accounting; Acute; Adipocytes; Adipose tissue; Adverse effects; Age; Agonist; Amenorrhea; Anorexia Nervosa; Apoptosis; Attention; Behavior Therapy; Body Weight; Body Weight decreased; Bone Density; Bone Mineral Contents; Bone Resorption; Brain; Cell Proliferation; Chronic; Clinical; Clinical Research; Data; Defect; Development; Diet; Disease; Double-Blind Method; Eating; Eating Disorders; Effectiveness; Energy Metabolism; Estrogens; Etiology; Explosion; Fasting; Fatty acid glycerol esters; Fertility; Food; Food deprivation (experimental); Foundations; Functional disorder; Future; Gastrointestinal tract structure; Goals; Grant; Growth; Growth Factor; Homeostasis; Hormones; Human; Hypothalamic structure; Immune; Immune response; In Vitro; Insulin Receptor; Insulin-Like Growth Factor I; Laboratories; Leptin; Leptin deficiency; Letters; Link; Long-Term Effects; Lymphocyte; Malnutrition; Mediating; Melanocortin 4 Receptor; Menstrual cycle; Modeling; Molecular; Neuraxis; Neurosecretory Systems; Obesity; Organ; Osteogenesis; Osteoporosis; Outcome; Ovulation; Paper; Pathogenesis; Pathway interactions; Patients; Peptide YY; Peptides; Peripheral; Peripheral Blood Mononuclear Cell; Personal Satisfaction; Pharmaceutical Preparations; Physiological; Physiology; Pilot Projects; Pituitary Gland; Placebos; Play; Production; Public Health; Publishing; Randomized; Recombinants; Regulation; Relative (related person); Research Design; Research Personnel; Rodent; Role; Safety; Signal Transduction; Somatotropin; Starvation; Structure; System; Testing; Therapeutic; Therapeutic Intervention; Thyroid Gland; Well in self; Woman; adiponectin; base; bone; bone health; bone metabolism; clinical application; cytokine; density; deprivation; diet and exercise; double-blind placebo controlled trial; energy balance; falls; feeding; food restriction; ghrelin; gonad function; human subject; immune function; improved; in vivo; insight; leptin receptor; open label; programs; randomized placebo controlled trial; recombinant methionyl human leptin; reproductive; reproductive hormone; research study; resistin; response; treatment duration

The adipoeyte-secreted hormone leptin signals the amount of energy stored in adipose tissue to the central nervous system. We have shown, in the context of this grant, that leptin administration to normalize the relative leptin deficiency induced by short term energy deficiency results in normalization of reproductive and other neuroendocrine defects. We have also shown that altering leptin levels within the normal physiological range, or into supraphysiological levels, has no effect on the same outcomes. Thus, in humans, leptin serves as a critical link between the sufficiency of energy stores and the integrity of the hypothalamic-pituitary- peripheral axes in states of leptin deficiency only. We have subsequently hypothesized that the abnormalities in the reproductive and other neuroendocrine axes in women with hypothalamic amenorrhea (HA), a condition associated with low leptin levels, may also be related to the chronic hypoleptinemia induced by negative energy balance. In a recently completed, open-label, small pilot study using historical controls, we found that leptin replacement to correct the relative leptin deficiency in women with HA resulted in follicular growth and ovulation and significantly improved hormone levels, providing preliminary evidence that leptin may contribute to the etiology of the amenorrhea and that leptin replacement may be a potential treatment for disease states associated with relative leptin deficiency. The goal of this proposal is to confirm and extend these preliminary findings by performing a randomized, double-blinded, placebo-controlled trial of leptin treatment in women with HA and leptin deficiency which would eliminate potential bias and confounding and would verify safety and efficacy of leptin as a new treatment for HA. Since HA accounts for over 30% of amenorrhea in reproductive-aged women and can have significant deleterious effects on fertility, bone health, and overall well-being, this study would have considerable clinical impact if leptin becomes a new, more physiologic, therapeutic option for HA. This is particularly relevant since currently available treatment options for HA have side effects, are not well accepted by some patients, and have suboptimal effectiveness for complications such as osteoporosis. Results of this study will not only help elucidate the pathophysiology of HA but will also provide important new information on leptin physiology in neuroendocrine regulation, bone metabolism and immune function at large, using HA as a model of chronic leptin deficiency. Thus, findings of this study to elucidate leptin physiology may also have applications in the pathophysiology (and possibly therapeutics) of other leptin related diseases, including obesity, a major public health problem.

脂肪细胞分泌的激素瘦素将脂肪组织中储存的能量的量发送到中枢神经系统。 神经系统我们已经表明，在这项资助的背景下，瘦素管理，以正常化， 由短期能量缺乏引起的相对瘦素缺乏导致生殖和 其他神经内分泌缺陷我们还表明，在正常的生理条件下改变瘦素水平， 范围，或超生理水平，对相同的结果没有影响。因此，在人类中， 作为能量储存充足和下丘脑-垂体完整性之间的关键联系， 仅在瘦素缺乏状态下的外周轴。我们随后假设， 在下丘脑性闭经（HA）女性的生殖和其他神经内分泌轴中， 与低瘦素水平相关的疾病，也可能与由 负能量平衡在最近完成的一项使用历史对照的开放标签小型试点研究中，我们 研究发现，瘦素替代治疗可纠正HA女性的相对瘦素缺乏， 生长和排卵，并显着改善激素水平，提供了初步证据，瘦素， 可能与闭经的病因有关，瘦素替代可能是一种潜在的治疗方法 用于与相对瘦素缺乏相关的疾病。该提案的目的是确认和 通过进行一项随机、双盲、安慰剂对照试验， 在患有HA和瘦素缺乏症的女性中进行瘦素治疗，这将消除潜在的偏倚， 并将验证瘦素作为HA的新治疗的安全性和有效性。由于医管局占 超过30%的育龄妇女闭经，并可能对生育能力产生显著的有害影响， 骨骼健康和整体健康，如果瘦素成为一种有效的治疗方法，这项研究将产生相当大的临床影响。 HA的新的、更符合生理的治疗选择。这一点特别重要，因为目前 HA的治疗选择具有副作用，不被一些患者很好地接受，并且具有次优的 对骨质疏松症等并发症有效。这项研究的结果不仅有助于阐明 但也将提供重要的新信息瘦素生理学在神经内分泌 调节，骨代谢和免疫功能，使用HA作为慢性瘦素缺乏症的模型。 因此，这项研究的结果，以阐明瘦素生理学也可能有应用的病理生理学 (and可能是治疗剂）的其它瘦素相关疾病，包括肥胖症，这是一个主要的公共健康问题。