Hwa J J, Ghibaudi L, Compton D, Fawzi A B, Strader C D
Department of CNS and Cardiovascular Research, Schering-Plough Research Institute, Kenilworth, New Jersey 07033-0530, USA.
Horm Metab Res. 1996 Dec;28(12):659-63. doi: 10.1055/s-2007-979873.
Genetically obese (ob/ob) mice display a number of metabolic alterations, including decreased thermogenesis, hyperphagia, hyperglycemia and increased body fat. A single intracerebroventricular (i.c.v.) injection of these mice with leptin (0.01 to 1 microg) lowered food intake and body weight within 24 h. In addition, i.c.v. administration of leptin increased 22 h energy expenditure while reducing the respiratory quotient (RQ) in a dose-dependent manner. The leptin-induced decrease in RQ suggests a reduction in the fraction of total energy derived from carbohydrate oxidation and a corresponding increase in energy derived from fat oxidation. Our data suggest that leptin controls energy homeostasis through activation of receptor(s) in the central nervous system (CNS) that regulate both food intake and energy metabolism.
遗传性肥胖(ob/ob)小鼠表现出多种代谢改变,包括产热减少、食欲亢进、高血糖和体脂增加。向这些小鼠脑室内(i.c.v.)单次注射瘦素(0.01至1微克)可在24小时内降低食物摄入量和体重。此外,脑室内注射瘦素可增加22小时的能量消耗,同时以剂量依赖的方式降低呼吸商(RQ)。瘦素诱导的呼吸商降低表明,来自碳水化合物氧化的总能量比例减少,而来自脂肪氧化的能量相应增加。我们的数据表明,瘦素通过激活中枢神经系统(CNS)中的受体来控制能量平衡,这些受体调节食物摄入和能量代谢。