Astrup A, Lundsgaard C
Research Department of Human Nutrition, The Royal Veterinary and Agricultural University, Copenhagen, Denmark.
Exp Clin Endocrinol Diabetes. 1998;106 Suppl 2:29-34. doi: 10.1055/s-0029-1212034.
Obesity is characterised by pathophysiological defects affecting both sides of the energy balance equation. Individuals with a predisposition to obesity have impaired appetite control when diets are fat-rich and energy dense. They also exhibit a lower than expected resting metabolic rate (RMR). A low RMR, in concert with a sedentary lifestyle, contributes to a low total energy output, which may lead to obesity if continued over a period of years. A low metabolic rate seems to be genetically determined, and is partly caused by low sympathetic nervous system activity. Classical treatment programmes for obesity do not provide a satisfactory long-term outcome for the majority of patients. Patients who achieve only a small weight loss during dietary therapy, and have a tendency to weight regain, are characterised by lower energy expenditure, lower sympathetic activity, and a reduced ability to mobilise fat stores, compared with patients who are more successful at losing weight. It is reasonable to improve or normalise these traits by supporting the dietary approach with pharmacological manipulation of central and peripheral pathways. Agents which stimulate adrenergic neurons are particularly suitable because they offer mechanisms for inhibiting hunger and for stimulating energy expenditure, lipolysis and fat oxidation. Sympathomimetic compounds can reduce appetite and increase energy expenditure. Energy expenditure can be increased by 5-10% via stimulation of a combination of beta-adrenoceptors; beta3-adrenoceptors may predominate during chronic therapy. This increased energy expenditure increases the relative proportion of fat oxidation; as this is not fully compensated by increased energy intake, a negative energy balance occurs. This mechanism may be responsible for the long-term weight loss efficiency of agents like ephedrine/caffeine and sibutramine. Pharmacotherapy can be used to support short-term induction of weight loss or long-term weight maintenance. In the latter case, adrenergic agents enable a greater proportion of patients to maintain a satisfactory weight loss, compared with patients treated with conventional programmes alone. Pharmacotherapy which stabilises the size of fat stores at a lower level contributes indirectly to a pronounced improvement of risk factors, leading to a decreased potential for cardiovascular disease, type 2 diabetes and associated morbidity.
肥胖的特征是能量平衡等式双方都存在病理生理缺陷。易患肥胖症的个体在摄入富含脂肪且能量密集的饮食时,食欲控制会受损。他们的静息代谢率(RMR)也低于预期。低静息代谢率与久坐不动的生活方式共同导致总能量输出较低,如果这种情况持续数年,可能会导致肥胖。低代谢率似乎由基因决定,部分原因是交感神经系统活动较低。肥胖的传统治疗方案对大多数患者而言,无法提供令人满意的长期疗效。与减肥更成功的患者相比,在饮食治疗期间体重仅略有下降且有体重反弹倾向的患者,其能量消耗较低、交感神经活动较低,动员脂肪储备的能力也较低。通过对中枢和外周途径进行药理干预来辅助饮食疗法,改善或使这些特征正常化是合理的。刺激肾上腺素能神经元的药物特别合适,因为它们提供了抑制饥饿以及刺激能量消耗、脂肪分解和脂肪氧化的机制。拟交感化合物可减少食欲并增加能量消耗。通过刺激β-肾上腺素能受体的组合,能量消耗可增加5% - 10%;在长期治疗期间,β3-肾上腺素能受体可能起主要作用。这种增加的能量消耗会增加脂肪氧化的相对比例;由于能量摄入增加无法完全补偿这一增加,会出现能量负平衡。这种机制可能是麻黄碱/咖啡因和西布曲明等药物长期减肥效果的原因。药物治疗可用于辅助短期减肥诱导或长期体重维持。在后一种情况下,与仅接受传统方案治疗的患者相比,肾上腺素能药物能使更大比例的患者维持令人满意的体重减轻。将脂肪储备量稳定在较低水平的药物治疗间接有助于显著改善危险因素,降低心血管疾病、2型糖尿病及相关发病率的可能性。