Behavioural Neuroscience Laboratory, Institute of Psychological Sciences, University of Leeds, LS2 9JT, UK.
Dis Model Mech. 2012 Sep;5(5):621-6. doi: 10.1242/dmm.009621.
The ideal anti-obesity drug would produce sustained weight loss with minimal side effects. The mechanisms that regulate energy balance have substantial built-in redundancy, overlap considerably with other physiological functions, and are influenced by social, hedonic and psychological factors that limit the effectiveness of pharmacological interventions. It is therefore unsurprising that anti-obesity drug discovery programmes have been littered with false starts, failures in clinical development, and withdrawals due to adverse effects that were not fully appreciated at the time of launch. Drugs that target pathways in metabolic tissues, such as adipocytes, liver and skeletal muscle, have shown potential in preclinical studies but none has yet reached clinical development. Recent improvements in the understanding of peptidergic signalling of hunger and satiety from the gastrointestinal tract mediated by ghrelin, cholecystokinin (CCK), peptide YY (PYY) and glucagon-like peptide-1 (GLP-1), and of homeostatic mechanisms related to leptin and its upstream pathways in the hypothalamus, have opened up new possibilities. Although some have now reached clinical development, it is uncertain whether they will meet the strict regulatory hurdles required for licensing of an anti-obesity drug. However, GLP-1 receptor agonists have already succeeded in diabetes treatment and, owing to their attractive body-weight-lowering effects in humans, will perhaps also pave the way for other anti-obesity agents. To succeed in developing drugs that control body weight to the extent seen following surgical intervention, it seems obvious that a new paradigm is needed. In other therapeutic arenas, such as diabetes and hypertension, lower doses of multiple agents targeting different pathways often yield better results than strategies that modify one pathway alone. Some combination approaches using peptides and small molecules have now reached clinical trials, although recent regulatory experience suggests that large challenges lie ahead. In future, this polytherapeutic strategy could possibly rival surgery in terms of efficacy, safety and sustainability of weight loss.
理想的减肥药应具有最小的副作用,并能持续减轻体重。调节能量平衡的机制具有很大的冗余性,与其他生理功能有很大的重叠,并且受到社会、享乐和心理因素的影响,这些因素限制了药物干预的效果。因此,抗肥胖药物发现计划充满了错误的开始、临床开发失败以及因当时未充分认识到的不良反应而撤回并不令人惊讶。针对代谢组织(如脂肪细胞、肝脏和骨骼肌)中途径的药物在临床前研究中显示出了潜力,但没有一种药物已经进入临床开发。最近对胃肠道中饥饿和饱腹感的肽信号传导的理解有所改善,这些信号由生长激素释放肽(ghrelin)、胆囊收缩素(CCK)、肽 YY(PYY)和胰高血糖素样肽-1(GLP-1)介导,以及与瘦素及其在上丘脑的上游途径相关的稳态机制的理解有所改善,开辟了新的可能性。尽管其中一些药物现在已经进入临床开发阶段,但尚不确定它们是否能满足获得减肥药所需的严格监管障碍。然而,GLP-1 受体激动剂已在糖尿病治疗中取得成功,并且由于它们在人体中具有吸引人的体重减轻作用,它们也可能为其他抗肥胖药物铺平道路。为了成功开发能够控制体重的药物,达到手术干预后的程度,似乎需要一种新的模式。在其他治疗领域,如糖尿病和高血压,针对不同途径的多种药物的低剂量通常比单独改变一种途径的策略产生更好的效果。一些使用肽和小分子的联合方法现在已经进入临床试验,尽管最近的监管经验表明,前面还有很大的挑战。在未来,这种多疗法策略在疗效、安全性和减肥的可持续性方面可能与手术相媲美。