Molecular Nociception Group, Wolfson Institute for Biomedical Research, University College London, London WC1E 6BT, United Kingdom; email:
Annu Rev Pharmacol Toxicol. 2018 Jan 6;58:123-142. doi: 10.1146/annurev-pharmtox-010617-052554. Epub 2017 Oct 2.
Pain is an increasing clinical challenge affecting about half the population, with a substantial number of people suffering daily intense pain. Such suffering can be linked to the dramatic rise in opioid use and associated deaths in the United States. There is a pressing need for new analgesics with limited side effects. Here, we summarize what we know about the genetics of pain and implications for drug development. We make the case that chronic pain is not one but a set of disease states, with peripheral drive a key element in most. We argue that understanding redundancy and plasticity, hallmarks of the nervous system, is critical in developing analgesic drug strategies. We describe the exploitation of monogenic pain syndromes and genetic association studies to define analgesic targets, as well as issues associated with animal models of pain. We appraise present-day screening technologies and describe recent approaches to pain treatment that hold promise.
疼痛是一个日益严峻的临床挑战,影响了约一半的人口,其中相当一部分人每天都遭受着剧烈的疼痛。这种痛苦可能与美国阿片类药物使用的急剧增加和相关死亡有关。人们迫切需要副作用有限的新型镇痛药。在这里,我们总结了我们对疼痛遗传学及其对药物开发的影响的了解。我们认为慢性疼痛不是一种疾病,而是一组疾病状态,其中外周驱动是大多数疾病的关键因素。我们认为,了解冗余和可塑性是开发镇痛药策略的关键,冗余和可塑性是神经系统的标志。我们描述了利用单基因疼痛综合征和遗传关联研究来定义镇痛靶点,以及与疼痛动物模型相关的问题。我们评估了目前的筛选技术,并描述了最近有前途的疼痛治疗方法。