Autonomic Neuroscience Centre, University College Medical School, Rowland Hill Street, London NW3 2PF, UK; Department of Pharmacology and Therapeutics, The University of Melbourne, Australia.
Laboratory of Bioorganic Chemistry & Molecular Recognition Section, National Institute of Diabetes & Digestive & Kidney Diseases, National Institutes of Health, Bldg. 8A, Rm. B1A-19, Bethesda, MD 20892-0810, USA.
Curr Opin Pharmacol. 2017 Dec;37:131-141. doi: 10.1016/j.coph.2017.10.011. Epub 2017 Nov 14.
Purinergic receptors are implicated in the pathogenesis of gastrointestinal disorders and are being explored as potential therapeutic targets. Gut inflammation releases ATP that acts on neuronal, glial, epithelial and immune cells. Purinergic signalling in glia and neurons is implicated in enteric neuropathies. Inflammation activates glia to increase ATP release and alter purinergic signalling. ATP release causes neuron death and gut motor dysfunction in colitis via a P2X7-dependent neural-glial pathway and a glial purinergic-connexin-43 pathway. The latter pathway also mediates morphine-induced constipation and gut inflammation that may differ from opioid-induced constipation. P2X7R antagonists are protective in inflammatory bowel disease (IBD) models, where as AZD9056 is questionable in Crohn's disease, but is potentially beneficial for chronic abdominal pain. Drug targets under investigation for IBD, irritable bowel syndrome and motility disorders include P2X7R, P2X3R, P2YR, A/AAR, enzymes and transporters.
嘌呤能受体参与胃肠道疾病的发病机制,并被探索作为潜在的治疗靶点。肠道炎症释放作用于神经元、神经胶质细胞、上皮细胞和免疫细胞的 ATP。神经胶质细胞和神经元中的嘌呤能信号转导与肠神经病变有关。炎症激活神经胶质细胞增加 ATP 释放并改变嘌呤能信号转导。ATP 释放通过 P2X7 依赖的神经-神经胶质途径和神经胶质嘌呤能-连接蛋白 43 途径导致神经元死亡和结肠炎中的肠道运动功能障碍。后一种途径也介导吗啡引起的便秘和肠道炎症,其可能与阿片类药物引起的便秘不同。P2X7R 拮抗剂在炎症性肠病 (IBD) 模型中具有保护作用,而 AZD9056 在克罗恩病中存在争议,但对慢性腹痛可能有益。正在研究用于 IBD、肠易激综合征和运动障碍的药物靶点包括 P2X7R、P2X3R、P2YR、A/AAR、酶和转运体。