Akbarali H I, Inkisar A, Dewey W L
Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA, USA.
Neurogastroenterol Motil. 2014 Oct;26(10):1361-7. doi: 10.1111/nmo.12443.
Opioid-induced constipation is a major clinical problem. The effects of morphine, and other narcotics, on the gastrointestinal tract persist over long-term use thus limiting the clinical benefit of these excellent pain relievers. The effects of opioids in the gut, including morphine, are largely mediated by the μ-opioid receptors at the soma and nerve terminals of enteric neurons. Recent studies demonstrate that regional differences exist in both acute and chronic morphine along the gastrointestinal tract. While tolerance develops to the analgesic effects and upper gastrointestinal motility upon repeated morphine administration, tolerance does not develop in the colon with chronic opioids resulting in persistent constipation. Here, we review the mechanisms by which tolerance develops in the small but not the large intestine. The regional differences lie in the signaling and regulation of the μ-opioid receptor in the various segments of the gastrointestinal tract. The differential role of β-arrestin2 in tolerance development between central and enteric neurons defines the potential for therapeutic approaches in developing ligands with analgesic properties and minimal constipating effects.
阿片类药物引起的便秘是一个主要的临床问题。吗啡及其他麻醉药品对胃肠道的影响在长期使用过程中持续存在,从而限制了这些优秀止痛药的临床益处。阿片类药物(包括吗啡)在肠道中的作用很大程度上是由肠神经元的体细胞和神经末梢处的μ-阿片受体介导的。最近的研究表明,胃肠道中急性和慢性吗啡作用均存在区域差异。虽然重复给予吗啡后会对镇痛作用和上消化道动力产生耐受性,但慢性阿片类药物在结肠中不会产生耐受性,从而导致持续性便秘。在此,我们综述了小肠而非大肠产生耐受性的机制。区域差异在于胃肠道各段μ-阿片受体的信号传导和调节。β-抑制蛋白2在中枢神经元和肠神经元耐受性发展中的不同作用,为开发具有镇痛特性且便秘作用最小的配体的治疗方法提供了潜力。