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内脏痛。

Visceral Pain.

机构信息

Visceral Pain Research Group, College of Medicine and Public Health, Centre for Neuroscience, Flinders University, Bedford Park, South Australia 5042, Australia; email:

Centre for Nutrition and Gastrointestinal Diseases, University of Adelaide, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia 5000, Australia.

出版信息

Annu Rev Physiol. 2019 Feb 10;81:261-284. doi: 10.1146/annurev-physiol-020518-114525. Epub 2018 Oct 31.

Abstract

Most of us live blissfully unaware of the orchestrated function that our internal organs conduct. When this peace is interrupted, it is often by routine sensations of hunger and urge. However, for >20% of the global population, chronic visceral pain is an unpleasant and often excruciating reminder of the existence of our internal organs. In many cases, there is no obvious underlying pathological cause of the pain. Accordingly, chronic visceral pain is debilitating, reduces the quality of life of sufferers, and has large concomitant socioeconomic costs. In this review, we highlight key mechanisms underlying chronic abdominal and pelvic pain associated with functional and inflammatory disorders of the gastrointestinal and urinary tracts. This includes how the colon and bladder are innervated by specialized subclasses of spinal afferents, how these afferents become sensitized in highly dynamic signaling environments, and the subsequent development of neuroplasticity within visceral pain pathways. We also highlight key contributing factors, including alterations in commensal bacteria, altered mucosal permeability, epithelial interactions with afferent nerves, alterations in immune or stress responses, and cross talk between these two adjacent organs.

摘要

我们大多数人都幸福地生活在浑然不觉之中,不知道我们的内脏器官在有条不紊地运作。这种平静常常会被饥饿和便意等常规感觉所打破。然而,对于全球 20%以上的人口来说,慢性内脏疼痛是一种不愉快的、常常令人难以忍受的内部器官存在的提醒。在许多情况下,疼痛并没有明显的潜在病理原因。因此,慢性内脏疼痛使人虚弱,降低了患者的生活质量,并带来了巨大的社会经济成本。在这篇综述中,我们强调了与胃肠道和泌尿道功能和炎症性疾病相关的慢性腹痛和盆腔痛的关键机制。这包括结肠和膀胱如何被特定的脊髓传入神经类群支配,这些传入神经如何在高度动态的信号环境中变得敏感,以及内脏痛通路中随后发生的神经可塑性。我们还强调了关键的促成因素,包括共生细菌的改变、黏膜通透性的改变、上皮与传入神经的相互作用、免疫或应激反应的改变,以及这两个相邻器官之间的串扰。

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