Department of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Clinical Enteric Neurosciences Translational and Epidemiological Research (CENTER), Mayo Clinic, Rochester, Minnesota, USA.
Gut. 2018 Aug;67(8):1543-1552. doi: 10.1136/gutjnl-2018-316029. Epub 2018 Mar 21.
Functional gastrointestinal disorders (FGIDs) and IBDs are two of the most prevalent disorders of the GI tract and consume a significant proportion of healthcare resources. Recent studies have shown that membrane-bound guanylate cyclase-C (GC-C) receptors lining the GI tract may serve as novel therapeutic targets in the treatment of FGIDs and IBDs. GC-C receptor activation by its endogenous paracrine hormones uroguanylin and guanylin, and the resulting intracellular production of its downstream effector cyclic GMP, occurs in a pH-dependent manner and modulates key physiological functions. These include fluid and electrolyte homeostasis, maintenance of the intestinal barrier, anti-inflammatory activity and regulation of epithelial regeneration. Studies of the GC-C paracrine signalling axis have revealed the therapeutic potential of these receptors in treating GI disorders, including chronic idiopathic constipation and irritable bowel syndrome-constipation. This review focuses on the evolving understanding of GC-C function in health and disease, and strategies for translating these principles into new treatments for FGIDs and IBDs.
功能性胃肠病(FGIDs)和炎症性肠病(IBD)是胃肠道最常见的疾病之一,消耗了大量的医疗资源。最近的研究表明,胃肠道内的膜结合型鸟苷酸环化酶-C(GC-C)受体可能成为治疗 FGIDs 和 IBD 的新的治疗靶点。GC-C 受体通过其内源性旁分泌激素尿鸟苷素和鸟苷素激活,其下游效应物环鸟苷酸(cGMP)的产生是一种 pH 依赖性的方式,调节关键的生理功能。这些功能包括液体和电解质的稳态、肠道屏障的维持、抗炎活性和上皮细胞再生的调节。GC-C 旁分泌信号轴的研究揭示了这些受体在治疗胃肠道疾病方面的治疗潜力,包括慢性特发性便秘和肠易激综合征便秘型。本综述重点介绍了 GC-C 在健康和疾病中的作用的不断发展的认识,以及将这些原理转化为 FGIDs 和 IBD 新治疗方法的策略。
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