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• W2013078897 abstract "Pharmacology and clinical potential of guanylyl cyclase C agonists in the treatment of ulcerative colitis Giovanni M Pitari Department of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA, USA Abstract: Agonists of the transmembrane intestinal receptor guanylyl cyclase C (GCC) have recently attracted interest as promising human therapeutics. Peptide ligands that can specifically induce GCC signaling in the intestine include endogenous hormones guanylin and uroguanylin, diarrheagenic bacterial enterotoxins (ST), and synthetic drugs linaclotide, plecanatide, and SP-333. These agonists bind to GCC at intestinal epithelial surfaces and activate the receptor’s intracellular catalytic domain, an event initiating discrete biological responses upon conversion of guanosine-5&#39;-triphosphate to cyclic guanosine monophosphate. A principal action of GCC agonists in the colon is the promotion of mucosal homeostasis and its dependent barrier function. Herein, GCC agonists are being developed as new medications to treat inflammatory bowel diseases, pathological conditions characterized by mucosal barrier hyperpermeability, abnormal immune reactions, and chronic local inflammation. This review will present important concepts underlying the pharmacology and therapeutic utility of GCC agonists for patients with ulcerative colitis, one of the most prevalent inflammatory bowel disease disorders. Keywords: inflammatory bowel disease, GCC agonists, cyclic GMP" @default.
• W2013078897 created "2016-06-24" @default.
• W2013078897 creator A5022300126 @default.
• W2013078897 date "2013-04-01" @default.
• W2013078897 modified "2023-09-25" @default.
• W2013078897 title "Pharmacology and clinical potential of guanylyl cyclase C agonists in the treatment of ulcerative colitis" @default.
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• W2013078897 doi "https://doi.org/10.2147/dddt.s32252" @default.
• W2013078897 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3634396" @default.
• W2013078897 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23637522" @default.
• W2013078897 hasPublicationYear "2013" @default.
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