Attenuation of acute experimental colitis by preventing NPY Y1 receptor signaling

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 288; no. 3; pp. G550 - G556
• Main Authors: Hassani, Hessameh, Lucas, Guilherme, Rozell, Björn, Ernfors, Patrik
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.03.2005
• Subjects: Acute Disease; Amides - pharmacology; Animals; Capsaicin - pharmacology; Cellular Biology; Colitis - chemically induced; Colitis - pathology; Colitis - prevention & control; Coloring Agents; Dextran Sulfate; Evans Blue; Female; Immunohistochemistry; Intestinal Mucosa - pathology; Life Sciences; Medicin och hälsovetenskap; Mice; Receptors, Neuropeptide Y - antagonists & inhibitors; Receptors, Neuropeptide Y - biosynthesis; Receptors, Neuropeptide Y - genetics; Signal Transduction - physiology
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.00182.2004

Neuropeptide Y (NPY), a 36-amino acid peptide, is widely expressed in the central and peripheral nervous system. NPY is involved in the regulation of several physiological processes, including energy balance, food intake, and nociception. Recently, we showed that activation of the NPY Y1 receptor is required for cutaneous neurogenic inflammation. Because neurogenic inflammation could participate in colitis, the aim of this study was to investigate the role of the NPY Y1 receptor in acute colitis using mice genetically deficient of NPY Y1 receptor. In addition, the Y1 receptor antagonist H409/22, was also investigated. Animals received 5% dextran sulfate sodium (DSS) in drinking water for 7 days. One group of animals also received the Y1 receptor antagonist, administered intraperitoneally twice daily. Disease activity was assessed daily for 7 days in all groups. DSS induced colitis in all animals resulting in weight loss, diarrhea, epithelial damage, crypt shortening, and inflammatory infiltration. However, clinical manifestation of the disease was markedly attenuated in Y1 null mutant mice as well as in mice receiving the Y1 antagonist. Histological analysis showed that tissue damage and ulceration were less severe in Y1-deficient animals. Consistent with the clinical and histological data, capsaicin-induced plasma extravasation was significantly reduced in the gut of Y1 null mutant animals compared with treated wild-type animals. These data indicate that NPY and Y1 receptor are involved in intestinal inflammation and suggest that inhibition of NPY Y1 receptor signaling may provide a novel therapeutic approach in the treatment of colonic inflammation.