EndogenousCRFin rat large intestine mediates motor and secretory responses to stress

Male Restraint, Physical Colon Corticotropin-Releasing Hormone Clinical Sciences Medical Physiology Clinical sciences Enzyme-Linked Immunosorbent Assay Restraint Stress Polymerase Chain Reaction Rats, Sprague-Dawley stress 03 medical and health sciences Medical physiology Genetics Physical Animals 0303 health sciences Biomedical and Clinical Sciences colon Gastroenterology & Hepatology Animal Prevention Neurosciences Pharmacology and Pharmaceutical Sciences CRF Immunohistochemistry Rats Disease Models, Animal motility Disease Models ion secretion Psychological Sprague-Dawley Digestive Diseases Gastrointestinal Motility Stress, Psychological
DOI: 10.1111/nmo.12725 Publication Date: 2015-11-27T01:49:15Z
ABSTRACT
Abstract Background Corticotropin‐releasing factor ( CRF ) mediates our body's overall responses to stress. The role of central in stress‐stimulated colonic motility is well characterized. We hypothesized that transient perturbation expression enteric sufficient change stress‐induced motor and secretory responses. Methods Sprague–Dawley rats (adult, male) were subjected 1‐h partial restraint stress PRS euthanized at 0, 4, 8, 24 h. mRNA peptide levels the colon quantified by real‐time RT ‐ PCR , enzyme immuno‐assay immunohistochemistry. Double‐stranded RNA (ds designed target was injected into wall attain interference‐mediated inhibition expression. Ds for β ‐globin used as a control (dsControl). Four days after ds injection, . Fecal output measured. Ussing chamber techniques assess mucosal ion secretion transepithelial tissue conductance. Key Results Exposure elevated increased release rat colon. Injection inhibited basal prevented ‐induced increase expression, whereas dsControl‐injected colons remained high In treated with dsControl, caused significant fecal pellet output, baseline secretion, Inhibition Conclusions & Inferences These results provide direct evidence peripherally expressed prevents
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