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
AUTHORS (11)
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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