Stereotaxic Exposure of the Central Nucleus of the Amygdala to Corticosterone Increases Colonic Permeability and Reduces Nerve-Mediated Active Ion Transport in Rats
Autor: | Beverley Greenwood-Van Meerveld, Dawn K. Prusator, Anthony C. Johnson, Priya Hattay |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
medicine.medical_specialty
Amygdala lcsh:RC321-571 03 medical and health sciences chemistry.chemical_compound stress 0302 clinical medicine Corticosterone Internal medicine medicine rat lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Barrier function Original Research Intestinal permeability Forskolin colon Chemistry General Neuroscience Central nucleus of the amygdala corticosterone Visceral pain amygdala medicine.disease digestive system diseases medicine.anatomical_structure Endocrinology Hyperalgesia 030211 gastroenterology & hepatology medicine.symptom permeability 030217 neurology & neurosurgery Neuroscience |
Zdroj: | Frontiers in Neuroscience Frontiers in Neuroscience, Vol 12 (2018) |
ISSN: | 1662-453X 1662-4548 |
Popis: | Background: Irritable bowel syndrome (IBS) is characterized by visceral pain and abnormal bowel habits that are worsened during stress. Evidence also suggests altered intestinal barrier function in IBS. Previously, we demonstrated that stereotaxic application of the stress hormone corticosterone (CORT) onto the central nucleus of the amygdala (CeA) induces colonic hyperalgesia and anxiety-like behavior in a rat model, however the effect on intestinal permeability and mucosal function remain to be evaluated. Methods: Male Fischer 344 rats underwent bilateral stereotaxic implantation of CORT or inert cholesterol (CHOL)-containing micropellets (30 μg) onto the dorsal margin of the CeA. Seven days later, colonic tissue was isolated to assess tissue permeability in modified Ussing chambers via transepithelial electrical resistance (TEER) and macromolecular flux of horseradish peroxidase (HRP). Secretory responses to electrical field stimulation (EFS) of submucosal enteric nerves as well as activation with forskolin were used to assess movements of ions across the isolated colonic tissues. In a separate cohort, colonic histology, and mast cell infiltration was assessed. Key Results: Compared to CHOL-implanted controls, we determined that exposing the CeA to elevated levels of CORT significantly increased macromolecular flux across the colonic epithelial layer without changing TEER. Nerve-mediated but not cAMP-mediated active transport was inhibited in response to elevated amygdala CORT. There were no histological changes or increases in mast cell infiltration within colonic tissue from CORT treated animals. Conclusion and Inferences: These observations support a novel role for the CeA as a modulator of nerve-mediated colonic epithelial function. |
Databáze: | OpenAIRE |
Externí odkaz: |