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Acotiamide attenuates central urocortin 2-induced intestinal inflammatory responses, and urocortin 2 treatment reduces TNF-α productions in LPS-stimulated macrophage cell lines.
- Source :
-
Neurogastroenterology and motility [Neurogastroenterol Motil] 2020 Aug; Vol. 32 (8), pp. e13813. Date of Electronic Publication: 2020 Feb 07. - Publication Year :
- 2020
-
Abstract
- Background: To determine whether central and in vitro administration of urocortin 2 (Ucn 2) affected intestinal inflammatory responses in LPS-stimulated rat models and macrophage cell lines and acotiamide modified mucosal inflammation in this model.<br />Methods: Rats were divided into four groups. LPS-stimulated group (n = 4); LPS- and urocortin 2-treated group (n = 4); LPS- and acotiamide-treated group (n = 4); and LPS-, urocortin 2-, and acotiamide-treated group (n = 4). CD68-, CCR2-, and corticotropin-releasing hormone receptor type 2 (CRHR2)-positive cells were assessed by immunostaining. Myeloperoxidase (MPO) activity was measured. TNF-α, IL-6, and IL-4 levels were measured by ELISA method. Gastric emptying and small intestinal transit time were determined using Evans blue.<br />Key Results: Central administration of Ucn 2 significantly aggravated infiltrations of CD68- and CCR2-positive cells in the intestinal mucosa of LPS-stimulated rat models compared to those in LPS treatment alone. Interestingly, acotiamide treatment significantly reduced the migrations of both CD68- and CCR2-positive cells in the jejunum of central Ucn 2-treated LPS-stimulated rat models. Acotiamide significantly reduced the expression levels of IkB-α phosphorylation in LPS- and MCP-1-stimulated NR8383 cells. Central administration of Ucn 2 significantly delayed gastric emptying. In contrast, Ucn 2 stimulation significantly reduced TNF-α and IL-6 productions in LPS-stimulated NR8383 cells and astressin B reversed the inhibition of TNF-α production in stimulated NR8383 cells. Acotiamide (30 μmol/L) significantly reduced TNF-α and IL-6 productions in LPS- and MCP-1-stimulated NR8383 cells.<br />Conclusions and Inferences: Central and in vitro treatments of Ucn 2 affected intestinal inflammatory responses, respectively, and acotiamide improved them.<br /> (© 2020 John Wiley & Sons Ltd.)
- Subjects :
- Animals
Benzamides therapeutic use
Cell Line
Gastrointestinal Agents therapeutic use
Inflammation chemically induced
Inflammation metabolism
Interleukin-6 metabolism
Lipopolysaccharides
Macrophages metabolism
Male
Phosphorylation drug effects
Rats
Rats, Sprague-Dawley
Signal Transduction drug effects
Thiazoles therapeutic use
Benzamides pharmacology
Gastrointestinal Agents pharmacology
Inflammation drug therapy
Intestines drug effects
Macrophages drug effects
Thiazoles pharmacology
Tumor Necrosis Factor-alpha metabolism
Urocortins
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2982
- Volume :
- 32
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Neurogastroenterology and motility
- Publication Type :
- Academic Journal
- Accession number :
- 32030855
- Full Text :
- https://doi.org/10.1111/nmo.13813