miRNA-143 expression is associated with inflammation and time of exposure to amniotic fluid in experimental gastroschisis

•miR-143 is related with more inflammation and edema of intestinal loops of gastroschisis rat model.•Time of exposure of the amniotic fluid increases the intestinal damage.•miR-143 is a possible marker of gut inflammation. Gastroschisis (GS) is a congenital anomaly in the abdominal wall with the int...

Full description

Saved in:
Bibliographic Details
Published in:Clinics (São Paulo, Brazil) Vol. 78; p. 100311
Main Authors: Diniz, Ana Maria Bicudo, Gualberto, Igor José Nogueira, Lima, Luiza Almeida, Cirino, Mucio Luiz de Assis, Murakami, Rodrigo Kendi, Ishikiriama, Bella Luna Colombini, Ruano, Rodrigo, da Silva, Luiz Fernando Ferraz, Tirapelli, Daniela, Sbragia, Lourenço
Format: Journal Article
Language:English
Published: United States Elsevier España, S.L.U 01-01-2023
Faculdade de Medicina / USP
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:•miR-143 is related with more inflammation and edema of intestinal loops of gastroschisis rat model.•Time of exposure of the amniotic fluid increases the intestinal damage.•miR-143 is a possible marker of gut inflammation. Gastroschisis (GS) is a congenital anomaly in the abdominal wall with the intestinal loops exiting laterally to the umbilicus. The contact of the loops with Amniotic Fluid (AF) causes an inflammatory process in the exposed part, leading to an extended hospital stay and an increased risk of morbidity due to alterations related to intestinal motility. The authors aimed to evaluate the time of exposure to the AF in the experimental GS and to search for potential biomarkers of intestinal inflammation by measuring microRNAs. Rat fetuses were divided into three groups: a) CONTROL, b) GS reared on day 18 (GS = 18), and c) GS reared on day 19.5 (GS = 19) (term = 22 days). On day 21.5, the fetuses were removed for biometric parameters and biochemical analyses: 1) Biometrics: Body and Intestinal Weight (BW, IW), and intestinal-body weight ratio (IW/BW); 2) Descriptive histopathology and 3) miR-143 quantification by real-time Polymerase Chain Reaction (PCR). BW was higher in CONTROL than GS 18 and G19 (p < 0.05). IW, IW/BW, intestinal water, and mRNA-143 were higher in GS 18 and GS 19 than in CONTROL, and GS 18 was higher than GS 19 (p < 0.05). The average of the inflammation score from the intestinal wall with mucosal inflammation and intra-epithelial lymphocytes shows worst in GS 18 and GS 19 vs. CONTROL (p < 0.05). The tissue expression of mRNA-143 and the morphological changes in the intestine of GS worsened according to the time of exposure to AF, which could be a possible marker of fetal intestinal damage.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1807-5932
1980-5322
1980-5322
DOI:10.1016/j.clinsp.2023.100311