TY - JOUR
T1 - Maternal protein restriction impairs intestinal morphophysiology and antioxidant system in young male offspring rats
AU - Dos Santos, Isabela Baptista Leal
AU - Fioretto, Matheus Naia
AU - Jorge, Miguel Silingardi
AU - Barata, Luísa Annibal
AU - Ribeiro, Isabelle Tenori
AU - Franzolin, André Matheus Leandro
AU - Stoppa, Erick Guilherme
AU - Mattos, Renato
AU - Portela, Luiz Marcos Frediane
AU - Emílio Silva, Maycon Tavares
AU - Dos Santos, Sérgio Alexandre Alcântara
AU - de Arruda Miranda, José Ricardo
AU - Hiruma Lima, Clélia Akiko
AU - Justulin, Luis Antonio
N1 - Copyright © 2025 Elsevier Inc. All rights reserved.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - The developmental origins of health and disease (DOHaD) concept suggests that adverse conditions during gestation can influence the development and function of multiple organs, including the gastrointestinal tract. Maternal protein restriction (MPR) exposure has been associated with negative effects on reproduction, the endocrine system, and liver metabolic health. However, limited research has explored the impact of MPR on the offspring's intestinal morphophysiology. This study investigated the effects of gestational and lactational MPR on the duodenum and colon of young male offspring rats at postnatal (PND)21. We hypothesize that MPR affects intestinal morphophysiology and development early in life. Our findings revealed tachygastria in offspring exposed to MPR. The ultrastructural analysis uncovered a reduction in goblet cell numbers and changes in collagen deposition in the duodenum and colon. We also identified imbalances in inflammatory markers (IL-6 and TGF-β1) and antioxidant enzymes (CAT and SOD). These results demonstrate that MPR significantly affects gastrointestinal morphophysiology early in life by disrupting gastric motility and altering duodenal and colonic histoarchitecture, antioxidant defense, and inflammatory pathways. Such alterations may predispose the descendants to long-term gastrointestinal disorders, underscoring the importance of further research on the developmental origins of intestinal health and disease.
AB - The developmental origins of health and disease (DOHaD) concept suggests that adverse conditions during gestation can influence the development and function of multiple organs, including the gastrointestinal tract. Maternal protein restriction (MPR) exposure has been associated with negative effects on reproduction, the endocrine system, and liver metabolic health. However, limited research has explored the impact of MPR on the offspring's intestinal morphophysiology. This study investigated the effects of gestational and lactational MPR on the duodenum and colon of young male offspring rats at postnatal (PND)21. We hypothesize that MPR affects intestinal morphophysiology and development early in life. Our findings revealed tachygastria in offspring exposed to MPR. The ultrastructural analysis uncovered a reduction in goblet cell numbers and changes in collagen deposition in the duodenum and colon. We also identified imbalances in inflammatory markers (IL-6 and TGF-β1) and antioxidant enzymes (CAT and SOD). These results demonstrate that MPR significantly affects gastrointestinal morphophysiology early in life by disrupting gastric motility and altering duodenal and colonic histoarchitecture, antioxidant defense, and inflammatory pathways. Such alterations may predispose the descendants to long-term gastrointestinal disorders, underscoring the importance of further research on the developmental origins of intestinal health and disease.
KW - Animals
KW - Male
KW - Female
KW - Pregnancy
KW - Rats
KW - Antioxidants/metabolism
KW - Prenatal Exposure Delayed Effects/metabolism
KW - Diet, Protein-Restricted/adverse effects
KW - Duodenum/metabolism
KW - Colon/metabolism
KW - Intestines/pathology
UR - http://www.scopus.com/inward/record.url?scp=85218244293&partnerID=8YFLogxK
U2 - 10.1016/j.yexcr.2025.114464
DO - 10.1016/j.yexcr.2025.114464
M3 - Article
C2 - 39986598
SN - 0014-4827
VL - 446
SP - 114464
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 1
M1 - 114464
ER -