Intestinal Motility Dysfunction in Goto-Kakizaki Rats: Role of the Myenteric Plexus.
Goto-Kakizaki rats
cholinergic neuron
constipation
enteric nervous system
type 2 diabetes mellitus
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
28 Sep 2024
28 Sep 2024
Historique:
received:
03
09
2024
revised:
25
09
2024
accepted:
26
09
2024
medline:
15
10
2024
pubmed:
15
10
2024
entrez:
15
10
2024
Statut:
epublish
Résumé
Diabetes mellitus is associated with changes in intestinal morphology and the enteric nervous system. We previously reported constipation in Goto-Kakizaki (GK) rats, a non-obese model for type 2 diabetes mellitus. The morpho-quantitative analysis of myenteric plexus neurons in the small and large intestines of 120-day-old male GK rats was investigated. The diabetes was confirmed by high fasting blood glucose levels. The myenteric plexus was evaluated through wholemount immunofluorescence. The morpho-quantitative analyses included evaluating neuronal density (neurons per ganglion) of the total neuronal population, the cholinergic and nitrergic subpopulations, and enteric glial cells per ganglion. The cell body area of 100 neurons per segment per animal was measured. The total neurons and nitrergic subpopulation were unaltered in the GK rats' small and large intestines. The cholinergic subpopulation exhibited decreased density in the three segments of the small intestine and an increased number in the proximal colon of the GK rats. The number of enteric glial cells increased in the ileum of the GK rats, which could indicate enteric gliosis caused by the intestinal inflammatory state. The area of the cell body was increased in the total neuronal population of the jejunum and ileum of the GK rats. Frequency histograms of the cell body area distribution revealed the contribution of cholinergic neurons to larger areas in the jejunum and nitrergic neurons in the ileum. The constipation previously reported in GK rats might be explained by the decrease in the density of cholinergic neurons in the small intestine of this animal model.
Identifiants
pubmed: 39404390
pii: cells13191626
doi: 10.3390/cells13191626
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : São Paulo State Research Foundation (FAPESP)
ID : 2018/09868-7
Organisme : São Paulo State Research Foundation (FAPESP)
ID : 2019/01942-6
Organisme : São Paulo State Research Foundation (FAPESP)
ID : 2022/11249-9
Organisme : The National Council for Scientific and Technological Development (CNPq)
Organisme : Coordination of Superior Level Staff Improvement (CAPES)