Differential effects of fish-oil and cocoa-butter based high-fat/high-sucrose diets on endocrine pancreas morphology and function in mice.

cocoa butter fish oil glucagon high-fat/sucrose diet insulin α-cell β-cell

Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2024
Historique:
received: 23 07 2023
accepted: 29 01 2024
medline: 28 2 2024
pubmed: 28 2 2024
entrez: 28 2 2024
Statut: epublish

Résumé

A high-fat/high-sucrose diet leads to adverse metabolic changes that affect insulin sensitivity, function, and secretion. The source of fat in the diet might inhibit or increase this adverse effect. Fish oil and cocoa butter are a significant part of our diets. Yet comparisons of these commonly used fat sources with high sucrose on pancreas morphology and function are not made. This study investigated the comparative effects of a fish oil-based high-fat/high-sucrose diet (Fish-HFDS) versus a cocoa butter-based high-fat/high-sucrose diet (Cocoa-HFDS) on endocrine pancreas morphology and function in mice. C57BL/6 male mice (n=12) were randomly assigned to dietary intervention either Fish-HFDS (n=6) or Cocoa-HFDS (n=6) for 22 weeks. Intraperitoneal glucose and insulin tolerance tests (IP-GTT and IP-ITT) were performed after 20-21 weeks of dietary intervention. Plasma concentrations of c-peptide, insulin, glucagon, GLP-1, and leptin were measured by Milliplex kit. Pancreatic tissues were collected for immunohistochemistry to measure islet number and composition. Tissues were multi-labelled with antibodies against insulin and glucagon, also including expression on Pdx1-positive cells. Fish-HFDS-fed mice showed significantly reduced food intake and body weight gain compared to Cocoa-HFDS-fed mice. Fish-HFDS group had lower fasting blood glucose concentration and area under the curve (AUC) for both GTT and ITT. Plasma c-peptide, insulin, glucagon, and GLP-1 concentrations were increased in the Fish-HFDS group. Interestingly, mice fed the Fish-HFDS diet displayed higher plasma leptin concentration. Histochemical analysis revealed a significant increase in endocrine pancreas β-cells and islet numbers in mice fed Fish-HFDS compared to the Cocoa-HFDS group. Taken together, these findings suggest that in a high-fat/high-sucrose dietary setting, the source of the fat, especially fish oil, can ameliorate the effect of sucrose on glucose homeostasis and endocrine pancreas morphology and function.

Identifiants

pubmed: 38414818
doi: 10.3389/fendo.2024.1265799
pmc: PMC10897036
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1265799

Informations de copyright

Copyright © 2024 Albeloushi, Hasan, Arefanian, Sindhu, Al-Rashed, Kochumon, Abukhalaf, Jacob, Shenouda, Al Madhoun, Al-Mulla and Ahmad.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Shaima Albeloushi (S)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Amal Hasan (A)

Translational Research Department, Dasman Diabetes Institute, Dasman, Kuwait.

Hossein Arefanian (H)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Sardar Sindhu (S)

Animal and Imaging Core Facility, Dasman Diabetes Institute, Dasman, Kuwait.

Fatema Al-Rashed (F)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Shihab Kochumon (S)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Nermeen Abukhalaf (N)

Animal and Imaging Core Facility, Dasman Diabetes Institute, Dasman, Kuwait.

Texy Jacob (T)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Steve Shenouda (S)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Ashraf Al Madhoun (A)

Animal and Imaging Core Facility, Dasman Diabetes Institute, Dasman, Kuwait.

Fahd Al-Mulla (F)

Translational Research Department, Dasman Diabetes Institute, Dasman, Kuwait.

Rasheed Ahmad (R)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Classifications MeSH