# The effects of ketogenic and chitosan-based diets on submandibular salivary gland in rat model: a comparative histological study

**Authors:** Mahmoud Mohamed Aboulfotoh

PMC · DOI: 10.1186/s12903-024-03885-8 · 2024-01-31

## TL;DR

This study compares the effects of a ketogenic diet and chitosan supplementation on rat salivary glands, finding that chitosan helps reduce damage caused by the ketogenic diet.

## Contribution

The study provides a comparative histological analysis of the effects of a ketogenic diet and chitosan supplementation on rat submandibular salivary glands.

## Key findings

- A ketogenic diet significantly increased α-SMA and Congo red staining in rat salivary glands.
- Chitosan supplementation reduced the damaging effects of the ketogenic diet on salivary glands.
- There was no significant difference in staining between the control and chitosan groups.

## Abstract

This study was carried out in the submandibular salivary glands (SSGs) of rats to demonstrate the effect of a ketogenic diet (KD) in comparison with dietary chitosan supplementation.

Eighteen albino rats were randomly divided into three equal groups of six animals each. Rats in Group I were fed a balanced diet and considered controls. Meanwhile, those of Groups II and III were fed a KD, a balanced diet with high molecular weight chitosan, respectively. After 45 days, rats were euthanized, and the SSGs were dissected carefully for staining with hematoxylin and eosin (H&E), alpha-smooth muscle actin (α-SMA) immunohistochemical staining, and Congo red special stain. Quantitative data from α-SMA staining and Congo red staining were statistically analyzed using one-way ANOVA followed by Tukey’s multiple comparisons post hoc test.

Regarding Congo red and α-SMA staining, one-way ANOVA revealed a significant difference between the three groups. For α-SMA staining and Congo red staining, Group II had the highest mean values of 91.41 ± 3.30 and 68.10 ± 5.04, respectively, while Group I had the lowest values of 56.13 ± 3.96 and 16.87 ± 2.19, respectively. Group III had mean values of 60.70 ± 3.55 for α-SMA and 19.50 ± 1.78 for Congo red. Tukey’s multiple comparisons post hoc test revealed significant differences between groups I & II and between groups II & III (P < 0.05). Meanwhile, there was a nonsignificant difference between groups I and III (P > 0.05).

A KD has a deleterious effect on rats’ SSG whatever the test we used, and dietary chitosan supplementation ameliorates these damaging effects.

## Linked entities

- **Proteins:** ACTA1 (actin alpha 1, skeletal muscle)
- **Chemicals:** chitosan (PubChem CID 129662530)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Dag1 (dystroglycan 1) [NCBI Gene 114489], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Fgf7 (fibroblast growth factor 7) [NCBI Gene 29348] {aka Fgf5b, KGF/FGF7, Kgf}, Gcg (glucagon) [NCBI Gene 24952] {aka GLP-1, Glp1, Glp2}, Actg2 (actin gamma 2, smooth muscle) [NCBI Gene 25365] {aka ACTGE, SMGA}
- **Diseases:** anemia (MESH:D000740), GCTs (MESH:D007673), acidosis (MESH:D000138), glucose intolerance (MESH:D018149), nonalcoholic steatohepatitis (MESH:D065626), liver fibrosis (MESH:D008103), weight loss (MESH:D015431), cytotoxicity (MESH:D064420), SSG amyloidosis (MESH:D000686), starvation metabolic (MESH:D013217), type 2 diabetes mellitus (MESH:D003924), insulin resistance (MESH:D007333), ARRIVE (MESH:C536830), H&amp;E (MESH:D016751), epilepsy (MESH:D004827), seizures (MESH:D012640)
- **Chemicals:** formalin (MESH:D005557), 3, 3'diaminobenzidine (MESH:D015100), carbohydrates (MESH:D002241), Congo red B (-), water (MESH:D014867), hydrogen peroxide (MESH:D006861), fat (MESH:D005223), H&amp;E (MESH:D006371), cortisol (MESH:D006854), monosodium glutamate (MESH:D012970), acetone (MESH:D000096), GAGs (MESH:D006025), ketone bodies (MESH:D007657), glucose (MESH:D005947), chitin (MESH:D002686), alcohol (MESH:D000438), free fatty acids (MESH:D005230), Corn oil (MESH:D003314), starch (MESH:D013213), lipids (MESH:D008055), blood glucose (MESH:D001786), xylene (MESH:D014992), Congo red (MESH:D003224), acetoacetate (MESH:C016635), hematoxylin (MESH:D006416), cellulose (MESH:D002482), Chitosan (MESH:D048271), eosin (MESH:D004801), paraffin (MESH:D010232), glycogen (MESH:D006003), phenobarbital sodium salt (MESH:D010634), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Pleocyemata sp. (species) [taxon 6693]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10832202/full.md

---
Source: https://tomesphere.com/paper/PMC10832202