# Sleep recovery ameliorates submandibular salivary gland inflammation associated with paradoxical sleep deprivation in male Wistar rats

**Authors:** Jude Ijuo Abeje, Shehu-Tijani T. Shittu, Olayinka Olawale Asafa, Bimpe Bolarinwa, Taye J. Lasisi

PMC · DOI: 10.1590/1678-7757-2024-0133 · Journal of Applied Oral Science · 2024-01-13

## TL;DR

Sleep recovery helps reduce inflammation in salivary glands caused by sleep deprivation in rats.

## Contribution

The study shows that sleep recovery reduces inflammation in salivary glands after sleep deprivation.

## Key findings

- Total sleep deprivation increased inflammation markers in salivary glands compared to controls.
- Sleep recovery reduced the inflammatory impact in salivary glands caused by sleep deprivation.
- Partial sleep deprivation also increased inflammation markers in saliva and blood.

## Abstract

Submandibular salivary gland inflammation has been suggested as one of the mechanisms underlying impaired salivary secretion associated with sleep deprivation (SD). However, whether the salivary inflammatory response occurs to the same extent in paradoxical sleep deprivation with or without sleep recovery remains unknown.

This study evaluated the extent to which inflammation influences salivary impairments associated with paradoxical sleep deprivation with or without sleep recovery.

Male Wistar rats were randomly assigned into three groups as control, partial SD (PSD) with sleep recovery for four hours a day and total SD (TSD). Paradoxical SD was carried out for seven days in the SD groups, after which saliva, blood, and submandibular gland samples were taken. Levels of interleukin-6 (IL-6), tumour necrosis factor-alpha (TNF-α), and nitrite were determined in saliva, serum, and the submandibular salivary gland. Leucocyte count and neutrophil-lymphocyte ratio were determined in all groups. One-way ANOVA and the Tukey's post hoc tests were used for data analysis. P-values < 0.05 were considered statistically significant.

Levels of TNF-α, IL-6, and nitrite in the submandibular salivary glands were significantly higher in the TSD groups (p=0.04,p<0.001, p=0.03, respectively) than in the control. Saliva level of TNF-α was higher in the PSD and TSD groups (p=0.003 and p=0.01 respectively) than in the control. Neutrophil-lymphocyte ratio was significantly higher in both PSD and TSD groups than in the control (p<0.01 for both).

While total SD produced higher inflammatory response in the submandibular salivary gland, four-hour sleep recovery ameliorated this impact. This finding suggests that sleep recovery is crucial to improve inflammatory salivary gland dysfunction induced by sleep deprivation.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Chemicals:** nitrite (PubChem CID 946)

## Full-text entities

- **Genes:** Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}
- **Diseases:** inflammatory salivary gland dysfunction (MESH:D012466), gland (MESH:D000307), inflammation (MESH:D007249), salivary gland inflammation (MESH:D012793), PSD (MESH:D012892)
- **Chemicals:** nitrite (MESH:D009573)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11816956/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11816956/full.md

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Source: https://tomesphere.com/paper/PMC11816956