Red Bull Energy Drink Impact on Salivary Glands in Wistar Rats: Can Blueberry Extract Reverse the Damage?

Author:

Alghamdi Samar A.1ORCID,Hindi Emad A.23ORCID,Abuljadayel Layla4ORCID,Alwafi Hanadi5,Bagher Amina M.6ORCID,Khunkar Sahar7,Bakhsh Nadia8,Ali Soad9ORCID,Mirza Linda10,Alrafiah Aziza R.11ORCID,Alsomali Nimah I.12

Affiliation:

1. Department of Oral Biology, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia

2. Department of Clinical Anatomy, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia

3. Neuroscience and Geroscience Research Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah 21589, Saudi Arabia

4. Department of Dental Public Health, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia

5. Department of Pediatric and Prevention Dentistry, Batterjee Medical College, Jeddah 21442, Saudi Arabia

6. Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia

7. Department of Restorative, King Abdulaziz University Hospital, Jeddah 21589, Saudi Arabia

8. AGD Department, King Abdulaziz University Hospital, Jeddah 21589, Saudi Arabia

9. Department of Histology and Cell Biology, Faculty of Medicine, Assuit University, Assuit 98467, Egypt

10. King Abdullah Medical Complex, Ministry of Health, Jeddah 23816, Saudi Arabia

11. Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia

12. Research Center, King Fahad Medical City, Riyadh 11525, Saudi Arabia

Abstract

Energy drink (ED) consumption has become increasingly popular. Due to a lack of evidence, it was crucial to assess the effects of Red Bull (RB) consumption on the rat submandibular salivary gland and the potential therapeutic impact of blueberry (BB). Thirty rats were randomly assigned to five groups. Group 1 (Control) received distilled water. Group 2 (RB) received RB (10 mL/100 g/day) for 8 weeks. Group 3 (BB) rats were administered BB (500 mg/day for 8 weeks). Group 4 (RB + BB (L)) received RB for 8 weeks, and from the 5th week, were concurrently given BB (250 mg/day) for 4 weeks. Group 5 (RB + BB (H)) received RB for 8 weeks, and from the 5th week, were concurrently given BB (500 mg/day) for 4 weeks. At the end of the experiment, blood samples were collected, the animals were euthanized, and their submandibular salivary glands were harvested. Oxidative stress markers (MDA, GPx, CAT, and SOD) were assessed in both serum and tissue. Inflammatory markers (TNF-α, IL-6, and IL-10) were quantified in tissue. Submandibular gland specimens were prepared for light microscopy, and immunohistochemical staining was performed using anti-α-SMA. RB consumption resulted in a significant increase in MDA, TNF-α, IL-6, and IL-10, while GPx, CAT, and SOD levels decreased significantly. Degenerative changes in the gland’s structure were observed in the RB group. A significant increase in α-SMA immunoreaction was detected in myoepithelial cells. Administration of BB, particularly at a high dose, ameliorated the aforementioned findings. In conclusion, blueberry administration exhibited therapeutic effects due to its antioxidative and anti-inflammatory properties.

Funder

Deanship of Scientific Research

Publisher

MDPI AG

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