Anti-aging trait of whey protein against brain damage of senile rats

Springer Science and Business Media LLC - Tập 8 - Trang 8-20 - 2022
Mohamed E. El-Beeh1,2, Ashraf A. El-Badawi2,3, Ali H. Amin2,4, Sameer H. Qari1, Mohamed Fawzy Ramadan5, Wessam M. Filfilan2, Hassan I. H. El-Sayyad1
1Biology Department, El-Jumum University College, Umm Al-Qura University, Makkah, Saudi Arabia
2Department of Zoology, Faculty of Science, Mansoura University, Mansoura, Egypt
3Central Laboratory for Aquaculture Research, Sharkia, Egypt
4Deanship of Scientific Research, Umm Al-Qura University, Makkah, Saudi Arabia
5Department of Clinical Nutrition, College of Applied Medical Sciences, Umm Al-Qura University, Makkah, Saudi Arabia

Tóm tắt

Aging mammalian results in impaired bio-functions and neurological disorders. The current study investigated whether whey protein (WP) syrup supplementation may improve age-related changes in diseased brain indicators like tau protein, β-amyloid and α-amylase. The study was carried out in conjunction with immunohistochemistry, histology, and flow cytometry of apoptosis. At the ages of 8 and 30 months, Wistar albino rats (Rattus novergicus) were divided into four groups (n = 8; G1; 8 months old rats; G2, 8 months old rats supplemented WP; G3, 30 months old rats; G4, 30 months old rats supplemented WP), with or without whey syrup administration. For 2 months, oral whey supplementation in 2 mL/kg doses is given twice a day every 12 h. Rats were sacrificed, and their brains were subjected to biochemical, histological, immunohistochemistry, and flow cytometric investigations. Aged rats had lower levels of superoxide dismutase (SOD), adenosine triphosphate (ATP), serotonin (5-HT), and dopamine (DA). These observations were parallel with increased inflammatory markers [tumor necrosis factor α- and 5-lipoxygenase (5-LO)], lipid peroxidation products (MDA), as well as apoptotic marker caspase-3, annexin-v, tau protein, β-amyloid, and α-amylase. Whey administration to aged rats reduced inflammatory and oxidative stress markers as well as improved neurotransmitters, tau protein, β-amyloid, and α-amylase. The advantages of supplementation were validated by improved histology and immunohistochemistry in aged rats’ cerebrum, cerebellum, and hippocampus. In addition, apoptosis was reduced, according to flow cytometry analysis of annexin-v. In conclusion, WP contains amino acids and bioactive compounds that could decrease brain oxidative stress and restore normal metabolic function. Furthermore, increased antioxidant defense and DA and 5-HT neurotransmitters, while decreasing brain tau protein and β-amyloid, were associated with better histology in aged rats’ cerebrum, cerebellum, and hippocampus.

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