Protective Effects of Whey Protein Hydrolysate, Treadmill Exercise, and Their Combination against Scopolamine-Induced Cognitive Deficit in Mice.
Yeok Boo ChangEun Jin JungHyung-Joo SuhHyeon-Son ChoiPublished in: Foods (Basel, Switzerland) (2023)
In this study, the potential of whey protein hydrolysate (WPH) and treadmill exercise to prevent cognitive decline was investigated, along with their neuroprotective mechanisms. Cognitive dysfunction was induced in mice with 1 mg/kg of scopolamine, followed by the administration of WPH at 100 and 200 mg/kg and/or treadmill exercise at 15 m/min for 30 min five days per week. Both WPH administration and treadmill exercise significantly improved the memory of mice with scopolamine-induced cognitive impairment, which was attributed to several key mechanisms, including a reduction in oxidative stress based on decreased levels of reactive oxygen species and malondialdehyde in the brain tissue and an increase in acetylcholine by increasing choline acyltransferase and decreasing acetylcholine esterase levels. Exercise and WPH also exerted neuroprotective effects by inhibiting the hyperphosphorylation of tau proteins, enhancing the expression of the brain-derived neurotrophic factor, and inhibiting apoptosis by reducing the Bax/Bcl2 ratio in conjunction with the downregulation of the mitogen-activated protein kinase pathway. Moreover, the impact of WPH and treadmill exercise extended to the gut microbiome, suggesting a potential link with cognitive improvement. These findings suggest that both WPH intake and treadmill exercise are effective strategies for mitigating cognitive impairment, providing promising avenues for treating neurodegenerative diseases.
Keyphrases
- high intensity
- oxidative stress
- cognitive impairment
- cognitive decline
- physical activity
- resistance training
- diabetic rats
- high glucose
- signaling pathway
- reactive oxygen species
- mild cognitive impairment
- drug induced
- cell death
- randomized controlled trial
- white matter
- climate change
- cell proliferation
- multiple sclerosis
- mass spectrometry
- binding protein
- tyrosine kinase
- working memory
- ischemia reperfusion injury
- small molecule
- functional connectivity
- brain injury