Intermittent Metabolic Switching and Vascular Cognitive Impairment.
Vismitha RajeevNishat I TabassumDavid Y FannChristopher P ChenMitchell K P LaiThiruma Valavan ArumugamPublished in: Journal of obesity & metabolic syndrome (2024)
Intermittent fasting (IF), a dietary pattern alternating between eating and fasting periods within a 24-hour cycle, has garnered recognition for its potential to enhance both healthspan and lifespan in animal models and humans. It also shows promise in alleviating age-related diseases, including neurodegeneration. Vascular cognitive impairment (VCI) spans a severity range from mild cognitive deficits to severe cognitive deficits and loss of function in vascular dementia. Chronic cerebral hypoperfusion has emerged as a significant contributor to VCI, instigating vascular pathologies such as microbleeds, blood-brain barrier dysfunction, neuronal loss, and white matter lesions. Preclinical studies in rodents strongly suggest that IF has the potential to attenuate pathological mechanisms, including excitotoxicity, oxidative stress, inflammation, and cell death pathways in VCI models. Hence, this supports evaluating IF in clinical trials for both existing and at-risk VCI patients. This review compiles existing data supporting IF's potential in treating VCI-related vascular and neuronal pathologies, emphasizing the mechanisms by which IF may mitigate these issues. Hence providing a comprehensive overview of the available data supporting IF's potential in treating VCI by emphasizing the underlying mechanisms that make IF a promising intervention for VCI.
Keyphrases
- cognitive impairment
- oxidative stress
- blood brain barrier
- clinical trial
- cell death
- cerebral ischemia
- white matter
- big data
- end stage renal disease
- blood pressure
- newly diagnosed
- ejection fraction
- stem cells
- chronic kidney disease
- mild cognitive impairment
- physical activity
- subarachnoid hemorrhage
- risk assessment
- dna damage
- type diabetes
- prognostic factors
- adipose tissue
- bone marrow
- ischemia reperfusion injury
- drug induced
- signaling pathway
- patient reported outcomes
- cell therapy
- diabetic rats
- climate change
- endoplasmic reticulum stress