Move Your Body toward Healthy Aging: Potential Neuroprotective Mechanisms of Irisin in Alzheimer's Disease.
Tatiani Bellettini-SantosHemily Batista-SilvaClairton Marcolongo PereiraFernanda Cristina de Abreu Quintela-CastroRafael Mazioli BarcelosKelly Cristina Mota Braga ChiepeJoamyr Victor Rossoni JuniorRoberta Passamani-AmbrosioBruno Spalenza da SilvaOrlando Chiarelli-NetoMichelle Lima GarcezPublished in: International journal of molecular sciences (2023)
Alzheimer's disease (AD) is the leading cause of dementia in older adults, having a significant global burden and increasing prevalence. Current treatments for AD only provide symptomatic relief and do not cure the disease. Physical activity has been extensively studied as a potential preventive measure against cognitive decline and AD. Recent research has identified a hormone called irisin, which is produced during exercise, that has shown promising effects on cognitive function. Irisin acts on the brain by promoting neuroprotection by enhancing the growth and survival of neurons. It also plays a role in metabolism, energy regulation, and glucose homeostasis. Furthermore, irisin has been found to modulate autophagy, which is a cellular process involved in the clearance of protein aggregates, which are a hallmark of AD. Additionally, irisin has been shown to protect against cell death, apoptosis, oxidative stress, and neuroinflammation, all of which are implicated in AD pathogenesis. However, further research is needed to fully understand the mechanisms and therapeutic potential of irisin in AD. Despite the current gaps in knowledge, irisin holds promise as a potential therapeutic target for slowing cognitive decline and improving quality of life in AD patients.
Keyphrases
- cognitive decline
- mild cognitive impairment
- cell death
- oxidative stress
- physical activity
- cerebral ischemia
- endoplasmic reticulum stress
- end stage renal disease
- healthcare
- risk factors
- body mass index
- chronic kidney disease
- spinal cord
- newly diagnosed
- machine learning
- risk assessment
- depressive symptoms
- cognitive impairment
- induced apoptosis
- spinal cord injury
- insulin resistance
- cell proliferation
- dna damage
- artificial intelligence
- brain injury
- white matter
- blood brain barrier
- lps induced
- multiple sclerosis
- resistance training
- resting state
- protein protein
- patient reported outcomes
- skeletal muscle
- sleep quality
- inflammatory response
- weight loss