Abstract

Lifestyle factors emerge as key modifiers of the risk and progression of Alzheimer's disease (AD), the most prevalent senile dementia. Stress accelerates, whereas positive lifestyle factors such as physical and mental exercise, slow the progression of AD symptoms and neuropathological hallmarks in humans and genetic mouse models of the condition. Positive lifestyle factors are thought to improve brain function and delay ageing through the induction of a mild stress response as opposed to excessive stress reactions causing the harmful effects of adverse stressors. This suggests that stress mediators can be targeted for the development of improved treatment for AD. This review discussed the involvement of glucocorticoids, corticotrophin-releasing hormone (CRH) and cholinergic stress reactions, through the induction of a protective splice variant of synaptic acetylcholinesterase (AChE-R), in the progression of AD symptoms and neuropathological hallmarks and the impact of lifestyle factors. It is concluded that CRH is likely to play a critical, dose-dependent role in AD progression, protective at low doses but harmful at high doses, whereas an excess of glucocorticoids may only exacerbate some aspects of the disease. AChE-R shows a promising therapeutic potential which needs to be further investigated.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call