Affiliation:
1. Department of Pharmacology, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur,
603203, India
Abstract
Background:
Alzheimer’s disease (AD) is an age-dependent neurodegenerative disease
with progressive cognition and memory loss, insomnia, and other abnormal behavioral changes.
Amongst various hypotheses for AD pathophysiology, occupational stress-induced Alzheimer’s
has recently been reported in many AD cases.
Objective:
Studies pertaining to the same suggest that stress leads to insomnia or sleep disruption,
which further leads to neuroinflammation due to oxidative stress, both of which are major harbingers
of AD. Additionally, overall sleep deficit is associated with progressive cognitive and memory
decline, which adds more inconvenience to Alzheimer’s disease. Based on this, any triumphant AD
management needs a pharmacological intervention that can not only antagonize the amyloid betainduced
neurotoxicity but also correct the sleep-wake cycle disruption. Chronobiotic therapeutics
like melatonin offer vital neuroprotective effects by eliciting its action through more than one of
the pathologies of AD. This is also bolstered by the finding that endogenous melatonin levels are
lower in AD patients. This melatonin replacement therapy can be especially useful in AD treatment,
but only in the early phases of the disease and in cases where the melatonin receptors are intact
and functioning.
Conclusion:
To negate such limitations and extend the action and therapeutic efficacy of melatonin-
mediated actions towards AD treatment, melatonin analogue like tasimelteon can pose a high
therapeutic value in AD treatment superior to that provided by melatonin. This review encapsulates
all details about how AD is believed to occur and how current situations influence it, along with
how melatonin and tasimelteon act towards treating Alzheimer’s.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology (medical),Pharmacology,Toxicology
Cited by
2 articles.
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