Key result
Aspirin-based multi-target directed ligands show potential in regulating Alzheimer's disease pathology through the modulation of neuroinflammation and oxidative stress.
Why the study?
Currently available treatments address individual Alzheimer's disease pathology but are not disease-modifying, prompting interest in aspirin-based multi-target directed ligands to regulate neuroinflammation and oxidative stress.
Aspirin-based multi-target directed ligands may have potential in regulating Alzheimer's disease pathology by targeting neuroinflammation and oxidative stress.
Does not support clinical use in Alzheimer's; leaves open whether aspirin-based ligands alter disease progression.
Alzheimer's disease (AD) is one of the most common forms of dementia. AD is associated with memory loss and cognitive decline. Several research works have been carried out to treat AD. However, currently available treatment options are only useful in the treatment of the individual pathology of AD but not useful in disease modification. Recent research works have identified the associated effects of neuroinflammation, oxidative stress, and glial cell dysfunction in AD pathology. Aspirin is one of the most commonly used NSAIDs in the treatment of several inflammatory diseases. Aspirin inhibits cyclooxygenase (COX) enzymes through an irreversible pathway. However, aspirin also exhibits other important pharmacological properties. This review aims to highlight the potential of aspirin-based multi-target directed ligands in the regulation of AD pathology through the regulation of neuroinflammation and oxidative stress.
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S et al. (2026) conducted a review in Alzheimer's disease. Aspirin-based multi-target directed ligands was evaluated. Aspirin-based multi-target directed ligands show potential in regulating Alzheimer's disease pathology through the modulation of neuroinflammation and oxidative stress.
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