M1 agonists as a Potential Disease-Modifying Therapy for Alzheimer's Disease

Antonella Caccamo, Abraham Fisher, Frank M. Laferla

Research output: Contribution to journalReview article

51 Scopus citations

Abstract

Cholinergic deficit is a cardinal feature of Alzheimer's disease, and cholinesterase inhibitors represent one of the most prominent means of mitigating this dysfunction. Cholinesterase inhibitors provide mild symptomatic relief, although they lose their efficacy over time most likely because they are not disease-modifying agents. An alternative strategy for restoring cholinergic function and attenuating the cognitive decline involves acting on the receptors on which acetylcholine acts. Stimulation of muscarinic acetylcholine receptors and in particular the Ml subtype has been shown to have a beneficial effect in restoring cognition in patients with Alzheimer's disease and in attenuating A|3 and tau pathology in different animal models. In this review, we discuss the role of Ml agonists as a potential disease-modifying therapy for Alzheimer's disease.

Original languageEnglish (US)
Pages (from-to)112-117
Number of pages6
JournalCurrent Alzheimer research
Volume6
Issue number2
DOIs
StatePublished - Apr 1 2009

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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