Pharmacological targeting of microglia dynamics in Alzheimer's disease: Preclinical and clinical evidence.

Pharmacol Res

School of Pharmacy, Department of Biology, University of Rome "Tor Vergata", Rome, Italy; Laboratory Pharmacology of Synaptic Plasticity, European Brain Research (EBRI) Institute, Rome, Italy. Electronic address:

Published: October 2022

AI Article Synopsis

  • Many clinical trials on anti-amyloid agents for Alzheimer's disease have failed, calling the amyloid hypothesis into question.
  • Researchers are now focusing on microglia, non-neuronal cells that are crucial for brain development and synaptic remodeling, as potential targets for new treatments.
  • The review discusses how microglia contribute to synaptic loss and neuroinflammation in Alzheimer's, suggesting that targeting these cells could lead to effective disease-modifying therapies.

Article Abstract

Numerous clinical trials of anti-amyloid agents for Alzheimer's disease (AD) were so far unsuccessful thereby challenging the validity of the amyloid hypothesis. This lack of progress has encouraged researchers to investigate alternative mechanisms in non-neuronal cells, among which microglia represent nowadays an attractive target. Microglia play a key role in the developing brain and contribute to synaptic remodeling in the mature brain. On the other hand, the intimate relationship between microglia and synapses led to the so-called synaptic stripping hypothesis, a process in which microglia selectively remove synapses from injured neurons. Synaptic stripping, along with the induction of a microglia-mediated chronic neuroinflammatory environment, promote the progressive synaptic degeneration in AD. Therefore, targeting microglia may pave the way for a new disease modifying approach. This review provides an overview of the pathophysiological roles of the microglia cells in AD and describes putative targets for pharmacological intervention. It also provides evidence for microglia-targeted strategies in preclinical AD studies and in early clinical trials.

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Source
http://dx.doi.org/10.1016/j.phrs.2022.106404DOI Listing

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