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Cited by 259

The DOI matches its Crossref record; 207 of the 207 references it cites were found in a registry or an index.

ATP as a multi-target danger signal in the brain

Open access
Rodrigues, Ricardo J., Tomé, Angelo R., Cunha, Rodrigo A.·2015·Frontiers in Neuroscience

Abstract

ATP is released in an activity-dependent manner from different cell types in the brain, fulfilling different roles as a neurotransmitter, neuromodulator, in astrocyte-to-neuron communication, propagating astrocytic responses and formatting microglia responses. This involves the activation of different ATP P2 receptors (P2R) as well as adenosine receptors upon extracellular ATP catabolism by ecto-nucleotidases. Notably, brain noxious stimuli trigger a sustained increase of extracellular ATP, which plays a key role as danger signal in the brain. This involves a combined action of extracellular ATP in different cell types, namely increasing the susceptibility of neurons to damage, promoting astrogliosis and recruiting and formatting microglia to mount neuroinflammatory responses. Such actions involve the activation of different receptors, as heralded by neuroprotective effects resulting from blockade mainly of P2X7R, P2Y1R and adenosine A2A receptors (A2AR), which hierarchy, cooperation and/or redundancy is still not resolved. These pleiotropic functions of ATP as a danger signal in brain damage prompt a therapeutic interest to multi-target different purinergic receptors to provide maximal opportunities for neuroprotection.

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Metadata

Authors
Rodrigues, R. J., Tomé, A. R., & Cunha, R. A.
Venue
Frontiers in Neuroscience
Published
2015-04-28
Volume
9
Pages
148-148
ISSN
1662-453X (ISSN-L)
OpenAlex
W1985611042
Cited by
259
References
207
FWCI
22.92
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: ATP as a multi-target danger signal in the brain. https://app.cochat.ai/papers/10.3389/fnins.2015.00148
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Rodrigues, R. J., Tomé, A. R., & Cunha, R. A. (2015). ATP as a multi-target danger signal in the brain. Frontiers in Neuroscience. https://doi.org/10.3389/fnins.2015.00148

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