Purinergic receptor

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Revision as of 09:41, 17 August 2010 by Terence158 (Talk) (condensed and fixed some grammar)

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Purinergic receptors, also known as purinoceptors, are a family of newly characterized plasma membrane molecules involved in several cellular functions such as vascular reactivity, apoptosis and cytokine secretion. These functions have not been well characterized and the effect of the extracellular microenvironment on their function is also poorly understood.

Fibroblasts share several features with smooth muscle cells and are an important constituent of the atherosclerotic plaque.

These receptors have their effect of high glucose concentration on ATP-mediated responses in human fibroblasts.

The members of the family include the following:

Name Activation Class
P1 receptors adenosine G protein-coupled receptors
P2Y receptors nucleotides G protein-coupled receptors
P2X receptors ATP ligand-gated ion channel

Inhibitors

Inhibitors of purinergic receptors include clopidogrel, prasugrel and ticlopidine, as well as the investigational drug ticagrelor. All of these are antiplatelet agents that block P2Y12 receptors.

External links

pt:Receptor purinérgico zh:嘌呤受体