There have been many advances in our knowledge about different aspects of P2Y receptor signaling since the last review published by our International Union of Pharmacol. subcommittee. More receptor subtypes have been cloned and characterized and most orphan receptors deorphanized, so that it is now possible to provide a basis for a future subdivision of P2Y receptor subtypes. More is known about the functional elements of the P2Y receptor mols. and the signaling pathways involved, including interactions with ion channels. There have been substantial developments in the design of selective agonists and antagonists to some of the P2Y receptor subtypes. There are new findings about the mechanisms underlying nucleotide release and ectoenzymic nucleotide breakdown. Interactions between P2Y receptors and receptors to other signaling mols. have been explored as well as P2Y-mediated control of gene transcription. The distribution and roles of P2Y receptor subtypes in many different cell types are better understood and P2Y receptor-related compds. are being explored for therapeutic purposes. These and other advances are discussed in the present review

International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy / M.P. Abbracchio, G. Burnstock, J.M. Boeynaems, E.A. Barnard, J.L. Boyer, C. Kennedy, G.E. Knight, M. Fumagalli, C. Gachet, K.A. Jacobson, G.A. Weisman. - In: PHARMACOLOGICAL REVIEWS. - ISSN 0031-6997. - 58:3(2006 Sep), pp. 281-341. [10.1124/pr.58.3.3]

International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy

M.P. Abbracchio
Primo
;
M. Fumagalli;
2006

Abstract

There have been many advances in our knowledge about different aspects of P2Y receptor signaling since the last review published by our International Union of Pharmacol. subcommittee. More receptor subtypes have been cloned and characterized and most orphan receptors deorphanized, so that it is now possible to provide a basis for a future subdivision of P2Y receptor subtypes. More is known about the functional elements of the P2Y receptor mols. and the signaling pathways involved, including interactions with ion channels. There have been substantial developments in the design of selective agonists and antagonists to some of the P2Y receptor subtypes. There are new findings about the mechanisms underlying nucleotide release and ectoenzymic nucleotide breakdown. Interactions between P2Y receptors and receptors to other signaling mols. have been explored as well as P2Y-mediated control of gene transcription. The distribution and roles of P2Y receptor subtypes in many different cell types are better understood and P2Y receptor-related compds. are being explored for therapeutic purposes. These and other advances are discussed in the present review
English
Settore BIO/14 - Farmacologia
Articolo
Esperti anonimi
set-2006
Williams & Wilkins
58
3
281
341
Periodico con rilevanza internazionale
AN 2006:1072689
info:eu-repo/semantics/article
International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy / M.P. Abbracchio, G. Burnstock, J.M. Boeynaems, E.A. Barnard, J.L. Boyer, C. Kennedy, G.E. Knight, M. Fumagalli, C. Gachet, K.A. Jacobson, G.A. Weisman. - In: PHARMACOLOGICAL REVIEWS. - ISSN 0031-6997. - 58:3(2006 Sep), pp. 281-341. [10.1124/pr.58.3.3]
none
Prodotti della ricerca::01 - Articolo su periodico
11
262
Article (author)
Periodico con Impact Factor
M.P. Abbracchio, G. Burnstock, J.M. Boeynaems, E.A. Barnard, J.L. Boyer, C. Kennedy, G.E. Knight, M. Fumagalli, C. Gachet, K.A. Jacobson, G.A. Weisman
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/25916
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