Cargando…

The role of ATP and adenosine in the brain under normoxic and ischemic conditions

By taking advantage of some recently synthesized compounds that are able to block ecto-ATPase activity, we demonstrated that adenosine triphosphate (ATP) in the hippocampus exerts an inhibitory action independent of its degradation to adenosine. In addition, tonic activation of P2 receptors contribu...

Descripción completa

Detalles Bibliográficos
Autores principales: Pedata, F., Melani, A., Pugliese, A. M., Coppi, E., Cipriani, S., Traini, C.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2072927/
https://www.ncbi.nlm.nih.gov/pubmed/18404443
http://dx.doi.org/10.1007/s11302-007-9085-8
_version_ 1782137805038682112
author Pedata, F.
Melani, A.
Pugliese, A. M.
Coppi, E.
Cipriani, S.
Traini, C.
author_facet Pedata, F.
Melani, A.
Pugliese, A. M.
Coppi, E.
Cipriani, S.
Traini, C.
author_sort Pedata, F.
collection PubMed
description By taking advantage of some recently synthesized compounds that are able to block ecto-ATPase activity, we demonstrated that adenosine triphosphate (ATP) in the hippocampus exerts an inhibitory action independent of its degradation to adenosine. In addition, tonic activation of P2 receptors contributes to the normally recorded excitatory neurotransmission. The role of P2 receptors becomes critical during ischemia when extracellular ATP concentrations increase. Under such conditions, P2 antagonism is protective. Although ATP exerts a detrimental role under ischemia, it also exerts a trophic role in terms of cell division and differentiation. We recently reported that ATP is spontaneously released from human mesenchymal stem cells (hMSCs) in culture. Moreover, it decreases hMSC proliferation rate at early stages of culture. Increased hMSC differentiation could account for an ATP-induced decrease in cell proliferation. ATP as a homeostatic regulator might exert a different effect on cell trophism according to the rate of its efflux and receptor expression during the cell life cycle. During ischemia, adenosine formed by intracellular ATP escapes from cells through the equilibrative transporter. The protective role of adenosine A(1) receptors during ischemia is well accepted. However, the use of selective A(1) agonists is hampered by unwanted peripheral effects, thus attention has been focused on A(2A) and A(3) receptors. The protective effects of A(2A) antagonists in brain ischemia may be largely due to reduced glutamate outflow from neurones and glial cells. Reduced activation of p38 mitogen-activated protein kinases that are involved in neuronal death through transcriptional mechanisms may also contribute to protection by A(2A) antagonism. Evidence that A(3) receptor antagonism may be protective after ischemia is also reported.
format Text
id pubmed-2072927
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Springer Netherlands
record_format MEDLINE/PubMed
spelling pubmed-20729272008-02-27 The role of ATP and adenosine in the brain under normoxic and ischemic conditions Pedata, F. Melani, A. Pugliese, A. M. Coppi, E. Cipriani, S. Traini, C. Purinergic Signal Original Article By taking advantage of some recently synthesized compounds that are able to block ecto-ATPase activity, we demonstrated that adenosine triphosphate (ATP) in the hippocampus exerts an inhibitory action independent of its degradation to adenosine. In addition, tonic activation of P2 receptors contributes to the normally recorded excitatory neurotransmission. The role of P2 receptors becomes critical during ischemia when extracellular ATP concentrations increase. Under such conditions, P2 antagonism is protective. Although ATP exerts a detrimental role under ischemia, it also exerts a trophic role in terms of cell division and differentiation. We recently reported that ATP is spontaneously released from human mesenchymal stem cells (hMSCs) in culture. Moreover, it decreases hMSC proliferation rate at early stages of culture. Increased hMSC differentiation could account for an ATP-induced decrease in cell proliferation. ATP as a homeostatic regulator might exert a different effect on cell trophism according to the rate of its efflux and receptor expression during the cell life cycle. During ischemia, adenosine formed by intracellular ATP escapes from cells through the equilibrative transporter. The protective role of adenosine A(1) receptors during ischemia is well accepted. However, the use of selective A(1) agonists is hampered by unwanted peripheral effects, thus attention has been focused on A(2A) and A(3) receptors. The protective effects of A(2A) antagonists in brain ischemia may be largely due to reduced glutamate outflow from neurones and glial cells. Reduced activation of p38 mitogen-activated protein kinases that are involved in neuronal death through transcriptional mechanisms may also contribute to protection by A(2A) antagonism. Evidence that A(3) receptor antagonism may be protective after ischemia is also reported. Springer Netherlands 2007-10-11 2007-09 /pmc/articles/PMC2072927/ /pubmed/18404443 http://dx.doi.org/10.1007/s11302-007-9085-8 Text en © Springer Science+Business Media B.V. 2007
spellingShingle Original Article
Pedata, F.
Melani, A.
Pugliese, A. M.
Coppi, E.
Cipriani, S.
Traini, C.
The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title_full The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title_fullStr The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title_full_unstemmed The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title_short The role of ATP and adenosine in the brain under normoxic and ischemic conditions
title_sort role of atp and adenosine in the brain under normoxic and ischemic conditions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2072927/
https://www.ncbi.nlm.nih.gov/pubmed/18404443
http://dx.doi.org/10.1007/s11302-007-9085-8
work_keys_str_mv AT pedataf theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT melania theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT puglieseam theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT coppie theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT ciprianis theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT trainic theroleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT pedataf roleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT melania roleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT puglieseam roleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT coppie roleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT ciprianis roleofatpandadenosineinthebrainundernormoxicandischemicconditions
AT trainic roleofatpandadenosineinthebrainundernormoxicandischemicconditions