Cargando…

Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor

PURPOSE: Since the adenosine A3 receptor (A3R) is considered to be of high clinical importance in the diagnosis and treatment of ischaemic conditions (heart and brain), glaucoma, asthma, arthritis, cancer and inflammation, a suitable and selective A3R PET tracer such as [(18)F]FE@SUPPY would be of h...

Descripción completa

Detalles Bibliográficos
Autores principales: Haeusler, D., Grassinger, L., Fuchshuber, F., Hörleinsberger, W. J., Höftberger, R., Leisser, I., Girschele, F., Shanab, K., Spreitzer, H., Gerdenitsch, W., Hacker, M., Wadsak, W., Mitterhauser, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382535/
https://www.ncbi.nlm.nih.gov/pubmed/25739834
http://dx.doi.org/10.1007/s00259-014-2985-2
_version_ 1782364598021652480
author Haeusler, D.
Grassinger, L.
Fuchshuber, F.
Hörleinsberger, W. J.
Höftberger, R.
Leisser, I.
Girschele, F.
Shanab, K.
Spreitzer, H.
Gerdenitsch, W.
Hacker, M.
Wadsak, W.
Mitterhauser, Markus
author_facet Haeusler, D.
Grassinger, L.
Fuchshuber, F.
Hörleinsberger, W. J.
Höftberger, R.
Leisser, I.
Girschele, F.
Shanab, K.
Spreitzer, H.
Gerdenitsch, W.
Hacker, M.
Wadsak, W.
Mitterhauser, Markus
author_sort Haeusler, D.
collection PubMed
description PURPOSE: Since the adenosine A3 receptor (A3R) is considered to be of high clinical importance in the diagnosis and treatment of ischaemic conditions (heart and brain), glaucoma, asthma, arthritis, cancer and inflammation, a suitable and selective A3R PET tracer such as [(18)F]FE@SUPPY would be of high clinical value for clinicians as well as patients. A3R was discovered in the late 1990s, but there is still little known regarding its distribution in the CNS and periphery. Hence, in autoradiographic experiments the distribution of A3R in human brain and rat tissues was investigated and the specific binding of the A3R antagonist FE@SUPPY and MRS1523 compared. Immunohistochemical staining (IHC) experiments were also performed to validate the autoradiographic findings. METHODS: For autoradiographic competition experiments human post-mortem brain and rat tissues were incubated with [(125)I]AB-MECA and highly selective compounds to block the other adenosine receptor subtypes. Additionally, IHC was performed with an A3 antibody. RESULTS: Specific A3R binding of MRS1523 and FE@SUPPY was found in all rat peripheral tissues examined with the highest amounts in the spleen (44.0 % and 46.4 %), lung (44.5 % and 45.0 %), heart (39.9 % and 42.9 %) and testes (27.4 % and 29.5 %, respectively). Low amounts of A3R were found in rat brain tissues (5.9 % and 5.6 %, respectively) and human brain tissues (thalamus 8.0 % and 9.1 %, putamen 7.8 % and 8.2 %, cerebellum 6.0 % and 7.8 %, hippocampus 5.7 % and 5.6 %, caudate nucleus 4.9 % and 6.4 %, cortex 4.9 % and 6.3 %, respectively). The outcome of the A3 antibody staining experiments complemented the results of the autoradiographic experiments. CONCLUSION: The presence of A3R protein was verified in central and peripheral tissues by autoradiography and IHC. The specificity and selectivity of FE@SUPPY was confirmed by direct comparison with MRS1523, providing further evidence that [(18)F]FE@SUPPY may be a suitable A3 PET tracer for use in humans.
format Online
Article
Text
id pubmed-4382535
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-43825352015-04-07 Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor Haeusler, D. Grassinger, L. Fuchshuber, F. Hörleinsberger, W. J. Höftberger, R. Leisser, I. Girschele, F. Shanab, K. Spreitzer, H. Gerdenitsch, W. Hacker, M. Wadsak, W. Mitterhauser, Markus Eur J Nucl Med Mol Imaging Original Article PURPOSE: Since the adenosine A3 receptor (A3R) is considered to be of high clinical importance in the diagnosis and treatment of ischaemic conditions (heart and brain), glaucoma, asthma, arthritis, cancer and inflammation, a suitable and selective A3R PET tracer such as [(18)F]FE@SUPPY would be of high clinical value for clinicians as well as patients. A3R was discovered in the late 1990s, but there is still little known regarding its distribution in the CNS and periphery. Hence, in autoradiographic experiments the distribution of A3R in human brain and rat tissues was investigated and the specific binding of the A3R antagonist FE@SUPPY and MRS1523 compared. Immunohistochemical staining (IHC) experiments were also performed to validate the autoradiographic findings. METHODS: For autoradiographic competition experiments human post-mortem brain and rat tissues were incubated with [(125)I]AB-MECA and highly selective compounds to block the other adenosine receptor subtypes. Additionally, IHC was performed with an A3 antibody. RESULTS: Specific A3R binding of MRS1523 and FE@SUPPY was found in all rat peripheral tissues examined with the highest amounts in the spleen (44.0 % and 46.4 %), lung (44.5 % and 45.0 %), heart (39.9 % and 42.9 %) and testes (27.4 % and 29.5 %, respectively). Low amounts of A3R were found in rat brain tissues (5.9 % and 5.6 %, respectively) and human brain tissues (thalamus 8.0 % and 9.1 %, putamen 7.8 % and 8.2 %, cerebellum 6.0 % and 7.8 %, hippocampus 5.7 % and 5.6 %, caudate nucleus 4.9 % and 6.4 %, cortex 4.9 % and 6.3 %, respectively). The outcome of the A3 antibody staining experiments complemented the results of the autoradiographic experiments. CONCLUSION: The presence of A3R protein was verified in central and peripheral tissues by autoradiography and IHC. The specificity and selectivity of FE@SUPPY was confirmed by direct comparison with MRS1523, providing further evidence that [(18)F]FE@SUPPY may be a suitable A3 PET tracer for use in humans. Springer Berlin Heidelberg 2015-03-05 2015 /pmc/articles/PMC4382535/ /pubmed/25739834 http://dx.doi.org/10.1007/s00259-014-2985-2 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Haeusler, D.
Grassinger, L.
Fuchshuber, F.
Hörleinsberger, W. J.
Höftberger, R.
Leisser, I.
Girschele, F.
Shanab, K.
Spreitzer, H.
Gerdenitsch, W.
Hacker, M.
Wadsak, W.
Mitterhauser, Markus
Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title_full Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title_fullStr Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title_full_unstemmed Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title_short Hide and seek: a comparative autoradiographic in vitro investigation of the adenosine A3 receptor
title_sort hide and seek: a comparative autoradiographic in vitro investigation of the adenosine a3 receptor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382535/
https://www.ncbi.nlm.nih.gov/pubmed/25739834
http://dx.doi.org/10.1007/s00259-014-2985-2
work_keys_str_mv AT haeuslerd hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT grassingerl hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT fuchshuberf hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT horleinsbergerwj hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT hoftbergerr hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT leisseri hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT girschelef hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT shanabk hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT spreitzerh hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT gerdenitschw hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT hackerm hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT wadsakw hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor
AT mitterhausermarkus hideandseekacomparativeautoradiographicinvitroinvestigationoftheadenosinea3receptor