Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus

Somatostatin-14 (SS) significantly increased inositol-1,4,5-triphosphate (IP3) accumulation in rat hypothalamic, striatal, frontoparietal cortical and hippocampal slices. However, this stimulation of IP3accumulation by SS was highest in the frontoparietal cortex and hippocampus. The effect was alrea...

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Autores: Muñoz Acedo, Gema, Izquierdo Claros, Rosa María, Sánchez Alonso, Jesús Adolfo, Hoyo Medinilla, María Nancy del, Pérez Albarsanz, Miguel A, Arilla Ferreiro, Eduardo
Tipo de recurso: artículo
Fecha de publicación:1995
País:España
Institución:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/2282
Acceso en línea:http://hdl.handle.net/10017/2282
https://dx.doi.org/10.1016/0304-3940(95)11896-5
Access Level:acceso abierto
Palabra clave:Somatostatin
Inositol-1-4-5-trisphosphate
Brain
Rat
Bioquímica
Ciencia
Biochemistry
Science
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spelling Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampusMuñoz Acedo, GemaIzquierdo Claros, Rosa MaríaSánchez Alonso, Jesús AdolfoHoyo Medinilla, María Nancy delPérez Albarsanz, Miguel AArilla Ferreiro, EduardoSomatostatinInositol-1-4-5-trisphosphateBrainRatBioquímicaCienciaBiochemistryScienceSomatostatin-14 (SS) significantly increased inositol-1,4,5-triphosphate (IP3) accumulation in rat hypothalamic, striatal, frontoparietal cortical and hippocampal slices. However, this stimulation of IP3accumulation by SS was highest in the frontoparietal cortex and hippocampus. The effect was already significant with 0.01 μM in the frontoparietal cortex (P < 0.05) and hippocampus (P < 0.05) and the maximal accumulation was evident with 0.1 μM SS, in all areas studied. A concentration of 1 μM SS, lacked this effect in hypothalamus and striatum. SS rapidly increased IP3 accumulation in all brain areas studied. This effect was maximal at 15 s of incubation and decreased subsequently. At 60 s incubation, levels were still elevated in frontoparietal cortex and hippocampus but had returned to basal values in hypothalamus and striatum. Somatostatin-28 (SS-28) and the SS analogues, D-Trp8-D-Cys14 and SMS 201–995, also significantly stimulated IP3 accumulation although the effect of SMS 201–995 was greater than that of SS in the striatum in comparison with controls (P < 0.001 and P < 0.01, respectively). These results suggest that SS action at the hypothalamus, striatum, frontoparietal cortex and hippocampus is mediated at least in part by the accumulation of IP3, which may initiate intracellular processes responsible for some biological SS effects.Ministerio de Educación y CienciaElsevier19951995-01-01journal articlehttp://purl.org/coar/resource_type/c_6501NAhttp://purl.org/coar/version/c_be7fb7dd8ff6fe43info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10017/2282https://dx.doi.org/10.1016/0304-3940(95)11896-5reponame:e_Buah Biblioteca Digital Universidad de Alcaláinstname:Universidad de Alcalá (UAH)InglésengMinisterio de Educación y Ciencia Not available Not availableopen accesshttp://purl.org/coar/access_right/c_abf2Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:ebuah.uah.es:10017/22822026-06-18T11:13:07Z
dc.title.none.fl_str_mv Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
title Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
spellingShingle Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
Muñoz Acedo, Gema
Somatostatin
Inositol-1-4-5-trisphosphate
Brain
Rat
Bioquímica
Ciencia
Biochemistry
Science
title_short Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
title_full Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
title_fullStr Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
title_full_unstemmed Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
title_sort Effect of somatostatin on the mass accumulation of inositol-1,4,5- trisphosphate in rat hypothalamus, striatum, frontoparietal cortex and hippocampus
dc.creator.none.fl_str_mv Muñoz Acedo, Gema
Izquierdo Claros, Rosa María
Sánchez Alonso, Jesús Adolfo
Hoyo Medinilla, María Nancy del
Pérez Albarsanz, Miguel A
Arilla Ferreiro, Eduardo
author Muñoz Acedo, Gema
author_facet Muñoz Acedo, Gema
Izquierdo Claros, Rosa María
Sánchez Alonso, Jesús Adolfo
Hoyo Medinilla, María Nancy del
Pérez Albarsanz, Miguel A
Arilla Ferreiro, Eduardo
author_role author
author2 Izquierdo Claros, Rosa María
Sánchez Alonso, Jesús Adolfo
Hoyo Medinilla, María Nancy del
Pérez Albarsanz, Miguel A
Arilla Ferreiro, Eduardo
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Somatostatin
Inositol-1-4-5-trisphosphate
Brain
Rat
Bioquímica
Ciencia
Biochemistry
Science
topic Somatostatin
Inositol-1-4-5-trisphosphate
Brain
Rat
Bioquímica
Ciencia
Biochemistry
Science
description Somatostatin-14 (SS) significantly increased inositol-1,4,5-triphosphate (IP3) accumulation in rat hypothalamic, striatal, frontoparietal cortical and hippocampal slices. However, this stimulation of IP3accumulation by SS was highest in the frontoparietal cortex and hippocampus. The effect was already significant with 0.01 μM in the frontoparietal cortex (P < 0.05) and hippocampus (P < 0.05) and the maximal accumulation was evident with 0.1 μM SS, in all areas studied. A concentration of 1 μM SS, lacked this effect in hypothalamus and striatum. SS rapidly increased IP3 accumulation in all brain areas studied. This effect was maximal at 15 s of incubation and decreased subsequently. At 60 s incubation, levels were still elevated in frontoparietal cortex and hippocampus but had returned to basal values in hypothalamus and striatum. Somatostatin-28 (SS-28) and the SS analogues, D-Trp8-D-Cys14 and SMS 201–995, also significantly stimulated IP3 accumulation although the effect of SMS 201–995 was greater than that of SS in the striatum in comparison with controls (P < 0.001 and P < 0.01, respectively). These results suggest that SS action at the hypothalamus, striatum, frontoparietal cortex and hippocampus is mediated at least in part by the accumulation of IP3, which may initiate intracellular processes responsible for some biological SS effects.
publishDate 1995
dc.date.none.fl_str_mv 1995
1995-01-01
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
NA
http://purl.org/coar/version/c_be7fb7dd8ff6fe43
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv http://hdl.handle.net/10017/2282
https://dx.doi.org/10.1016/0304-3940(95)11896-5
url http://hdl.handle.net/10017/2282
https://dx.doi.org/10.1016/0304-3940(95)11896-5
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.relation.none.fl_str_mv Ministerio de Educación y Ciencia Not available Not available
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:e_Buah Biblioteca Digital Universidad de Alcalá
instname:Universidad de Alcalá (UAH)
instname_str Universidad de Alcalá (UAH)
reponame_str e_Buah Biblioteca Digital Universidad de Alcalá
collection e_Buah Biblioteca Digital Universidad de Alcalá
repository.name.fl_str_mv
repository.mail.fl_str_mv
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