Fluoxetine modulates norepinephrine contractile effect on rat vas deferens
- Autores
- Busch, Lucila; Wald, Miriam Ruth; Sterin, Leonor Josefina; Borda, Enri Santiago
- Año de publicación
- 2000
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The aim of this study was to evaluate whether the antidepressant drug fluoxetine could modify rat vas deferens response to norepinephrine (NE), and to compare its effect with that of desipramine and cocaine. Results showed that 10-5 M fluoxetine produced a super-sensibility of vas deferens to NE. This result was the same as those obtained for 10-6 M desipramine or cocaine. Since the effect was Na+- and Cl--dependent, an inhibitory mechanism of neuronal NE transport was suggested. Fluoxetine did not modify [3H]prazosin k(d) or B(max) in rat vas deferens, reinforcing the hypothesis of a pre-synaptic site of action. On the other hand fluoxetine inhibited NE maximal effect. This inhibitory effect could be related to an antagonism of calcium entry through the voltage-dependent calcium channel, since it was partially reverted by increasing calcium concentration and, besides, the drug was able to inhibit the calcium concentration-response curve also. Contractions induced by 5-hydroxytryptamine (5-HT) were not modified in the presence of fluoxetine. It is concluded that fluoxetine modulates rat vas deferens response to low NE concentrations in the same manner as the selective inhibitor of NE neuronal uptake desipramine. This peripheral effect could participate in the modulation of the male reproductive tract observed by these drugs when used in clinical trials.
Fil: Busch, Lucila. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina
Fil: Wald, Miriam Ruth. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Sterin, Leonor Josefina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Borda, Enri Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina - Materia
-
Fluoxetine
Neuronal Uptake
Norepinephrine
Vas Deferens - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/39146
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Fluoxetine modulates norepinephrine contractile effect on rat vas deferensBusch, LucilaWald, Miriam RuthSterin, Leonor JosefinaBorda, Enri SantiagoFluoxetineNeuronal UptakeNorepinephrineVas Deferenshttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3The aim of this study was to evaluate whether the antidepressant drug fluoxetine could modify rat vas deferens response to norepinephrine (NE), and to compare its effect with that of desipramine and cocaine. Results showed that 10-5 M fluoxetine produced a super-sensibility of vas deferens to NE. This result was the same as those obtained for 10-6 M desipramine or cocaine. Since the effect was Na+- and Cl--dependent, an inhibitory mechanism of neuronal NE transport was suggested. Fluoxetine did not modify [3H]prazosin k(d) or B(max) in rat vas deferens, reinforcing the hypothesis of a pre-synaptic site of action. On the other hand fluoxetine inhibited NE maximal effect. This inhibitory effect could be related to an antagonism of calcium entry through the voltage-dependent calcium channel, since it was partially reverted by increasing calcium concentration and, besides, the drug was able to inhibit the calcium concentration-response curve also. Contractions induced by 5-hydroxytryptamine (5-HT) were not modified in the presence of fluoxetine. It is concluded that fluoxetine modulates rat vas deferens response to low NE concentrations in the same manner as the selective inhibitor of NE neuronal uptake desipramine. This peripheral effect could participate in the modulation of the male reproductive tract observed by these drugs when used in clinical trials.Fil: Busch, Lucila. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; ArgentinaFil: Wald, Miriam Ruth. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Sterin, Leonor Josefina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Borda, Enri Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; ArgentinaAcademic Press Ltd - Elsevier Science Ltd2000-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/39146Busch, Lucila; Wald, Miriam Ruth; Sterin, Leonor Josefina; Borda, Enri Santiago; Fluoxetine modulates norepinephrine contractile effect on rat vas deferens; Academic Press Ltd - Elsevier Science Ltd; Pharmacological Research; 41; 1; 1-2000; 39-451043-6618CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1006/phrs.1999.0559info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1043661899905595info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:05:32Zoai:ri.conicet.gov.ar:11336/39146instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:05:32.373CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
title |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
spellingShingle |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens Busch, Lucila Fluoxetine Neuronal Uptake Norepinephrine Vas Deferens |
title_short |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
title_full |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
title_fullStr |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
title_full_unstemmed |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
title_sort |
Fluoxetine modulates norepinephrine contractile effect on rat vas deferens |
dc.creator.none.fl_str_mv |
Busch, Lucila Wald, Miriam Ruth Sterin, Leonor Josefina Borda, Enri Santiago |
author |
Busch, Lucila |
author_facet |
Busch, Lucila Wald, Miriam Ruth Sterin, Leonor Josefina Borda, Enri Santiago |
author_role |
author |
author2 |
Wald, Miriam Ruth Sterin, Leonor Josefina Borda, Enri Santiago |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Fluoxetine Neuronal Uptake Norepinephrine Vas Deferens |
topic |
Fluoxetine Neuronal Uptake Norepinephrine Vas Deferens |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
The aim of this study was to evaluate whether the antidepressant drug fluoxetine could modify rat vas deferens response to norepinephrine (NE), and to compare its effect with that of desipramine and cocaine. Results showed that 10-5 M fluoxetine produced a super-sensibility of vas deferens to NE. This result was the same as those obtained for 10-6 M desipramine or cocaine. Since the effect was Na+- and Cl--dependent, an inhibitory mechanism of neuronal NE transport was suggested. Fluoxetine did not modify [3H]prazosin k(d) or B(max) in rat vas deferens, reinforcing the hypothesis of a pre-synaptic site of action. On the other hand fluoxetine inhibited NE maximal effect. This inhibitory effect could be related to an antagonism of calcium entry through the voltage-dependent calcium channel, since it was partially reverted by increasing calcium concentration and, besides, the drug was able to inhibit the calcium concentration-response curve also. Contractions induced by 5-hydroxytryptamine (5-HT) were not modified in the presence of fluoxetine. It is concluded that fluoxetine modulates rat vas deferens response to low NE concentrations in the same manner as the selective inhibitor of NE neuronal uptake desipramine. This peripheral effect could participate in the modulation of the male reproductive tract observed by these drugs when used in clinical trials. Fil: Busch, Lucila. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina Fil: Wald, Miriam Ruth. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Sterin, Leonor Josefina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Borda, Enri Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Odontología. Cátedra de Farmacología; Argentina |
description |
The aim of this study was to evaluate whether the antidepressant drug fluoxetine could modify rat vas deferens response to norepinephrine (NE), and to compare its effect with that of desipramine and cocaine. Results showed that 10-5 M fluoxetine produced a super-sensibility of vas deferens to NE. This result was the same as those obtained for 10-6 M desipramine or cocaine. Since the effect was Na+- and Cl--dependent, an inhibitory mechanism of neuronal NE transport was suggested. Fluoxetine did not modify [3H]prazosin k(d) or B(max) in rat vas deferens, reinforcing the hypothesis of a pre-synaptic site of action. On the other hand fluoxetine inhibited NE maximal effect. This inhibitory effect could be related to an antagonism of calcium entry through the voltage-dependent calcium channel, since it was partially reverted by increasing calcium concentration and, besides, the drug was able to inhibit the calcium concentration-response curve also. Contractions induced by 5-hydroxytryptamine (5-HT) were not modified in the presence of fluoxetine. It is concluded that fluoxetine modulates rat vas deferens response to low NE concentrations in the same manner as the selective inhibitor of NE neuronal uptake desipramine. This peripheral effect could participate in the modulation of the male reproductive tract observed by these drugs when used in clinical trials. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/39146 Busch, Lucila; Wald, Miriam Ruth; Sterin, Leonor Josefina; Borda, Enri Santiago; Fluoxetine modulates norepinephrine contractile effect on rat vas deferens; Academic Press Ltd - Elsevier Science Ltd; Pharmacological Research; 41; 1; 1-2000; 39-45 1043-6618 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/39146 |
identifier_str_mv |
Busch, Lucila; Wald, Miriam Ruth; Sterin, Leonor Josefina; Borda, Enri Santiago; Fluoxetine modulates norepinephrine contractile effect on rat vas deferens; Academic Press Ltd - Elsevier Science Ltd; Pharmacological Research; 41; 1; 1-2000; 39-45 1043-6618 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1006/phrs.1999.0559 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1043661899905595 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Academic Press Ltd - Elsevier Science Ltd |
publisher.none.fl_str_mv |
Academic Press Ltd - Elsevier Science Ltd |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269915676934144 |
score |
13.13397 |