Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release
- Autores
- Muchnik, Salomon; Losavio, Adriana Silvia; De Lorenzo, Silvana
- Año de publicación
- 2002
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Objectives: The aim of this work was to further investigate the effect of sera from sporadic amyotrophic lateral sclerosis (ALS) patients on miniature end-plate potentials (MEPP) frequency, by the mouse passive transfer model, and to study whether the transferred serum induces any change in the sensitivity of the L-type voltage-dependent calcium channels (VDCC) to its specific blocker Nitrendipine. Methods: A total of 35 CF1 mice were divided into 3 groups: (a) ALS group receiving sera from 15 patients that had been clinically and electromyographycally diagnosed as having sporadic ALS; (b) normal group receiving sera from 13 healthy volunteers and from 3 disease control patients, and (c) control group, which was kept untreated. Animals in groups (a) and (b) received daily intraperitoneal injection of 0.5-1ml of serum for 3 days, and 24h later the left hemidiaphragm was excised for electrophysiological recordings. Results: Analysis of MEPPs frequency recorded from ALS group showed that 3 of them induced an increase in spontaneous neurotransmitter release while in 4 a decrease was observed, suggesting that sera alter spontaneous secretion as result of an increased or decreased Ca2+ influx through the normally involved N-type or L-type VDCC, respectively. When the effect of Nitrendipine, an L-type VDCC blocker, was studied on ALS sera-injected mice, we found variable responses to the drug: only two mice showed control sensitivity to Nitrendipine, while in 7 its action was lower and surprisingly in 4 was greater than that without the drug. Conclusions: These results suggest that ALS sera contain factor(s) that are able to modify spontaneous neurotransmitter release by altering calcium current through L-type and N-type VDCC, and even inducing changes in the sensitivity to the L-type VDCC blocker.
Fil: Muchnik, Salomon. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Losavio, Adriana Silvia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: De Lorenzo, Silvana. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina - Materia
-
AMYOTROPHIC LATERAL SCLEROSIS
CALCIUM CHANNELS
NITRENDIPINE
SPONTANEOUS ACETYLCHOLINE RELEASE
TEMPERATURE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/100650
Ver los metadatos del registro completo
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Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine releaseMuchnik, SalomonLosavio, Adriana SilviaDe Lorenzo, SilvanaAMYOTROPHIC LATERAL SCLEROSISCALCIUM CHANNELSNITRENDIPINESPONTANEOUS ACETYLCHOLINE RELEASETEMPERATUREhttps://purl.org/becyt/ford/3.5https://purl.org/becyt/ford/3Objectives: The aim of this work was to further investigate the effect of sera from sporadic amyotrophic lateral sclerosis (ALS) patients on miniature end-plate potentials (MEPP) frequency, by the mouse passive transfer model, and to study whether the transferred serum induces any change in the sensitivity of the L-type voltage-dependent calcium channels (VDCC) to its specific blocker Nitrendipine. Methods: A total of 35 CF1 mice were divided into 3 groups: (a) ALS group receiving sera from 15 patients that had been clinically and electromyographycally diagnosed as having sporadic ALS; (b) normal group receiving sera from 13 healthy volunteers and from 3 disease control patients, and (c) control group, which was kept untreated. Animals in groups (a) and (b) received daily intraperitoneal injection of 0.5-1ml of serum for 3 days, and 24h later the left hemidiaphragm was excised for electrophysiological recordings. Results: Analysis of MEPPs frequency recorded from ALS group showed that 3 of them induced an increase in spontaneous neurotransmitter release while in 4 a decrease was observed, suggesting that sera alter spontaneous secretion as result of an increased or decreased Ca2+ influx through the normally involved N-type or L-type VDCC, respectively. When the effect of Nitrendipine, an L-type VDCC blocker, was studied on ALS sera-injected mice, we found variable responses to the drug: only two mice showed control sensitivity to Nitrendipine, while in 7 its action was lower and surprisingly in 4 was greater than that without the drug. Conclusions: These results suggest that ALS sera contain factor(s) that are able to modify spontaneous neurotransmitter release by altering calcium current through L-type and N-type VDCC, and even inducing changes in the sensitivity to the L-type VDCC blocker.Fil: Muchnik, Salomon. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Losavio, Adriana Silvia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: De Lorenzo, Silvana. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaElsevier Ireland2002-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/100650Muchnik, Salomon; Losavio, Adriana Silvia; De Lorenzo, Silvana; Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release; Elsevier Ireland; Clinical Neurophysiology; 113; 7; 12-2002; 1066-10711388-2457CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1388245702001086info:eu-repo/semantics/altIdentifier/doi/10.1016/S1388-2457(02)00108-6info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:49:36Zoai:ri.conicet.gov.ar:11336/100650instacron: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:34982025-11-05 10:49:37.233CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| title |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| spellingShingle |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release Muchnik, Salomon AMYOTROPHIC LATERAL SCLEROSIS CALCIUM CHANNELS NITRENDIPINE SPONTANEOUS ACETYLCHOLINE RELEASE TEMPERATURE |
| title_short |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| title_full |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| title_fullStr |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| title_full_unstemmed |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| title_sort |
Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release |
| dc.creator.none.fl_str_mv |
Muchnik, Salomon Losavio, Adriana Silvia De Lorenzo, Silvana |
| author |
Muchnik, Salomon |
| author_facet |
Muchnik, Salomon Losavio, Adriana Silvia De Lorenzo, Silvana |
| author_role |
author |
| author2 |
Losavio, Adriana Silvia De Lorenzo, Silvana |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
AMYOTROPHIC LATERAL SCLEROSIS CALCIUM CHANNELS NITRENDIPINE SPONTANEOUS ACETYLCHOLINE RELEASE TEMPERATURE |
| topic |
AMYOTROPHIC LATERAL SCLEROSIS CALCIUM CHANNELS NITRENDIPINE SPONTANEOUS ACETYLCHOLINE RELEASE TEMPERATURE |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.5 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
Objectives: The aim of this work was to further investigate the effect of sera from sporadic amyotrophic lateral sclerosis (ALS) patients on miniature end-plate potentials (MEPP) frequency, by the mouse passive transfer model, and to study whether the transferred serum induces any change in the sensitivity of the L-type voltage-dependent calcium channels (VDCC) to its specific blocker Nitrendipine. Methods: A total of 35 CF1 mice were divided into 3 groups: (a) ALS group receiving sera from 15 patients that had been clinically and electromyographycally diagnosed as having sporadic ALS; (b) normal group receiving sera from 13 healthy volunteers and from 3 disease control patients, and (c) control group, which was kept untreated. Animals in groups (a) and (b) received daily intraperitoneal injection of 0.5-1ml of serum for 3 days, and 24h later the left hemidiaphragm was excised for electrophysiological recordings. Results: Analysis of MEPPs frequency recorded from ALS group showed that 3 of them induced an increase in spontaneous neurotransmitter release while in 4 a decrease was observed, suggesting that sera alter spontaneous secretion as result of an increased or decreased Ca2+ influx through the normally involved N-type or L-type VDCC, respectively. When the effect of Nitrendipine, an L-type VDCC blocker, was studied on ALS sera-injected mice, we found variable responses to the drug: only two mice showed control sensitivity to Nitrendipine, while in 7 its action was lower and surprisingly in 4 was greater than that without the drug. Conclusions: These results suggest that ALS sera contain factor(s) that are able to modify spontaneous neurotransmitter release by altering calcium current through L-type and N-type VDCC, and even inducing changes in the sensitivity to the L-type VDCC blocker. Fil: Muchnik, Salomon. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Losavio, Adriana Silvia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: De Lorenzo, Silvana. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina |
| description |
Objectives: The aim of this work was to further investigate the effect of sera from sporadic amyotrophic lateral sclerosis (ALS) patients on miniature end-plate potentials (MEPP) frequency, by the mouse passive transfer model, and to study whether the transferred serum induces any change in the sensitivity of the L-type voltage-dependent calcium channels (VDCC) to its specific blocker Nitrendipine. Methods: A total of 35 CF1 mice were divided into 3 groups: (a) ALS group receiving sera from 15 patients that had been clinically and electromyographycally diagnosed as having sporadic ALS; (b) normal group receiving sera from 13 healthy volunteers and from 3 disease control patients, and (c) control group, which was kept untreated. Animals in groups (a) and (b) received daily intraperitoneal injection of 0.5-1ml of serum for 3 days, and 24h later the left hemidiaphragm was excised for electrophysiological recordings. Results: Analysis of MEPPs frequency recorded from ALS group showed that 3 of them induced an increase in spontaneous neurotransmitter release while in 4 a decrease was observed, suggesting that sera alter spontaneous secretion as result of an increased or decreased Ca2+ influx through the normally involved N-type or L-type VDCC, respectively. When the effect of Nitrendipine, an L-type VDCC blocker, was studied on ALS sera-injected mice, we found variable responses to the drug: only two mice showed control sensitivity to Nitrendipine, while in 7 its action was lower and surprisingly in 4 was greater than that without the drug. Conclusions: These results suggest that ALS sera contain factor(s) that are able to modify spontaneous neurotransmitter release by altering calcium current through L-type and N-type VDCC, and even inducing changes in the sensitivity to the L-type VDCC blocker. |
| publishDate |
2002 |
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2002-12 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/100650 Muchnik, Salomon; Losavio, Adriana Silvia; De Lorenzo, Silvana; Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release; Elsevier Ireland; Clinical Neurophysiology; 113; 7; 12-2002; 1066-1071 1388-2457 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/100650 |
| identifier_str_mv |
Muchnik, Salomon; Losavio, Adriana Silvia; De Lorenzo, Silvana; Effect of amyotrophic lateral sclerosis serum on calcium channels related to spontaneous acetylcholine release; Elsevier Ireland; Clinical Neurophysiology; 113; 7; 12-2002; 1066-1071 1388-2457 CONICET Digital CONICET |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1388245702001086 info:eu-repo/semantics/altIdentifier/doi/10.1016/S1388-2457(02)00108-6 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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Elsevier Ireland |
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Elsevier Ireland |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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