Neural modulation of behavioral state transitions in foraging strategies in C. elegans
- Autores
- Blanco, Maria Gabriela; Florman, Jeremy; Alkema, Mark; de Rosa, Maria Jose; Rayes, Diego Hernán
- Año de publicación
- 2023
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Adequate feeding behavior is essential for animal survival and it is regulated not only by the digestive system but also by the nervous system (NS). The NS allows the animal to respond flexibly to changes in the environment depending on the availability of food and the nutritional internal state. Despite feeding behaviors have been studied for decades, understanding the mechanisms involved in different animals´ responses to food depending on its internal state (satiated or fasted/stressed) is still a major challenge. Referred to as the “happiness hormone”, serotonin (5-HT) has been shown to increase with food stimulus and modulate feeding in different animals, suggesting that the role of 5-HT is conserved in nature. On the other hand, noradrenaline (NA), implicated in triggering a stress response, is involved in appetite control by reducing food ingestion. Interestingly, there are reports showing that a lesion of the serotonergic system enhances the effect of noradrenergic drugs. These findings indicate an interaction between serotonergic and noradrenergic signaling. However, the mechanism and relevance of this interplay are not entirely clear. Therefore, our goal is to investigate the molecular processes underlying this interaction. The complexity of the mammalian brain complicates the study of neuronal processes. The nematode Caenorhabditis elegans is suitable for understanding neuronal signaling because of its simple and well-described nervous system. We found that during prolonged fasting, animals decrease their locomotion, which can be resumed by adding tyramine (TA), the analog of NA in invertebrates. 5-HT produces the opposite effect by reducing locomotion, suggesting that 5-HT acts antagonistically to TA. Moreover, it has been shown that when the environment improves and fasted animals encounter food, they release 5-HT to slow their locomotion and promote feeding. Interestingly, we found that this slowing response and the activity of the serotonergic neurons upon food encounter are enhanced in TA-deficient mutants compared to wild-type animals. Given that we also show that TA levels decrease during fasting, we hypothesize that this disinhibits the serotonergic neurons and favors their activity upon refeeding, allowing the animal to exploit the new source of food. Considering the conservation of neuronal components, we believe that our results may contribute to the understanding of the nervous control of state dependent foraging strategies
Fil: Blanco, Maria Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Florman, Jeremy. University of Massachusetts; Estados Unidos
Fil: Alkema, Mark. University of Massachusetts; Estados Unidos
Fil: de Rosa, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Rayes, Diego Hernán. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
24th International C. elegans Conference
Glasgow
Reino Unido
Genetics Society of America - Materia
-
C. ELEGANS
BIOAMINES
NEURONAL CIRCUITS
FEEDING BEHAVIOR - 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:11336/241421
Ver los metadatos del registro completo
id |
CONICETDig_8709351517ad1355345ebd5a1b3d3c4b |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/241421 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Neural modulation of behavioral state transitions in foraging strategies in C. elegansBlanco, Maria GabrielaFlorman, JeremyAlkema, Markde Rosa, Maria JoseRayes, Diego HernánC. ELEGANSBIOAMINESNEURONAL CIRCUITSFEEDING BEHAVIORhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Adequate feeding behavior is essential for animal survival and it is regulated not only by the digestive system but also by the nervous system (NS). The NS allows the animal to respond flexibly to changes in the environment depending on the availability of food and the nutritional internal state. Despite feeding behaviors have been studied for decades, understanding the mechanisms involved in different animals´ responses to food depending on its internal state (satiated or fasted/stressed) is still a major challenge. Referred to as the “happiness hormone”, serotonin (5-HT) has been shown to increase with food stimulus and modulate feeding in different animals, suggesting that the role of 5-HT is conserved in nature. On the other hand, noradrenaline (NA), implicated in triggering a stress response, is involved in appetite control by reducing food ingestion. Interestingly, there are reports showing that a lesion of the serotonergic system enhances the effect of noradrenergic drugs. These findings indicate an interaction between serotonergic and noradrenergic signaling. However, the mechanism and relevance of this interplay are not entirely clear. Therefore, our goal is to investigate the molecular processes underlying this interaction. The complexity of the mammalian brain complicates the study of neuronal processes. The nematode Caenorhabditis elegans is suitable for understanding neuronal signaling because of its simple and well-described nervous system. We found that during prolonged fasting, animals decrease their locomotion, which can be resumed by adding tyramine (TA), the analog of NA in invertebrates. 5-HT produces the opposite effect by reducing locomotion, suggesting that 5-HT acts antagonistically to TA. Moreover, it has been shown that when the environment improves and fasted animals encounter food, they release 5-HT to slow their locomotion and promote feeding. Interestingly, we found that this slowing response and the activity of the serotonergic neurons upon food encounter are enhanced in TA-deficient mutants compared to wild-type animals. Given that we also show that TA levels decrease during fasting, we hypothesize that this disinhibits the serotonergic neurons and favors their activity upon refeeding, allowing the animal to exploit the new source of food. Considering the conservation of neuronal components, we believe that our results may contribute to the understanding of the nervous control of state dependent foraging strategiesFil: Blanco, Maria Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Florman, Jeremy. University of Massachusetts; Estados UnidosFil: Alkema, Mark. University of Massachusetts; Estados UnidosFil: de Rosa, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Rayes, Diego Hernán. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina24th International C. elegans ConferenceGlasgowReino UnidoGenetics Society of AmericaGenetics Society of America2023info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectConferenciaJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/241421Neural modulation of behavioral state transitions in foraging strategies in C. elegans; 24th International C. elegans Conference; Glasgow; Reino Unido; 2023; 380-380CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://genetics-gsa.org/celegans2023/Internacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:45:53Zoai:ri.conicet.gov.ar:11336/241421instacron: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:34982025-09-29 09:45:53.655CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
title |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
spellingShingle |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans Blanco, Maria Gabriela C. ELEGANS BIOAMINES NEURONAL CIRCUITS FEEDING BEHAVIOR |
title_short |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
title_full |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
title_fullStr |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
title_full_unstemmed |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
title_sort |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans |
dc.creator.none.fl_str_mv |
Blanco, Maria Gabriela Florman, Jeremy Alkema, Mark de Rosa, Maria Jose Rayes, Diego Hernán |
author |
Blanco, Maria Gabriela |
author_facet |
Blanco, Maria Gabriela Florman, Jeremy Alkema, Mark de Rosa, Maria Jose Rayes, Diego Hernán |
author_role |
author |
author2 |
Florman, Jeremy Alkema, Mark de Rosa, Maria Jose Rayes, Diego Hernán |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
C. ELEGANS BIOAMINES NEURONAL CIRCUITS FEEDING BEHAVIOR |
topic |
C. ELEGANS BIOAMINES NEURONAL CIRCUITS FEEDING BEHAVIOR |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Adequate feeding behavior is essential for animal survival and it is regulated not only by the digestive system but also by the nervous system (NS). The NS allows the animal to respond flexibly to changes in the environment depending on the availability of food and the nutritional internal state. Despite feeding behaviors have been studied for decades, understanding the mechanisms involved in different animals´ responses to food depending on its internal state (satiated or fasted/stressed) is still a major challenge. Referred to as the “happiness hormone”, serotonin (5-HT) has been shown to increase with food stimulus and modulate feeding in different animals, suggesting that the role of 5-HT is conserved in nature. On the other hand, noradrenaline (NA), implicated in triggering a stress response, is involved in appetite control by reducing food ingestion. Interestingly, there are reports showing that a lesion of the serotonergic system enhances the effect of noradrenergic drugs. These findings indicate an interaction between serotonergic and noradrenergic signaling. However, the mechanism and relevance of this interplay are not entirely clear. Therefore, our goal is to investigate the molecular processes underlying this interaction. The complexity of the mammalian brain complicates the study of neuronal processes. The nematode Caenorhabditis elegans is suitable for understanding neuronal signaling because of its simple and well-described nervous system. We found that during prolonged fasting, animals decrease their locomotion, which can be resumed by adding tyramine (TA), the analog of NA in invertebrates. 5-HT produces the opposite effect by reducing locomotion, suggesting that 5-HT acts antagonistically to TA. Moreover, it has been shown that when the environment improves and fasted animals encounter food, they release 5-HT to slow their locomotion and promote feeding. Interestingly, we found that this slowing response and the activity of the serotonergic neurons upon food encounter are enhanced in TA-deficient mutants compared to wild-type animals. Given that we also show that TA levels decrease during fasting, we hypothesize that this disinhibits the serotonergic neurons and favors their activity upon refeeding, allowing the animal to exploit the new source of food. Considering the conservation of neuronal components, we believe that our results may contribute to the understanding of the nervous control of state dependent foraging strategies Fil: Blanco, Maria Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Florman, Jeremy. University of Massachusetts; Estados Unidos Fil: Alkema, Mark. University of Massachusetts; Estados Unidos Fil: de Rosa, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Rayes, Diego Hernán. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina 24th International C. elegans Conference Glasgow Reino Unido Genetics Society of America |
description |
Adequate feeding behavior is essential for animal survival and it is regulated not only by the digestive system but also by the nervous system (NS). The NS allows the animal to respond flexibly to changes in the environment depending on the availability of food and the nutritional internal state. Despite feeding behaviors have been studied for decades, understanding the mechanisms involved in different animals´ responses to food depending on its internal state (satiated or fasted/stressed) is still a major challenge. Referred to as the “happiness hormone”, serotonin (5-HT) has been shown to increase with food stimulus and modulate feeding in different animals, suggesting that the role of 5-HT is conserved in nature. On the other hand, noradrenaline (NA), implicated in triggering a stress response, is involved in appetite control by reducing food ingestion. Interestingly, there are reports showing that a lesion of the serotonergic system enhances the effect of noradrenergic drugs. These findings indicate an interaction between serotonergic and noradrenergic signaling. However, the mechanism and relevance of this interplay are not entirely clear. Therefore, our goal is to investigate the molecular processes underlying this interaction. The complexity of the mammalian brain complicates the study of neuronal processes. The nematode Caenorhabditis elegans is suitable for understanding neuronal signaling because of its simple and well-described nervous system. We found that during prolonged fasting, animals decrease their locomotion, which can be resumed by adding tyramine (TA), the analog of NA in invertebrates. 5-HT produces the opposite effect by reducing locomotion, suggesting that 5-HT acts antagonistically to TA. Moreover, it has been shown that when the environment improves and fasted animals encounter food, they release 5-HT to slow their locomotion and promote feeding. Interestingly, we found that this slowing response and the activity of the serotonergic neurons upon food encounter are enhanced in TA-deficient mutants compared to wild-type animals. Given that we also show that TA levels decrease during fasting, we hypothesize that this disinhibits the serotonergic neurons and favors their activity upon refeeding, allowing the animal to exploit the new source of food. Considering the conservation of neuronal components, we believe that our results may contribute to the understanding of the nervous control of state dependent foraging strategies |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Conferencia Journal http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/241421 Neural modulation of behavioral state transitions in foraging strategies in C. elegans; 24th International C. elegans Conference; Glasgow; Reino Unido; 2023; 380-380 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/241421 |
identifier_str_mv |
Neural modulation of behavioral state transitions in foraging strategies in C. elegans; 24th International C. elegans Conference; Glasgow; Reino Unido; 2023; 380-380 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://genetics-gsa.org/celegans2023/ |
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 application/pdf |
dc.coverage.none.fl_str_mv |
Internacional |
dc.publisher.none.fl_str_mv |
Genetics Society of America |
publisher.none.fl_str_mv |
Genetics Society of America |
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 |
_version_ |
1844613434090455040 |
score |
13.070432 |