Why Deprivation Makes Food Taste Better?
- Autores
- Blanco, Maria Gabriela; Florman, Jeremy; Lacour, Ailin; de Rosa, Maria Jose; Alkema, Mark; Rayes, Diego Hernán
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- The phenomenon of food tasting better after deprivation is conserved across many species. In C. elegans, an enhanced slowing response is ob- served when encountering food after 30 minutes of food deprivation (Sawin et al., 2000). This response is mediated by a large increase in serotonin (5-HT) release from the NSM and ADF neurons (Iwanir et al., 2016; Rhoades et al, 2019). We found that this slowing response and the activity of serotonergic neurons upon food exposure are further enhanced in tyramine (TA)-deficient mutants. TA levels decrease during fasting, and C. elegans reduces its locomotion rate after prolonged fasting (>30 minutes). This reduction in locomotion can be counteracted by the addition of exogenous TA, highlighting the role of TA in regulating movement. In contrast, serotonin (5-HT) decreases locomotion, indicating an antagonistic relationship between 5-HT and TA. We found that tyramine exerts an inhibitory effect on the NSM neuron by activating the tyramine GPCR receptors SER-2 and TYRA-2 Downregulation of tyramine during food deprivation leads to the disinhibition of serotonergic signaling and increased NSM activity upon re-encountering food. This disinhibition provides molecular and neural insights into the enhanced slowing response, enabling the worm to efficiently exploit a new food source. The antagonistic crosstalk between TA and 5-HT illustrates how the nervous system controls discrete behavioral state transitions during foraging. This mechanism may explain why food is perceived as more rewarding or appealing in states of hunger, offering a neural basis for the enhanced sensory experience of food after deprivation.
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 Massachussets. Medical School. Department Of Neurobiology; Estados Unidos
Fil: Lacour, Ailin. 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: 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: Alkema, Mark. University Of Massachussets. Medical School. Department Of Neurobiology; Estados Unidos
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
25th International Worm meeting
Davis
Estados Unidos
Genetics Society of America - Materia
-
neuronal activity
feeding
hunger
serotonin - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/282485
Ver los metadatos del registro completo
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Why Deprivation Makes Food Taste Better?Blanco, Maria GabrielaFlorman, JeremyLacour, Ailinde Rosa, Maria JoseAlkema, MarkRayes, Diego Hernánneuronal activityfeedinghungerserotoninhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The phenomenon of food tasting better after deprivation is conserved across many species. In C. elegans, an enhanced slowing response is ob- served when encountering food after 30 minutes of food deprivation (Sawin et al., 2000). This response is mediated by a large increase in serotonin (5-HT) release from the NSM and ADF neurons (Iwanir et al., 2016; Rhoades et al, 2019). We found that this slowing response and the activity of serotonergic neurons upon food exposure are further enhanced in tyramine (TA)-deficient mutants. TA levels decrease during fasting, and C. elegans reduces its locomotion rate after prolonged fasting (>30 minutes). This reduction in locomotion can be counteracted by the addition of exogenous TA, highlighting the role of TA in regulating movement. In contrast, serotonin (5-HT) decreases locomotion, indicating an antagonistic relationship between 5-HT and TA. We found that tyramine exerts an inhibitory effect on the NSM neuron by activating the tyramine GPCR receptors SER-2 and TYRA-2 Downregulation of tyramine during food deprivation leads to the disinhibition of serotonergic signaling and increased NSM activity upon re-encountering food. This disinhibition provides molecular and neural insights into the enhanced slowing response, enabling the worm to efficiently exploit a new food source. The antagonistic crosstalk between TA and 5-HT illustrates how the nervous system controls discrete behavioral state transitions during foraging. This mechanism may explain why food is perceived as more rewarding or appealing in states of hunger, offering a neural basis for the enhanced sensory experience of food after deprivation.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; ArgentinaFil: Florman, Jeremy. University Of Massachussets. Medical School. Department Of Neurobiology; Estados UnidosFil: Lacour, Ailin. 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: 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: Alkema, Mark. University Of Massachussets. Medical School. Department Of Neurobiology; Estados UnidosFil: 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; Argentina25th International Worm meetingDavisEstados UnidosGenetics Society of AmericaGenetics Society of America2025info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/282485Why Deprivation Makes Food Taste Better?; 25th International Worm meeting; Davis; Estados Unidos; 2025; 51-51CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://genetics-gsa.org/worm-2025/download-program-and-abstract-books/Internacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-05-13T11:22:12Zoai:ri.conicet.gov.ar:11336/282485instacron: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:34982026-05-13 11:22:12.497CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Why Deprivation Makes Food Taste Better? |
| title |
Why Deprivation Makes Food Taste Better? |
| spellingShingle |
Why Deprivation Makes Food Taste Better? Blanco, Maria Gabriela neuronal activity feeding hunger serotonin |
| title_short |
Why Deprivation Makes Food Taste Better? |
| title_full |
Why Deprivation Makes Food Taste Better? |
| title_fullStr |
Why Deprivation Makes Food Taste Better? |
| title_full_unstemmed |
Why Deprivation Makes Food Taste Better? |
| title_sort |
Why Deprivation Makes Food Taste Better? |
| dc.creator.none.fl_str_mv |
Blanco, Maria Gabriela Florman, Jeremy Lacour, Ailin de Rosa, Maria Jose Alkema, Mark Rayes, Diego Hernán |
| author |
Blanco, Maria Gabriela |
| author_facet |
Blanco, Maria Gabriela Florman, Jeremy Lacour, Ailin de Rosa, Maria Jose Alkema, Mark Rayes, Diego Hernán |
| author_role |
author |
| author2 |
Florman, Jeremy Lacour, Ailin de Rosa, Maria Jose Alkema, Mark Rayes, Diego Hernán |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
neuronal activity feeding hunger serotonin |
| topic |
neuronal activity feeding hunger serotonin |
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https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
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The phenomenon of food tasting better after deprivation is conserved across many species. In C. elegans, an enhanced slowing response is ob- served when encountering food after 30 minutes of food deprivation (Sawin et al., 2000). This response is mediated by a large increase in serotonin (5-HT) release from the NSM and ADF neurons (Iwanir et al., 2016; Rhoades et al, 2019). We found that this slowing response and the activity of serotonergic neurons upon food exposure are further enhanced in tyramine (TA)-deficient mutants. TA levels decrease during fasting, and C. elegans reduces its locomotion rate after prolonged fasting (>30 minutes). This reduction in locomotion can be counteracted by the addition of exogenous TA, highlighting the role of TA in regulating movement. In contrast, serotonin (5-HT) decreases locomotion, indicating an antagonistic relationship between 5-HT and TA. We found that tyramine exerts an inhibitory effect on the NSM neuron by activating the tyramine GPCR receptors SER-2 and TYRA-2 Downregulation of tyramine during food deprivation leads to the disinhibition of serotonergic signaling and increased NSM activity upon re-encountering food. This disinhibition provides molecular and neural insights into the enhanced slowing response, enabling the worm to efficiently exploit a new food source. The antagonistic crosstalk between TA and 5-HT illustrates how the nervous system controls discrete behavioral state transitions during foraging. This mechanism may explain why food is perceived as more rewarding or appealing in states of hunger, offering a neural basis for the enhanced sensory experience of food after deprivation. 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 Massachussets. Medical School. Department Of Neurobiology; Estados Unidos Fil: Lacour, Ailin. 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: 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: Alkema, Mark. University Of Massachussets. Medical School. Department Of Neurobiology; Estados Unidos 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 25th International Worm meeting Davis Estados Unidos Genetics Society of America |
| description |
The phenomenon of food tasting better after deprivation is conserved across many species. In C. elegans, an enhanced slowing response is ob- served when encountering food after 30 minutes of food deprivation (Sawin et al., 2000). This response is mediated by a large increase in serotonin (5-HT) release from the NSM and ADF neurons (Iwanir et al., 2016; Rhoades et al, 2019). We found that this slowing response and the activity of serotonergic neurons upon food exposure are further enhanced in tyramine (TA)-deficient mutants. TA levels decrease during fasting, and C. elegans reduces its locomotion rate after prolonged fasting (>30 minutes). This reduction in locomotion can be counteracted by the addition of exogenous TA, highlighting the role of TA in regulating movement. In contrast, serotonin (5-HT) decreases locomotion, indicating an antagonistic relationship between 5-HT and TA. We found that tyramine exerts an inhibitory effect on the NSM neuron by activating the tyramine GPCR receptors SER-2 and TYRA-2 Downregulation of tyramine during food deprivation leads to the disinhibition of serotonergic signaling and increased NSM activity upon re-encountering food. This disinhibition provides molecular and neural insights into the enhanced slowing response, enabling the worm to efficiently exploit a new food source. The antagonistic crosstalk between TA and 5-HT illustrates how the nervous system controls discrete behavioral state transitions during foraging. This mechanism may explain why food is perceived as more rewarding or appealing in states of hunger, offering a neural basis for the enhanced sensory experience of food after deprivation. |
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