Impact of A118G polymorphism on the Mu opioid receptor function in pain
- Autores
- López Soto, Eduardo Javier; Agosti, Francina; Catanesi, Cecilia Inés; Raingo, Jesica
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mu Opioid Receptor (MOR) activation by exogenous or endogenous agonists causes reduction of pain threshold after a noxious stimulus, relieving pain sensation.MOR is encoded by OPRM1 gene and its messenger RNA suffers extensible modifications by alternative splicing and single nucleotide polymorphisms (SNPs). A118G (N40D) is the most frequent encoding MOR SNP in humans. In this review we discuss the impact of this polymorphism at molecular, cellular and clinical levels. Since some SNPs are unequally distributed among human populations, we also discuss the utility of A118G as an ethnicity marker among worldwide human populations. As an example, we evaluate A118G frequency in an Argentinean humanpopulation and compare it with worldwide frequencies extracted from HapMap database.
Instituto Multidisciplinario de Biología Celular - Materia
-
Medicina
Mu-opioid receptor
A118g polymorphism
N40d polymorphism
Voltage-gated calcium channel
Population studies - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/98211
Ver los metadatos del registro completo
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Impact of A118G polymorphism on the Mu opioid receptor function in painLópez Soto, Eduardo JavierAgosti, FrancinaCatanesi, Cecilia InésRaingo, JesicaMedicinaMu-opioid receptorA118g polymorphismN40d polymorphismVoltage-gated calcium channelPopulation studiesMu Opioid Receptor (MOR) activation by exogenous or endogenous agonists causes reduction of pain threshold after a noxious stimulus, relieving pain sensation.MOR is encoded by <i>OPRM1</i> gene and its messenger RNA suffers extensible modifications by alternative splicing and single nucleotide polymorphisms (SNPs). A118G (N40D) is the most frequent encoding MOR SNP in humans. In this review we discuss the impact of this polymorphism at molecular, cellular and clinical levels. Since some SNPs are unequally distributed among human populations, we also discuss the utility of A118G as an ethnicity marker among worldwide human populations. As an example, we evaluate A118G frequency in an Argentinean humanpopulation and compare it with worldwide frequencies extracted from HapMap database.Instituto Multidisciplinario de Biología Celular2013-07-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1-6http://sedici.unlp.edu.ar/handle/10915/98211enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/85028info:eu-repo/semantics/altIdentifier/url/https://www.omicsonline.org/open-access/impact-of-ag-polymorphism-on-the-mu-opioid-receptor-function-in-pain-2167-0846.1000119.php?aid=15830info:eu-repo/semantics/altIdentifier/issn/2167-0846info:eu-repo/semantics/altIdentifier/doi/10.4172/2167-0846.1000119info:eu-repo/semantics/altIdentifier/hdl/11336/85028info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-22T17:01:21Zoai:sedici.unlp.edu.ar:10915/98211Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-22 17:01:21.493SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| title |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| spellingShingle |
Impact of A118G polymorphism on the Mu opioid receptor function in pain López Soto, Eduardo Javier Medicina Mu-opioid receptor A118g polymorphism N40d polymorphism Voltage-gated calcium channel Population studies |
| title_short |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| title_full |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| title_fullStr |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| title_full_unstemmed |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| title_sort |
Impact of A118G polymorphism on the Mu opioid receptor function in pain |
| dc.creator.none.fl_str_mv |
López Soto, Eduardo Javier Agosti, Francina Catanesi, Cecilia Inés Raingo, Jesica |
| author |
López Soto, Eduardo Javier |
| author_facet |
López Soto, Eduardo Javier Agosti, Francina Catanesi, Cecilia Inés Raingo, Jesica |
| author_role |
author |
| author2 |
Agosti, Francina Catanesi, Cecilia Inés Raingo, Jesica |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
Medicina Mu-opioid receptor A118g polymorphism N40d polymorphism Voltage-gated calcium channel Population studies |
| topic |
Medicina Mu-opioid receptor A118g polymorphism N40d polymorphism Voltage-gated calcium channel Population studies |
| dc.description.none.fl_txt_mv |
Mu Opioid Receptor (MOR) activation by exogenous or endogenous agonists causes reduction of pain threshold after a noxious stimulus, relieving pain sensation.MOR is encoded by <i>OPRM1</i> gene and its messenger RNA suffers extensible modifications by alternative splicing and single nucleotide polymorphisms (SNPs). A118G (N40D) is the most frequent encoding MOR SNP in humans. In this review we discuss the impact of this polymorphism at molecular, cellular and clinical levels. Since some SNPs are unequally distributed among human populations, we also discuss the utility of A118G as an ethnicity marker among worldwide human populations. As an example, we evaluate A118G frequency in an Argentinean humanpopulation and compare it with worldwide frequencies extracted from HapMap database. Instituto Multidisciplinario de Biología Celular |
| description |
Mu Opioid Receptor (MOR) activation by exogenous or endogenous agonists causes reduction of pain threshold after a noxious stimulus, relieving pain sensation.MOR is encoded by <i>OPRM1</i> gene and its messenger RNA suffers extensible modifications by alternative splicing and single nucleotide polymorphisms (SNPs). A118G (N40D) is the most frequent encoding MOR SNP in humans. In this review we discuss the impact of this polymorphism at molecular, cellular and clinical levels. Since some SNPs are unequally distributed among human populations, we also discuss the utility of A118G as an ethnicity marker among worldwide human populations. As an example, we evaluate A118G frequency in an Argentinean humanpopulation and compare it with worldwide frequencies extracted from HapMap database. |
| publishDate |
2013 |
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2013-07-07 |
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http://sedici.unlp.edu.ar/handle/10915/98211 |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/85028 info:eu-repo/semantics/altIdentifier/url/https://www.omicsonline.org/open-access/impact-of-ag-polymorphism-on-the-mu-opioid-receptor-function-in-pain-2167-0846.1000119.php?aid=15830 info:eu-repo/semantics/altIdentifier/issn/2167-0846 info:eu-repo/semantics/altIdentifier/doi/10.4172/2167-0846.1000119 info:eu-repo/semantics/altIdentifier/hdl/11336/85028 |
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