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Relevant bibliographies by topics / Opioidní receptor

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Dissertations / Theses

Academic literature on the topic 'Opioidní receptor'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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Dissertations / Theses on the topic "Opioidní receptor"

1

Zhang, Shengwen. "The opioid receptor-like receptor ORL1 signaling and interaction with opioid receptors /." Cincinnati, Ohio : University of Cincinnati, 2002. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=ucin1029419843.

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2

ZHANG, SHENGWEN. "THE OPIOID RECEPTOR-LIKE RECEPTOR ORL1: SIGNALING AND INTERACTION WITH OPIOID RECEPTORS." University of Cincinnati / OhioLINK, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1029419843.

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3

Rudén, Ludvig. "Neurobiology of opioid addiction." Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-15735.

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Since the use of opioids started to emerge for analgesic reasons in the 19th century with the synthetization of morphine, opioids have been studied rigorously to better understand its effects on the brain. This thesis shows that both the analgesic effects and the reinforcing effects of opioids are mediated by the same receptor, the mu opioid receptor (MOR). MOR activity has been correlated to both primary and secondary reinforcers and should be considered to cause positive reinforcement together with increases in dopamine transmission for all drugs of abuse, and not only in relation to opioids

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4

Martínez, Navarro Miriam 1990. "Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system." Doctoral thesis, Universitat Pompeu Fabra, 2019. http://hdl.handle.net/10803/665963.

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La alta variabilidad interindividual en las manifestaciones de dolor neuropático puede conducir a una respuesta diferencial de los pacientes a los tratamientos, y sugiere la idoneidad de terapias más personalizadas en lugar de pautas generales. En esta tesis hemos estudiado en primer lugar la influencia de los rasgos conductuales en las manifestaciones del dolor neuropático crónico utilizando aproximaciones conductuales, electrofisiológicas y genéticas. El sistema opioide endógeno es una diana terapéutica crucial para el tratamiento del dolor inflamatorio y nociceptivo moderado o intenso. Sin

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5

Nascimento, Ana Isabel Reis. "Participação dos receptores delta e kappa -opioides centrais no controle do apetite por sódio em ratos estimulados a ingerir solução salina hipertônica." reponame:Repositório Institucional da FIOCRUZ, 2015. https://www.arca.fiocruz.br/handle/icict/11934.

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Submitted by Ana Maria Fiscina Sampaio (fiscina@bahia.fiocruz.br) on 2015-10-13T12:34:40Z No. of bitstreams: 1 Ana Isabel Reis Nascimento. Participação...2015.pdf: 1631129 bytes, checksum: d14aa063c882bb96ee29f85751abf2e6 (MD5)<br>Approved for entry into archive by Ana Maria Fiscina Sampaio (fiscina@bahia.fiocruz.br) on 2015-10-13T12:34:59Z (GMT) No. of bitstreams: 1 Ana Isabel Reis Nascimento. Participação...2015.pdf: 1631129 bytes, checksum: d14aa063c882bb96ee29f85751abf2e6 (MD5)<br>Made available in DSpace on 2015-10-13T12:34:59Z (GMT). No. of bitstreams: 1 Ana Isabel Reis Nascimento. Parti

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6

Szekeres, Philip Graham. "Studies on the activation of G proteins by opioid receptors and receptor-mimetic peptides." Thesis, Loughborough University, 1995. https://dspace.lboro.ac.uk/2134/12440.

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7

Yoo, Ji Hoon. "Receptor studies in opioid receptor and opioid peptide gene knockout mice." Thesis, University of Surrey, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493210.

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is postulated that dynorphin inhibits the cocaine-induced increase in striatal dopamine levels, that may contribute to dynorphin's ability to prevent cocaine induced conditioned place preference and to attenuate an increase in locomotor activity. In this thesis interactions between dynorphin and the dopaminergic system in cocaine addiction have been addressed using preprodynorphin gene knockout mice treated with a chronic "binge" cocaine protocol.

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8

Olson, Keith Mathew, and Keith Mathew Olson. "Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling." Diss., The University of Arizona, 2017. http://hdl.handle.net/10150/626669.

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Most clinical opioids produce analgesia through the Mu Opioid Receptor (MOR) providing the only effective treatment for chronic pain patients. These studies explore three pre-clinical strategies to improve MOR analgesia and minimize side effects: 1) compounds that target G-protein Coupled Receptors (GPCRs) heterodimers, such as heterodimerization between the Delta Opioid Receptor (DOR) and MOR (MDOR); 2) multi-functional compounds that target multiple receptor systems for synergistic effects, such as a MOR agonist and a the serotonin reuptake transporter (SERT) inhibitor; or 3) biased agonists

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9

Macedo, Cristina Gomes de 1964. "Mecanismos opióides centrais envolvidos no efeito protetor da testosterona no desenvolvimento da dor da ATM em ratos." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/290572.

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Orientador: Claudia Herrera Tambeli<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba<br>Made available in DSpace on 2018-08-20T01:36:46Z (GMT). No. of bitstreams: 1 Macedo_CristinaGomesde_M.pdf: 777542 bytes, checksum: 9fba5bed6fd851b4349bf4812dda8d33 (MD5) Previous issue date: 2012<br>Resumo: Disfunções temporomandibulares são condições dolorosas que envolvem a articulação temporomandibular e os músculos mastigatórios com maior prevalência, severidade e duração no sexo feminino. Recentemente foi demonstrado que a testosterona apresenta um

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10

Smith, Caroline Jackson. "Development of oxytocin, vasopressin V1a, and mu-opioid receptor expression in the rat brain: Implications for the regulation of juvenile social novelty-seeking behavior." Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107311.

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Thesis advisor: Alexa H. Veemena<br>Across species, the juvenile period is characterized by increased social interaction with peers and heightened novelty-seeking behavior, as compared to any other life stage. These behaviors are likely to be highly adaptive during this developmental phase. Still, an excessive novelty-seeking phenotype may predispose individuals to risk-taking and substance abuse, while too little social engagement and low novelty-seeking are characteristics of neuropsychiatry disorders such as autism. The over-arching aim of this dissertation research has been to elucidate th

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