نتایج جستجو برای: oprm1 gene

تعداد نتایج: 1141821  

Journal: :Molecular Pain 2009
Kate L Holliday Barbara I Nicholl Gary J Macfarlane Wendy Thomson Kelly A Davies John McBeth

Genetic risk factors for pain sensitivity may also play a role in susceptibility to chronic pain disorders, in which subjects have low pain thresholds. The aim of this study was to determine if proposed functional single nucleotide polymorphisms (SNPs) in the GTP cyclohydrolase (GCH1) and mu opioid receptor (OPRM1) genes previously associated with pain sensitivity affect susceptibility to chron...

2017
Aline Hajj Lucine Halepian Nada El Osta Georges Chahine Joseph Kattan Lydia Rabbaa Khabbaz

Despite increased attention on assessment and management, pain remains the most persistent symptom in patients with cancer, in particular in end-of-life settings, with detrimental impact on their quality-of-life (QOL). We conducted this study to evaluate the added value of determining some genetic and non-genetic factors to optimize cancer pain treatment. Eighty-nine patients were included in t...

Journal: :Genes, brain, and behavior 2011
A M Dlugos A Hamidovic C Hodgkinson P H Shen D Goldman A A Palmer H de Wit

The μ-opioid receptor is involved in the rewarding effects of not only opioids like morphine but also psychostimulants like amphetamine. This study aimed to investigate associations between subjective response to amphetamine and genetic polymorphisms and haplotypes in the μ-opioid receptor including the exonic variant rs1799971 (Asp40Asn). One hundred and sixty-two Caucasian volunteers particip...

Journal: :Pharmacology Biochemistry and Behavior 2014

2011
Mary R. Lee Courtney L. Gallen Xiaochu Zhang Colin A. Hodgkinson David Goldman Elliot A. Stein Christina S. Barr

Previous reports on the functional effects (i.e., gain or loss of function), and phenotypic outcomes (e.g., changes in addiction vulnerability and stress response) of a commonly occurring functional single nucleotide polymorphism (SNP) of the mu-opioid receptor (OPRM1 A118G) have been inconsistent. Here we examine the effect of this polymorphism on implicit reward learning. We used a probabilis...

2012
Grace Su Yin Pang Farida Ithnin Yin Yee Wong Jing Bo Wang Yvonne Lim Alex Tiong Heng Sia Caroline Guat Lay Lee

BACKGROUND Fentanyl-induced emesis (FIE) is a distressing adverse effect in the postoperative setting. The genetic basis of FIE remains largely unknown, therefore, we examined whether it was associated with specific genetic variants of OPRM1, the gene encoding the main receptor target of fentanyl. METHODS In this prospective case-control study, 193 women undergoing gynaecological surgery unde...

2012
Shailendra Kapoor Fiammetta Cosci Giuly Bertoli

Correspondence: Shailendra Kapoor 2300 E Cary Street, Richmond, VA 23223, USA Email [email protected] I read with great interest the article by Cosci et al in a recent issue of your journal. The article provides for highly interesting reading and is very thought-provoking. Interestingly, the past few years have seen the emergence of extensive data that establish a close association bet...

Journal: :Brain, behavior and evolution 2010
Peter Cruz-Gordillo Olivier Fedrigo Gregory A Wray Courtney C Babbitt

The various means by which the body perceives, transmits, and resolves the experiences of pain and nociception are mediated by a host of molecules, including neuropeptides within the opioid gene signaling pathway. The peptide ligands and receptors encoded by this group of genes have been linked to behavioral disorders as well as a number of psychiatric affective disorders. Our aim was to explor...

Journal: :Addiction biology 2014
Elliot C Nelson Michael T Lynskey Andrew C Heath Naomi Wray Arpana Agrawal Fiona L Shand Anjali K Henders Leanne Wallace Alexandre A Todorov Andrew J Schrage Pamela A F Madden Louisa Degenhardt Nicholas G Martin Grant W Montgomery

Genes encoding the opioid receptors (OPRM1, OPRD1 and OPRK1) are obvious candidates for involvement in risk for heroin dependence. Prior association studies commonly had samples of modest size, included limited single nucleotide polymorphism (SNP) coverage of these genes and yielded inconsistent results. Participants for the current investigation included 1459 heroin-dependent cases ascertained...

2013
Pang-Ying Shih

Background: Parkinson’s disease (PD) is a complex disorder that involves multiple genetic and environmental factors. Several candidate genes have been speculated to be involved in the development of PD. We conducted a case-control study to investigate the association between PD and single nucleotide polymorphisms (SNP) at the OPRM1, DAT, COMT and DRD2 genes in a Taiwanese population. Methods: T...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید