Literature DB >> 10949117

Five exon 1 variants of mu opioid receptor and vulnerability to alcohol dependence.

N Gscheidel1, T Sander, B Wendel, P Heere, L G Schmidt, H Rommelspacher, M R Hoehe, J Samochowiec.   

Abstract

The human mu opioid receptor (hMOR) gene is a prime candidate gene responsible for addictive disorders. The present association study tested the hypothesis that hMOR exon 1 variants elicit susceptibility to alcohol dependence. We have analyzed five nucleotide changes in exon 1 of the hMOR gene. Three of them are in the 5'untranslated region of exon 1 at positions -172G/T,-111C/T and -3 8C/A, the remaining two variants cause amino acid substitutions: +17C/T (Ala6Val) and +118A/G (Asn40Asp). Our population-based association study included 327 German alcohol-dependent subjects and 340 ethnically matched controls. The lack of an allelic association suggests that the analyzed hMOR exon 1 variants do not contribute a common and substantial effect to the genetically determined vulnerability of alcohol dependence.

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Year:  2000        PMID: 10949117

Source DB:  PubMed          Journal:  Pol J Pharmacol        ISSN: 1230-6002


  8 in total

Review 1.  Candidate gene polymorphisms predicting individual sensitivity to opioids.

Authors:  Shinya Kasai; Masakazu Hayashida; Ichiro Sora; Kazutaka Ikeda
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2007-11-13       Impact factor: 3.000

2.  A rapid screening method for a single nucleotide polymorphism (SNP) in the human MOR gene.

Authors:  S Grösch; E Niederberger; J Lötsch; C Skarke; G Geisslinger
Journal:  Br J Clin Pharmacol       Date:  2001-12       Impact factor: 4.335

Review 3.  The genetics of the opioid system and specific drug addictions.

Authors:  Orna Levran; Vadim Yuferov; Mary Jeanne Kreek
Journal:  Hum Genet       Date:  2012-05-01       Impact factor: 4.132

4.  Testing multiple levels of influence in the intergenerational transmission of alcohol disorders from a developmental perspective: the example of alcohol use promoting peers and μ-opioid receptor M1 variation.

Authors:  Laurie Chassin; Matthew R Lee; Young Il Cho; Frances L Wang; Arpana Agrawal; Kenneth J Sher; Michael T Lynskey
Journal:  Dev Psychopathol       Date:  2012-08

5.  Association between Val66Met brain-derived neurotrophic factor (BDNF) gene polymorphism and post-treatment relapse in alcohol dependence.

Authors:  Marcin Wojnar; Kirk J Brower; Stephen Strobbe; Mark Ilgen; Halina Matsumoto; Izabela Nowosad; Elzbieta Sliwerska; Margit Burmeister
Journal:  Alcohol Clin Exp Res       Date:  2009-01-27       Impact factor: 3.455

Review 6.  OPRM1 SNP (A118G): involvement in disease development, treatment response, and animal models.

Authors:  Stephen D Mague; Julie A Blendy
Journal:  Drug Alcohol Depend       Date:  2010-01-13       Impact factor: 4.492

7.  The opioid peptides enkephalin and beta-endorphin in alcohol dependence.

Authors:  Ildiko Racz; Britta Schürmann; Anna Karpushova; Martin Reuter; Sven Cichon; Christian Montag; Robert Fürst; Christian Schütz; Petra E Franke; Jana Strohmaier; Thomas F Wienker; Lars Terenius; Urban Osby; Agneta Gunnar; Wolfgang Maier; Andras Bilkei-Gorzó; Markus Nöthen; Andreas Zimmer
Journal:  Biol Psychiatry       Date:  2008-06-27       Impact factor: 13.382

8.  Genetic Analysis of Mu and Kappa Opioid Receptor and COMT Enzyme in Cancer Pain Tunisian Patients Under Opioid Treatment.

Authors:  Imen Chatti; Jean-Baptiste Woillard; Amira Mili; Isabelle Creveaux; Ilhem Ben Charfeddine; Jihène Feki; Sarah Langlais; Leila Ben Fatma; Ali Saad; Moez Gribaa; Frédéric Libert
Journal:  Iran J Public Health       Date:  2017-12       Impact factor: 1.429

  8 in total

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