Association Study of Two Cannabinoid Receptor Genes, CNR1 and CNR2, with Methamphetamine Dependence

被引:13
|
作者
Okahisa, Y.
Kodama, M.
Takaki, M.
Inada, T. [2 ]
Uchimura, N. [3 ]
Yamada, M. [4 ]
Iwata, N. [5 ]
Iyo, M. [6 ]
Sora, I. [7 ]
Ozaki, N. [8 ]
Ujike, H. [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Neuropsychiat, Kita Ku, Okayama 7008558, Japan
[2] Seiwa Hosp, Tokyo, Japan
[3] Kurume Univ, Grad Sch Med, Dept Neuropsychiat, Kurume, Fukuoka 830, Japan
[4] Natl Ctr Neurol & Psychiat, Dept Psychogeriatr, Natl Inst Mental Hlth, Kodaira, Tokyo, Japan
[5] Fujita Hlth Univ, Dept Psychiat, Sch Med, Houmei, Japan
[6] Chiba Univ, Grad Sch Med, Dept Psychiat, Chiba, Japan
[7] Tohoku Univ, Grad Sch Med, Dept Neurosci, Div Psychobiol, Sendai, Miyagi 980, Japan
[8] Nagoya Univ, Grad Sch Med, Dept Psychiat, Nagoya, Aichi 4648601, Japan
基金
日本学术振兴会;
关键词
Substance abuse; methamphetamine; cannabinoid receptor 1; cannabinoid receptor 2; case-control association; ENDOCANNABINOID SYSTEM; FUNCTIONAL EXPRESSION; CB1; RECEPTORS; DRUG; BRAIN; LOCALIZATION; RISK; POLYMORPHISMS; INVOLVEMENT; ALCOHOLISM;
D O I
10.2174/157015911795017191
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several studies have suggested that the endocannabinoid system plays significant roles in the vulnerability to psychiatric disorders including drug abuse. To examine the possible association of the CNR1 and CNR2 genes, which encode cannabinoid receptors CB1 and CB2, with methamphetamine dependence, we investigated three single nucleotide polymorphisms (SNPs) (rs806379, rs1535255, rs2023239) in intron 2 of the CNR1 gene and a nonsynonymous SNP, Q63R, in the CNR2 gene. The study samples consisted of 223 patients with methamphetamine dependence and 292 age-and sex-matched controls. There were no significant differences between the patients and controls in genotypic or allelic distribution of any SNP of the CNR1 and CNR2 genes. We also analyzed the clinical features of methamphetamine dependence. Rs806379 of the CNR1 gene showed a significant association with the phenotype of latency of psychosis after the first consumption of methamphetamine. Patients with the T allele or T-positive genotypes (T/T or A/T) may develop a rapid onset of psychosis after methamphetamine abuse. The present study suggests a possibility that genetic variants of the CNR1 gene may produce a liability to the complication of psychotic state after abuse of methamphetamine; however, our findings need to be confirmed by future replications.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 50 条
  • [21] Comparative study of CNR1 and CNR2 cannabinoid receptors expression levels in COVID-19 patients with and without diabetes mellitus: Recommendations for future research targets
    Aghamahdi, Fatemeh
    Sha, Arman
    Rostami, Sayeh
    Mokhames, Zakiye
    Safavi, Mahshid
    Yaslianifard, Somayeh
    Siami, Zeinab
    Kabir, Kourosh
    Azizi, Gholamreza
    Bakhtiyari, Mahmood
    Mozhgani, Sayed-Hamidreza
    DIABETES & METABOLIC SYNDROME-CLINICAL RESEARCH & REVIEWS, 2022, 16 (05)
  • [22] Association study between cannabinoid receptor gene (CNR1) and pathogenesis and psychotic symptoms of mood disorders
    Tsai, SJ
    Wang, YC
    Hong, CJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (03): : 219 - 221
  • [23] Polymorphisms of the human cannabinoid receptor gene (CNR1) in multiple sclerosis
    Ortíz, P
    González, MP
    Arriaga, A
    Sánchez, AJ
    Merino, JAG
    MULTIPLE SCLEROSIS, 2004, 10 (7032): : S208 - S208
  • [24] Association of the Cannabinoid Receptor Gene (CNR1) With ADHD and Post-Traumatic Stress Disorder
    Lu, Ake T.
    Ogdie, Matthew N.
    Jarvelin, Marjo-Ritta
    Moilanen, Irma K.
    Loo, Sandra K.
    McCracken, James T.
    McGough, James J.
    Yang, May H.
    Peltonen, Leena
    Nelson, Stanley F.
    Cantor, Rita M.
    Smalley, Susan L.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2008, 147B (08) : 1488 - 1494
  • [25] Genetic variability in the endocannabinoid system and 12-week clinical response to citalopram treatment: the role of the CNR1, CNR2 and FAAH genes
    Mitjans, Marina
    Gasto, Cristobal
    Catalan, Rosa
    Fananas, Lourdes
    Arias, Barbara
    JOURNAL OF PSYCHOPHARMACOLOGY, 2012, 26 (10) : 1391 - 1398
  • [26] THE ANALYSIS OF GENETIC VARIABILITY AT COMT, CNR1, CNR2 AND FAAH GENES ON CANNABIS USE, SCHIZOTYPY AND PSYCHOTIC-LIKE EXPERIENCES: A STUDY IN A SPANISH GENERAL POPULATION
    Arias, Barbara
    Fatjo-Vilas, Mar
    Estrada, Gemma
    Aguilera, MCarmen
    Mitjans, Marina
    Moya, Jorge
    Ibanez, Ignacio
    Villa, Helena
    Ruiperez, MAngeles
    Ortet, Generos
    Fananas, Lourdes
    SCHIZOPHRENIA RESEARCH, 2010, 117 (2-3) : 307 - 308
  • [27] (AAT)n repeat in the cannabinoid receptor gene, CNR1:: association with schizophrenia in a Spanish population
    Martinez-Gras, Isabel
    Hoenicka, Janet
    Ponce, Guillermo
    Rodriguez-Jimenez, Roberto
    Angel Jimenez-Arriero, Miguel
    Perez-Hernandez, Elena
    Ampuero, Israel
    Antonio Ramos-Atance, Jose
    Palomo, Tomas
    Rubio, Gabriel
    EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2006, 256 (07) : 437 - 441
  • [28] (AAT)n repeat in the cannabinoid receptor gene, CNR1: association with schizophrenia in a Spanish population
    Isabel Martínez-Gras
    Janet Hoenicka
    Guillermo Ponce
    Roberto Rodríguez–Jiménez
    Miguel Angel Jiménez-Arriero
    Elena Pérez-Hernandez
    Israel Ampuero
    Jose Antonio Ramos-Atance
    Tomas Palomo
    Gabriel Rubio
    European Archives of Psychiatry and Clinical Neuroscience, 2006, 256 : 437 - 441
  • [29] The cannabinoid receptor 1 gene (CNR1) and multiple sclerosis: an association study in two case-control groups from Spain
    Ramil, E.
    Sanchez, A. J.
    Gonzalez-Perez, P.
    Rodriguez-Antiguedad, A.
    Gomez-Lozano, N.
    Ortiz, P.
    Arroyo, R.
    De las Heras, V.
    Vilches, C.
    Garcia-Merino, A.
    MULTIPLE SCLEROSIS JOURNAL, 2010, 16 (02) : 139 - 146
  • [30] Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene
    Gadzicki, D
    Müller-Vahl, KR
    Heller, D
    Ossege, S
    Nöthen, MM
    Hebebrand, J
    Stuhrmann, M
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 127B (01) : 97 - 103